PAPSS1
Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1
Also known as: ATPSK1, PAPS1_HUMAN, PAPSS
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43252
- Gene
- PAPSS1
- Ensembl
- ENSG00000138801
- Chromosome
- 4
- Canonical length
- 624 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli rim,Mitotic chromosome
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Three-prime-phosphoadenosine 5-prime-phosphosulfate (PAPS) is the sulfate donor cosubstrate for all sulfotransferase (SULT) enzymes (Xu et al., 2000 [PubMed 10679223]). SULTs catalyze the sulfate conjugation of many endogenous and exogenous compounds, including drugs and other xenobiotics. In humans, PAPS is synthesized from adenosine 5-prime triphosphate (ATP) and inorganic sulfate by 2 isoforms, PAPSS1 and PAPSS2 (MIM 603005).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
624 residues, UniProt reviewed canonical sequence.
>O43252|PAPSS1
1 MEIPGSLCKK VKLSNNAQNW GMQRATNVTY QAHHVSRNKR GQVVGTRGGF RGCTVWLTGL
61 SGAGKTTVSM ALEEYLVCHG IPCYTLDGDN IRQGLNKNLG FSPEDREENV RRIAEVAKLF
121 ADAGLVCITS FISPYTQDRN NARQIHEGAS LPFFEVFVDA PLHVCEQRDV KGLYKKARAG
181 EIKGFTGIDS EYEKPEAPEL VLKTDSCDVN DCVQQVVELL QERDIVPVDA SYEVKELYVP
241 ENKLHLAKTD AETLPALKIN KVDMQWVQVL AEGWATPLNG FMREREYLQC LHFDCLLDGG
301 VINLSVPIVL TATHEDKERL DGCTAFALMY EGRRVAILRN PEFFEHRKEE RCARQWGTTC
361 KNHPYIKMVM EQGDWLIGGD LQVLDRVYWN DGLDQYRLTP TELKQKFKDM NADAVFAFQL
421 RNPVHNGHAL LMQDTHKQLL ERGYRRPVLL LHPLGGWTKD DDVPLMWRMK QHAAVLEEGV
481 LNPETTVVAI FPSPMMYAGP TEVQWHCRAR MVAGANFYIV GRDPAGMPHP ETGKDLYEPS
541 HGAKVLTMAP GLITLEIVPF RVAAYNKKKK RMDYYDSEHH EDFEFISGTR MRKLAREGQK
601 PPEGFMAPKA WTVLTEYYKS LEKALocalizationUniProt · AlphaFold · HPA
Whether an antibody against PAPSS1 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)
- 0.26
- Highest tissue expression
- 108 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 108 nTPM
- salivary gland: 62 nTPM
- stomach: 59 nTPM
- hippocampal formation: 50 nTPM
- midbrain: 49 nTPM
- tonsil: 48 nTPM
Single-cell type
- endometrial glandular cells: 944 nCPM
- endometrial luminal cells: 388 nCPM
- mucous neck cells: 310 nCPM
- neutrophils: 261 nCPM
- gastric chief cells: 249 nCPM
- megakaryocytes: 247 nCPM
Immune cell
- eosinophil: 361 nTPM
- basophil: 323 nTPM
- non-classical monocyte: 61 nTPM
- intermediate monocyte: 56 nTPM
- neutrophil: 56 nTPM
- myeloid DC: 51 nTPM
Brain region
- white matter: 103 nTPM
- medulla oblongata: 76 nTPM
- spinal cord: 72 nTPM
- cerebellum: 62 nTPM
- pons: 58 nTPM
- basal ganglia: 55 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)
- 0.79
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.74
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
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
- 3'-phosphoadenosine 5'-phosphosulfate biosynthetic process
- skeletal system development
- sulfate assimilation
Molecular functions
- adenylylsulfate kinase activity
- ATP binding
- nucleotidyltransferase activity
- protein homodimerization activity
- sulfate adenylyltransferase (ATP) activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PAPSS1 as an antibody target. Whether an autoantibody or antibody against PAPSS1 could matter depends on whether native PAPSS1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PAPSS1 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 PAPSS1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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