Structure of PDB 4bng Chain E Binding Site BS01

Receptor Information
>4bng Chain E (length=254) Species: 158879 (Staphylococcus aureus subsp. aureus N315) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
NLENKTYVIMGIANKRSIAFGVAKVLDQLGAKLVFTYRKERSRKELEKLL
EQLNQPEAHLYQIDVQSDEEVINGFEQIGKDVGNIDGVYHSIAFANMEDL
RGRFSETSREGFLLAQDISSYSLTIVAHEAKKLMPEGGSIVATTYLGGEF
AVQNYNVMGVAKASLEANVKYLALDLGPDNIRVNAISAGPIRTLSAKGVG
GFNTILKEIEERAPLKRNVDQVEVGKTAAYLLSDLSSGVTGENIHVDSGF
HAIK
Ligand information
Ligand ID5PP
InChIInChI=1S/C17H20O2/c1-2-3-5-8-14-11-12-17(16(18)13-14)19-15-9-6-4-7-10-15/h4,6-7,9-13,18H,2-3,5,8H2,1H3
InChIKeyOJLYTHOKCYLPMA-UHFFFAOYSA-N
SMILES
SoftwareSMILES
CACTVS 3.341CCCCCc1ccc(Oc2ccccc2)c(O)c1
OpenEye OEToolkits 1.5.0CCCCCc1ccc(c(c1)O)Oc2ccccc2
ACDLabs 10.04O(c1ccccc1)c2ccc(cc2O)CCCCC
FormulaC17 H20 O2
Name5-PENTYL-2-PHENOXYPHENOL
ChEMBLCHEMBL1224745
DrugBankDB07178
ZINCZINC000014961108
PDB chain4bng Chain E Residue 1257 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB4bng Rational Optimization of Drug-Target Residence Time: Insights from Inhibitor Binding to the S. Aureus Fabi Enzyme-Product Complex.
Resolution2.2 Å
Binding residue
(original residue number in PDB)		A95 Y147 Y157 M160 S197 A198 V201
Binding residue
(residue number reindexed from 1)		A93 Y145 Y155 M158 S195 A196 V199
Annotation score1
Binding affinityMOAD: Ki=0.04nM
Enzymatic activity
Catalytic site (original residue number in PDB) Y147 Y157 M160 K164 K199
Catalytic site (residue number reindexed from 1) Y145 Y155 M158 K162 K197
Enzyme Commision number 1.3.1.39: enoyl-[acyl-carrier-protein] reductase (NADPH, Re-specific).
Gene Ontology
Molecular Function
GO:0000166 nucleotide binding
GO:0004318 enoyl-[acyl-carrier-protein] reductase (NADH) activity
GO:0016491 oxidoreductase activity
GO:0042802 identical protein binding
GO:0141148 enoyl-[acyl-carrier-protein] reductase (NADPH) activity
Biological Process
GO:0006633 fatty acid biosynthetic process

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Molecular Function
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Biological Process
External links
PDB RCSB:4bng, PDBe:4bng, PDBj:4bng
PDBsum4bng
PubMed23697754
UniProtA0A0H3JLH9

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