Enzyme

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EC Tree
     1. Oxidoreductases
        1.17 Acting on CH or CH2 groups
            1.17.7 With an iron-sulfur protein as acceptor
ID:1.17.7.1
Description:(E)-4-hydroxy-3-methylbut-2-enyl-diphosphate synthase (ferredoxin).
Alternative Name: 4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase.
(E)-4-hydroxy-3-methylbut-2-enyl diphosphate synthase.
Cath: 3.20.20.20; 3.30.413.10;

3D structure

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References

External Links

UniProtKB Enzyme Link: UniProtKB 1.17.7.1
BRENDA Enzyme Link: BRENDA 1.17.7.1
KEGG Enzyme Link: KEGG1.17.7.1
BioCyc Enzyme Link: BioCyc 1.17.7.1
ExPASy Enzyme Link: ExPASy1.17.7.1
EC2PDB Enzyme Link: EC2PDB 1.17.7.1
ExplorEnz Enzyme Link: ExplorEnz 1.17.7.1
PRIAM enzyme-specific profiles Link: PRIAM 1.17.7.1
IntEnz Enzyme Link: IntEnz 1.17.7.1
MEDLINE Enzyme Link: MEDLINE 1.17.7.1
MSA:

1.17.7.1;

Phylogenetic Tree:

1.17.7.1;

Uniprot:
M-CSA:
RHEA:26119 (2E)-4-hydroxy-3-methylbut-2-enyl diphosphate + H2O + 2 oxidized [2Fe-2S]-[ferredoxin] = 2-C-methyl-D-erythritol 2,4-cyclic diphosphate + H(+) + 2 reduced [2Fe-2S]-[ferredoxin]
RULE(radius=1) ([*:1]-[CH;+0:2]=[C;H0;+0:3](-[*:4])-[*:5].[*:6]-[OH;+0:7]).[*:8]-[Fe+;H0:9]-[*:10].[*:11]-[Fe+;H0:12]-[*:13].[OH2;+0:14]>>[*:1]-[CH;+0:2](-[OH;+0:14])-[C;H0;+0:3](-[*:4])(-[*:5])-[O;H0;+0:7]-[*:6].[*:8]-[Fe;H0;+0:9]-[*:10].[*:11]-[Fe;H0;+0:12]-[*:13]
Reaction
Core-to-Core More

References

TitleAuthorsDatePubMed ID
Isoprenoid biosynthesis in plant chloroplasts via the MEP pathway: direct thylakoid/ferredoxin-dependent photoreduction of GcpE/IspG.Seemann M, Tse Sum Bui B, Wolff M, Miginiac-Maslow M, Rohmer M2006 Mar 616480720
Cyanobacterial non-mevalonate pathway: (E)-4-hydroxy-3-methylbut-2-enyl diphosphate synthase interacts with ferredoxin in Thermosynechococcus elongatus BP-1.Okada K, Hase T2005 May 2715792953
Isoprenoid biosynthesis in chloroplasts via the methylerythritol phosphate pathway: the (E)-4-hydroxy-3-methylbut-2-enyl diphosphate synthase (GcpE) from Arabidopsis thaliana is a [4Fe-4S] protein.Seemann M, Wegner P, Schünemann V, Bui BT, Wolff M, Marquet A, Trautwein AX, Rohmer M2005 Mar15650872