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・ Ndudi Ebi
・ Nduduzo Makhathini
・ Ndue Marashi
・ Ndue Paluca
・ Ndue Përlleshi
・ Ndue Ukaj
・ Nduese Essien
・ NDUFA10
・ NDUFA11
・ NDUFA12
・ NDUFA13
・ NDUFA2
・ NDUFA3
・ NDUFA4
・ NDUFA4L2
NDUFA5
・ NDUFA6
・ NDUFA7
・ NDUFA8
・ NDUFA9
・ NDUFAB1
・ NDUFAF1
・ NDUFB1
・ NDUFB10
・ NDUFB11
・ NDUFB2
・ NDUFB3
・ NDUFB4
・ NDUFB5
・ NDUFB6


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NDUFA5 : ウィキペディア英語版
NDUFA5

NADH dehydrogenase () 1 alpha subcomplex subunit 5 is an enzyme that in humans is encoded by the ''NDUFA5'' gene.〔(【引用サイトリンク】 url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4698 )〕 The NDUFA5 protein is a subunit of NADH dehydrogenase (ubiquinone), which is located in the mitochondrial inner membrane and is the largest of the five complexes of the electron transport chain.
==Structure==
The NDUFA5 gene is located on the q arm of chromosome 7 and it spans 64,655 base pairs.〔 The gene produces a 13.5 kDa protein composed of 116 amino acids.〔(【引用サイトリンク】 work = Cardiac Organellar Protein Atlas Knowledgebase (COPaKB) )〕 NDUFA5 is a subunit of the enzyme NADH dehydrogenase (ubiquinone), the largest of the respiratory complexes. The structure is L-shaped with a long, hydrophobic transmembrane domain and a hydrophilic domain for the peripheral arm that includes all the known redox centers and the NADH binding site.〔 It has been noted that the N-terminal hydrophobic domain has the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular subunits of Complex I. The highly conserved two-domain structure suggests that this feature is critical for the protein function and that the hydrophobic domain acts as an anchor for the NADH dehydrogenase (ubiquinone) complex at the inner mitochondrial membrane. NDUFA5 is one of about 31 hydrophobic subunits that form the transmembrane region of Complex I. The protein localizes to the inner mitochondrial membrane as part of the 7 component-containing, water-soluble iron-sulfur protein (IP) fraction of complex I, although its specific role is unknown. It is assumed to undergo post-translational removal of the initiator methionine and N-acetylation of the next amino acid. The predicted secondary structure is primarily alpha helix, but the carboxy-terminal half of the protein has high potential to adopt a coiled-coil form. The amino-terminal part contains a putative beta sheet rich in hydrophobic amino acids that may serve as mitochondrial import signal. Related pseudogenes have also been identified on four other chromosomes.〔

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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