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人泛醇 - 细胞色素c还原酶核心I蛋白基因的完整编码序列、内含子/外显子组织及染色体定位。

Complete coding sequence, intron/exon organization, and chromosomal location of the gene for the core I protein of human ubiquinol-cytochrome c reductase.

作者信息

Hoffman G G, Lee S, Christiano A M, Chung-Honet L C, Cheng W, Katchman S, Uitto J, Greenspan D S

机构信息

Department of Pathology and Laboratory Medicine, University of Wisconsin, Madison 53706.

出版信息

J Biol Chem. 1993 Oct 5;268(28):21113-9.

PMID:8407948
Abstract

Core I protein is a nuclear-encoded component of the ubiquinol-cytochrome c reductase complex of the mitochondrial respiratory chain. We have located the gene for the human core I protein in the p21 region of chromosome 3, just upstream of the COL7A1 gene which encodes type VII collagen. The core I gene, which has been sequenced in its entirety, is comprised of 10,417 base pairs, from the major transcription start site to the polyadenylation signal, and contains 13 exons. The predicted polypeptide contains 480 amino acids, of which the first 34 are predicted to constitute a typical mitochondrial leader peptide containing 6 positively charged arginine residues. The predicted human protein shows significant homology with core I protein from Saccharomyces cerevisiae, rather high homology (64% similarity, 46% identity) with the processing enhancing protein, which functions as core I protein in Neurospora crassa, and, surprisingly, highest homology with the small subunit of the mitochondrial processing peptidase of rat (74% similarity, 55% identity). The predicted human sequence is 87% identical to the reported bovine core I sequence predicted from cDNA cloning, up to residue 298, but the two predicted sequences are widely divergent after that point.

摘要

核心I蛋白是线粒体呼吸链泛醇-细胞色素c还原酶复合体的一种核编码成分。我们已将人类核心I蛋白的基因定位在3号染色体的p21区域,就在编码VII型胶原的COL7A1基因的上游。已对核心I基因进行了全序列测定,它从主要转录起始位点到多聚腺苷酸化信号由10,417个碱基对组成,包含13个外显子。预测的多肽含有480个氨基酸,其中前34个预计构成一个典型的线粒体前导肽,含有6个带正电荷的精氨酸残基。预测的人类蛋白与酿酒酵母的核心I蛋白有显著同源性,与粗糙脉孢菌中起核心I蛋白作用的加工增强蛋白有相当高的同源性(64%相似性,46%同一性),而且令人惊讶的是,与大鼠线粒体加工肽酶的小亚基有最高的同源性(74%相似性,55%同一性)。预测的人类序列与从cDNA克隆预测的已报道牛核心I序列在第298位残基之前有87%的同一性,但在该位点之后,这两个预测序列有很大差异。

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