EC Number   |
Title |
Organism |
|---|
   3.7.1.18 | Asymmetric synthesis of 3-substituted cyclohexylamine derivatives from prochiral diketones via three biocatalytic steps |
Rhodococcus sp. |
| 3.7.1.18 | Asymmetric synthesis of 3-substituted cyclohexylamine derivatives from prochiral diketones via three biocatalytic steps |
Rhodococcus sp. NCIMB 9784 |
| 3.7.1.18 | On the resolution of chiral substrates by a retro-Claisenase enzyme: biotransformations of heteroannular bicyclic beta-diketones by 6-oxocamphor hydrolase |
Rhodococcus sp. |
| 3.7.1.18 | On the resolution of chiral substrates by a retro-Claisenase enzyme: biotransformations of heteroannular bicyclic beta-diketones by 6-oxocamphor hydrolase |
Rhodococcus sp. NCIMB 9784 |
| 3.7.1.18 | Structure of 6-oxo camphor hydrolase H122A mutant bound to its natural product, (2S,4S)-alpha-campholinic acid. Mutant structure suggests an atypical mode of transition state binding for a crotonase homolog |
Rhodococcus sp. |
| 3.7.1.18 | Structure of 6-oxo camphor hydrolase H122A mutant bound to its natural product, (2S,4S)-alpha-campholinic acid. Mutant structure suggests an atypical mode of transition state binding for a crotonase homolog |
Rhodococcus sp. NCIMB 9784 |
| 3.7.1.18 | The 2-A crystal structure of 6-oxo camphor hydrolase: new structural diversity in the crotonase superfamily |
Rhodococcus erythropolis |
| 3.7.1.18 | The desymmetrization of bicyclic beta -diketones by an enzymatic retro-Claisen reaction. A new reaction of the crotonase superfamily |
Rhodococcus sp. |
| 3.7.1.18 | The desymmetrization of bicyclic beta -diketones by an enzymatic retro-Claisen reaction. A new reaction of the crotonase superfamily |
Rhodococcus sp. NCIMB 9784 |
