EC Number   |
Inhibitors |
Structure |
|---|
   3.4.21.104 | alpha-2-Macroglobulin |
forms a stable complex with the enzyme, inhibits at a large molar excess, 40fold |
 |
| 3.4.21.104 | alpha-2-Macroglobulin |
inhibition of recombinant, not native, enzyme at large molar excess |
|
| 3.4.21.104 | anti-thrombin III |
recombinant enzyme, inhibition only in presence of heparin |
|
| 3.4.21.104 | benzyloxycarbonyl-D-Phe-Pro-methoxypropylboroglycinepinanediol ester |
- |
  |
| 3.4.21.104 | C1 inhibitor |
abolishes activity at a 1:1 inhibitor:protease concentration |
|
| 3.4.21.104 | C1 inhibitor |
recombinant enzyme, at pH 7.4, inhibitor from human, the protease-serpin complex in highly unstable at alkaline pH |
|
| 3.4.21.104 | C1-inhibitor |
forms equimolar complexes with the enzyme and inhibits its proteolytic activity |
|
| 3.4.21.104 | C1-inhibitor |
forms a stable complex with the enzyme, 1-3fold excess completely inactivates |
|
| 3.4.21.104 | C1-inhibitor |
linear relationship between inhibition and the molar ratio of inhibitor:enzyme up to about 50% inhibition |
|
| 3.4.21.104 | C1-inhibitor |
- |
|
