EC Number   |
Inhibitors |
Structure |
|---|
  2.4.1.218 | Ca2+ |
10 mM, 24.4% inhibition |
   |
| 2.4.1.218 | Co2+ |
10 mM, 54.2% inhibition |
|
| 2.4.1.218 | dichlorophen |
- |
|
| 2.4.1.218 | Hg2+ |
10 mM, complete inhibition, reversed by addition of 20 mM 2-mercaptoethanol |
|
| 2.4.1.218 | hydroquinone |
Glu274 is acting as an acidic backbone acceptor residue. Lys262, a basic amino acid from the active site of wheat Hydroquinone glucosyltransferase interacts with the hydroxyl group of hydroquinone and behaves as a side chain donor molecule. Asp264 is also observed as an interacting residue from the active site of hydroquinone glucosyltransferase. It binds to the hydroxyl group of hydroquinone inhibitor and donates hydrogen ion from its side chain group |
|
| 2.4.1.218 | Mn2+ |
10 mM, 24.7% inhibition |
|
| 2.4.1.218 | more |
enzyme molecular docking of urease inhibitors hydroquinone, phenyl phosphorodiamate, and N-(n-butyl) phosphorothiocic triamide, three-dimensional structure analysis using homology modeling, and interactions analysis, overview |
|
| 2.4.1.218 | N-(n-butyl) phosphorothiocic triamide |
Glu274 is acting as an acidic backbone donor residue and interacts with the amino group of the inhibitor |
|
| 2.4.1.218 | phenyl phosphorodiamate |
Glu395 is directly interacting with amino group of the inhibitor |
|
| 2.4.1.218 | Zn2+ |
10 mM, 87.4% inhibition |
|
