首页> 美国卫生研究院文献>Biochemical Journal >The 12.3 kDa subunit of complex I (respiratory-chain NADH dehydrogenase) from Neurospora crassa: cDNA cloning and chromosomal mapping of the gene.
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The 12.3 kDa subunit of complex I (respiratory-chain NADH dehydrogenase) from Neurospora crassa: cDNA cloning and chromosomal mapping of the gene.

机译:粗糙神经孢菌的复合体I(呼吸链NADH脱氢酶)的12.3 kDa亚基:该基因的cDNA克隆和染色体作图。

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摘要

The 12.3 kDa subunit of complex I (respiratory-chain NADH dehydrogenase) is a nuclear-coded protein of the hydrophobic fragment of the enzyme. We have isolated and sequenced a full-length cDNA clone coding for this polypeptide. The deduced protein is 104 amino acid residues long with a molecular mass of 12305 Da. This particular subunit of complex I lacks a cleavable mitochondrial targeting sequence. In agreement with its localization within complex I, we have found that this subunit behaves like an intrinsic membrane protein. Nevertheless, the deduced protein is rather hydrophilic, exhibiting no hydrophobic domain long enough to traverse a membrane in an alpha-helical conformation. The 12.3 kDa subunit shows a significant similarity to the hinge protein of complex III, suggesting that these two polypeptides may be involved in identical functions. This complex I subunit is coded for by a single gene. Applying restriction-fragment-length-polymorphism mapping, we located the gene on the right side of the centromere in linkage group I, linked to the lys-4 locus.
机译:复合物I(呼吸链NADH脱氢酶)的12.3 kDa亚基是该酶疏水片段的核编码蛋白。我们已经分离并测序了编码该多肽的全长cDNA克隆。推导的蛋白质长104个氨基酸残基,分子量为12305 Da。复合物I的这个特定亚基缺乏可切割的线粒体靶向序列。与它在复合体I中的定位一致,我们发现该亚基的行为类似于内在的膜蛋白。然而,推导的蛋白质是相当亲水的,没有表现出足够长的疏水结构域以足以以α-螺旋构象穿过膜。 12.3 kDa亚基显示出与复合物III的铰链蛋白的显着相似性,表明这两个多肽可能参与相同的功能。这个复杂的I亚基由单个基因编码。应用限制性片段长度多态性图谱,我们将基因定位在连接组I的着丝粒右侧,与lys-4基因座相连。

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