CHMP2A
Charged multivesicular body protein 2a
Also known as: BC-2, CHM2A_HUMAN, CHMP2, VPS2, VPS2A
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43633
- Gene
- CHMP2A
- Ensembl
- ENSG00000130724
- Chromosome
- 19
- Canonical length
- 222 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane,Cytosol
OverviewNCBI Gene
CHMP2A belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
222 residues, UniProt reviewed canonical sequence.
>O43633|CHMP2A
1 MDLLFGRRKT PEELLRQNQR ALNRAMRELD RERQKLETQE KKIIADIKKM AKQGQMDAVR
61 IMAKDLVRTR RYVRKFVLMR ANIQAVSLKI QTLKSNNSMA QAMKGVTKAM GTMNRQLKLP
121 QIQKIMMEFE RQAEIMDMKE EMMNDAIDDA MGDEEDEEES DAVVSQVLDE LGLSLTDELS
181 NLPSTGGSLS VAAGGKKAEA AASALADADA DLEERLKNLR RDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CHMP2A 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)
- 0.47
- Highest tissue expression
- 213 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 213 nTPM
- adrenal gland: 176 nTPM
- choroid plexus: 175 nTPM
- heart muscle: 172 nTPM
- basal ganglia: 164 nTPM
- kidney: 164 nTPM
Single-cell type
- esophageal apical cells: 1,199 nCPM
- syncytiotrophoblasts: 612 nCPM
- esophageal suprabasal cells: 602 nCPM
- enterocytes: 550 nCPM
- colonocytes: 496 nCPM
- extravillous trophoblasts: 401 nCPM
Immune cell
- neutrophil: 799 nTPM
- eosinophil: 346 nTPM
- basophil: 276 nTPM
- classical monocyte: 245 nTPM
- non-classical monocyte: 243 nTPM
- intermediate monocyte: 231 nTPM
Brain region
- white matter: 89 nTPM
- medulla oblongata: 86 nTPM
- cerebellum: 84 nTPM
- cerebral cortex: 84 nTPM
- spinal cord: 79 nTPM
- thalamus: 78 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CHMP2A.
Disease | ImmuneIEDB
Conditions an epitope on CHMP2A was assayed in.
- rheumatoid arthritis B cell
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
- 0.13
- gnomAD missense Z
- 0.9
- DepMap mean gene effect
- -1.84
- DepMap dependency class
- pan
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
- autophagosome maturation
- autophagy
- endosome transport via multivesicular body sorting pathway
- ESCRT III complex disassembly
- establishment of protein localization
- exit from mitosis
- late endosome to lysosome transport
- late endosome to vacuole transport
- macroautophagy
- membrane fission
- membrane invagination
- midbody abscission
- mitotic metaphase chromosome alignment
- multivesicular body assembly
- multivesicular body sorting pathway
- multivesicular body-lysosome fusion
- negative regulation of centriole elongation
- nuclear membrane reassembly
- nucleus organization
- plasma membrane repair
- positive regulation of exosomal secretion
- protein homooligomerization
- protein polymerization
- protein transport
- regulation of centrosome duplication
- regulation of mitotic spindle assembly
- ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway
- vesicle fusion with vacuole
- viral budding from plasma membrane
- viral budding via host ESCRT complex
- viral release from host cell
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CHMP2A 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 CHMP2A as an antibody target. Whether an autoantibody or antibody against CHMP2A could matter depends on whether native CHMP2A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CHMP2A 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 CHMP2A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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