Structure of PDB 2zuq Chain A Binding Site BS01
Receptor Information
>2zuq Chain A (length=148) Species:
83333
(Escherichia coli K-12) [
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QGRGAWLLMAFTALALELTALWFQHVMLLKPSVLCIYERVALFGVLGAAL
IGAIAPKTPLRYVAMVIWLYSAFRGVQLTYEHTMLQLYPSPFATCDFMVL
PLDKWVPQVFVASGDCAERQWDFLGLEMPQWLLGIFIAYLIVAVLVVI
Ligand information
Ligand ID
UQ1
InChI
InChI=1S/C14H18O4/c1-8(2)6-7-10-9(3)11(15)13(17-4)14(18-5)12(10)16/h6H,7H2,1-5H3
InChIKey
SOECUQMRSRVZQQ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
COC1=C(OC)C(=O)C(=C(C)C1=O)CC=C(C)C
OpenEye OEToolkits 1.5.0
CC1=C(C(=O)C(=C(C1=O)OC)OC)CC=C(C)C
ACDLabs 10.04
O=C1C(=C(C(=O)C(OC)=C1OC)C)C\C=C(/C)C
Formula
C14 H18 O4
Name
UBIQUINONE-1
ChEMBL
CHEMBL1236594
DrugBank
DB08689
ZINC
ZINC000001559692
PDB chain
2zuq Chain A Residue 177 [
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Receptor-Ligand Complex Structure
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PDB
2zuq
Dynamic nature of disulphide bond formation catalysts revealed by crystal structures of DsbB
Resolution
3.3 Å
Binding residue
(original residue number in PDB)
A29 P40 S41 C44 M142 L146
Binding residue
(residue number reindexed from 1)
A20 P31 S32 C35 M128 L132
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
S41 C44 R48 C104 C130
Catalytic site (residue number reindexed from 1)
S32 C35 R39 C95 C116
Enzyme Commision number
1.8.5.-
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0009055
electron transfer activity
GO:0015035
protein-disulfide reductase activity
GO:0016491
oxidoreductase activity
GO:0016672
oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor
GO:0048039
ubiquinone binding
Biological Process
GO:0006457
protein folding
GO:0009408
response to heat
Cellular Component
GO:0005886
plasma membrane
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2zuq
,
PDBe:2zuq
,
PDBj:2zuq
PDBsum
2zuq
PubMed
19214188
UniProt
P0A6M2
|DSBB_ECOLI Disulfide bond formation protein B (Gene Name=dsbB)
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