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・ NDUFB1
・ NDUFB10
・ NDUFB11
・ NDUFB2
・ NDUFB3
・ NDUFB4
・ NDUFB5
・ NDUFB6
・ NDUFB7
・ NDUFB8
・ NDUFB9
・ NDUFC1
・ NDUFC2
・ NDUFS1
・ NDUFS2
NDUFS3
・ NDUFS4
・ NDUFS5
・ NDUFS6
・ NDUFS7
・ NDUFS8
・ NDUFV1
・ NDUFV2
・ NDUFV3
・ Nduga language
・ Nduga Regency
・ Ndugumbi
・ Nduguti
・ Nduka Anyanwu
・ Nduka Awazie


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NDUFS3 : ウィキペディア英語版
NDUFS3

NADH dehydrogenase () iron-sulfur protein 3, mitochondrial is an enzyme that in humans is encoded by the ''NDUFS3'' gene on chromosome 11.〔(【引用サイトリンク】 url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4722 )〕 This gene encodes one of the iron-sulfur protein (IP) components of mitochondrial NADH:ubiquinone oxidoreductase (complex I). Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency.〔
== Structure ==

The ''NDUFS3'' gene encodes a protein subunit consisting of 263 amino acids. This protein is synthesized in the cytoplasm and then transported to the mitochondria via a signal peptide. Two mutations that occur in its highly conserved C-terminal region, T145I and R199W, are causally linked to Leigh syndrome and optic atrophy. Nonetheless, despite its crucial biological role, the human NDUFS3 remains structurally poorly understood.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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