RAP2B
Ras-related protein Rap-2b
Also known as: RAP2B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P61225
- Gene
- RAP2B
- Ensembl
- ENSG00000181467
- Chromosome
- 3
- Canonical length
- 183 aa
- Protein class
- Enzymes, Predicted intracellular proteins
OverviewNCBI Gene
This intronless gene belongs to a family of RAS-related genes. The proteins encoded by these genes share approximately 50% amino acid identity with the classical RAS proteins and have numerous structural features in common. The most striking difference between the RAP and RAS proteins resides in their 61st amino acid: glutamine in RAS is replaced by threonine in RAP proteins. Evidence suggests that this protein may be polyisoprenylated and palmitoylated. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
183 residues, UniProt reviewed canonical sequence.
>P61225|RAP2B
1 MREYKVVVLG SGGVGKSALT VQFVTGSFIE KYDPTIEDFY RKEIEVDSSP SVLEILDTAG
61 TEQFASMRDL YIKNGQGFIL VYSLVNQQSF QDIKPMRDQI IRVKRYERVP MILVGNKVDL
121 EGEREVSYGE GKALAEEWSC PFMETSAKNK ASVDELFAEI VRQMNYAAQP NGDEGCCSAC
181 VILLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RAP2B 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
- 0
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 15 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 15 nTPM
- esophagus: 14 nTPM
- stomach: 8.2 nTPM
- placenta: 8.1 nTPM
- urinary bladder: 7.6 nTPM
- spleen: 7.1 nTPM
Single-cell type
- platelets: 811 nCPM
- epididymal basal cells: 634 nCPM
- ocular epithelial cells: 587 nCPM
- urothelial cells: 398 nCPM
- esophageal apical cells: 382 nCPM
- suprabasal keratinocytes: 227 nCPM
Immune cell
- basophil: 28 nTPM
- intermediate monocyte: 28 nTPM
- non-classical monocyte: 28 nTPM
- gdT-cell: 20 nTPM
- classical monocyte: 18 nTPM
- memory CD8 T-cell: 17 nTPM
Brain region
- hippocampal formation: 28 nTPM
- hypothalamus: 20 nTPM
- cerebral cortex: 18 nTPM
- basal ganglia: 17 nTPM
- white matter: 14 nTPM
- midbrain: 13 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)
- 0.8
- gnomAD pLI
- 0.49
- gnomAD missense Z
- 2.25
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of cell migration
- platelet activation
- platelet aggregation
- Rap protein signal transduction
- regulation of protein tyrosine kinase activity
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RAP2B 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 RAP2B as an antibody target. Whether an autoantibody or antibody against RAP2B could matter depends on whether native RAP2B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RAP2B 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 RAP2B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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