UAP1
UDP-N-acetylhexosamine pyrophosphorylase
Also known as: AgX, AGX1, SPAG2, UAP1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q16222
- Gene
- UAP1
- Ensembl
- ENSG00000117143
- Chromosome
- 1
- Canonical length
- 522 aa
- Protein class
- Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables identical protein binding activity and protein serine pyrophosphorylase activity. Involved in antiviral innate immune response and positive regulation of type I interferon production. Located in nucleoplasm and plasma membrane. Is active in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
522 residues, UniProt reviewed canonical sequence.
>Q16222|UAP1
1 MNINDLKLTL SKAGQEHLLR FWNELEEAQQ VELYAELQAM NFEELNFFFQ KAIEGFNQSS
61 HQKNVDARME PVPREVLGSA TRDQDQLQAW ESEGLFQISQ NKVAVLLLAG GQGTRLGVAY
121 PKGMYDVGLP SRKTLFQIQA ERILKLQQVA EKYYGNKCII PWYIMTSGRT MESTKEFFTK
181 HKYFGLKKEN VIFFQQGMLP AMSFDGKIIL EEKNKVSMAP DGNGGLYRAL AAQNIVEDME
241 QRGIWSIHVY CVDNILVKVA DPRFIGFCIQ KGADCGAKVV EKTNPTEPVG VVCRVDGVYQ
301 VVEYSEISLA TAQKRSSDGR LLFNAGNIAN HFFTVPFLRD VVNVYEPQLQ HHVAQKKIPY
361 VDTQGQLIKP DKPNGIKMEK FVFDIFQFAK KFVVYEVLRE DEFSPLKNAD SQNGKDNPTT
421 ARHALMSLHH CWVLNAGGHF IDENGSRLPA IPRSATNGKS ETITADVNHN LKDANDVPIQ
481 CEISPLISYA GEGLESYVAD KEFHAPLIID ENGVHELVKN GILocalizationUniProt · AlphaFold · HPA
Whether an antibody against UAP1 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)
- 0.25
- Highest tissue expression
- 94 nTPM
Expression across tissuesHPA
Tissue
- liver: 94 nTPM
- adipose tissue: 54 nTPM
- testis: 52 nTPM
- urinary bladder: 43 nTPM
- salivary gland: 42 nTPM
- pancreas: 39 nTPM
Single-cell type
- fibroblasts: 396 nCPM
- late primary spermatocytes: 314 nCPM
- epicardial cells: 307 nCPM
- salivary acinar cells: 303 nCPM
- pancreatic acinar cells: 302 nCPM
- breast lactating cells: 269 nCPM
Immune cell
- MAIT T-cell: 13 nTPM
- memory CD8 T-cell: 11 nTPM
- gdT-cell: 11 nTPM
- naive CD8 T-cell: 7.6 nTPM
- eosinophil: 7.4 nTPM
- naive B-cell: 6.9 nTPM
Brain region
- midbrain: 20 nTPM
- choroid plexus: 18 nTPM
- thalamus: 16 nTPM
- cerebellum: 16 nTPM
- cerebral cortex: 15 nTPM
- hypothalamus: 15 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)
- 0.54
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 1.02
- DepMap mean gene effect
- -0.32
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- antiviral innate immune response
- positive regulation of type I interferon production
- UDP-N-acetylglucosamine biosynthetic process
Molecular functions
- identical protein binding
- UDP-N-acetylglucosamine diphosphorylase activity
- protein serine pyrophosphorylase activity
- UDP-N-acetylgalactosamine diphosphorylase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads UAP1 as an antibody target. Whether an autoantibody or antibody against UAP1 could matter depends on whether native UAP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
UAP1 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 UAP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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