EC Number   |
Inhibitors |
Structure |
|---|
    3.1.3.3 | 1-(3-sulfopropyl)pyridin-1-ium |
- |
   |
| 3.1.3.3 | BeF3- |
at 50°C, the hydrolytic activity of is markedly inhibited (more than 95%) in the presence of both BeCl2 and NaF. The latter is provided at concentrations that yield predominantly BeF3- in situ. Either BeCl2 or NaF alone has a much smaller inhibitory effect (35 or 20%, respectively). Similar inhibition by BeF3- is observed at room temperature or at 70°C |
|
| 3.1.3.3 | Ca2+ |
inhibition even in presence of Mg2+, replacement of sixfold coordinated Mg2+ in active site by Ca2+ results in sevenfold coordinated metal ion, explaining the inhibitory effect of Ca2+ |
|
| 3.1.3.3 | Ca2+ |
less than 50% activity at 1 mM |
|
| 3.1.3.3 | Ca2+ |
- |
|
| 3.1.3.3 | Cd2+ |
- |
|
| 3.1.3.3 | chlorpromazine |
- |
|
| 3.1.3.3 | Clorobiocin |
displays bactericidal activity and kills intracellular bacteria in a dose-dependent manner, highly specific in the ability to inhibit isoform SerB2 in comparison with human phosphoserine phosphatase |
|
| 3.1.3.3 | Cu2+ |
less than 50% activity at 1 mM |
|
| 3.1.3.3 | Cu2+ |
- |
|
