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第二个与gapA基因相似的大肠杆菌基因。

A second Escherichia coli gene with similarity to gapA.

作者信息

Hidalgo E, Limón A, Aguilar J

机构信息

Department of Biochemistry, Faculty of Pharmacy, University of Barcelona, Spain.

出版信息

Microbiologia. 1996 Mar;12(1):99-106.

PMID:9019141
Abstract

An open reading frame has been found downstream of the ald gene at 31 min in the Escherichia coli chromosome and has been designated gapC because of its high similarity with gapA (min 39, encoding glyceraldehyde-3-phosphate dehydrogenase), and with gapB (min 62, a gene with high similarity to gapA, encoding erythrose-4-phosphate dehydrogenase). The gapC gene (min 31) encodes a polypeptide of 204 amino acids, 126 residues shorter than glyceraldehyde-3-phosphate dehydrogenase. In this 204-codon open reading frame several amino acids important for catalysis are conserved. However, the cofactor binding site is lost. The results illustrate a case of a gene, encoding a glycolytic enzyme, for which at least three copies maintaining a certain degree of similarity are apparent in the E. coli genome. It seems likely that the genes encode products with different cellular functions. The origin of these three copies of the gap gene by horizontal transfer or by duplication of an ancestral gene is discussed.

摘要

在大肠杆菌染色体上31分钟处的ald基因下游发现了一个开放阅读框,因其与gapA(39分钟处,编码甘油醛-3-磷酸脱氢酶)以及gapB(62分钟处,与gapA高度相似的基因,编码赤藓糖-4-磷酸脱氢酶)具有高度相似性,故而被命名为gapC。gapC基因(31分钟处)编码一个由204个氨基酸组成的多肽,比甘油醛-3-磷酸脱氢酶少126个残基。在这个204密码子的开放阅读框中,几个对催化作用至关重要的氨基酸是保守的。然而,辅因子结合位点缺失。这些结果说明了一个编码糖酵解酶的基因的情况,在大肠杆菌基因组中至少有三个保持一定程度相似性的拷贝是明显的。似乎这些基因编码具有不同细胞功能的产物。讨论了这三个gap基因拷贝是通过水平转移还是祖先基因的复制产生的。

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