Structure of PDB 3dva Chain A Binding Site BS01
Receptor Information
>3dva Chain A (length=365) Species:
1422
(Geobacillus stearothermophilus) [
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TFQFPFAEQLEKVAEQFPTFQILNEEGEVVNEEAMPELSDEQLKELMRRM
VYTRILDQRSISLNRQGRLGFYAPTAGQEASQIASHFALEKEDFILPGYR
DVPQIIWHGLPLYQAFLFSRGHFHGNQIPEGVNVLPPQIIIGAQYIQAAG
VALGLKMRGKKAVAITYTGDGGTSQGDFYEGINFAGAFKAPAIFVVQNNR
FAASTPVEKQTVAKTLAQKAVAAGIPGIQVDGMDPLAVYAAVKAARERAI
NGEGPTLIETLCFRYGPHTMSGDDPTRYRSKELENEWAKKDPLVRFRKFL
EAKGLWSEEEENNVIEQAKEEIKEAIKKADETPKQKVTDLISIMFEELPF
NLKEQYEIYKEKESK
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
3dva Chain A Residue 1368 [
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Receptor-Ligand Complex Structure
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PDB
3dva
Snapshots of catalysis in the e1 subunit of the pyruvate dehydrogenase multienzyme complex
Resolution
2.35 Å
Binding residue
(original residue number in PDB)
D173 N202 F204
Binding residue
(residue number reindexed from 1)
D170 N199 F201
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S65 I142 R267 H271 T272 Y281
Catalytic site (residue number reindexed from 1)
S62 I139 R264 H268 T269 Y278
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
View graph for
Biological Process
External links
PDB
RCSB:3dva
,
PDBe:3dva
,
PDBj:3dva
PDBsum
3dva
PubMed
19081062
UniProt
P21873
|ODPA_GEOSE Pyruvate dehydrogenase E1 component subunit alpha (Gene Name=pdhA)
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