Homo sapiens Protein: CYCS | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-294739.5 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | CYCS | ||||||||||||||||||||||
Protein Name | cytochrome c, somatic | ||||||||||||||||||||||
Synonyms | |||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000387279 | ||||||||||||||||||||||
InnateDB Gene | IDBG-10008 (CYCS) | ||||||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||||||
Function | Electron carrier protein. The oxidized form of the cytochrome c heme group can accept an electron from the heme group of the cytochrome c1 subunit of cytochrome reductase. Cytochrome c then transfers this electron to the cytochrome oxidase complex, the final protein carrier in the mitochondrial electron-transport chain.Plays a role in apoptosis. Suppression of the anti- apoptotic members or activation of the pro-apoptotic members of the Bcl-2 family leads to altered mitochondrial membrane permeability resulting in release of cytochrome c into the cytosol. Binding of cytochrome c to Apaf-1 triggers the activation of caspase-9, which then accelerates apoptosis by activating other caspases. | ||||||||||||||||||||||
Subcellular Localization | Mitochondrion intermembrane space. Note=Loosely associated with the inner membrane. | ||||||||||||||||||||||
Disease Associations | Thrombocytopenia 4 (THC4) [MIM:612004]: Thrombocytopenia is defined by a decrease in the number of platelets in circulating blood, resulting in the potential for increased bleeding and decreased ability for clotting. {ECO:0000269PubMed:18345000}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||||||
Tissue Specificity | |||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 30 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||
InterPro |
IPR002327
Cytochrome c, class IA/ IB IPR003088 Cytochrome c domain IPR009056 Cytochrome c-like domain |
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PFAM |
PF00034
PF13442 |
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PRINTS |
PR00604
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PIRSF | |||||||||||||||||||||||
SMART | |||||||||||||||||||||||
TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | P99999 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-P99999 | ||||||||||||||||||||||
TrEMBL | Q6LER6 | ||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 54205 | ||||||||||||||||||||||
UniGene | Hs.660527 | ||||||||||||||||||||||
RefSeq | |||||||||||||||||||||||
HUGO | HGNC:19986 | ||||||||||||||||||||||
OMIM | 123970 | ||||||||||||||||||||||
CCDS | CCDS5393 | ||||||||||||||||||||||
HPRD | 00479 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AC004129 AC007487 AK311836 AL713681 BC005299 BC008475 BC008477 BC009578 BC009579 BC009582 BC009587 BC009602 BC009607 BC014359 BC014361 BC015130 BC016006 BC021994 BC022330 BC067222 BC068464 BC070156 BC070346 BC071761 BT006946 CH236948 CH471073 D00265 JF919224 M22877 | ||||||||||||||||||||||
GenPept | AAA35732 AAH05299 AAH08475 AAH08477 AAH09578 AAH09579 AAH09582 AAH09587 AAH09602 AAH09607 AAH14359 AAH14361 AAH15130 AAH16006 AAH21994 AAH22330 AAH67222 AAH68464 AAH70156 AAH70346 AAH71761 AAP35592 AAQ96844 AEP27189 BAA00187 BAG34778 CAD28485 EAL24239 EAW93822 EAW93823 EAW93824 | ||||||||||||||||||||||