TPSB2
Tryptase beta-2
Also known as: TRYB2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P20231
- Gene
- TPSB2
- Ensembl
- ENSG00000197253
- Chromosome
- 16
- Canonical length
- 275 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted secreted proteins
- Secretome location
- Secreted to blood
- Quaternary structure
- Homotetramer
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. These genes are characterized by several distinct features. They have a highly conserved 3' UTR and contain tandem repeat sequences at the 5' flank and 3' UTR which are thought to play a role in regulation of the mRNA stability. These genes have an intron immediately upstream of the initiator Met codon, which separates the site of transcription initiation from protein coding sequence. This feature is characteristic of tryptases but is unusual in other genes. The alleles of this gene exhibit an unusual amount of sequence variation, such that the alleles were once thought to represent two separate genes, beta II and beta III. Beta tryptases appear to be the main isoenzymes expressed in mast cells, whereas in basophils, alpha-tryptases predominate. 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
275 residues, UniProt reviewed canonical sequence.
>P20231|TPSB2
1 MLNLLLLALP VLASRAYAAP APGQALQRVG IVGGQEAPRS KWPWQVSLRV RDRYWMHFCG
61 GSLIHPQWVL TAAHCVGPDV KDLAALRVQL REQHLYYQDQ LLPVSRIIVH PQFYTAQIGA
121 DIALLELEEP VNVSSHVHTV TLPPASETFP PGMPCWVTGW GDVDNDERLP PPFPLKQVKV
181 PIMENHICDA KYHLGAYTGD DVRIVRDDML CAGNTRRDSC QGDSGGPLVC KVNGTWLQAG
241 VVSWGEGCAQ PNRPGIYTRV TYYLDWIHHY VPKKPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TPSB2 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 141 nTPM
Expression across tissuesHPA
Tissue
- small intestine: 141 nTPM
- urinary bladder: 123 nTPM
- lung: 122 nTPM
- skin: 116 nTPM
- stomach: 100 nTPM
- gallbladder: 98 nTPM
Single-cell type
- mast cells: 13,412 nCPM
- pancreatic acinar cells: 27 nCPM
- gastric chief cells: 21 nCPM
- pancreatic islet cells: 14 nCPM
- pancreatic duct cells: 9.2 nCPM
- smooth muscle cells: 7.4 nCPM
Immune cell
- basophil: 5 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- choroid plexus: 1.6 nTPM
- basal ganglia: 0.9 nTPM
- spinal cord: 0.7 nTPM
- hippocampal formation: 0.6 nTPM
- hypothalamus: 0.6 nTPM
- pons: 0.6 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)
- 1.9
- gnomAD pLI
- 0
- gnomAD missense Z
- -2.04
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
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TPSB2 as an antibody target. Whether an autoantibody or antibody against TPSB2 could matter depends on whether native TPSB2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TPSB2 is annotated as secreted, so native TPSB2 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label TPSB2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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