Structure of PDB 5sci Chain H Binding Site BS02
Receptor Information
>5sci Chain H (length=425) Species:
9606
(Homo sapiens) [
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GTAFFQQQQLPAAMADTFLEHLCLLDIDSEPVAARSTSIIATIGPASRSV
ERLKEMIKAGMNIARLNFSHGSHEYHAESIANVREAVESFAGSPLSYRPV
AIALDTKGPGSGPGLSEQDVRDLRFGVEHGVDIVFASFVRKASDVAAVRA
ALGPEGHGIKIISKIENHEGVKRFDEILEVSDGIMVARGDLGIEIPAEKV
FLAQKMMIGRCNLAGKPVVCATQMLESMITKPRPTRAETSDVANAVLDGA
DCIMLSGETAKGNFPVEAVKMQHAIAREAEAAVYHRQLFEELRRAAPLSR
DPTEVTAIGAVEAAFKCCAAAIIVLTTTGRSAQLLSRYRPRAAVIAVTRS
AQAARQVHLCRGVFPLLYREPPEAIWADDVDRRVQFGIESGKLRGFLRVG
DLVIVVTGWRPGSGYTNIMRVLSIS
Ligand information
Ligand ID
OXL
InChI
InChI=1S/C2H2O4/c3-1(4)2(5)6/h(H,3,4)(H,5,6)/p-2
InChIKey
MUBZPKHOEPUJKR-UHFFFAOYSA-L
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
[O-]C(=O)C([O-])=O
OpenEye OEToolkits 1.5.0
C(=O)(C(=O)[O-])[O-]
Formula
C2 O4
Name
OXALATE ION
ChEMBL
DrugBank
ZINC
PDB chain
5sci Chain H Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
5sci
Anthraquinone derivatives as ADP-competitive inhibitors of liver pyruvate kinase.
Resolution
2.155 Å
Binding residue
(original residue number in PDB)
K282 E284 A305 G307 D308 T340
Binding residue
(residue number reindexed from 1)
K164 E166 A187 G189 D190 T222
Annotation score
2
Enzymatic activity
Enzyme Commision number
2.7.1.40
: pyruvate kinase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0004743
pyruvate kinase activity
GO:0030955
potassium ion binding
Biological Process
GO:0006096
glycolytic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:5sci
,
PDBe:5sci
,
PDBj:5sci
PDBsum
5sci
PubMed
35290845
UniProt
P30613
|KPYR_HUMAN Pyruvate kinase PKLR (Gene Name=PKLR)
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