| Entry |
|
| Name |
caffeate 3,4-dioxygenase |
| Class |
Oxidoreductases;
Acting on single donors with O2 as oxidant and incorporation of
oxygen into the substrate (oxygenases). The oxygen incorporated need
not be derived from O2;
With incorporation of two atoms of oxygen
 |
| Sysname |
3,4-dihydroxy-trans-cinnamate:oxygen 3,4-oxidoreductase
(decyclizing) |
| Reaction(IUBMB) |
3,4-dihydroxy-trans-cinnamate + O2 =
3-(2-carboxyethenyl)-cis,cis-muconate [RN:R03365] |
| Reaction(KEGG) |
R03365
 |
| Substrate |
3,4-dihydroxy-trans-cinnamate [CPD:C01197];
O2 [CPD:C00007] |
| Product |
3-(2-carboxyethenyl)-cis,cis-muconate [CPD:C04366] |
| Pathway |
PATH: ec00940 Phenylpropanoid biosynthesis |
Reference Authors Title
Journal Organism
|
1 [PMID:5776526]
Seidman MM, Toms A, Wood JM.
Influence of side-chain substituents on the position of cleavage of
the benzene ring by Pseudomonas fluorescens.
J. Bacteriol. 97 (1969) 1192-7.
Pseudomonas fluorescens |
| Other DBs |
ExplorEnz - The Enzyme Database: 1.13.11.22
IUBMB Enzyme Nomenclature: 1.13.11.22
ExPASy - ENZYME nomenclature database: 1.13.11.22
BRENDA, the Enzyme Database: 1.13.11.22
CAS: 37256-61-4 |