TAPBP
Tapasin
Also known as: TAPA, TPSN_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O15533
- Gene
- TAPBP
- Ensembl
- ENSG00000231925
- Chromosome
- 6
- Canonical length
- 448 aa
- Protein class
- Disease related genes, Human disease related genes, Plasma proteins, Potential drug targets, Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Nucleoli,Plasma membrane,Mitochondria
OverviewNCBI Gene
This gene encodes a transmembrane glycoprotein which mediates interaction between newly assembled major histocompatibility complex (MHC) class I molecules and the transporter associated with antigen processing (TAP), which is required for the transport of antigenic peptides across the endoplasmic reticulum membrane. This interaction is essential for optimal peptide loading on the MHC class I molecule. Up to four complexes of MHC class I and this protein may be bound to a single TAP molecule. This protein contains a C-terminal double-lysine motif (KKKAE) known to maintain membrane proteins in the endoplasmic reticulum. This gene lies within the major histocompatibility complex on chromosome 6. Alternative splicing results in three transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
448 residues, UniProt reviewed canonical sequence.
>O15533|TAPBP
1 MKSLSLLLAV ALGLATAVSA GPAVIECWFV EDASGKGLAK RPGALLLRQG PGEPPPRPDL
61 DPELYLSVHD PAGALQAAFR RYPRGAPAPH CEMSRFVPLP ASAKWASGLT PAQNCPRALD
121 GAWLMVSISS PVLSLSSLLR PQPEPQQEPV LITMATVVLT VLTHTPAPRV RLGQDALLDL
181 SFAYMPPTSE AASSLAPGPP PFGLEWRRQH LGKGHLLLAA TPGLNGQMPA AQEGAVAFAA
241 WDDDEPWGPW TGNGTFWLPT VQPFQEGTYL ATIHLPYLQG QVTLELAVYK PPKVSLMPAT
301 LARAAPGEAP PELLCLVSHF YPSGGLEVEW ELRGGPGGRS QKAEGQRWLS ALRHHSDGSV
361 SLSGHLQPPP VTTEQHGARY ACRIHHPSLP ASGRSAEVTL EVAGLSGPSL EDSVGLFLSA
421 FLLLGLFKAL GWAAVYLSTC KDSKKKAELocalizationUniProt · AlphaFold · HPA
Whether an antibody against TAPBP 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 68 nTPM
Expression across tissuesHPA
Tissue
- spleen: 68 nTPM
- lung: 49 nTPM
- small intestine: 48 nTPM
- duodenum: 46 nTPM
- adrenal gland: 45 nTPM
- liver: 40 nTPM
Single-cell type
- podocytes: 96 nCPM
- papillary tip epithelial cells: 87 nCPM
- choroid plexus epithelial cells: 58 nCPM
- renal collecting duct principal cells: 56 nCPM
- microglia: 52 nCPM
- ependymal cells: 51 nCPM
Immune cell
- eosinophil: 168 nTPM
- NK-cell: 155 nTPM
- basophil: 149 nTPM
- total PBMC: 141 nTPM
- gdT-cell: 134 nTPM
- non-classical monocyte: 134 nTPM
Brain region
- midbrain: 14 nTPM
- thalamus: 12 nTPM
- choroid plexus: 11 nTPM
- medulla oblongata: 11 nTPM
- basal ganglia: 11 nTPM
- cerebral cortex: 9.5 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TAPBP.
Disease | AllUniProt
Conditions TAPBP is implicated in, by any mechanism.
- MHC class I deficiency 3 (MHC1D3) MIM:620814
Disease | GeneticClinVar
2 pathogenic / likely-pathogenic of 396 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- MHC class I deficiency 3
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)
- 1.18
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.76
- DepMap mean gene effect
- -0.16
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- antigen processing and presentation of endogenous peptide antigen via MHC class I
- antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent
- peptide antigen assembly with MHC class I protein complex
- protein-containing complex assembly
- regulation of gene expression
- regulation of protein complex stability
- retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum
- MHC class Ib protein complex assembly
- peptide antigen stabilization
Molecular functions
- MHC class I protein binding
- MHC class I protein complex binding
- molecular adaptor activity
- peptide antigen binding
- protein folding chaperone
- TAP complex binding
- TAP1 binding
- TAP2 binding
- unfolded protein binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TAPBP 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 TAPBP as an antibody target. Whether an autoantibody or antibody against TAPBP could matter depends on whether native TAPBP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TAPBP 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 TAPBP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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