Structure of PDB 4bnf Chain H Binding Site BS02
Receptor Information
>4bnf Chain H (length=254) Species:
158879
(Staphylococcus aureus subsp. aureus N315) [
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NLENKTYVIMGIANKRSIAFGVAKVLDQLGAKLVFTYRKERSRKELEKLL
EQLNQPEAHLYQIDVQSDEEVINGFEQIGKDVGNIDGVYHSIAFANMEDL
RGRFSETSREGFLLAQDISSYSLTIVAHEAKKLMPEGGSIVATTYLGGEF
AVQNYNVMGVAKASLEANVKYLALDLGPDNIRVNAISAGPIRTLSAKGVG
GFNTILKEIEERAPLKRNVDQVEVGKTAAYLLSDLSSGVTGENIHVDSGF
HAIK
Ligand information
Ligand ID
PV4
InChI
InChI=1S/C15H16O2/c1-2-6-12-9-10-15(14(16)11-12)17-13-7-4-3-5-8-13/h3-5,7-11,16H,2,6H2,1H3
InChIKey
JOZACDNAOCTHDN-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
CCCc1ccc(Oc2ccccc2)c(O)c1
ACDLabs 12.01
O(c1ccccc1)c2ccc(cc2O)CCC
OpenEye OEToolkits 1.9.2
CCCc1ccc(c(c1)O)Oc2ccccc2
Formula
C15 H16 O2
Name
2-phenoxy-5-propyl-phenol
ChEMBL
DrugBank
ZINC
ZINC000034962079
PDB chain
4bnf Chain H Residue 1258 [
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Receptor-Ligand Complex Structure
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PDB
4bnf
Rational Optimization of Drug-Target Residence Time: Insights from Inhibitor Binding to the S. Aureus Fabi Enzyme-Product Complex.
Resolution
2.3 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 score
1
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:4bnf
,
PDBe:4bnf
,
PDBj:4bnf
PDBsum
4bnf
PubMed
23697754
UniProt
A0A0H3JLH9
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