3.7.1.18	733048	Asymmetric synthesis of 3-substituted cyclohexylamine derivatives from prochiral diketones via three biocatalytic steps	Adv. Synth. Catal.	355	1703-1708	2013	Rhodococcus sp.	
3.7.1.18	733048	Asymmetric synthesis of 3-substituted cyclohexylamine derivatives from prochiral diketones via three biocatalytic steps	Adv. Synth. Catal.	355	1703-1708	2013	Rhodococcus sp. NCIMB 9784	
3.7.1.18	718527	On the resolution of chiral substrates by a retro-Claisenase enzyme: biotransformations of heteroannular bicyclic beta-diketones by 6-oxocamphor hydrolase	Adv. Synth. Catal.	349	1353-1360	2007	Rhodococcus sp.	
3.7.1.18	718527	On the resolution of chiral substrates by a retro-Claisenase enzyme: biotransformations of heteroannular bicyclic beta-diketones by 6-oxocamphor hydrolase	Adv. Synth. Catal.	349	1353-1360	2007	Rhodococcus sp. NCIMB 9784	
3.7.1.18	719819	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	J. Biol. Chem.	279	31312-31317	2004	Rhodococcus sp.	
3.7.1.18	719819	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	J. Biol. Chem.	279	31312-31317	2004	Rhodococcus sp. NCIMB 9784	
3.7.1.18	719814	The 2-A crystal structure of 6-oxo camphor hydrolase: new structural diversity in the crotonase superfamily	J. Biol. Chem.	278	1744-1750	2003	Rhodococcus erythropolis	
3.7.1.18	719804	The desymmetrization of bicyclic beta -diketones by an enzymatic retro-Claisen reaction. A new reaction of the crotonase superfamily	J. Biol. Chem.	276	12565-12572	2001	Rhodococcus sp.	
3.7.1.18	719804	The desymmetrization of bicyclic beta -diketones by an enzymatic retro-Claisen reaction. A new reaction of the crotonase superfamily	J. Biol. Chem.	276	12565-12572	2001	Rhodococcus sp. NCIMB 9784