EC Number   |
Inhibitors |
Structure |
|---|
   1.11.1.B2 | azide |
no inhibition |
   |
| 1.11.1.B2 | azide |
uncompetitive; uncompetitive inhibition, inhibition constant: 50 nM |
|
| 1.11.1.B2 | Br- |
inhibition of mutant enzyme S402A between pH 3.5 and 4.5: concentrations greater than 0.2 mM inhibit, between pH 5.0 and 5.5: concentrations above 0.5 mM inhibit, between pH 6.0 and 6.3: 0.5 mM does not inhibit the mutant enzyme |
|
| 1.11.1.B2 | Cl- |
pH 4.1: mixed type inhibition with respect to H2O2, pH 3.1: competitive inhibition |
|
| 1.11.1.B2 | F- |
0.3 mM, 50% inhibition of brominating activity |
|
| 1.11.1.B2 | F- |
0.18 mM, 50% inhibition |
|
| 1.11.1.B2 | H2O2 |
above 50 mM |
|
| 1.11.1.B2 | hydrazine |
uncompetitive; uncompetitive inhibition, inhibition constant: 0.3 mM |
|
| 1.11.1.B2 | hydroxylamine |
competitive and uncompetitive inhibition; inhibits rVCPO both competitively and uncompetitively. The competitive inhibition constant: 0.04 mM, uncompetitive inhibition 0.08 mM |
|
| 1.11.1.B2 | KCN |
0.01 mM, 50% inhibition |
|
