TPSG1
Tryptase gamma
Also known as: PRSS31, TMT, TRYG1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NRR2
- Gene
- TPSG1
- Ensembl
- ENSG00000116176
- Chromosome
- 16
- Canonical length
- 321 aa
- Protein class
- Enzymes, Predicted membrane proteins
OverviewNCBI Gene
Tryptases comprise a family of trypsin-like serine proteases, the peptidase family S1. Tryptases are enzymatically active only as heparin-stabilized tetramers, and they are resistant to all known endogenous proteinase inhibitors. Several tryptase genes are clustered on chromosome 16p13.3. There is uncertainty regarding the number of genes in this cluster. Currently four functional genes - alpha I, beta I, beta II and gamma I - have been identified. And beta I has an allelic variant named alpha II, beta II has an allelic variant beta III, also gamma I has an allelic variant gamma II. Beta tryptases appear to be the main isoenzymes expressed in mast cells; whereas in basophils, alpha-tryptases predominant. This gene differs from other members of the tryptase gene family in that it has C-terminal hydrophobic domain, which may serve as a membrane anchor. Tryptases have been implicated as mediators in the pathogenesis of asthma and other allergic and inflammatory disorders. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
321 residues, UniProt reviewed canonical sequence.
>Q9NRR2|TPSG1
1 MALGACGLLL LLAVPGVSLR TLQPGCGRPQ VSDAGGRIVG GHAAPAGAWP WQASLRLRRV
61 HVCGGSLLSP QWVLTAAHCF SGSLNSSDYQ VHLGELEITL SPHFSTVRQI ILHSSPSGQP
121 GTSGDIALVE LSVPVTLSSR ILPVCLPEAS DDFCPGIRCW VTGWGYTREG EPLPPPYSLR
181 EVKVSVVDTE TCRRDYPGPG GSILQPDMLC ARGPGDACQD DSGGPLVCQV NGAWVQAGTV
241 SWGEGCGRPN RPGVYTRVPA YVNWIRRHIT ASGGSESGYP RLPLLAGFFL PGLFLLLVSC
301 VLLAKCLLHP SADGTPFPAP DLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TPSG1 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.35
- Highest tissue expression
- 14 nTPM
Expression across tissuesHPA
Tissue
- colon: 14 nTPM
- duodenum: 13 nTPM
- small intestine: 8.7 nTPM
- rectum: 8.3 nTPM
- pituitary gland: 2.9 nTPM
- breast: 2.8 nTPM
Single-cell type
- goblet cells: 269 nCPM
- mast cells: 32 nCPM
- colonocytes: 3.7 nCPM
- vascular smooth muscle cells: 2.5 nCPM
- enteric transient amplifying cells: 2.3 nCPM
- epicardial cells: 2.3 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- basal ganglia: 3.7 nTPM
- hypothalamus: 1.4 nTPM
- amygdala: 1.2 nTPM
- cerebral cortex: 0.9 nTPM
- pons: 0.9 nTPM
- thalamus: 0.9 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)
- 1.97
- gnomAD pLI
- 0
- gnomAD missense Z
- -2.45
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TPSG1 as an antibody target. Whether an autoantibody or antibody against TPSG1 could matter depends on whether native TPSG1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TPSG1 is annotated at the cell surface, where native TPSG1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label TPSG1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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