Structure of PDB 1kf6 Chain C Binding Site BS01
Receptor Information
>1kf6 Chain C (length=130) Species:
562
(Escherichia coli) [
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TTKRKPYVRPMTSTWWKKLPFYRFYMLREGTAVPAVWFSIELIFGLFALK
NGPEAWAGFVDFLQNPVIVIINLITLAAALLHTKTWFELAPKAANIIVKD
EKMGPEPIIKSLWAVTVVATIVILFVALYW
Ligand information
Ligand ID
HQO
InChI
InChI=1S/C16H21NO2/c1-2-3-4-5-6-9-13-12-16(18)14-10-7-8-11-15(14)17(13)19/h7-8,10-12,18H,2-6,9H2,1H3
InChIKey
NZPACTGCRWDXCJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
CCCCCCCc1cc(O)c2ccccc2[n+]1[O-]
OpenEye OEToolkits 1.5.0
CCCCCCCc1cc(c2ccccc2[n+]1[O-])O
ACDLabs 10.04
[O-][n+]2c1ccccc1c(O)cc2CCCCCCC
Formula
C16 H21 N O2
Name
2-HEPTYL-4-HYDROXY QUINOLINE N-OXIDE;
2-HEPTYL-1-OXY-QUINOLIN-4-OL
ChEMBL
CHEMBL1233401
DrugBank
DB07918
ZINC
ZINC000001529909
PDB chain
1kf6 Chain C Residue 700 [
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Receptor-Ligand Complex Structure
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PDB
1kf6
Crystallographic studies of the Escherichia coli quinol-fumarate reductase with inhibitors bound to the quinol-binding site.
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
R28 E29
Binding residue
(residue number reindexed from 1)
R28 E29
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=6.70,Ki=0.2uM
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000104
succinate dehydrogenase activity
Biological Process
GO:0006113
fermentation
GO:0009061
anaerobic respiration
GO:0019645
anaerobic electron transport chain
GO:0044780
bacterial-type flagellum assembly
Cellular Component
GO:0005886
plasma membrane
GO:0016020
membrane
GO:0045283
fumarate reductase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1kf6
,
PDBe:1kf6
,
PDBj:1kf6
PDBsum
1kf6
PubMed
11850430
UniProt
P0A8Q0
|FRDC_ECOLI Fumarate reductase subunit C (Gene Name=frdC)
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