ULBP1
UL16-binding protein 1
Also known as: RAET1I, ULBP1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BZM6
- Gene
- ULBP1
- Ensembl
- ENSG00000111981
- Chromosome
- 6
- Canonical length
- 244 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Plasma membrane,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a ligand of natural killer group 2, member D (NKG2D), an immune system-activating receptor on NK cells and T-cells. Binding of the encoded ligand to NKG2D leads to activation of several signal transduction pathways, including those of JAK2, STAT5, ERK and PI3K kinase/Akt. Also, in cytomegalovirus-infected cells, this ligand binds the UL16 glycoprotein and is prevented from activating the immune system. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]
Canonical amino-acid sequenceUniProt
244 residues, UniProt reviewed canonical sequence.
>Q9BZM6|ULBP1
1 MAAAASPAFL LCLPLLHLLS GWSRAGWVDT HCLCYDFIIT PKSRPEPQWC EVQGLVDERP
61 FLHYDCVNHK AKAFASLGKK VNVTKTWEEQ TETLRDVVDF LKGQLLDIQV ENLIPIEPLT
121 LQARMSCEHE AHGHGRGSWQ FLFNGQKFLL FDSNNRKWTA LHPGAKKMTE KWEKNRDVTM
181 FFQKISLGDC KMWLEEFLMY WEQMLDPTKP PSLAPGTTQP KAMATTLSPW SLLIIFLCFI
241 LAGRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ULBP1 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
- 0
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 3.6 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 3.6 nTPM
- testis: 3.2 nTPM
- lung: 1.5 nTPM
- placenta: 0.5 nTPM
- hippocampal formation: 0.4 nTPM
- thyroid gland: 0.4 nTPM
Single-cell type
- ocular epithelial cells: 16 nCPM
- epididymal basal cells: 4.2 nCPM
- cdc: 3.3 nCPM
- esophageal apical cells: 2.9 nCPM
- esophageal suprabasal cells: 2.6 nCPM
- breast secretory cells: 1.9 nCPM
Immune cell
- non-classical monocyte: 0.6 nTPM
- intermediate monocyte: 0.4 nTPM
- memory B-cell: 0.1 nTPM
- neutrophil: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
Brain region
- cerebellum: 10 nTPM
- cerebral cortex: 4.9 nTPM
- hippocampal formation: 4.3 nTPM
- pons: 2.1 nTPM
- midbrain: 1.4 nTPM
- white matter: 1.4 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)
- 1.52
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.22
- DepMap mean gene effect
- 0.05
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% 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 via ER pathway, TAP-independent
- antigen processing and presentation of endogenous peptide antigen via MHC class Ib
- immune response
- natural killer cell activation
- natural killer cell mediated cytotoxicity
- positive regulation of T cell mediated cytotoxicity
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ULBP1 as an antibody target. Whether an autoantibody or antibody against ULBP1 could matter depends on whether native ULBP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ULBP1 is annotated at the cell surface, where native ULBP1 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 ULBP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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