MGP Database

MGP002379

Ontology/Pathway Information

Entrez Gene ID5471
Gene Namephosphoribosyl pyrophosphate amidotransferase
Gene Symbol PPAT
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005829 TAS:ReactomeCcytosol
GO:0051539 IEA:UniProtKB-KWF4 iron, 4 sulfur cluster binding
GO:0004044 TAS:ProtIncFamidophosphoribosyltransferase activity
GO:0046872 IEA:UniProtKB-KWFmetal ion binding
GO:0035690 IEA:EnsemblPcellular response to drug
GO:0032869 IEA:EnsemblPcellular response to insulin stimulus
GO:0006189 IEA:UniProtKB-UniPathwayP'de novo' IMP biosynthetic process
GO:0000082 IEA:EnsemblPG1/S transition of mitotic cell cycle
GO:0006543 IEA:EnsemblPglutamine catabolic process
GO:0001822 IEA:EnsemblPkidney development
GO:0007595 IEA:EnsemblPlactation
GO:0060135 IEA:EnsemblPmaternal process involved in female pregnancy
GO:0055086 TAS:ReactomePnucleobase-containing small molecule metabolic process
GO:0009116 IEA:InterProPnucleoside metabolic process
GO:0031100 IEA:EnsemblPorgan regeneration
GO:0051289 IEA:EnsemblPprotein homotetramerization
GO:0009113 IEA:InterProPpurine nucleobase biosynthetic process
GO:0006144 TAS:ReactomePpurine nucleobase metabolic process
GO:0006164 TAS:ProtIncPpurine nucleotide biosynthetic process
GO:0009168 TAS:ReactomePpurine ribonucleoside monophosphate biosynthetic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_111217Metabolism
REACT_1698Metabolism of nucleotides
REACT_522Purine metabolism
REACT_1776Purine ribonucleoside monophosphate biosynthesis
SMP Pathway Links
SMP IDDescription
SMP001362-Hydroxyglutric Aciduria (D And L Form)
SMP002434-Hydroxybutyric Aciduria/Succinic Semialdehyde Dehydrogenase Deficiency
SMP00535Adenine phosphoribosyltransferase deficiency (APRT)
SMP00144Adenosine Deaminase Deficiency
SMP00167Adenylosuccinate Lyase Deficiency
SMP00168AICA-Ribosiduria
SMP00427Azathioprine Action Pathway
SMP00072Glutamate Metabolism
SMP00365Gout or Kelley-Seegmiller Syndrome
SMP00385Homocarnosinosis
SMP00339Hyperinsulinism-Hyperammonemia Syndrome
SMP00364Lesch-Nyhan Syndrome (LNS)
SMP00428Mercaptopurine Action Pathway
SMP00609Mercaptopurine Metabolism Pathway
SMP00536Mitochondrial DNA depletion syndrome
SMP00203Molybdenum Cofactor Deficiency
SMP00537Myoadenylate deaminase deficiency
SMP00050Purine Metabolism
SMP00210Purine Nucleoside Phosphorylase Deficiency
SMP00567Succinic semialdehyde dehydrogenase deficiency
SMP00430Thioguanine Action Pathway
SMP00220Xanthine Dehydrogenase Deficiency (Xanthinuria)
SMP00512Xanthinuria type I
SMP00513Xanthinuria type II
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