UPRT
Uracil phosphoribosyltransferase homolog
Also known as: DKFZp781E1243, FUR1, MGC23937, RP11-311P8.3, UPP_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96BW1
- Gene
- UPRT
- Ensembl
- ENSG00000094841
- Chromosome
- X
- Canonical length
- 309 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles
OverviewNCBI Gene
This gene encodes uracil phosphoribosyltransferase, which catalyzes the conversion of uracil and 5-phosphoribosyl-1-R-diphosphate to uridine monophosphate (UMP). This reaction is an important part of nucleotide metabolism, specifically the pyrimidine salvage pathway. The enzyme localizes to the nucleus and cytoplasm. The protein is a potential target for rational design of drugs to treat parasitic infections and cancer. [provided by RefSeq, Nov 2009]
Canonical amino-acid sequenceUniProt
309 residues, UniProt reviewed canonical sequence.
>Q96BW1|UPRT
1 MATELQCPDS MPCHNQQVNS ASTPSPEQLR PGDLILDHAG GNRASRAKVI LLTGYAHSSL
61 PAELDSGACG GSSLNSEGNS GSGDSSSYDA PAGNSFLEDC ELSRQIGAQL KLLPMNDQIR
121 ELQTIIRDKT ASRGDFMFSA DRLIRLVVEE GLNQLPYKEC MVTTPTGYKY EGVKFEKGNC
181 GVSIMRSGEA MEQGLRDCCR SIRIGKILIQ SDEETQRAKV YYAKFPPDIY RRKVLLMYPI
241 LSTGNTVIEA VKVLIEHGVQ PSVIILLSLF STPHGAKSII QEFPEITILT TEVHPVAPTH
301 FGQKYFGTDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against UPRT can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.43
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 13 nTPM
- bone marrow: 13 nTPM
- kidney: 11 nTPM
- adrenal gland: 10 nTPM
- duodenum: 10 nTPM
- tongue: 10 nTPM
Single-cell type
- esophageal apical cells: 105 nCPM
- parietal cells: 57 nCPM
- megakaryocytes: 43 nCPM
- choroid plexus epithelial cells: 42 nCPM
- somatotrophs: 40 nCPM
- epicardial cells: 39 nCPM
Immune cell
- non-classical monocyte: 18 nTPM
- NK-cell: 15 nTPM
- T-reg: 14 nTPM
- myeloid DC: 11 nTPM
- intermediate monocyte: 11 nTPM
- naive CD4 T-cell: 9.4 nTPM
Brain region
- midbrain: 12 nTPM
- hypothalamus: 12 nTPM
- choroid plexus: 12 nTPM
- pons: 11 nTPM
- white matter: 11 nTPM
- cerebral cortex: 10 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.56
- gnomAD pLI
- 0.58
- gnomAD missense Z
- 1.45
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of UPRT in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads UPRT as an antibody target. Whether an autoantibody or antibody against UPRT could matter depends on whether native UPRT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
UPRT is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label UPRT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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