Structure of PDB 1w85 Chain E Binding Site BS01
Receptor Information
>1w85 Chain E (length=350) Species:
1422
(Geobacillus stearothermophilus) [
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FQFPFAEQLEKVAEQFPTFQILNEEGEVVNEEAMPELSDEQLKELMRRMV
YTRILDQRSISLNRQGRLGFYAPTAGQEASQIASHFALEKEDFILPGYRD
VPQIIWHGLPLYQAFLFSRGHFHGNQIPEGVNVLPPQIIIGAQYIQAAGV
ALGLKMRGKKAVAITYTGDGGTSQGDFYEGINFAGAFKAPAIFVVQNNRK
QTVAKTLAQKAVAAGIPGIQVDGMDPLAVYAAVKAARERAINGEGPTLIE
TLCFRYGPHTMSGDDKELENEWAKKDPLVRFRKFLEAKGLWSEEEENNVI
EQAKEEIKEAIKKADETPKQKVTDLISIMFEELPFNLKEQYEIYKEKESK
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
1w85 Chain E Residue 1368 [
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Receptor-Ligand Complex Structure
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PDB
1w85
A molecular switch and proton wire synchronize the active sites in thiamine enzymes.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D173 N202
Binding residue
(residue number reindexed from 1)
D169 N198
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S65 I142 R267 H271 T272
Catalytic site (residue number reindexed from 1)
S61 I138 R255 H259 T260
Enzyme Commision number
1.2.4.1
: pyruvate dehydrogenase (acetyl-transferring).
Gene Ontology
Molecular Function
GO:0004739
pyruvate dehydrogenase (acetyl-transferring) activity
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0016624
oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor
Biological Process
GO:0009083
branched-chain amino acid catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1w85
,
PDBe:1w85
,
PDBj:1w85
PDBsum
1w85
PubMed
15514159
UniProt
P21873
|ODPA_GEOSE Pyruvate dehydrogenase E1 component subunit alpha (Gene Name=pdhA)
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