trpCF - Vibrio cholerae O1 biovar El Tor str. N16961

Tryptophan biosynthesis protein TrpCF

> trpCF - Vibrio cholerae O1 biovar El Tor str. N16961 [Tryptophan biosynthesis protein TrpCF]
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统计信息
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Metadata

Organism Source: 243277 - Vibrio cholerae O1 biovar El Tor str. N16961
EC Number: 4.1.1.48 / 5.3.1.24
Cluster:
Registry Model:

Reactions

reaction id name note
KEGG:R03508 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose-5-phosphate carboxy-lyase(cyclizing) 1-(2-Carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate <=> Indoleglycerol phosphate + CO2 + H2O
KEGG:R03509 N-(5-phospho-beta-D-ribosyl)anthranilate ketol-isomerase N-(5-Phospho-D-ribosyl)anthranilate <=> 1-(2-Carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate
BioCyc:IGPSYN-RXN PROTON + CARBOXYPHENYLAMINO-DEOXYRIBULOSE-P --> INDOLE-3-GLYCEROL-P + CARBON-DIOXIDE + WATER this is the fourth reaction in the tryptophan synthesis pathway
BioCyc:PRAISOM-RXN N-5-PHOSPHORIBOSYL-ANTHRANILATE --> CARBOXYPHENYLAMINO-DEOXYRIBULOSE-P This is the third step in the tryptophan synthesis pathway
Rhea:RHEA:21541 N-(5-phospho-β-D-ribosyl)anthranilate => 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate
Rhea:RHEA:21542 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate => N-(5-phospho-β-D-ribosyl)anthranilate
Rhea:RHEA:21543 N-(5-phospho-β-D-ribosyl)anthranilate <=> 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate
Rhea:RHEA:23477 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate + H+ => (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate + CO2 + H2O
Rhea:RHEA:23478 (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate + CO2 + H2O => 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate + H+
Rhea:RHEA:23479 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate + H+ <=> (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate + CO2 + H2O

Pathways

pathway id name
BioCyc:VCHO_ALL-CHORISMATE-PWY superpathway of chorismate metabolism
BioCyc:VCHO_PWY-6629 superpathway of L-tryptophan biosynthesis
BioCyc:VCHO_TRPSYN-PWY L-tryptophan biosynthesis
BioCyc:VCHO_COMPLETE-ARO-PWY superpathway of aromatic amino acid biosynthesis