Entity Details

Primary name C560_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ99643
EntryNameC560_HUMAN
FullNameSuccinate dehydrogenase cytochrome b560 subunit, mitochondrial
TaxID9606
Evidenceevidence at protein level
Length169
SequenceStatuscomplete
DateCreated1999-07-15
DateModified2021-06-02

Ontological Relatives

GenesSDHC

GO terms

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GOName
GO:0000104 succinate dehydrogenase activity
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0005749 mitochondrial respiratory chain complex II, succinate dehydrogenase complex (ubiquinone)
GO:0006099 tricarboxylic acid cycle
GO:0006121 mitochondrial electron transport, succinate to ubiquinone
GO:0009055 electron transfer activity
GO:0009060 aerobic respiration
GO:0016021 integral component of membrane
GO:0020037 heme binding
GO:0046872 metal ion binding

Subcellular Location

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Subcellular Location
Mitochondrion inner membrane

Domains

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DomainNameCategoryType
IPR000701 Succinate dehydrogenase/fumarate reductase type B, transmembrane subunitFamilyFamily
IPR014314 Succinate dehydrogenase, cytochrome b556 subunitFamilyFamily
IPR018495 Succinate dehydrogenase, cytochrome b subunit, conserved siteSiteConserved site
IPR034804 Fumarate reductase/succinate dehydrogenase, transmembrane subunitFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
605373 OMIMParagangliomas 3 (PGL3)A neural crest tumor usually derived from the chromoreceptor tissue of a paraganglion. Paragangliomas can develop at various body sites, including the head, neck, thorax and abdomen. Most commonly, they are located in the head and neck region, specifically at the carotid bifurcation, the jugular foramen, the vagal nerve, and in the middle ear. The disease is caused by variants affecting the gene represented in this entry.
606864 OMIMParaganglioma and gastric stromal sarcoma (PGGSS)Gastrointestinal stromal tumors may be sporadic or inherited in an autosomal dominant manner, alone or as a component of a syndrome associated with other tumors, such as in the context of neurofibromatosis type 1 (NF1). Patients have both gastrointestinal stromal tumors and paragangliomas. Susceptibility to the tumors was inherited in an apparently autosomal dominant manner, with incomplete penetrance. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB00139 Succinic acidDrugbanksmall molecule
DB04141 2-Hexyloxy-6-Hydroxymethyl-Tetrahydro-Pyran-3,4,5-TriolDrugbanksmall molecule
DB08689 Ubiquinone Q1Drugbanksmall molecule