Enzyme

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     1. Oxidoreductases
        1.14 Acting on paired donors, with incorporation or reduction of molecular oxygen
            1.14.19 With oxidation of a pair of donors resulting in the reduction of O2 to two molecules of water
ID:1.14.19.55
Description:4-hydroxybenzoate brominase (decarboxylating).

3D structure

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References

External Links

UniProtKB Enzyme Link: UniProtKB 1.14.19.55
BRENDA Enzyme Link: BRENDA 1.14.19.55
KEGG Enzyme Link: KEGG1.14.19.55
BioCyc Enzyme Link: BioCyc 1.14.19.55
ExPASy Enzyme Link: ExPASy1.14.19.55
EC2PDB Enzyme Link: EC2PDB 1.14.19.55
ExplorEnz Enzyme Link: ExplorEnz 1.14.19.55
PRIAM enzyme-specific profiles Link: PRIAM 1.14.19.55
IntEnz Enzyme Link: IntEnz 1.14.19.55
MEDLINE Enzyme Link: MEDLINE 1.14.19.55
MSA:

1.14.19.55;

Phylogenetic Tree:

1.14.19.55;

Uniprot:
M-CSA:
RHEA:56368 3,4-dihydroxybenzoate + 2 bromide + 5 H(+) + 2 NADPH + 2 O2 = 3,5-dibromobenzene-1,2-diol + CO2 + 4 H2O + 2 NADP(+)
RULE(radius=1) [*:1]-[C;H0;+0:2]1=[CH;+0:3]-[N;H0;+0:4](-[*:5])-[CH;+0:6]=[CH;+0:7]-[CH2;+0:8]-1.[*:9]-[N;H0;+0:10]1-[CH;+0:11]=[C;H0;+0:12](-[*:13])-[CH2;+0:14]-[CH;+0:15]=[CH;+0:16]-1.[*:17]:[cH;+0:18]:[*:19]:[c;H0;+0:20](:[*:21])-[C;H0;+0:22](=[*:23])-[OH;+0:24].[Br-;H0:25].[Br-;H0:26].[H+;H0:27].[H+;H0:28].[H+;H0:29].[H+;H0:30].[H+;H0:31].[O;H0;+0:32]=[O;H0;+0:33].[O;H0;+0:34]=[O;H0;+0:35]>>[*:1]-[c;H0;+0:2]1:[cH;+0:3]:[n+;H0:4](-[*:5]):[cH;+0:6]:[cH;+0:7]:[cH;+0:8]:1.[*:9]-[n+;H0:10]1:[cH;+0:11]:[c;H0;+0:12](-[*:13]):[cH;+0:14]:[cH;+0:15]:[cH;+0:16]:1.[*:17]:[c;H0;+0:18](-[Br;H0;+0:26]):[*:19]:[c;H0;+0:20](:[*:21])-[Br;H0;+0:25].[*:23]=[C;H0;+0:22]=[O;H0;+0:24].[OH2;+0:32].[OH2;+0:33].[OH2;+0:34].[OH2;+0:35]
Reaction
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References

TitleAuthorsDatePubMed ID
Enzymatic synthesis of polybrominated dioxins from the marine environment.Agarwal V, Moore BS2014 Sep 1925061970
Biosynthesis of polybrominated aromatic organic compounds by marine bacteria.Agarwal V, El Gamal AA, Yamanaka K, Poth D, Kersten RD, Schorn M, Allen EE, Moore BS2014 Aug24974229

RHEA:56348 4-hydroxybenzoate + 2 bromide + 5 H(+) + 2 NADPH + 2 O2 = 2,4-dibromophenol + CO2 + 4 H2O + 2 NADP(+)
RULE(radius=1) [*:1]-[C;H0;+0:2]1=[CH;+0:3]-[N;H0;+0:4](-[*:5])-[CH;+0:6]=[CH;+0:7]-[CH2;+0:8]-1.[*:9]-[N;H0;+0:10]1-[CH;+0:11]=[C;H0;+0:12](-[*:13])-[CH2;+0:14]-[CH;+0:15]=[CH;+0:16]-1.[*:17]:[c;H0;+0:18](:[*:19]:[cH;+0:20]:[*:21])-[C;H0;+0:22](=[*:23])-[OH;+0:24].[Br-;H0:25].[Br-;H0:26].[H+;H0:27].[H+;H0:28].[H+;H0:29].[H+;H0:30].[H+;H0:31].[O;H0;+0:32]=[O;H0;+0:33].[O;H0;+0:34]=[O;H0;+0:35]>>[*:1]-[c;H0;+0:2]1:[cH;+0:3]:[n+;H0:4](-[*:5]):[cH;+0:6]:[cH;+0:7]:[cH;+0:8]:1.[*:9]-[n+;H0:10]1:[cH;+0:11]:[c;H0;+0:12](-[*:13]):[cH;+0:14]:[cH;+0:15]:[cH;+0:16]:1.[*:17]:[c;H0;+0:18](-[Br;H0;+0:25]):[*:19]:[c;H0;+0:20](:[*:21])-[Br;H0;+0:26].[*:23]=[C;H0;+0:22]=[O;H0;+0:24].[OH2;+0:32].[OH2;+0:33].[OH2;+0:34].[OH2;+0:35]
Reaction
Core-to-Core More

References

TitleAuthorsDatePubMed ID
Enzymatic synthesis of polybrominated dioxins from the marine environment.Agarwal V, Moore BS2014 Sep 1925061970
Biosynthesis of polybrominated aromatic organic compounds by marine bacteria.Agarwal V, El Gamal AA, Yamanaka K, Poth D, Kersten RD, Schorn M, Allen EE, Moore BS2014 Aug24974229