5-oxoprolinase, ATP-hydrolysing

Summary
Gene Symbol
  • OPLAH
Aliases
  • 5-Opase
  • OPLA
Organism
Homo sapiens (human)
NCBI Gene
26873
HGNC
8149
PubChem
26873
Alliance of Genome Resources
JoGo
OPLAH
TogoVar
OPLAH
Annotation
Keyword
  • ATP-binding
  • Cytoplasm
  • Hydrolase
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
Proteins
Displaying 1 entry
UniProt Protein Name
O14841
  • 5-oxo-L-prolinase
  • Pyroglutamase
Gene Ontology (GO)
Displaying all 3 entries
GO Term Evidence Code PMID
cytosol
cytosol
cytosol
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
oxoprolinase
Functional Category
  • E: Amino acid transport and metabolism
  • I: Lipid transport and metabolism
  • K: Transcription
  • Q: Secondary metabolites biosynthesis, transport and catabolism
Disease
The Human Phenotype Ontology
Displaying all 8 entries
HPO ID HPO Term
HP:0000006 Autosomal dominant inheritance
HP:0000007 Autosomal recessive inheritance
HP:0002013 Vomiting
HP:0002014 Diarrhea
HP:0002027 Abdominal pain
HP:0003137 Prolinuria
HP:0004387 Enterocolitis
HP:0008672 Calcium oxalate nephrolithiasis
Displaying 1 entry
Disease ID Disease Name
OMIM:260005
  • 5-oxoprolinase deficiency

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026