EC Number   |
Inhibitors |
Structure |
|---|
   7.1.1.5 | 2-(n-heptyl)-4-hydroxyquinoline-N-oxide |
- |
   |
| 7.1.1.5 | 2-hydroxy-3-undecyl-1,4-naphthoquinone |
0.01 mM, 20% inhibition |
|
| 7.1.1.5 | 2n-heptyl-4-hydroxyquinoline N-oxide |
most potent inhibitor |
|
| 7.1.1.5 | antimycin A |
more than 10fold less effective than 2-(n-heptyl)-4-hydroxyquinoline-N-oxide, 39% residual activity at 0.01 mM |
|
| 7.1.1.5 | asolectin |
- |
|
| 7.1.1.5 | cyanide |
more than 90% of activity is inhibited by 0.01 mM cyanide |
|
| 7.1.1.5 | cyanide |
47% residual activity at 0.5 mM |
|
| 7.1.1.5 | cyanide |
the enzyme is easily inhibited by cyanide |
|
| 7.1.1.5 | Lipid |
addition of total lipids from Thermoplasma acidophilum decreases activity |
|
| 7.1.1.5 | more |
antimycin A, myxothiazol, methyl 3-methoxy-2-(2-styrylphenyl) propenate and stigmatellin (at concentration up to 0.030 mM) and Zn2+ at a concentration up to 1 mM, do not inhibit |
|
