Structure of PDB 4bnl Chain H Binding Site BS02
Receptor Information
>4bnl 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
W1G
InChI
InChI=1S/C15H14O2/c1-2-6-12-9-10-15(14(16)11-12)17-13-7-4-3-5-8-13/h2-5,7-11,16H,1,6H2
InChIKey
DBZGFSBCPYRHRA-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
Oc1cc(CC=C)ccc1Oc2ccccc2
ACDLabs 12.01
O(c1ccccc1)c2ccc(cc2O)C\C=C
OpenEye OEToolkits 1.9.2
C=CCc1ccc(c(c1)O)Oc2ccccc2
Formula
C15 H14 O2
Name
2-PHENOXY-5-(2-PROPENYL)PHENOL
ChEMBL
DrugBank
ZINC
ZINC000095921369
PDB chain
4bnl Chain H Residue 1258 [
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Receptor-Ligand Complex Structure
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PDB
4bnl
Rational Optimization of Drug-Target Residence Time: Insights from Inhibitor Binding to the S. Aureus Fabi Enzyme-Product Complex.
Resolution
2.15 Å
Binding residue
(original residue number in PDB)
L102 Y147 Y157 S197 V201
Binding residue
(residue number reindexed from 1)
L100 Y145 Y155 S195 V199
Annotation score
1
Binding affinity
MOAD
: Ki=110pM
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
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4bnl
,
PDBe:4bnl
,
PDBj:4bnl
PDBsum
4bnl
PubMed
23697754
UniProt
A0A0H3JLH9
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