COPS8
COP9 signalosome complex subunit 8
Also known as: COP9, CSN8, CSN8_HUMAN, MGC1297, SGN8
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99627
- Gene
- COPS8
- Ensembl
- ENSG00000198612
- Chromosome
- 2
- Canonical length
- 209 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is one of the eight subunits of COP9 signalosome, a highly conserved protein complex that functions as an important regulator in multiple signaling pathways. The structure and function of COP9 signalosome is similar to that of the 19S regulatory particle of 26S proteasome. COP9 signalosome has been shown to interact with SCF-type E3 ubiquitin ligases and act as a positive regulator of E3 ubiquitin ligases. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
209 residues, UniProt reviewed canonical sequence.
>Q99627|COPS8
1 MPVAVMAESA FSFKKLLDQC ENQELEAPGG IATPPVYGQL LALYLLHNDM NNARYLWKRI
61 PPAIKSANSE LGGIWSVGQR IWQRDFPGIY TTINAHQWSE TVQPIMEALR DATRRRAFAL
121 VSQAYTSIIA DDFAAFVGLP VEEAVKGILE QGWQADSTTR MVLPRKPVAG ALDVSFNKFI
181 PLSEPAPVPP IPNEQQLARL TDYVAFLENLocalizationUniProt · AlphaFold · HPA
Whether an antibody against COPS8 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)
- 0.36
- Highest tissue expression
- 160 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 160 nTPM
- tongue: 110 nTPM
- retina: 85 nTPM
- heart muscle: 78 nTPM
- cerebral cortex: 69 nTPM
- hypothalamus: 66 nTPM
Single-cell type
- oocytes: 1,110 nCPM
- decidual stromal cells: 201 nCPM
- differentiating spermatogonia: 187 nCPM
- melanocytes: 171 nCPM
- hepatic stellate cells: 129 nCPM
- ovarian stromal cells: 120 nCPM
Immune cell
- NK-cell: 72 nTPM
- MAIT T-cell: 71 nTPM
- T-reg: 71 nTPM
- total PBMC: 71 nTPM
- memory B-cell: 69 nTPM
- memory CD8 T-cell: 66 nTPM
Brain region
- hypothalamus: 100 nTPM
- hippocampal formation: 74 nTPM
- thalamus: 74 nTPM
- cerebral cortex: 73 nTPM
- white matter: 72 nTPM
- pons: 72 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)
- 0.49
- gnomAD pLI
- 0.72
- gnomAD missense Z
- 0.92
- DepMap mean gene effect
- -1.05
- DepMap dependency class
- common
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
- activation of NF-kappaB-inducing kinase activity
- COP9 signalosome assembly
- negative regulation of cell population proliferation
- protein deneddylation
- protein neddylation
- protein phosphorylation
- regulation of protein neddylation
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Proteasome component (PCI) domain
- CSN8/PSMD8/EIF3K
- CSN8/PSMD8/EIF3K family
- COP9 signalosome, subunit CSN8
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of COPS8 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 COPS8 as an antibody target. Whether an autoantibody or antibody against COPS8 could matter depends on whether native COPS8 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
COPS8 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 COPS8 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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