ITGB1BP1
Integrin beta-1-binding protein 1
Also known as: ICAP-1A, ICAP-1alpha, ICAP-1B, ICAP1, ICAP1A, ICAP1B, ITBP1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O14713
- Gene
- ITGB1BP1
- Ensembl
- ENSG00000119185
- Chromosome
- 2
- Canonical length
- 200 aa
- Protein class
- Predicted intracellular proteins, Transporters
- Subcellular location
- Nucleoplasm,Nuclear bodies,Cytosol
OverviewNCBI Gene
The cytoplasmic domains of integrins are essential for cell adhesion. The protein encoded by this gene binds to the beta1 integrin cytoplasmic domain. The interaction between this protein and beta1 integrin is highly specific. Two isoforms of this protein are derived from alternatively spliced transcripts. The shorter form of this protein does not interact with the beta1 integrin cytoplasmic domain. The longer form is a phosphoprotein and the extent of its phosphorylation is regulated by the cell-matrix interaction, suggesting an important role of this protein during integrin-dependent cell adhesion. Several transcript variants, some protein-coding and some non-protein coding, have been found for this gene. [provided by RefSeq, Jan 2016]
Canonical amino-acid sequenceUniProt
200 residues, UniProt reviewed canonical sequence.
>O14713|ITGB1BP1
1 MFRKGKKRHS SSSSQSSEIS TKSKSVDSSL GGLSRSSTVA SLDTDSTKSS GQSNNNSDTC
61 AEFRIKYVGA IEKLKLSEGK GLEGPLDLIN YIDVAQQDGK LPFVPPEEEF IMGVSKYGIK
121 VSTSDQYDVL HRHALYLIIR MVCYDDGLGA GKSLLALKTT DASNEEYSLW VYQCNSLEQA
181 QAICKVLSTA FDSVLTSEKPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ITGB1BP1 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)
- 0.42
- Highest tissue expression
- 107 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 107 nTPM
- breast: 57 nTPM
- kidney: 50 nTPM
- basal ganglia: 49 nTPM
- cerebral cortex: 44 nTPM
- choroid plexus: 44 nTPM
Single-cell type
- megakaryocytes: 167 nCPM
- adipocytes: 162 nCPM
- decidual stromal cells: 158 nCPM
- hepatic stellate cells: 149 nCPM
- melanocytes: 139 nCPM
- fibro-adipogenic progenitors: 137 nCPM
Immune cell
- basophil: 87 nTPM
- T-reg: 62 nTPM
- myeloid DC: 57 nTPM
- eosinophil: 56 nTPM
- gdT-cell: 55 nTPM
- intermediate monocyte: 54 nTPM
Brain region
- basal ganglia: 93 nTPM
- cerebral cortex: 79 nTPM
- thalamus: 75 nTPM
- white matter: 70 nTPM
- cerebellum: 67 nTPM
- pons: 66 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)
- 1.14
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.71
- DepMap mean gene effect
- 0.02
- 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
- activation of protein kinase B activity
- biomineral tissue development
- blood vessel diameter maintenance
- blood vessel endothelial cell proliferation involved in sprouting angiogenesis
- cell differentiation
- cell migration
- cell-matrix adhesion
- cellular response to fibroblast growth factor stimulus
- cellular response to vascular endothelial growth factor stimulus
- integrin activation
- integrin-mediated signaling pathway
- intracellular signal transduction
- myoblast migration
- negative regulation of cell adhesion involved in substrate-bound cell migration
- negative regulation of cell migration involved in sprouting angiogenesis
- negative regulation of cell population proliferation
- negative regulation of ERK1 and ERK2 cascade
- negative regulation of fibroblast migration
- negative regulation of focal adhesion assembly
- negative regulation of protein binding
- negative regulation of protein kinase activity
- negative regulation of protein targeting to membrane
- negative regulation of substrate adhesion-dependent cell spreading
- Notch signaling pathway
- positive regulation of cell division
- positive regulation of cell population proliferation
- positive regulation of endothelial cell migration
- positive regulation of focal adhesion assembly
- positive regulation of Notch signaling pathway
- positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
- positive regulation of protein targeting to membrane
- positive regulation of stress fiber assembly
- positive regulation of transcription by RNA polymerase II
- protein localization to plasma membrane
- receptor clustering
- regulation of cell adhesion mediated by integrin
- regulation of GTPase activity
- regulation of integrin-mediated signaling pathway
- tube formation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- PTB/PI domain
- Integrin binding protein, ICAP-1
- Beta-1 integrin binding protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ITGB1BP1 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 ITGB1BP1 as an antibody target. Whether an autoantibody or antibody against ITGB1BP1 could matter depends on whether native ITGB1BP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ITGB1BP1 is annotated at the cell surface, where native ITGB1BP1 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 ITGB1BP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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