CCS
Copper chaperone for superoxide dismutase
Also known as: CCS_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O14618
- Gene
- CCS
- Ensembl
- ENSG00000173992
- Chromosome
- 11
- Canonical length
- 274 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Copper chaperone for superoxide dismutase specifically delivers Cu to copper/zinc superoxide dismutase and may activate copper/zinc superoxide dismutase through direct insertion of the Cu cofactor. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
274 residues, UniProt reviewed canonical sequence.
>O14618|CCS
1 MASDSGNQGT LCTLEFAVQM TCQSCVDAVR KSLQGVAGVQ DVEVHLEDQM VLVHTTLPSQ
61 EVQALLEGTG RQAVLKGMGS GQLQNLGAAV AILGGPGTVQ GVVRFLQLTP ERCLIEGTID
121 GLEPGLHGLH VHQYGDLTNN CNSCGNHFNP DGASHGGPQD SDRHRGDLGN VRADADGRAI
181 FRMEDEQLKV WDVIGRSLII DEGEDDLGRG GHPLSKITGN SGERLACGII ARSAGLFQNP
241 KQICSCDGLT IWEERGRPIA GKGRKESAQP PAHLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCS 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)
- 0.29
- Highest tissue expression
- 90 nTPM
Expression across tissuesHPA
Tissue
- liver: 90 nTPM
- adrenal gland: 45 nTPM
- ovary: 44 nTPM
- colon: 43 nTPM
- choroid plexus: 40 nTPM
- prostate: 39 nTPM
Single-cell type
- platelets: 288 nCPM
- hepatocytes: 194 nCPM
- bergmann glia: 170 nCPM
- rod photoreceptor cells: 112 nCPM
- hofbauer cells: 100 nCPM
- decidual stromal cells: 98 nCPM
Immune cell
- plasmacytoid DC: 84 nTPM
- eosinophil: 60 nTPM
- memory B-cell: 33 nTPM
- myeloid DC: 31 nTPM
- classical monocyte: 27 nTPM
- naive B-cell: 25 nTPM
Brain region
- white matter: 38 nTPM
- cerebellum: 35 nTPM
- cerebral cortex: 35 nTPM
- medulla oblongata: 34 nTPM
- hypothalamus: 32 nTPM
- midbrain: 31 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)
- 1.37
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.4
- DepMap mean gene effect
- -0.21
- 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
Molecular functions
- cadherin binding
- copper ion binding
- protein-disulfide reductase activity
- superoxide dismutase copper chaperone activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Superoxide dismutase, copper/zinc binding domain
- Heavy metal-associated domain, HMA
- Superoxide dismutase, copper/zinc, binding site
- Superoxide dismutase (Cu/Zn) / superoxide dismutase copper chaperone
- Heavy metal-associated domain superfamily
- Superoxide dismutase-like, copper/zinc binding domain superfamily
- Copper/zinc superoxide dismutase (SODC)
- Heavy-metal-associated domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CCS 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 CCS as an antibody target. Whether an autoantibody or antibody against CCS could matter depends on whether native CCS is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCS 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 CCS as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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