Adenine phosphoribosyltransferase

APRT
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesAPRT, AMP, APRTD, adenine phosphoribosyltransferase
External IDsOMIM: 102600; MGI: 88061; HomoloGene: 413; GeneCards: APRT; OMA:APRT - orthologs
Orthologs
SpeciesHumanMouse
Entrez

353

11821

Ensembl

ENSG00000198931

ENSMUSG00000006589

UniProt

P07741

P08030

RefSeq (mRNA)

NM_001030018
NM_000485

NM_009698

RefSeq (protein)

NP_000476
NP_001025189

NP_033828

Location (UCSC)Chr 16: 88.81 – 88.81 MbChr 8: 123.3 – 123.3 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Adenine phosphoribosyltransferase (APRTase) is an enzyme encoded by the APRT gene, found in humans on chromosome 16. It is part of the Type I PRTase family and is involved in the nucleotide salvage pathway, which provides an alternative to nucleotide biosynthesis de novo in humans and most other animals. In parasitic protozoa such as giardia, APRTase provides the sole mechanism by which AMP can be produced. APRTase deficiency contributes to the formation of kidney stones (urolithiasis) and to potential kidney failure.