Entry
Name
chloromuconate cycloisomerase;
muconate cycloisomerase II;
2-chloro-2,5-dihydro-5-oxofuran-2-acetate lyase (decyclizing);
2-chloro-2,5-dihydro-5-oxofuran-2-acetate lyase (ring-opening)
Class
Isomerases;
Intramolecular lyases;
Intramolecular lyases (only sub-subclass identified to date)
BRITE hierarchy
Sysname
(2R)-2-chloro-2,5-dihydro-5-oxofuran-2-acetate lyase (ring-opening)
Reaction(IUBMB)
(2R)-2-chloro-2,5-dihydro-5-oxofuran-2-acetate = 3-chloro-cis,cis-muconate [RN:
R04259 ]
Reaction(KEGG)
Substrate
(2R)-2-chloro-2,5-dihydro-5-oxofuran-2-acetate [CPD:
C04522 ]
Product
3-chloro-cis,cis-muconate [CPD:
C03585 ]
Comment
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 on 2-chloro-cis,cis-muconate. Not identical with EC
5.5.1.1 (muconate cycloisomerase) or EC
5.5.1.11 (dichloromuconate cycloisomerase).
History
EC 5.5.1.7 created 1983
Pathway
ec00361 Chlorocyclohexane and chlorobenzene degradation
ec01120 Microbial metabolism in diverse environments
Orthology
K01860 chloromuconate cycloisomerase
Genes
PKC : PKB_3274(clcb1) PKB_3623(clcb3)
REU : Reut_D6465 Reut_D6474
BPT : Bpet1535(catB2) Bpet3749(catB5)
Taxonomy
Reference
Authors
Schmidt E, Knackmuss HJ.
Title
Chemical structure and biodegradability of halogenated aromatic compounds. Conversion of chlorinated muconic acids into maleoylacetic acid.
Journal
Reference
Authors
Kaulmann U, Kaschabek SR, Schlomann M
Title
Mechanism of chloride elimination from 3-chloro- and 2,4-dichloro-cis,cis-muconate: new insight obtained from analysis of muconate cycloisomerase variant CatB-K169A.
Journal
Reference
Authors
Kajander T, Lehtio L, Schlomann M, Goldman A
Title
The structure of Pseudomonas P51 Cl-muconate lactonizing enzyme: co-evolution of structure and dynamics with the dehalogenation function.
Journal
Sequence
Other DBs
ExplorEnz - The Enzyme Database: 5.5.1.7
ExPASy - ENZYME nomenclature database: 5.5.1.7
UM-BBD (Biocatalysis/Biodegradation Database): 5.5.1.7
BRENDA, the Enzyme Database: 5.5.1.7
LinkDB
All DBs