CBX5
Chromobox protein homolog 5
Also known as: CBX5_HUMAN, HP1, HP1-ALPHA, HP1Hs-alpha
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P45973
- Gene
- CBX5
- Ensembl
- ENSG00000094916
- Chromosome
- 12
- Canonical length
- 191 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a highly conserved nonhistone protein, which is a member of the heterochromatin protein family. The protein is enriched in the heterochromatin and associated with centromeres. The protein has a single N-terminal chromodomain which can bind to histone proteins via methylated lysine residues, and a C-terminal chromo shadow-domain (CSD) which is responsible for the homodimerization and interaction with a number of chromatin-associated nonhistone proteins. The encoded product is involved in the formation of functional kinetochore through interaction with essential kinetochore proteins. The gene has a pseudogene located on chromosome 3. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
191 residues, UniProt reviewed canonical sequence.
>P45973|CBX5
1 MGKKTKRTAD SSSSEDEEEY VVEKVLDRRV VKGQVEYLLK WKGFSEEHNT WEPEKNLDCP
61 ELISEFMKKY KKMKEGENNK PREKSESNKR KSNFSNSADD IKSKKKREQS NDIARGFERG
121 LEPEKIIGAT DSCGDLMFLM KWKDTDEADL VLAKEANVKC PQIVIAFYEE RLTWHAYPED
181 AENKEKETAK SLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CBX5 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.48
- Highest tissue expression
- 112 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 112 nTPM
- thymus: 29 nTPM
- cerebral cortex: 25 nTPM
- parathyroid gland: 24 nTPM
- testis: 24 nTPM
- thyroid gland: 22 nTPM
Single-cell type
- choroid plexus epithelial cells: 511 nCPM
- late primary spermatocytes: 312 nCPM
- megakaryocyte progenitors: 207 nCPM
- corticotrophs: 207 nCPM
- erythrocyte progenitors: 200 nCPM
- early primary spermatocytes: 163 nCPM
Immune cell
- plasmacytoid DC: 22 nTPM
- naive B-cell: 14 nTPM
- memory B-cell: 12 nTPM
- T-reg: 10 nTPM
- myeloid DC: 9.4 nTPM
- non-classical monocyte: 8.2 nTPM
Brain region
- choroid plexus: 275 nTPM
- hypothalamus: 138 nTPM
- white matter: 114 nTPM
- midbrain: 112 nTPM
- spinal cord: 110 nTPM
- thalamus: 109 nTPM
ReferencesPubMed · IEDB
Publications for CBX5 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
1 publication
- Clinical significance of autoantibodies to the pericentromeric heterochromatin protein 1a protein.
2013 · Eur J Intern Med · RCR 0.2 · 4 citations
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
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)
- 0.35
- gnomAD pLI
- 0.93
- gnomAD missense Z
- 2.53
- 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
- chromosome condensation
- DNA damage response
- heterochromatin formation
- heterochromatin organization
- negative regulation of DNA-templated transcription
- negative regulation of transcription by RNA polymerase II
- protein localization to heterochromatin
Molecular functions
- chromatin binding
- DNA-binding transcription factor binding
- histone deacetylase binding
- histone H1K26me1 reader activity
- histone H1K26me2 reader activity
- histone H3K9me2/3 reader activity
- identical protein binding
- protein-containing complex binding
- protein-macromolecule adaptor activity
- ribonucleoprotein complex binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CBX5 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 CBX5 as an antibody target. Whether an autoantibody or antibody against CBX5 could matter depends on whether native CBX5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CBX5 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 CBX5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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