MGP Database

MGP002303

Ontology/Pathway Information

Entrez Gene ID5313
Gene Namepyruvate kinase, liver and RBC
Gene Symbol PKLR
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005829 TAS:ReactomeCcytosol
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0005524 IEA:UniProtKB-KWFATP binding
GO:0000287 IEA:InterProFmagnesium ion binding
GO:0030955 IEA:InterProFpotassium ion binding
GO:0004743 NAS:UniProtKBFpyruvate kinase activity
GO:0006754 IEA:EnsemblPATP biosynthetic process
GO:0005975 TAS:ReactomePcarbohydrate metabolic process
GO:0032869 IEA:EnsemblPcellular response to insulin stimulus
GO:0031018 TAS:ReactomePendocrine pancreas development
GO:0006112 TAS:ReactomePenergy reserve metabolic process
GO:0006006 TAS:ReactomePglucose metabolic process
GO:0006096 TAS:ReactomePglycolytic process
GO:0031325 TAS:ReactomePpositive regulation of cellular metabolic process
GO:0042866 IEA:EnsemblPpyruvate biosynthetic process
GO:0033198 IEA:EnsemblPresponse to ATP
GO:0051591 IEA:EnsemblPresponse to cAMP
GO:0009749 IEA:EnsemblPresponse to glucose
GO:0009408 IEA:EnsemblPresponse to heat
GO:0001666 IEA:EnsemblPresponse to hypoxia
GO:0010226 IEA:EnsemblPresponse to lithium ion
GO:0007584 IEA:EnsemblPresponse to nutrient
GO:0051707 IEA:EnsemblPresponse to other organism
GO:0044281 TAS:ReactomePsmall molecule metabolic process
SMP Pathway Links
SMP IDDescription
SMP00572Fanconi-bickel syndrome
SMP00531Glycogenosis, Type VII. Tarui disease
SMP00040Glycolysis
SMP00196Leigh Syndrome
SMP00558Primary hyperoxaluria II, PH2
SMP00334Pyruvate Decarboxylase E1 Component Deficiency (PDHE1 Deficiency)
SMP00212Pyruvate Dehydrogenase Complex Deficiency
SMP00559Pyruvate kinase deficiency
SMP00060Pyruvate Metabolism
SMP00654Warburg Effect
  logo