3.7.1.18: 6-oxocamphor hydrolase
This is an abbreviated version!
For detailed information about 6-oxocamphor hydrolase, go to the full flat file.
Word Map on EC 3.7.1.18
-
3.7.1.18
-
crotonase
-
desymmetrization
-
beta-diketones
-
bicyclic
-
diketone
-
rhodococcus
-
ncimb
-
prochiral
-
enol
-
hexamer
-
anabaena
-
trimer
-
dyad
-
carbon-carbon
- 3.7.1.18
- crotonase
-
desymmetrization
- beta-diketones
-
bicyclic
- diketone
- rhodococcus
-
ncimb
-
prochiral
-
enol
-
hexamer
- anabaena
- trimer
-
dyad
-
carbon-carbon
Reaction
Synonyms
6-oxo camphor hydrolase, CaMK, OCH, retro-Claisenase
ECTree
Advanced search results
Reaction
Reaction on EC 3.7.1.18 - 6-oxocamphor hydrolase
Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
bornane-2,6-dione + H2O = [(1S)-4-hydroxy-2,2,3-trimethylcyclopent-3-enyl]acetate
analysis of the molecular determinants of both mechanism and enantiotopic selectivity in reactions catalysed by OCH and reaction mechanism, putative Asp154-His145 dyad, overview
-
bornane-2,6-dione + H2O = [(1S)-4-hydroxy-2,2,3-trimethylcyclopent-3-enyl]acetate
involvement of five residues, His45, His122, His145, Asp154, and Glu244, in catalysis, catalytic His145/Asp154 dyad. The the pendant acetate of the product (2S,4S)-alpha-campholinic acid hydrogen bonded to a His145/Asp154 dyad and the endocyclic carbonyl of the cyclopentane ring hydrogen bonds to Trp40, prochiral selectivity, base-catalyzed mechanism of C-C bond cleavage, overview
bornane-2,6-dione + H2O = [(1S)-4-hydroxy-2,2,3-trimethylcyclopent-3-enyl]acetate
mechanism of carbon-carbon bond cleavage by 6-oxo camphor hydrolase
-
bornane-2,6-dione + H2O = [(1S)-4-hydroxy-2,2,3-trimethylcyclopent-3-enyl]acetate
analysis of the molecular determinants of both mechanism and enantiotopic selectivity in reactions catalysed by OCH and reaction mechanism, putative Asp154-His145 dyad, overview
-
-
bornane-2,6-dione + H2O = [(1S)-4-hydroxy-2,2,3-trimethylcyclopent-3-enyl]acetate
involvement of five residues, His45, His122, His145, Asp154, and Glu244, in catalysis, catalytic His145/Asp154 dyad. The the pendant acetate of the product (2S,4S)-alpha-campholinic acid hydrogen bonded to a His145/Asp154 dyad and the endocyclic carbonyl of the cyclopentane ring hydrogen bonds to Trp40, prochiral selectivity, base-catalyzed mechanism of C-C bond cleavage, overview
-
-