Due to scheduled maintenance work, this service may not be available on Monday January 22nd between 08.00 am and 9.00 am CEST
To improve security and privacy, we are moving our web pages and services from HTTP to HTTPS.
To give users of web services time to transition to HTTPS, we will support separate HTTP and HTTPS services until the end of 2017.
From January 2018 most HTTP traffic will be automatically redirected to HTTPS. [more...] View this page in https
ENZYME entry: EC 126.96.36.199
View entry in original ENZYME format
View entry in raw text format (no links)
in this entry
|Bornane-2,6-dione + H(2)O <=> ((1S)-4-hydroxy-2,2,3-trimethylcyclopent-3-enyl)acetate|
- Isolated from Rhodococcus sp.
- The bornane ring system is cleaved by a retro-Claisen reaction to
give the enol of alpha-campholonate.
- When separate from the enzyme the enol is tautomerised to the keto
form as a 6:1 mixture of ((1S,3R)-2,2,3-trimethyl-4-
oxocyclopentyl)acetate and ((1S,3S)-2,2,3-trimethyl-4-
|PRIAM enzyme-specific profiles||188.8.131.52|
|KEGG Ligand Database for Enzyme Nomenclature||184.108.40.206|
|IUBMB Enzyme Nomenclature||220.127.116.11|
|MEDLINE||Find literature relating to 18.104.22.168|
, with possibility to download in different formats, align etc.
entries corresponding to 3.7.1.-
entries corresponding to 3.7.-.-
entries corresponding to 3.-.-.-