Activating Compound | Comment | Organism | Structure |
---|---|---|---|
DTT | - |
Vigna radiata var. radiata | |
DTT | - |
Hordeum vulgare | |
DTT | - |
Spinacia oleracea | |
DTT | - |
Pisum sativum | |
DTT | - |
Zea mays | |
DTT | - |
Solanum tuberosum | |
DTT | - |
Nicotiana tabacum | |
DTT | - |
Glycine max | |
DTT | - |
Lithospermum erythrorhizon | |
DTT | - |
Arabidopsis thaliana | |
DTT | - |
Picea abies | |
DTT | - |
Brassica napus | |
DTT | - |
Arachis hypogaea | |
DTT | - |
Medicago sativa | |
DTT | - |
Daucus carota | |
DTT | - |
Solanum lycopersicum | |
DTT | - |
Helianthus tuberosus | |
DTT | - |
Raphanus sativus | |
DTT | - |
Gossypium hirsutum | |
DTT | - |
Ochromonas malhamensis | |
DTT | - |
Hevea brasiliensis | |
DTT | - |
Persea americana | |
DTT | - |
Cucumis melo | |
DTT | - |
Cannabis sativa | |
DTT | - |
Sinapis alba | |
DTT | - |
Ipomoea batatas | |
DTT | - |
Malus domestica | |
DTT | - |
Dunaliella salina | |
DTT | - |
Euphorbia lathyris | |
DTT | - |
Nepeta cataria | |
DTT | - |
Pimpinella anisum | |
DTT | - |
Parthenium argentatum | |
DTT | - |
Gossypium barbadense | |
DTT | - |
Artemisia annua | |
DTT | - |
Nicotiana benthamiana | |
DTT | - |
Stevia rebaudiana | |
DTT | - |
Salvia miltiorrhiza | |
DTT | - |
Taraxacum brevicorniculatum | |
DTT | - |
Solanum virginianum | |
DTT | - |
Bixa orellana | |
EDTA | increases the apparent HMGR activity in sweet potato extracts | Ipomoea batatas |
Inhibitors | Comment | Organism | Structure |
---|---|---|---|
EDTA | inhibits the subsequent reactions of the mevalonate pathway in Hevea latex | Hevea brasiliensis |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
endoplasmic reticulum membrane | - |
Vigna radiata var. radiata | 5789 | - |
endoplasmic reticulum membrane | - |
Hordeum vulgare | 5789 | - |
endoplasmic reticulum membrane | - |
Spinacia oleracea | 5789 | - |
endoplasmic reticulum membrane | - |
Pisum sativum | 5789 | - |
endoplasmic reticulum membrane | - |
Zea mays | 5789 | - |
endoplasmic reticulum membrane | - |
Solanum tuberosum | 5789 | - |
endoplasmic reticulum membrane | - |
Nicotiana tabacum | 5789 | - |
endoplasmic reticulum membrane | - |
Glycine max | 5789 | - |
endoplasmic reticulum membrane | - |
Lithospermum erythrorhizon | 5789 | - |
endoplasmic reticulum membrane | - |
Picea abies | 5789 | - |
endoplasmic reticulum membrane | - |
Brassica napus | 5789 | - |
endoplasmic reticulum membrane | - |
Arachis hypogaea | 5789 | - |
endoplasmic reticulum membrane | - |
Medicago sativa | 5789 | - |
endoplasmic reticulum membrane | - |
Daucus carota | 5789 | - |
endoplasmic reticulum membrane | - |
Solanum lycopersicum | 5789 | - |
endoplasmic reticulum membrane | - |
Helianthus tuberosus | 5789 | - |
endoplasmic reticulum membrane | - |
Raphanus sativus | 5789 | - |
endoplasmic reticulum membrane | - |
Gossypium hirsutum | 5789 | - |
endoplasmic reticulum membrane | - |
Ochromonas malhamensis | 5789 | - |
endoplasmic reticulum membrane | - |
Hevea brasiliensis | 5789 | - |
endoplasmic reticulum membrane | - |
Persea americana | 5789 | - |
endoplasmic reticulum membrane | - |
Cucumis melo | 5789 | - |
endoplasmic reticulum membrane | - |
Cannabis sativa | 5789 | - |
endoplasmic reticulum membrane | - |
Sinapis alba | 5789 | - |
endoplasmic reticulum membrane | - |
Ipomoea batatas | 5789 | - |
endoplasmic reticulum membrane | - |
Malus domestica | 5789 | - |
endoplasmic reticulum membrane | - |
Dunaliella salina | 5789 | - |
endoplasmic reticulum membrane | - |
Euphorbia lathyris | 5789 | - |
endoplasmic reticulum membrane | - |
Nepeta cataria | 5789 | - |
endoplasmic reticulum membrane | - |
Pimpinella anisum | 5789 | - |
endoplasmic reticulum membrane | - |
Parthenium argentatum | 5789 | - |
endoplasmic reticulum membrane | - |
Gossypium barbadense | 5789 | - |
endoplasmic reticulum membrane | - |
Artemisia annua | 5789 | - |
endoplasmic reticulum membrane | - |
Nicotiana benthamiana | 5789 | - |
endoplasmic reticulum membrane | - |
Stevia rebaudiana | 5789 | - |
endoplasmic reticulum membrane | - |
Salvia miltiorrhiza | 5789 | - |
endoplasmic reticulum membrane | - |
Taraxacum brevicorniculatum | 5789 | - |
endoplasmic reticulum membrane | - |
Solanum virginianum | 5789 | - |
endoplasmic reticulum membrane | - |
Bixa orellana | 5789 | - |
endoplasmic reticulum membrane | the enzyme spans the endoplasmic reticulum membrane twice. Both the N-terminal region and the highly conserved catalytic domain are in the cytosol, whereas only a short stretch of the protein is in the endoplasmic reticulum lumen. Insertion in the endoplasmic reticulum membrane is mediated by the signal recognition particle (SRP) that recognizes the two hydrophobic sequences which will become membrane spanning segments | Arabidopsis thaliana | 5789 | - |
microsome | the HMGR activity is detected in the final microsomal pellet after ultracentrifugation | Arabidopsis thaliana | - |
- |
Metals/Ions | Comment | Organism | Structure |
---|---|---|---|
Ca2+ | activates | Vigna radiata var. radiata | |
Ca2+ | activates | Hordeum vulgare | |
Ca2+ | activates | Spinacia oleracea | |
Ca2+ | activates | Pisum sativum | |
Ca2+ | activates | Zea mays | |
Ca2+ | activates | Solanum tuberosum | |
Ca2+ | activates | Nicotiana tabacum | |
Ca2+ | activates | Glycine max | |
Ca2+ | activates | Lithospermum erythrorhizon | |
Ca2+ | activates | Arabidopsis thaliana | |
Ca2+ | activates | Picea abies | |
Ca2+ | activates | Brassica napus | |
Ca2+ | activates | Arachis hypogaea | |
Ca2+ | activates | Medicago sativa | |
Ca2+ | activates | Daucus carota | |
Ca2+ | activates | Solanum lycopersicum | |
Ca2+ | activates | Helianthus tuberosus | |
Ca2+ | activates | Raphanus sativus | |
Ca2+ | activates | Gossypium hirsutum | |
Ca2+ | activates | Ochromonas malhamensis | |
Ca2+ | activates | Hevea brasiliensis | |
Ca2+ | activates | Persea americana | |
Ca2+ | activates | Cucumis melo | |
Ca2+ | activates | Cannabis sativa | |
Ca2+ | activates | Sinapis alba | |
Ca2+ | activates | Ipomoea batatas | |
Ca2+ | activates | Malus domestica | |
Ca2+ | activates | Dunaliella salina | |
Ca2+ | activates | Euphorbia lathyris | |
Ca2+ | activates | Nepeta cataria | |
Ca2+ | activates | Pimpinella anisum | |
Ca2+ | activates | Parthenium argentatum | |
Ca2+ | activates | Gossypium barbadense | |
Ca2+ | activates | Artemisia annua | |
Ca2+ | activates | Nicotiana benthamiana | |
Ca2+ | activates | Stevia rebaudiana | |
Ca2+ | activates | Salvia miltiorrhiza | |
Ca2+ | activates | Taraxacum brevicorniculatum | |
Ca2+ | activates | Solanum virginianum | |
Ca2+ | activates | Bixa orellana |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
(R)-mevalonate + CoA + 2 NADP+ | Vigna radiata var. radiata | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Hordeum vulgare | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Spinacia oleracea | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Pisum sativum | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Zea mays | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Solanum tuberosum | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Nicotiana tabacum | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Glycine max | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Lithospermum erythrorhizon | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Arabidopsis thaliana | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Picea abies | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Brassica napus | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Arachis hypogaea | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Medicago sativa | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Daucus carota | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Solanum lycopersicum | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Helianthus tuberosus | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Raphanus sativus | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Gossypium hirsutum | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Ochromonas malhamensis | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Hevea brasiliensis | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Persea americana | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Cucumis melo | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Cannabis sativa | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Sinapis alba | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Ipomoea batatas | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Malus domestica | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Dunaliella salina | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Euphorbia lathyris | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Nepeta cataria | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Pimpinella anisum | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Parthenium argentatum | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Gossypium barbadense | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Artemisia annua | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Nicotiana benthamiana | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Stevia rebaudiana | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Salvia miltiorrhiza | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Taraxacum brevicorniculatum | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Solanum virginianum | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | Bixa orellana | - |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Vigna radiata var. radiata | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Hordeum vulgare | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Spinacia oleracea | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Pisum sativum | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Zea mays | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Solanum tuberosum | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Nicotiana tabacum | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Glycine max | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Lithospermum erythrorhizon | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Arabidopsis thaliana | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Picea abies | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Brassica napus | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Arachis hypogaea | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Medicago sativa | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Daucus carota | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Solanum lycopersicum | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Helianthus tuberosus | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Raphanus sativus | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Gossypium hirsutum | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Ochromonas malhamensis | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Hevea brasiliensis | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Persea americana | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Cucumis melo | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Cannabis sativa | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Sinapis alba | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Ipomoea batatas | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Malus domestica | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Dunaliella salina | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Euphorbia lathyris | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Nepeta cataria | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Pimpinella anisum | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Parthenium argentatum | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Gossypium barbadense | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Artemisia annua | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Nicotiana benthamiana | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Stevia rebaudiana | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Salvia miltiorrhiza | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Taraxacum brevicorniculatum | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Solanum virginianum | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | Bixa orellana | - |
(R)-mevalonate + CoA + 2 NADP+ | - |
r |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Arabidopsis thaliana | - |
- |
- |
Arachis hypogaea | - |
- |
- |
Artemisia annua | - |
- |
- |
Bixa orellana | - |
- |
- |
Brassica napus | - |
- |
- |
Cannabis sativa | - |
- |
- |
Cucumis melo | - |
- |
- |
Daucus carota | - |
- |
- |
Dunaliella salina | - |
- |
- |
Euphorbia lathyris | - |
- |
- |
Glycine max | - |
- |
- |
Gossypium barbadense | - |
- |
- |
Gossypium hirsutum | - |
- |
- |
Helianthus tuberosus | - |
- |
- |
Hevea brasiliensis | - |
- |
- |
Hordeum vulgare | - |
- |
- |
Ipomoea batatas | - |
- |
- |
Lithospermum erythrorhizon | - |
- |
- |
Malus domestica | - |
- |
- |
Medicago sativa | - |
- |
- |
Nepeta cataria | - |
- |
- |
Nicotiana benthamiana | - |
- |
- |
Nicotiana tabacum | - |
- |
- |
Ochromonas malhamensis | - |
- |
- |
Parthenium argentatum | - |
- |
- |
Persea americana | - |
- |
- |
Picea abies | - |
- |
- |
Pimpinella anisum | - |
- |
- |
Pisum sativum | - |
- |
- |
Raphanus sativus | - |
- |
- |
Salvia miltiorrhiza | - |
- |
- |
Sinapis alba | - |
- |
- |
Solanum lycopersicum | - |
- |
- |
Solanum tuberosum | - |
- |
- |
Solanum virginianum | - |
- |
- |
Spinacia oleracea | - |
- |
- |
Stevia rebaudiana | - |
- |
- |
Taraxacum brevicorniculatum | - |
- |
- |
Vigna radiata var. radiata | - |
- |
- |
Zea mays | - |
- |
- |
Oxidation Stability | Organism |
---|---|
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Vigna radiata var. radiata |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Hordeum vulgare |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Spinacia oleracea |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Pisum sativum |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Zea mays |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Solanum tuberosum |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Nicotiana tabacum |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Glycine max |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Lithospermum erythrorhizon |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Arabidopsis thaliana |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Picea abies |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Brassica napus |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Arachis hypogaea |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Medicago sativa |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Daucus carota |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Solanum lycopersicum |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Helianthus tuberosus |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Raphanus sativus |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Gossypium hirsutum |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Ochromonas malhamensis |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Hevea brasiliensis |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Persea americana |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Cucumis melo |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Cannabis sativa |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Sinapis alba |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Ipomoea batatas |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Malus domestica |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Dunaliella salina |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Euphorbia lathyris |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Nepeta cataria |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Pimpinella anisum |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Parthenium argentatum |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Gossypium barbadense |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Artemisia annua |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Nicotiana benthamiana |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Stevia rebaudiana |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Salvia miltiorrhiza |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Taraxacum brevicorniculatum |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Solanum virginianum |
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose | Bixa orellana |
Posttranslational Modification | Comment | Organism |
---|---|---|
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Vigna radiata var. radiata |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Hordeum vulgare |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Spinacia oleracea |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Pisum sativum |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Zea mays |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Solanum tuberosum |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Nicotiana tabacum |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Glycine max |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Lithospermum erythrorhizon |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Arabidopsis thaliana |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Picea abies |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Brassica napus |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Arachis hypogaea |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Medicago sativa |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Daucus carota |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Solanum lycopersicum |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Helianthus tuberosus |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Raphanus sativus |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Gossypium hirsutum |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Ochromonas malhamensis |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Hevea brasiliensis |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Persea americana |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Cucumis melo |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Cannabis sativa |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Sinapis alba |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Ipomoea batatas |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Malus domestica |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Dunaliella salina |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Euphorbia lathyris |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Nepeta cataria |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Pimpinella anisum |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Parthenium argentatum |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Gossypium barbadense |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Artemisia annua |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Nicotiana benthamiana |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Stevia rebaudiana |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Salvia miltiorrhiza |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Taraxacum brevicorniculatum |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Solanum virginianum |
additional information | protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated | Bixa orellana |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Vigna radiata var. radiata |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Hordeum vulgare |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Spinacia oleracea |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Pisum sativum |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Zea mays |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Solanum tuberosum |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Nicotiana tabacum |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Glycine max |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Lithospermum erythrorhizon |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Arabidopsis thaliana |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Picea abies |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Brassica napus |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Arachis hypogaea |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Medicago sativa |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Daucus carota |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Solanum lycopersicum |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Helianthus tuberosus |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Raphanus sativus |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Gossypium hirsutum |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Ochromonas malhamensis |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Hevea brasiliensis |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Persea americana |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Cucumis melo |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Cannabis sativa |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Sinapis alba |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Ipomoea batatas |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Malus domestica |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Dunaliella salina |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Euphorbia lathyris |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Nepeta cataria |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Pimpinella anisum |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Parthenium argentatum |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Gossypium barbadense |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Artemisia annua |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Nicotiana benthamiana |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Stevia rebaudiana |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Salvia miltiorrhiza |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Taraxacum brevicorniculatum |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Solanum virginianum |
phosphoprotein | phosphorylation at a conserved site of the catalytic domain of enzyme HMGR | Bixa orellana |
Purification (Comment) | Organism |
---|---|
native enzyme by ultracentrifugation | Arabidopsis thaliana |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
bark | - |
Parthenium argentatum | - |
BY-2 cell | - |
Nicotiana tabacum | - |
callus | - |
Nicotiana tabacum | - |
callus | - |
Picea abies | - |
callus | - |
Nepeta cataria | - |
callus | - |
Bixa orellana | - |
cell culture | - |
Nicotiana tabacum | - |
cell culture | - |
Glycine max | - |
cell culture | - |
Lithospermum erythrorhizon | - |
cell culture | - |
Picea abies | - |
cell culture | - |
Daucus carota | - |
cell culture | - |
Ochromonas malhamensis | - |
cell culture | - |
Dunaliella salina | - |
cell culture | - |
Pimpinella anisum | - |
cell suspension culture | - |
Solanum virginianum | - |
cotyledon | - |
Glycine max | - |
exocarp | - |
Malus domestica | - |
fruit | - |
Solanum lycopersicum | - |
fruit | - |
Cucumis melo | - |
hairy root | - |
Lithospermum erythrorhizon | - |
hairy root | - |
Medicago sativa | - |
hairy root | - |
Salvia miltiorrhiza | - |
hypocotyl | - |
Glycine max | - |
KY-14 cell | - |
Nicotiana tabacum | - |
latex | - |
Hevea brasiliensis | - |
latex | - |
Euphorbia lathyris | - |
latex | - |
Taraxacum brevicorniculatum | - |
leaf | - |
Vigna radiata var. radiata | - |
leaf | - |
Spinacia oleracea | - |
leaf | - |
Picea abies | - |
leaf | - |
Solanum lycopersicum | - |
leaf | - |
Cannabis sativa | - |
leaf | - |
Euphorbia lathyris | - |
leaf | - |
Nepeta cataria | - |
leaf | - |
Artemisia annua | - |
leaf | - |
Nicotiana benthamiana | - |
leaf | - |
Stevia rebaudiana | - |
leaf | - |
Bixa orellana | - |
leaf | expanded | Nicotiana tabacum | - |
leaf | fully expanded | Parthenium argentatum | - |
leaf | rosette leaves and fully expanded leaves | Arabidopsis thaliana | - |
mesocarp | - |
Persea americana | - |
pericarp | - |
Cucumis melo | - |
root | - |
Glycine max | - |
root | - |
Ipomoea batatas | - |
seed | - |
Arabidopsis thaliana | - |
seed | - |
Persea americana | - |
seed | developing | Nicotiana tabacum | - |
seed | developing | Brassica napus | - |
seedling | - |
Hordeum vulgare | - |
seedling | - |
Picea abies | - |
seedling | - |
Raphanus sativus | - |
seedling | etiolated | Zea mays | - |
seedling | green | Arachis hypogaea | - |
seedling | green | Sinapis alba | - |
seedling | aerial part and full seedling | Nicotiana tabacum | - |
seedling | apical part | Glycine max | - |
seedling | etiolated and green seedlings | Pisum sativum | - |
seedling | green seedling, aerial part and root | Arabidopsis thaliana | - |
stele | - |
Gossypium hirsutum | - |
stele | - |
Gossypium barbadense | - |
stem | - |
Euphorbia lathyris | - |
stem | lower | Parthenium argentatum | - |
tuber | - |
Solanum tuberosum | - |
tuber | explants | Helianthus tuberosus | - |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
(R)-mevalonate + CoA + 2 NADP+ | - |
Vigna radiata var. radiata | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Hordeum vulgare | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Spinacia oleracea | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Pisum sativum | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Zea mays | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Solanum tuberosum | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Nicotiana tabacum | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Glycine max | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Lithospermum erythrorhizon | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Arabidopsis thaliana | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Picea abies | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Brassica napus | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Arachis hypogaea | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Medicago sativa | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Daucus carota | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Solanum lycopersicum | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Helianthus tuberosus | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Raphanus sativus | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Gossypium hirsutum | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Ochromonas malhamensis | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Hevea brasiliensis | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Persea americana | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Cucumis melo | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Cannabis sativa | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Sinapis alba | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Ipomoea batatas | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Malus domestica | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Dunaliella salina | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Euphorbia lathyris | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Nepeta cataria | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Pimpinella anisum | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Parthenium argentatum | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Gossypium barbadense | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Artemisia annua | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Nicotiana benthamiana | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Stevia rebaudiana | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Salvia miltiorrhiza | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Taraxacum brevicorniculatum | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Solanum virginianum | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(R)-mevalonate + CoA + 2 NADP+ | - |
Bixa orellana | (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Vigna radiata var. radiata | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Hordeum vulgare | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Spinacia oleracea | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Pisum sativum | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Zea mays | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Solanum tuberosum | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Nicotiana tabacum | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Glycine max | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Lithospermum erythrorhizon | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Arabidopsis thaliana | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Picea abies | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Brassica napus | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Arachis hypogaea | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Medicago sativa | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Daucus carota | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Solanum lycopersicum | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Helianthus tuberosus | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Raphanus sativus | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Gossypium hirsutum | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Ochromonas malhamensis | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Hevea brasiliensis | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Persea americana | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Cucumis melo | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Cannabis sativa | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Sinapis alba | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Ipomoea batatas | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Malus domestica | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Dunaliella salina | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Euphorbia lathyris | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Nepeta cataria | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Pimpinella anisum | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Parthenium argentatum | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Gossypium barbadense | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Artemisia annua | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Nicotiana benthamiana | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Stevia rebaudiana | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Salvia miltiorrhiza | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Taraxacum brevicorniculatum | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Solanum virginianum | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ | - |
Bixa orellana | (R)-mevalonate + CoA + 2 NADP+ | - |
r | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Vigna radiata var. radiata | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Hordeum vulgare | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Spinacia oleracea | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Pisum sativum | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Zea mays | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Solanum tuberosum | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Nicotiana tabacum | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Glycine max | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Lithospermum erythrorhizon | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Arabidopsis thaliana | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Picea abies | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Brassica napus | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Arachis hypogaea | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Medicago sativa | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Daucus carota | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Solanum lycopersicum | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Helianthus tuberosus | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Raphanus sativus | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Gossypium hirsutum | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Ochromonas malhamensis | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Hevea brasiliensis | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Persea americana | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Cucumis melo | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Cannabis sativa | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Sinapis alba | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Ipomoea batatas | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Malus domestica | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Dunaliella salina | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Euphorbia lathyris | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Nepeta cataria | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Pimpinella anisum | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Parthenium argentatum | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Gossypium barbadense | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Artemisia annua | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Nicotiana benthamiana | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Stevia rebaudiana | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Salvia miltiorrhiza | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Taraxacum brevicorniculatum | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Solanum virginianum | ? | - |
? | |
additional information | assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC | Bixa orellana | ? | - |
? |
Subunits | Comment | Organism |
---|---|---|
? | x * 63000-70000 | Vigna radiata var. radiata |
? | x * 63000-70000 | Hordeum vulgare |
? | x * 63000-70000 | Spinacia oleracea |
? | x * 63000-70000 | Pisum sativum |
? | x * 63000-70000 | Zea mays |
? | x * 63000-70000 | Solanum tuberosum |
? | x * 63000-70000 | Nicotiana tabacum |
? | x * 63000-70000 | Glycine max |
? | x * 63000-70000 | Lithospermum erythrorhizon |
? | x * 63000-70000 | Arabidopsis thaliana |
? | x * 63000-70000 | Picea abies |
? | x * 63000-70000 | Brassica napus |
? | x * 63000-70000 | Arachis hypogaea |
? | x * 63000-70000 | Medicago sativa |
? | x * 63000-70000 | Daucus carota |
? | x * 63000-70000 | Solanum lycopersicum |
? | x * 63000-70000 | Helianthus tuberosus |
? | x * 63000-70000 | Raphanus sativus |
? | x * 63000-70000 | Gossypium hirsutum |
? | x * 63000-70000 | Ochromonas malhamensis |
? | x * 63000-70000 | Hevea brasiliensis |
? | x * 63000-70000 | Persea americana |
? | x * 63000-70000 | Cucumis melo |
? | x * 63000-70000 | Cannabis sativa |
? | x * 63000-70000 | Sinapis alba |
? | x * 63000-70000 | Ipomoea batatas |
? | x * 63000-70000 | Malus domestica |
? | x * 63000-70000 | Dunaliella salina |
? | x * 63000-70000 | Euphorbia lathyris |
? | x * 63000-70000 | Nepeta cataria |
? | x * 63000-70000 | Pimpinella anisum |
? | x * 63000-70000 | Parthenium argentatum |
? | x * 63000-70000 | Gossypium barbadense |
? | x * 63000-70000 | Artemisia annua |
? | x * 63000-70000 | Nicotiana benthamiana |
? | x * 63000-70000 | Stevia rebaudiana |
? | x * 63000-70000 | Salvia miltiorrhiza |
? | x * 63000-70000 | Taraxacum brevicorniculatum |
? | x * 63000-70000 | Solanum virginianum |
? | x * 63000-70000 | Bixa orellana |
Synonyms | Comment | Organism |
---|---|---|
3-hydroxy-3-methylglutaryl CoA reductase | - |
Vigna radiata var. radiata |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Hordeum vulgare |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Spinacia oleracea |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Pisum sativum |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Zea mays |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Solanum tuberosum |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Nicotiana tabacum |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Glycine max |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Lithospermum erythrorhizon |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Arabidopsis thaliana |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Picea abies |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Brassica napus |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Arachis hypogaea |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Medicago sativa |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Daucus carota |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Solanum lycopersicum |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Helianthus tuberosus |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Raphanus sativus |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Gossypium hirsutum |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Ochromonas malhamensis |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Hevea brasiliensis |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Persea americana |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Cucumis melo |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Cannabis sativa |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Sinapis alba |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Ipomoea batatas |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Malus domestica |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Dunaliella salina |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Euphorbia lathyris |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Nepeta cataria |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Pimpinella anisum |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Parthenium argentatum |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Gossypium barbadense |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Artemisia annua |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Nicotiana benthamiana |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Stevia rebaudiana |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Salvia miltiorrhiza |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Taraxacum brevicorniculatum |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Solanum virginianum |
3-hydroxy-3-methylglutaryl CoA reductase | - |
Bixa orellana |
HMGR | - |
Vigna radiata var. radiata |
HMGR | - |
Hordeum vulgare |
HMGR | - |
Spinacia oleracea |
HMGR | - |
Pisum sativum |
HMGR | - |
Zea mays |
HMGR | - |
Solanum tuberosum |
HMGR | - |
Nicotiana tabacum |
HMGR | - |
Glycine max |
HMGR | - |
Lithospermum erythrorhizon |
HMGR | - |
Arabidopsis thaliana |
HMGR | - |
Picea abies |
HMGR | - |
Brassica napus |
HMGR | - |
Arachis hypogaea |
HMGR | - |
Medicago sativa |
HMGR | - |
Daucus carota |
HMGR | - |
Solanum lycopersicum |
HMGR | - |
Helianthus tuberosus |
HMGR | - |
Raphanus sativus |
HMGR | - |
Gossypium hirsutum |
HMGR | - |
Ochromonas malhamensis |
HMGR | - |
Hevea brasiliensis |
HMGR | - |
Persea americana |
HMGR | - |
Cucumis melo |
HMGR | - |
Cannabis sativa |
HMGR | - |
Sinapis alba |
HMGR | - |
Ipomoea batatas |
HMGR | - |
Malus domestica |
HMGR | - |
Dunaliella salina |
HMGR | - |
Euphorbia lathyris |
HMGR | - |
Nepeta cataria |
HMGR | - |
Pimpinella anisum |
HMGR | - |
Parthenium argentatum |
HMGR | - |
Gossypium barbadense |
HMGR | - |
Artemisia annua |
HMGR | - |
Nicotiana benthamiana |
HMGR | - |
Stevia rebaudiana |
HMGR | - |
Salvia miltiorrhiza |
HMGR | - |
Taraxacum brevicorniculatum |
HMGR | - |
Solanum virginianum |
HMGR | - |
Bixa orellana |
Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|
37 | - |
assay at | Vigna radiata var. radiata |
37 | - |
assay at | Hordeum vulgare |
37 | - |
assay at | Spinacia oleracea |
37 | - |
assay at | Pisum sativum |
37 | - |
assay at | Zea mays |
37 | - |
assay at | Solanum tuberosum |
37 | - |
assay at | Nicotiana tabacum |
37 | - |
assay at | Glycine max |
37 | - |
assay at | Lithospermum erythrorhizon |
37 | - |
assay at | Arabidopsis thaliana |
37 | - |
assay at | Picea abies |
37 | - |
assay at | Brassica napus |
37 | - |
assay at | Arachis hypogaea |
37 | - |
assay at | Medicago sativa |
37 | - |
assay at | Daucus carota |
37 | - |
assay at | Solanum lycopersicum |
37 | - |
assay at | Helianthus tuberosus |
37 | - |
assay at | Raphanus sativus |
37 | - |
assay at | Gossypium hirsutum |
37 | - |
assay at | Ochromonas malhamensis |
37 | - |
assay at | Hevea brasiliensis |
37 | - |
assay at | Persea americana |
37 | - |
assay at | Cucumis melo |
37 | - |
assay at | Cannabis sativa |
37 | - |
assay at | Sinapis alba |
37 | - |
assay at | Ipomoea batatas |
37 | - |
assay at | Malus domestica |
37 | - |
assay at | Dunaliella salina |
37 | - |
assay at | Euphorbia lathyris |
37 | - |
assay at | Nepeta cataria |
37 | - |
assay at | Pimpinella anisum |
37 | - |
assay at | Parthenium argentatum |
37 | - |
assay at | Gossypium barbadense |
37 | - |
assay at | Artemisia annua |
37 | - |
assay at | Nicotiana benthamiana |
37 | - |
assay at | Stevia rebaudiana |
37 | - |
assay at | Salvia miltiorrhiza |
37 | - |
assay at | Taraxacum brevicorniculatum |
37 | - |
assay at | Solanum virginianum |
37 | - |
assay at | Bixa orellana |
pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|
additional information | - |
two pH optima are found, corresponding to HMGR from the heavy or the light fractions: pH 7.0 and pH 75, respectively | Parthenium argentatum |
additional information | - |
two pH optima are found, corresponding to HMGR from the heavy or the light fractions: pH 7.9 and pH 6.9, respectively | Pisum sativum |
6.8 | - |
- |
Hevea brasiliensis |
6.9 | - |
- |
Pisum sativum |
7 | - |
- |
Parthenium argentatum |
7.2 | - |
assay at | Vigna radiata var. radiata |
7.2 | - |
assay at | Hordeum vulgare |
7.2 | - |
assay at | Spinacia oleracea |
7.2 | - |
assay at | Zea mays |
7.2 | - |
assay at | Solanum tuberosum |
7.2 | - |
assay at | Nicotiana tabacum |
7.2 | - |
assay at | Glycine max |
7.2 | - |
assay at | Lithospermum erythrorhizon |
7.2 | - |
assay at | Arabidopsis thaliana |
7.2 | - |
assay at | Picea abies |
7.2 | - |
assay at | Brassica napus |
7.2 | - |
assay at | Arachis hypogaea |
7.2 | - |
assay at | Medicago sativa |
7.2 | - |
assay at | Daucus carota |
7.2 | - |
assay at | Solanum lycopersicum |
7.2 | - |
assay at | Helianthus tuberosus |
7.2 | - |
assay at | Gossypium hirsutum |
7.2 | - |
assay at | Ochromonas malhamensis |
7.2 | - |
assay at | Persea americana |
7.2 | - |
assay at | Cucumis melo |
7.2 | - |
assay at | Cannabis sativa |
7.2 | - |
assay at | Sinapis alba |
7.2 | - |
assay at | Ipomoea batatas |
7.2 | - |
assay at | Malus domestica |
7.2 | - |
assay at | Dunaliella salina |
7.2 | - |
assay at | Euphorbia lathyris |
7.2 | - |
assay at | Nepeta cataria |
7.2 | - |
assay at | Pimpinella anisum |
7.2 | - |
assay at | Gossypium barbadense |
7.2 | - |
assay at | Artemisia annua |
7.2 | - |
assay at | Nicotiana benthamiana |
7.2 | - |
assay at | Stevia rebaudiana |
7.2 | - |
assay at | Salvia miltiorrhiza |
7.2 | - |
assay at | Taraxacum brevicorniculatum |
7.2 | - |
assay at | Solanum virginianum |
7.2 | - |
assay at | Bixa orellana |
7.3 | 7.5 | - |
Raphanus sativus |
7.5 | - |
- |
Parthenium argentatum |
7.9 | - |
- |
Pisum sativum |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
NADP+ | - |
Vigna radiata var. radiata | |
NADP+ | - |
Hordeum vulgare | |
NADP+ | - |
Spinacia oleracea | |
NADP+ | - |
Pisum sativum | |
NADP+ | - |
Zea mays | |
NADP+ | - |
Solanum tuberosum | |
NADP+ | - |
Nicotiana tabacum | |
NADP+ | - |
Glycine max | |
NADP+ | - |
Lithospermum erythrorhizon | |
NADP+ | - |
Arabidopsis thaliana | |
NADP+ | - |
Picea abies | |
NADP+ | - |
Brassica napus | |
NADP+ | - |
Arachis hypogaea | |
NADP+ | - |
Medicago sativa | |
NADP+ | - |
Daucus carota | |
NADP+ | - |
Solanum lycopersicum | |
NADP+ | - |
Helianthus tuberosus | |
NADP+ | - |
Raphanus sativus | |
NADP+ | - |
Gossypium hirsutum | |
NADP+ | - |
Ochromonas malhamensis | |
NADP+ | - |
Hevea brasiliensis | |
NADP+ | - |
Persea americana | |
NADP+ | - |
Cucumis melo | |
NADP+ | - |
Cannabis sativa | |
NADP+ | - |
Sinapis alba | |
NADP+ | - |
Ipomoea batatas | |
NADP+ | - |
Malus domestica | |
NADP+ | - |
Dunaliella salina | |
NADP+ | - |
Euphorbia lathyris | |
NADP+ | - |
Nepeta cataria | |
NADP+ | - |
Pimpinella anisum | |
NADP+ | - |
Parthenium argentatum | |
NADP+ | - |
Gossypium barbadense | |
NADP+ | - |
Artemisia annua | |
NADP+ | - |
Nicotiana benthamiana | |
NADP+ | - |
Stevia rebaudiana | |
NADP+ | - |
Salvia miltiorrhiza | |
NADP+ | - |
Taraxacum brevicorniculatum | |
NADP+ | - |
Solanum virginianum | |
NADP+ | - |
Bixa orellana | |
NADPH | - |
Vigna radiata var. radiata | |
NADPH | - |
Hordeum vulgare | |
NADPH | - |
Spinacia oleracea | |
NADPH | - |
Pisum sativum | |
NADPH | - |
Zea mays | |
NADPH | - |
Solanum tuberosum | |
NADPH | - |
Nicotiana tabacum | |
NADPH | - |
Glycine max | |
NADPH | - |
Lithospermum erythrorhizon | |
NADPH | - |
Arabidopsis thaliana | |
NADPH | - |
Picea abies | |
NADPH | - |
Brassica napus | |
NADPH | - |
Arachis hypogaea | |
NADPH | - |
Medicago sativa | |
NADPH | - |
Daucus carota | |
NADPH | - |
Solanum lycopersicum | |
NADPH | - |
Helianthus tuberosus | |
NADPH | - |
Raphanus sativus | |
NADPH | - |
Gossypium hirsutum | |
NADPH | - |
Ochromonas malhamensis | |
NADPH | - |
Hevea brasiliensis | |
NADPH | - |
Persea americana | |
NADPH | - |
Cucumis melo | |
NADPH | - |
Cannabis sativa | |
NADPH | - |
Sinapis alba | |
NADPH | - |
Ipomoea batatas | |
NADPH | - |
Malus domestica | |
NADPH | - |
Dunaliella salina | |
NADPH | - |
Euphorbia lathyris | |
NADPH | - |
Nepeta cataria | |
NADPH | - |
Pimpinella anisum | |
NADPH | - |
Parthenium argentatum | |
NADPH | - |
Gossypium barbadense | |
NADPH | - |
Artemisia annua | |
NADPH | - |
Nicotiana benthamiana | |
NADPH | - |
Stevia rebaudiana | |
NADPH | - |
Salvia miltiorrhiza | |
NADPH | - |
Taraxacum brevicorniculatum | |
NADPH | - |
Solanum virginianum | |
NADPH | - |
Bixa orellana |
General Information | Comment | Organism |
---|---|---|
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Vigna radiata var. radiata |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Hordeum vulgare |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Spinacia oleracea |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Pisum sativum |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Zea mays |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Solanum tuberosum |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Nicotiana tabacum |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Glycine max |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Lithospermum erythrorhizon |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Arabidopsis thaliana |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Picea abies |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Brassica napus |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Arachis hypogaea |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Medicago sativa |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Daucus carota |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Solanum lycopersicum |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Helianthus tuberosus |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Raphanus sativus |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Gossypium hirsutum |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Ochromonas malhamensis |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Hevea brasiliensis |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Persea americana |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Cucumis melo |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Cannabis sativa |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Sinapis alba |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Ipomoea batatas |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Malus domestica |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Dunaliella salina |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Euphorbia lathyris |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Nepeta cataria |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Pimpinella anisum |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Parthenium argentatum |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Gossypium barbadense |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Artemisia annua |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Nicotiana benthamiana |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Stevia rebaudiana |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Salvia miltiorrhiza |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Taraxacum brevicorniculatum |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Solanum virginianum |
evolution | not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family | Bixa orellana |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Vigna radiata var. radiata |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Hordeum vulgare |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Spinacia oleracea |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Pisum sativum |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Zea mays |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Solanum tuberosum |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Nicotiana tabacum |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Glycine max |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Lithospermum erythrorhizon |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Arabidopsis thaliana |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Picea abies |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Brassica napus |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Arachis hypogaea |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Medicago sativa |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Daucus carota |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Solanum lycopersicum |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Helianthus tuberosus |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Raphanus sativus |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Gossypium hirsutum |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Ochromonas malhamensis |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Hevea brasiliensis |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Persea americana |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Cucumis melo |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Cannabis sativa |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Sinapis alba |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Ipomoea batatas |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Malus domestica |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Dunaliella salina |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Euphorbia lathyris |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Nepeta cataria |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Pimpinella anisum |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Parthenium argentatum |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Gossypium barbadense |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Artemisia annua |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Nicotiana benthamiana |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Stevia rebaudiana |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Salvia miltiorrhiza |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Taraxacum brevicorniculatum |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Solanum virginianum |
metabolism | HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes | Bixa orellana |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Vigna radiata var. radiata |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Hordeum vulgare |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Spinacia oleracea |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Pisum sativum |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Zea mays |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Solanum tuberosum |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Nicotiana tabacum |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Glycine max |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Lithospermum erythrorhizon |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Picea abies |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Brassica napus |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Arachis hypogaea |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Medicago sativa |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Daucus carota |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Solanum lycopersicum |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Helianthus tuberosus |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Raphanus sativus |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Gossypium hirsutum |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Ochromonas malhamensis |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Hevea brasiliensis |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Persea americana |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Cucumis melo |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Cannabis sativa |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Sinapis alba |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Ipomoea batatas |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Malus domestica |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Dunaliella salina |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Euphorbia lathyris |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Nepeta cataria |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Pimpinella anisum |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Parthenium argentatum |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Gossypium barbadense |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Artemisia annua |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Nicotiana benthamiana |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Stevia rebaudiana |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Salvia miltiorrhiza |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Taraxacum brevicorniculatum |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Solanum virginianum |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated | Bixa orellana |
physiological function | in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated. Protein phosphatase 2A (PP2A) is both a transcriptional and a posttranslational regulator of HMGR in Arabidopsis thaliana | Arabidopsis thaliana |