EC Number |
Inhibitors |
Structure |
---|
3.4.24.3 | 1,10-phenanthroline |
activity restored by Co2+, Mn2+, Ca2+, Cu2+, Ni2+ and Zn2+ |
|
3.4.24.3 | 1,10-phenanthroline |
- |
|
3.4.24.3 | 1,10-phenanthroline |
The half maximal inhibitory concentrations of the catalytic domains for 1,10-phenanthroline are significantly decreased in the presence of the N-terminal His6-tag |
|
3.4.24.3 | 1,10-phenanthroline |
The half maximal inhibitory concentrations of the catalytic domains for 1,10-phenanthroline are significantly decreased for both isoforms ColG and ColH in the presence of the N-terminal His6-tag |
|
3.4.24.3 | 2-(1-benzyl-3-naphthalen-1-yl-ureido)-3-methyl-butyric acid |
- |
|
3.4.24.3 | 2-(1-benzyl-3-naphthalen-1-yl-ureido)-N-hydroxy-3-methyl-butyramide |
- |
|
3.4.24.3 | 2-(3-benzoyl-1-benzyl-thioureido)-N-hydroxy-3-methyl-butyramide |
- |
|
3.4.24.3 | 2-(benzyl[[(2,4-difluorophenyl)amino]carbonyl]amino)-3-methylbutanoic acid |
- |
|
3.4.24.3 | 2-(benzyl[[(2,4-difluorophenyl)amino]carbonyl]amino)-N-hydroxy-3-methylbutanamide |
- |
|
3.4.24.3 | 2-(benzyl[[(2,4-difluorophenyl)amino]carbonyl]amino)-N-hydroxypropanamide |
- |
|