Structure of PDB 4bnj Chain H Binding Site BS01
Receptor Information
>4bnj Chain H (length=255) Species:
158879
(Staphylococcus aureus subsp. aureus N315) [
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VNLENKTYVIMGIANKRSIAFGVAKVLDQLGAKLVFTYRKERSRKELEKL
LEQLNQPEAHLYQIDVQSDEEVINGFEQIGKDVGNIDGVYHSIAFANMED
LRGRFSETSREGFLLAQDISSYSLTIVAHEAKKLMPEGGSIVATTYLGGE
FAVQNYNVMGVAKASLEANVKYLALDLGPDNIRVNAISAGPIRTLSAKGV
GGFNTILKEIEERAPLKRNVDQVEVGKTAAYLLSDLSSGVTGENIHVDSG
FHAIK
Ligand information
Ligand ID
MJ5
InChI
InChI=1S/C13H12O2/c1-10-7-8-13(12(14)9-10)15-11-5-3-2-4-6-11/h2-9,14H,1H3
InChIKey
HUPPMDCSGSHZHI-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O(c1ccccc1)c2ccc(cc2O)C
CACTVS 3.370
Cc1ccc(Oc2ccccc2)c(O)c1
OpenEye OEToolkits 1.7.6
Cc1ccc(c(c1)O)Oc2ccccc2
Formula
C13 H12 O2
Name
5-methyl-2-phenoxyphenol
ChEMBL
CHEMBL148755
DrugBank
ZINC
ZINC000013559002
PDB chain
4bnj Chain H Residue 1257 [
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Receptor-Ligand Complex Structure
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PDB
4bnj
Rational Optimization of Drug-Target Residence Time: Insights from Inhibitor Binding to the S. Aureus Fabi Enzyme-Product Complex.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
A95 Y147 Y157 M160 S197 A198 V201
Binding residue
(residue number reindexed from 1)
A94 Y146 Y156 M159 S196 A197 V200
Annotation score
1
Binding affinity
MOAD
: Ki=380pM
Enzymatic activity
Catalytic site (original residue number in PDB)
Y147 Y157 M160 K164 K199
Catalytic site (residue number reindexed from 1)
Y146 Y156 M159 K163 K198
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:4bnj
,
PDBe:4bnj
,
PDBj:4bnj
PDBsum
4bnj
PubMed
23697754
UniProt
A0A0H3JLH9
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