|Superclasses:||Reactions Classified By Conversion Type → Simple Reactions → Chemical Reactions|
|Reactions Classified By Substrate → Small-Molecule Reactions|
EC Number: 18.104.22.168
Enzymes and Genes:
|Pseudomonas reinekei :||muconate cycloisomerase I
In Pathway: chlorosalicylate degradation
The reaction direction shown, that is, A + B ↔ C + D versus C + D ↔ A + B, is in accordance with the Enzyme Commission system.
Most BioCyc compounds have been protonated to a reference pH value of 7.3, and some reactions have been computationally balanced for hydrogen by adding free protons. Please see the PGDB Concepts Guide for more information.
Mass balance status: Balanced.
Enzyme Commission Primary Name: chloromuconate cycloisomerase
Enzyme Commission Synonyms: muconate cycloisomerase II
Standard Gibbs Free Energy (ΔrG'° in kcal/mol): 1.9617538 [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 22.214.171.124 (muconate cycloisomerase) or EC 126.96.36.199 (dichloromuconate cycloisomerase).
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
©2015 SRI International, 333 Ravenswood Avenue, Menlo Park, CA 94025-3493