Structure of PDB 4cv0 Chain D Binding Site BS02
Receptor Information
>4cv0 Chain D (length=254) Species:
1280
(Staphylococcus aureus) [
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NLENKTYVIMGIANKRSIAFGVAKVLDQLGAKLVFTYRKERSRKELEKLL
EQLNQPEAHLYQIDVQSDEEVINGFEQIGKDVGNIDGVYHSIAFANMEDL
RGRFSETSREGFLLAQDISSYSLTIVAHEAKKLMPEGGSIVATTYLGGEF
AVQNYNVMGVAKASLEANVKYLALDLGPDNIRVNAISAGPIRTLSAKGVG
GFNTILKEIEERAPLKRNVDQVEVGKTAAYLLSDLSSGVTGENIHVDSGF
HAIK
Ligand information
Ligand ID
PT6
InChI
InChI=1S/C19H20N2O2S/c1-14-15(4-2-6-18(14)20)13-21-9-7-16(12-19(21)22)23-10-8-17-5-3-11-24-17/h2-7,9,11-12H,8,10,13,20H2,1H3
InChIKey
YCLREGRRHGLOAK-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
Cc1c(cccc1N)CN2C=CC(=CC2=O)OCCc3cccs3
ACDLabs 12.01
O=C2C=C(OCCc1sccc1)C=CN2Cc3cccc(N)c3C
CACTVS 3.385
Cc1c(N)cccc1CN2C=CC(=CC2=O)OCCc3sccc3
Formula
C19 H20 N2 O2 S
Name
1-(3-amino-2-methylbenzyl)-4-[2-(thiophen-2-yl)ethoxy]pyridin-2(1H)-one
ChEMBL
CHEMBL488937
DrugBank
DB12347
ZINC
ZINC000016696900
PDB chain
4cv0 Chain D Residue 1258 [
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Receptor-Ligand Complex Structure
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PDB
4cv0
Rational Design of Broad Spectrum Antibacterial Activity Based on a Clinically Relevant Enoyl-Acyl Carrier Protein (Acp) Reductase Inhibitor.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
A95 F96 A97 L102 Y147 Y157 M160 S197 V201 F204
Binding residue
(residue number reindexed from 1)
A93 F94 A95 L100 Y145 Y155 M158 S195 V199 F202
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
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4cv0
,
PDBe:4cv0
,
PDBj:4cv0
PDBsum
4cv0
PubMed
24739388
UniProt
A0A0H3JLH9
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