|Superclasses:||Reactions Classified By Conversion Type → Simple Reactions → Chemical Reactions|
|Reactions Classified By Substrate → Small-Molecule Reactions|
EC Number: 188.8.131.52
Enzymes and Genes:
|Cupriavidus sp. PS12 :||chloromuconate cycloisomerase
|Pseudomonas knackmussii :||chloromuconate cycloisomerase
|Pseudomonas sp. P51 :||chloromuconate cycloisomerase
|Ralstonia eutropha JMP134 :||chloromuconate cycloisomerase I
chloromuconate cycloisomerase II : tfdDII
In Pathway: 4-chlorocatechol degradation
Note that this reaction equation differs from the official Enzyme Commission reaction equation for this EC number, which can be found here .
The reaction direction shown, that is, A + B ↔ C + D versus C + D ↔ A + B, is in accordance with the Enzyme Commission system.
Mass balance status: Balanced.
Enzyme Commission Primary Name: chloromuconate cycloisomerase
Enzyme Commission Synonyms: muconate cycloisomerase II
Standard Gibbs Free Energy (ΔrG'° in kcal/mol): -7.4241257 [Latendresse13]
Enzyme Commission Summary:
Requires Mn2+. The product of cycloisomerization of 3-chloro-cis,cis-muconate spontaneously eliminates chloride to produce cis-4-carboxymethylenebut-2-en-4-olide. Also acts (in the reverse direction) on 2-chloro-cis,cis-muconate. Not identical with EC 184.108.40.206 (muconate cycloisomerase) or EC 220.127.116.11 (dichloromuconate cycloisomerase).
Unification Links: KEGG:R05391
Schmidt80: Schmidt E, Knackmuss HJ (1980). "Chemical structure and biodegradability of halogenated aromatic compounds. Conversion of chlorinated muconic acids into maleoylacetic acid." Biochem J 192(1);339-47. PMID: 7305906
©2014 SRI International, 333 Ravenswood Avenue, Menlo Park, CA 94025-3493