Structure of PDB 3uic Chain C Binding Site BS02
Receptor Information
>3uic Chain C (length=259) Species:
119856
(Francisella tularensis subsp. tularensis) [
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GFLAGKKILITGLLSNKSIAYGIAKAMHREGAELAFTYVGQFKDRVEKLC
AEFNPAAVLPCDVISDQEIKDLFVELGKVWDGLDAIVHSIAFAPRDQLEG
NFIDCVTREGFSIAHDISAYSFAALAKEGRSMMKNRNASMVALTYIGAEK
AMPSYNTMGVAKASLEATVRYTALALGEDGIKVNAVSAGPIKTLAASGIS
NFKKMLDYNAMVSPLKKNVDIMEVGNTVAFLCSDMATGITGEVVHVDAGY
HCVSMGNVL
Ligand information
Ligand ID
09T
InChI
InChI=1S/C16H14Cl2N2/c1-10-5-15-16(6-11(10)2)20(9-19-15)8-12-3-4-13(17)14(18)7-12/h3-7,9H,8H2,1-2H3
InChIKey
PCJBTWVYIQBUCM-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.2
Cc1cc2c(cc1C)n(cn2)Cc3ccc(c(c3)Cl)Cl
CACTVS 3.370
Cc1cc2ncn(Cc3ccc(Cl)c(Cl)c3)c2cc1C
ACDLabs 12.01
Clc1ccc(cc1Cl)Cn2c3cc(c(cc3nc2)C)C
Formula
C16 H14 Cl2 N2
Name
1-(3,4-dichlorobenzyl)-5,6-dimethyl-1H-benzimidazole
ChEMBL
CHEMBL1945507
DrugBank
ZINC
ZINC000004747684
PDB chain
3uic Chain C Residue 262 [
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Receptor-Ligand Complex Structure
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PDB
3uic
Structural and enzymatic analyses reveal the binding mode of a novel series of Francisella tularensis enoyl reductase (FabI) inhibitors.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
A92 F93 Y146 Y156 A196 I200 F203
Binding residue
(residue number reindexed from 1)
A91 F92 Y145 Y155 A195 I199 F202
Annotation score
1
Binding affinity
BindingDB: Ki=360nM
Enzymatic activity
Catalytic site (original residue number in PDB)
M28 A33 C51 N55 P56 A57 D117 T145 Y156 M159 K163 T194
Catalytic site (residue number reindexed from 1)
M27 A32 C50 N54 P55 A56 D116 T144 Y155 M158 K162 T193
Enzyme Commision number
1.3.1.9
: enoyl-[acyl-carrier-protein] reductase (NADH).
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004318
enoyl-[acyl-carrier-protein] reductase (NADH) activity
GO:0016491
oxidoreductase activity
Biological Process
GO:0006633
fatty acid biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3uic
,
PDBe:3uic
,
PDBj:3uic
PDBsum
3uic
PubMed
22642319
UniProt
Q5NGQ3
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