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大肠杆菌谷氨酰胺-tRNA合成酶:单个氨基酸替换可放宽对rRNA的特异性。

Escherichia coli glutaminyl-tRNA synthetase: a single amino acid replacement relaxes rRNA specificity.

作者信息

Uemura H, Conley J, Yamao F, Rogers J, Söll D

机构信息

Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06511.

出版信息

Protein Seq Data Anal. 1988;1(6):479-85.

PMID:2464170
Abstract

We described previously the isolation, by genetic selection, of a mutant of Escherichia coli glutaminyl-tRNA synthetase that misaminoacylates supFtRNATyr with glutamine. The single amino acid change responsible for the mischarging phenotype was identified at amino acid 235 in the translated glnS gene. The mutant, called glnS7, has an Asp----Asn change, and studies with the purified glnS7 gene product show it may mischarge a number of presumably different tRNAs. We have carried out extensive homology searches that show E. coli glutaminyl-tRNA synthetase shares regions of homology with other aminoacyl-tRNA synthetases, although little apparent similarity at the site of the glnS7 mutation. In addition to the conserved 'HIGH' motif implicated in aminoacyl adenylate formation, there are regions of homology of glutaminyl-tRNA synthetase with other synthetases which may be involved in tRNA binding. These include short stretches of homology in sequences acting as a tRNA 'anchor' as well as homology of some aminoacyl-tRNA synthetases to a recently identified motif in ribonucleoproteins. Therefore, our results show that E. coli glutaminyl-tRNA synthetase may share with other aminoacyl-tRNA synthetases regions responsible for tRNA binding, while other regions of the protein, of which the glnS7 mutation may be a component, are responsible for tRNA discrimination.

摘要

我们先前描述了通过基因筛选分离出的大肠杆菌谷氨酰胺-tRNA合成酶突变体,该突变体用谷氨酰胺错误地对supFtRNATyr进行氨基酰化。导致错误充电表型的单个氨基酸变化在翻译后的glnS基因的第235位氨基酸处被鉴定出来。该突变体称为glnS7,发生了天冬氨酸(Asp)到天冬酰胺(Asn)的变化,对纯化的glnS7基因产物的研究表明它可能会错误地对许多可能不同的tRNA进行氨基酰化。我们进行了广泛的同源性搜索,结果表明大肠杆菌谷氨酰胺-tRNA合成酶与其他氨基酰-tRNA合成酶存在同源区域,尽管在glnS7突变位点几乎没有明显的相似性。除了与氨基酰腺苷酸形成有关的保守“HIGH”基序外,谷氨酰胺-tRNA合成酶与其他合成酶的同源区域可能参与tRNA结合。这些区域包括作为tRNA“锚定”序列的短同源片段,以及一些氨基酰-tRNA合成酶与核糖核蛋白中最近鉴定的基序的同源性。因此,我们的结果表明,大肠杆菌谷氨酰胺-tRNA合成酶可能与其他氨基酰-tRNA合成酶共享负责tRNA结合的区域,而蛋白质的其他区域(glnS7突变可能是其中一部分)则负责tRNA识别。

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