Structure of PDB 4bnn Chain H Binding Site BS01
Receptor Information
>4bnn 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
JUS
InChI
InChI=1S/C19H21NO2/c1-2-3-4-5-8-15-11-12-19(17(21)13-15)22-18-10-7-6-9-16(18)14-20/h6-7,9-13,21H,2-5,8H2,1H3
InChIKey
RPZKERMNVCALKE-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.370
CCCCCCc1ccc(Oc2ccccc2C#N)c(O)c1
OpenEye OEToolkits 1.7.6
CCCCCCc1ccc(c(c1)O)Oc2ccccc2C#N
ACDLabs 12.01
N#Cc2c(Oc1ccc(cc1O)CCCCCC)cccc2
Formula
C19 H21 N O2
Name
2-(2-CYANOPHENOXY)-5-HEXYLPHENOL
ChEMBL
CHEMBL3360252
DrugBank
ZINC
ZINC000095921221
PDB chain
4bnn Chain H Residue 1257 [
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Receptor-Ligand Complex Structure
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PDB
4bnn
Rational Optimization of Drug-Target Residence Time: Insights from Inhibitor Binding to the S. Aureus Fabi Enzyme-Product Complex.
Resolution
2.25 Å
Binding residue
(original residue number in PDB)
A95 Y147 Y157 S197 A198 V201 I207
Binding residue
(residue number reindexed from 1)
A93 Y145 Y155 S195 A196 V199 I205
Annotation score
1
Binding affinity
MOAD
: Ki=120pM
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:4bnn
,
PDBe:4bnn
,
PDBj:4bnn
PDBsum
4bnn
PubMed
23697754
UniProt
A0A0H3JLH9
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