Enzyme

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     1. Oxidoreductases
        1.1 Acting on the CH-OH group of donors
            1.1.1 With NAD+ or NADP+ as acceptor
ID:1.1.1.110
Description:Aromatic 2-oxoacid reductase.
Alternative Name: Indolelactate dehydrogenase.
Indole-3-lactate dehydrogenase.
(R)-aromatic lactate dehydrogenase.
(R)-4-hydroxyphenyllactate dehydrogenase.

3D structure

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References

External Links

UniProtKB Enzyme Link: UniProtKB 1.1.1.110
BRENDA Enzyme Link: BRENDA 1.1.1.110
KEGG Enzyme Link: KEGG1.1.1.110
BioCyc Enzyme Link: BioCyc 1.1.1.110
ExPASy Enzyme Link: ExPASy1.1.1.110
EC2PDB Enzyme Link: EC2PDB 1.1.1.110
ExplorEnz Enzyme Link: ExplorEnz 1.1.1.110
PRIAM enzyme-specific profiles Link: PRIAM 1.1.1.110
IntEnz Enzyme Link: IntEnz 1.1.1.110
MEDLINE Enzyme Link: MEDLINE 1.1.1.110
MSA:

1.1.1.110;

Phylogenetic Tree:

1.1.1.110;

Uniprot:
M-CSA:
RHEA:10780 (2R)-2-hydroxy-3-(4-hydroxyphenyl)propanoate + NAD(+) = 3-(4-hydroxyphenyl)pyruvate + H(+) + NADH
RULE(radius=1) [*:1]-[CH;+0:2](-[*:3])-[OH;+0:4].[*:5]-[n+;H0:6]1:[cH;+0:7]:[cH;+0:8]:[cH;+0:9]:[c;H0;+0:10](-[*:11]):[cH;+0:12]:1>>[*:1]-[C;H0;+0:2](-[*:3])=[O;H0;+0:4].[*:5]-[N;H0;+0:6]1-[CH;+0:7]=[CH;+0:8]-[CH2;+0:9]-[C;H0;+0:10](-[*:11])=[CH;+0:12]-1
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References

TitleAuthorsDatePubMed ID
Nontargeted in vitro metabolomics for high-throughput identification of novel enzymes in Escherichia coli.Sévin DC, Fuhrer T, Zamboni N, Sauer U2017 Feb27941785
Purification, cloning and functional expression of hydroxyphenylpyruvate reductase involved in rosmarinic acid biosynthesis in cell cultures of Coleus blumei.Kim KH, Janiak V, Petersen M2004 Feb15284489
HPPR encodes the hydroxyphenylpyruvate reductase required for the biosynthesis of hydrophilic phenolic acids in Salvia miltiorrhiza.Wang GQ, Chen JF, Yi B, Tan HX, Zhang L, Chen WS2017 Dec29329649
Molecular cloning and characterization of tyrosine aminotransferase and hydroxyphenylpyruvate reductase, and rosmarinic acid accumulation in Scutellaria baicalensis.Kim YB, Uddina MR, Kim Y, Park CG, Park SU2014 Sep25918800

RHEA:20133 3-(indol-3-yl)lactate + NAD(+) = H(+) + indole-3-pyruvate + NADH
RULE(radius=1) [*:1]-[CH;+0:2](-[*:3])-[OH;+0:4].[*:5]-[n+;H0:6]1:[cH;+0:7]:[cH;+0:8]:[cH;+0:9]:[c;H0;+0:10](-[*:11]):[cH;+0:12]:1>>[*:1]-[C;H0;+0:2](-[*:3])=[O;H0;+0:4].[*:5]-[N;H0;+0:6]1-[CH;+0:7]=[CH;+0:8]-[CH2;+0:9]-[C;H0;+0:10](-[*:11])=[CH;+0:12]-1
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References

TitleAuthorsDatePubMed ID
On the occurrence of enoate reductase and 2-oxo-carboxylate reductase in clostridia and some observations on the amino acid fermentation by Peptostreptococcus anaerobius.Giesel H, Simon H1983 Aug6354130
A gut bacterial pathway metabolizes aromatic amino acids into nine circulating metabolites.Dodd D, Spitzer MH, Van Treuren W, Merrill BD, Hryckowian AJ, Higginbottom SK, Le A, Cowan TM, Nolan GP, Fischbach MA, Sonnenburg JL2017 Nov 3029168502
Indolelactate dehydrogenase from Clostridium sporogenes.Jean M, DeMoss RD1968 Apr4384683
The involvement of coenzyme A esters in the dehydration of (R)-phenyllactate to (E)-cinnamate by Clostridium sporogenes.Dickert S, Pierik AJ, Linder D, Buckel W2000 Jun10849007

RHEA:38351 (R)-3-phenyllactate + NAD(+) = 3-phenylpyruvate + H(+) + NADH
RULE(radius=1) [*:1]-[CH;+0:2](-[*:3])-[OH;+0:4].[*:5]-[n+;H0:6]1:[cH;+0:7]:[cH;+0:8]:[cH;+0:9]:[c;H0;+0:10](-[*:11]):[cH;+0:12]:1>>[*:1]-[C;H0;+0:2](-[*:3])=[O;H0;+0:4].[*:5]-[N;H0;+0:6]1-[CH;+0:7]=[CH;+0:8]-[CH2;+0:9]-[C;H0;+0:10](-[*:11])=[CH;+0:12]-1
Reaction
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References

TitleAuthorsDatePubMed ID
The involvement of coenzyme A esters in the dehydration of (R)-phenyllactate to (E)-cinnamate by Clostridium sporogenes.Dickert S, Pierik AJ, Linder D, Buckel W2000 Jun10849007
Molecular characterization of phenyllactate dehydratase and its initiator from Clostridium sporogenes.Dickert S, Pierik AJ, Buckel W2002 Apr11967068