Structure of PDB 4bnu Chain C Binding Site BS01
Receptor Information
>4bnu Chain C (length=251) Species:
208964
(Pseudomonas aeruginosa PAO1) [
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HHHHHHSSGVNLYFQSMSLQGKVALVTGASRGIGQAIALELGRLGAVVIG
TATSASGAEKIAETLKANGVEGAGLVLDVSSDESVAATLEHIQQHLGQPL
IVVNNAGDEWFDVVNTNLNSLYRLSKAVLRGMTKARWGRIINIGSVVGAM
GNAGQTNYAAAKAGLEGFTRALAREVGSRAITVNAVAPGFIDTDMTRELP
EAQREALLGQIPLGRLGQAEEIAKVVGFLASDGAAYVTGATVPVNGGMYM
S
Ligand information
Ligand ID
9KQ
InChI
InChI=1S/C16H11N5/c1-2-6-12(7-3-1)15-19-14-9-5-4-8-13(14)16(20-15)21-10-17-18-11-21/h1-11H
InChIKey
PNPWQEYBCDBCSQ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.370
OpenEye OEToolkits 1.7.6
c1ccc(cc1)c2nc3ccccc3c(n2)n4cnnc4
ACDLabs 12.01
n1c(nc(c2ccccc12)n3cnnc3)c4ccccc4
Formula
C16 H11 N5
Name
2-phenyl-4-(1,2,4-triazol-4-yl)quinazoline
ChEMBL
CHEMBL3988703
DrugBank
ZINC
ZINC000008726387
PDB chain
4bnu Chain D Residue 1248 [
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Receptor-Ligand Complex Structure
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PDB
4bnu
Discovery of an Allosteric Inhibitor Binding Site in 3-Oxo-Acyl-Acp Reductase from Pseudomonas Aeruginosa
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
V110 L114 G160 G163
Binding residue
(residue number reindexed from 1)
V114 L118 G164 G167
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G16 S141 Y154 K158
Catalytic site (residue number reindexed from 1)
G32 S145 Y158 K162
Enzyme Commision number
1.1.1.100
: 3-oxoacyl-[acyl-carrier-protein] reductase.
Gene Ontology
Molecular Function
GO:0004316
3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0050661
NADP binding
GO:0051287
NAD binding
Biological Process
GO:0006633
fatty acid biosynthetic process
GO:0030497
fatty acid elongation
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Molecular Function
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Biological Process
External links
PDB
RCSB:4bnu
,
PDBe:4bnu
,
PDBj:4bnu
PDBsum
4bnu
PubMed
24015914
UniProt
O54438
|FABG_PSEAE 3-oxoacyl-[acyl-carrier-protein] reductase FabG (Gene Name=fabG)
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