EC Number   |
Inhibitors |
Structure |
|---|
   2.7.1.172 | 1-deoxy-1-morpholin-4-yl-D-psicose |
- |
   |
| 2.7.1.172 | 1-deoxy-1-morpholin-4-yl-D-ribulose |
- |
|
| 2.7.1.172 | 1-deoxy-1-morpholino-D-ribulose |
0.25 mM, 50% inhibition |
|
| 2.7.1.172 | 1-deoxy-1-morpholinopsicose |
competitive inhibitor |
|
| 2.7.1.172 | 5'-p-[(fluorosulfonyl)benzoyl]adenosine |
incubation of 0.7 mg/ml Fn3KRP with 0.5 mM inhibitor results in significant activity loss compared with controls. The inhibitor inactivates Fn3KRP by modification of residues at the nucleotide-binding site |
|
| 2.7.1.172 | more |
neither fructosamines (fructoselysine and deoxymorpholinofructose) nor psicoselysine affect the enzymatic activity at concentrations up to 1 mM. No inhibition is observed with ribulosamines bound to the alpha-amino groups of glycine, valine or leucine, or with D-ribulose or D-erythrulose (all tested at 1 mM) |
|
| 2.7.1.172 | N6-D-psicosyl-L-lysine |
- |
|
| 2.7.1.172 | ribuloselysine |
0.1 mM, 50% inhibition |
|
