EC Number   |
Ki Value [mM] |
Ki Value maximum [mM] |
Inhibitor |
Reference |
|---|
    2.6.1.42 | -999 |
- |
more |
inhibition kinetics of L- and D-cyclserine, the inactivation follows pseudo-first-order kinetics, at least one molar equivalent of inhibitor binds to one molecule of enzyme for inactivation. Rapid inactivation by L-cycloserine with the second-order rate constant of inactivation kinact/KI_LCS of 7.32 M/s being greater than kinact/KI_DCS of 0.12 M/s |
758558 |
| 2.6.1.42 | 0.0082 |
- |
O-Benzylhydroxylamine |
competitive component of mixed-type inhibition, pH 7.4, 37°C |
661400 |
| 2.6.1.42 | 0.011 |
- |
O-(t-butyl)hydroxylamine |
competitive component of mixed-type inhibition, pH 7.4, 37°C |
661400 |
| 2.6.1.42 | 0.01424 |
- |
carboxymethoxylamine |
uncompetitive component of mixed-type inhibition, pH 7.4, 37°C |
661400 |
| 2.6.1.42 | 0.0209 |
- |
carboxymethoxylamine |
competitive component of mixed-type inhibition, pH 7.4, 37°C |
661400 |
| 2.6.1.42 | 0.0216 |
- |
O-allylhydroxylamine |
competitive component of mixed-type inhibition, pH 7.4, 37°C |
661400 |
| 2.6.1.42 | 0.0841 |
- |
O-Benzylhydroxylamine |
uncompetitive component of mixed-type inhibition, pH 7.4, 37°C |
661400 |
| 2.6.1.42 | 0.0856 |
- |
O-(t-butyl)hydroxylamine |
uncompetitive component of mixed-type inhibition, pH 7.4, 37°C |
661400 |
| 2.6.1.42 | 0.2 |
- |
O-allylhydroxylamine |
or higher, uncompetitive component of mixed-type inhibition, pH 7.4, 37°C |
661400 |
| 2.6.1.42 | 1.3 |
- |
gabapentin |
cytosolic isoform, reduced |
662423 |
