Structure of PDB 2pnq Chain A Binding Site BS02
Receptor Information
>2pnq Chain A (length=382) Species:
10116
(Rattus norvegicus) [
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LTPPQVNSILKANEYSFKVPEFDGKNVSSILGFDSNRLPANAPIEDRRSA
TTCLQTRGMLLGVFDGHAGCACSQAVSERLFYYIAVSLLPHETLLEIENA
VELLPILQWHKHPNDYFSKEASKLYFNGLRTYWQELIDLDIDVKEALINA
FKRLDNDISLEAQVGDPNSFLNYLVLRVAFSGATACVAHVDGVDLHVANT
GDSRAMLGVQEEDGSWSAVTLSNDHNAQNERELQRLKLEHPKNEAKSVVK
QDRLLGLLMPFRAFGDVKFKWSIDLQKRVIESGPDPPNYHTPPYLTAEPE
VTYHRLRPQDKFLVLATDGLWETMHRQDVVRIVGEYLTGMHHQQQNAATH
LIRHAVGYRDDITIIVVQFNSHVVGAYQNQEQ
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
2pnq Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
2pnq
Crystal structure of pyruvate dehydrogenase phosphatase 1 and its functional implications.
Resolution
1.81 Å
Binding residue
(original residue number in PDB)
D73 D347 D445
Binding residue
(residue number reindexed from 1)
D65 D318 D360
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.1.3.43
: [pyruvate dehydrogenase (acetyl-transferring)]-phosphatase.
Gene Ontology
Molecular Function
GO:0004722
protein serine/threonine phosphatase activity
GO:0043169
cation binding
Biological Process
GO:0006470
protein dephosphorylation
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Molecular Function
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Biological Process
External links
PDB
RCSB:2pnq
,
PDBe:2pnq
,
PDBj:2pnq
PDBsum
2pnq
PubMed
17532339
UniProt
O88483
|PDP1_RAT [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial (Gene Name=Pdp1)
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