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PVAR3D
fabI - P0AEK4
No structure available

Entry features
GENE fabI
DESCRIPTION NADH-dependent enoyl-ACP reductase
ORGANISM Escherichia coli (strain K12)
TAXONOMY Bacteria; Proteobacteria; Gammaproteobacteria; Enterobacterales;Enterobacteriaceae; Escherichia.
UNIPROT P0AEK4
Cross-references
STRING 316385.ECDH10B_1405
REFSEQ NP_415804.1; NC_000913.3; WP_000506490.1; NZ_LN832404.1
PATRIC fig|1411691.4.peg.991
KEGG ecj:JW1281; eco:b1288
EMBL AP009048; BAA14841.1; M97219; AAA17755.1; U00096; AAC74370.1; X78733; CAA55381.1
BioCyc/EcoCyc/MetaCyc EcoCyc:ENOYL-ACP-REDUCT-NADH-MONOMER; MetaCyc:ENOYL-ACP-REDUCT-NADH-MONOMER
INTACT P0AEK4
EC 1.3.1.9;
Drugbank DB01691 - Indole Naphthyridinone; DB01865 - 3-(6-Aminopyridin-3-Yl)-N-Methyl-N-[(1-Methyl-1h-Indol-2-Yl)Methyl]Acrylamide; DB02379 - Beta-D-Glucose; DB03030 - 4-(2-Thienyl)-1-(4-Methylbenzyl)-1h-Imidazole; DB03534 - 3-[(Acetyl-Methyl-Amino)-Methyl]-4-Amino-N-Methyl-N-(1-Methyl-1h-Indol-2-Ylmethyl)-Benzamide; DB08604 - Triclosan
CHEMBL CHEMBL1857
Active site 146 146 Proton acceptor; 156 156 Proton acceptor
PATHWAY Cofactor biosynthesis; biotin biosynthesis.

Gene Ontology

Molecular Function GO ID Term Evidence
GO:0004318 F:enoyl-[acyl-carrier-protein] reductase (NADH) activity IDA
GO:0016631 F:enoyl-[acyl-carrier-protein] reductase activity IEA
GO:0042802 F:identical protein binding IDA
Biological Process GO ID Term Evidence
GO:0008610 P:lipid biosynthetic process IDA
GO:0046677 P:response to antibiotic IEA
GO:0051289 P:protein homotetramerization IDA
GO:0030497 P:fatty acid elongation IDA
GO:0009102 P:biotin biosynthetic process IMP
Cellular Component GO ID Term Evidence
GO:0005829 C:cytosol IDA
GO:0016020 C:membrane HDA
Mutation panel
Mutation Phenotype Reference
Y156F

(non-resistant)

No effect on substrate reduction
PMID:NA
K201A

(non-resistant)

No effect on substrate reduction
PMID:NA
R204A

(non-resistant)

No effect on substrate reduction
PMID:NA
K205A

(non-resistant)

No effect on substrate reduction
PMID:NA
Sequence
Multiple sequence alignment Not Available
MSA Mutation Not Available