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Literature summary for 1.1.1.349 extracted from

  • Yabe, K.; Matsuyama, Y.; Ando, Y.; Nakajima, H.; Hamasaki, T.
    Stereochemistry during aflatoxin biosynthesis: Conversion of norsolorinic acid to averufin (1993), Appl. Environ. Microbiol., 59, 2486-2492.
    View publication on PubMedView publication on EuropePMC

Localization

Localization Comment Organism GeneOntology No. Textmining
cytosol
-
Aspergillus parasiticus 5829
-

Organism

Organism UniProt Comment Textmining
Aspergillus parasiticus
-
-
-
Aspergillus parasiticus NIAH-26
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(1'S)-averantin + NADP+
-
Aspergillus parasiticus norsolorinic acid + NADPH + H+
-
r
(1'S)-averantin + NADP+
-
Aspergillus parasiticus NIAH-26 norsolorinic acid + NADPH + H+
-
r
additional information the enzyme cannot use (1’R)-averantin as substrate in the reverse reaction Aspergillus parasiticus ?
-
?
additional information the enzyme cannot use (1’R)-averantin as substrate in the reverse reaction Aspergillus parasiticus NIAH-26 ?
-
?
norsolorinic acid + NADPH + H+
-
Aspergillus parasiticus (1'S)-averantin + NADP+
-
r
norsolorinic acid + NADPH + H+
-
Aspergillus parasiticus NIAH-26 (1'S)-averantin + NADP+
-
r

General Information

General Information Comment Organism
metabolism the enzyme is involved in the aflatoxin pathway Aspergillus parasiticus