Homo sapiens Protein: NDUFS8 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-61140.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | NDUFS8 | ||||||||||||||||||
Protein Name | NADH dehydrogenase (ubiquinone) Fe-S protein 8, 23kDa (NADH-coenzyme Q reductase) | ||||||||||||||||||
Synonyms | CI-23k; CI23KD; TYKY; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000315774 | ||||||||||||||||||
InnateDB Gene | IDBG-61138 (NDUFS8) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone (By similarity). May donate electrons to ubiquinone. {ECO:0000250}. | ||||||||||||||||||
Subcellular Localization | Mitochondrion {ECO:0000305}. | ||||||||||||||||||
Disease Associations | Leigh syndrome (LS) [MIM:256000]: An early-onset progressive neurodegenerative disorder characterized by the presence of focal, bilateral lesions in one or more areas of the central nervous system including the brainstem, thalamus, basal ganglia, cerebellum and spinal cord. Clinical features depend on which areas of the central nervous system are involved and include subacute onset of psychomotor retardation, hypotonia, ataxia, weakness, vision loss, eye movement abnormalities, seizures, and dysphagia. {ECO:0000269PubMed:9837812}. 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 27 experimentally validated interaction(s) in this database.
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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 |
IPR001450
4Fe-4S binding domain IPR010226 NADH-quinone oxidoreductase, chain I |
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PFAM |
PF00037
PF12797 PF12798 PF12800 PF12801 PF12837 PF12838 |
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PRINTS | |||||||||||||||||||
PIRSF | |||||||||||||||||||
SMART | |||||||||||||||||||
TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | O00217 | ||||||||||||||||||
PhosphoSite | PhosphoSite-O00217 | ||||||||||||||||||
TrEMBL | Q08E91 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 4728 | ||||||||||||||||||
UniGene | Hs.90443 | ||||||||||||||||||
RefSeq | NP_002487 | ||||||||||||||||||
HUGO | HGNC:7715 | ||||||||||||||||||
OMIM | 602141 | ||||||||||||||||||
CCDS | CCDS8176 | ||||||||||||||||||
HPRD | 03683 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AF038406 AK314546 AP002807 BC119753 BC119754 U65579 | ||||||||||||||||||
GenPept | AAB51776 AAC34273 AAI19754 AAI19755 BAG37133 | ||||||||||||||||||