TAPBPL
Tapasin-related protein
Also known as: FLJ10143, TAPBP-R, TAPBPR, TPSNR_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BX59
- Gene
- TAPBPL
- Ensembl
- ENSG00000139192
- Chromosome
- 12
- Canonical length
- 468 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins, Transporters
OverviewNCBI Gene
Tapasin, or TAPBP (MIM 601962), is a member of the variable-constant Ig superfamily that links major histocompatibility complex (MHC) class I molecules to the transporter associated with antigen processing (TAP; see MIM 170260) in the endoplasmic reticulum (ER). The TAPBP gene is located near the MHC complex on chromosome 6p21.3. TAPBPL is a member of the Ig superfamily that is localized on chromosome 12p13.3, a region somewhat paralogous to the MHC.[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
468 residues, UniProt reviewed canonical sequence.
>Q9BX59|TAPBPL
1 MGTQEGWCLL LCLALSGAAE TKPHPAEGQW RAVDVVLDCF LAKDGAHRGA LASSEDRARA
61 SLVLKQVPVL DDGSLEDFTD FQGGTLAQDD PPIIFEASVD LVQIPQAEAL LHADCSGKEV
121 TCEISRYFLQ MTETTVKTAA WFMANMQVSG GGPSISLVMK TPRVTKNEAL WHPTLNLPLS
181 PQGTVRTAVE FQVMTQTQSL SFLLGSSASL DCGFSMAPGL DLISVEWRLQ HKGRGQLVYS
241 WTAGQGQAVR KGATLEPAQL GMARDASLTL PGLTIQDEGT YICQITTSLY RAQQIIQLNI
301 QASPKVRLSL ANEALLPTLI CDIAGYYPLD VVVTWTREEL GGSPAQVSGA SFSSLRQSVA
361 GTYSISSSLT AEPGSAGATY TCQVTHISLE EPLGASTQVV PPERRTALGV IFASSLFLLA
421 LMFLGLQRRQ APTGLGLLQA ERWETTSCAD TQSSHLHEDR TARVSQPSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TAPBPL 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)
- 0.38
- Highest tissue expression
- 32 nTPM
Expression across tissuesHPA
Tissue
- salivary gland: 32 nTPM
- duodenum: 31 nTPM
- small intestine: 26 nTPM
- stomach: 22 nTPM
- gallbladder: 20 nTPM
- colon: 20 nTPM
Single-cell type
- enterocytes: 82 nCPM
- cardiomyocytes: 70 nCPM
- epididymal principal cells: 65 nCPM
- plasma cells: 65 nCPM
- colonocytes: 47 nCPM
- breast lactating cells: 46 nCPM
Immune cell
- basophil: 126 nTPM
- intermediate monocyte: 125 nTPM
- total PBMC: 124 nTPM
- NK-cell: 105 nTPM
- non-classical monocyte: 103 nTPM
- classical monocyte: 103 nTPM
Brain region
- choroid plexus: 14 nTPM
- medulla oblongata: 11 nTPM
- basal ganglia: 9 nTPM
- white matter: 8.8 nTPM
- spinal cord: 8.6 nTPM
- pons: 8.4 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)
- 1.22
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.78
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- peptide antigen assembly with MHC class I protein complex
- negative regulation of antigen processing and presentation of peptide antigen via MHC class I
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Immunoglobulin/major histocompatibility complex, conserved site
- Immunoglobulin C1-set
- Immunoglobulin domain subtype
- Immunoglobulin-like domain
- Immunoglobulin V-set domain
- Immunoglobulin-like fold
- Immunoglobulin-like domain superfamily
- Immune Recognition and Response Modulators
- Immunoglobulin C1-set domain
- Immunoglobulin V-set domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TAPBPL 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 TAPBPL as an antibody target. Whether an autoantibody or antibody against TAPBPL could matter depends on whether native TAPBPL is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TAPBPL is annotated at the cell surface, where native TAPBPL 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 TAPBPL as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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