EC Number   |
Substrates |
Organism |
Products |
Reversibility  |
|---|
   1.13.11.50 | more |
iron(II) complexes [Fe(L)(CH3CN)3](SO3CF3)2 of tris(2-pyridyl)-based ligands exhibit very similar chemical surroundings to the active site of the enzyme and mimic its functions |
Paraburkholderia xenovorans |
? |
- |
- |
| 1.13.11.50 | more |
Ni(II)-complex-adducts show regioselective oxidative cleavage of the aliphatic C-C bond using dioxygen via the substrate activation mechanism without changing the oxidation state of nickel(II) as similar to the wild type enzyme |
Acinetobacter johnsonii |
? |
- |
- |
| 1.13.11.50 | 1,1,1-trifluoro-2,4-pentanedione + O2 |
- |
Acinetobacter johnsonii |
? |
- |
? |
| 1.13.11.50 | 1,1,1-trifluoro-pentane-2,4-dione + O2 |
- |
Acinetobacter johnsonii |
? |
- |
? |
| 1.13.11.50 | 1,1-difluoro-2,4-pentanedione + O2 |
- |
Acinetobacter johnsonii |
? |
- |
? |
| 1.13.11.50 | 1,1-difluoropentane-2,4-dione + O2 |
- |
Acinetobacter johnsonii |
? |
- |
? |
| 1.13.11.50 | 1-phenyl-1,3-butanedione + O2 |
- |
Acinetobacter johnsonii |
? |
- |
? |
| 1.13.11.50 | 1-phenylbutane-1,3-dione + O2 |
- |
Acinetobacter johnsonii |
? |
- |
? |
| 1.13.11.50 | 2,4-dioxopentanoic acid ethyl ester + O2 |
- |
Acinetobacter johnsonii |
? |
- |
? |
| 1.13.11.50 | 2,4-dioxopentanoic acid ethyl ester + O2 |
poor substrate |
Acinetobacter johnsonii |
? |
- |
? |
