Significant Aspect of Rv0378 Gene of Mycobacterium tuberculosis H37Rv Reveals the PE_PGRS like Properties by Computational Approaches

Beg Ma, Athar F, Meena Ls
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引用次数: 8

Abstract

Rv0378 is a conserved hypothetical gene of Mycobacterium tuberculosis H37Rv (M. tuberculosis H37Rv). This gene has been predicted to possess some PE_PGRS like characteristics. M. tuberculosis H37Rv contains a group of PE_PGRS qualities, with various identified motifs, encoding firmly related proteins that are outstandingly rich in glycine and alanine. These genes are predicted to be one of the key regulators for the pathogenic mechanism of this bacterium by the evidence of their absence in other a virulent strain. This manuscript noted some of the most valuable aspects about hypothetical protein Rv0378 being function as a PE_PGRS protein. The major insights of this study include interaction study, modelling by using I-TASSER, validation of the model by RAMPAGE analysis and prediction of metal binding sites by using Insilico approaches. The study shows that this gene is majorly a coiled structure with very short lengths and had a similarity with other already confirmed PE_PGRS proteins. The structure is validated by the bioinformatics approach. Interaction study by STRING shows that this protein interacts with its neighboring partner and secE2 protein which is a transporter protein. Prediction of ligand binding site confirms that this gene binds with calcium and magnesium with very high affinity which focus our step ahead in the direction of this gene as PE_PGRS protein and essential for pathogenesis. This study will be helpful in the experimental design to work in this field and if found correct as predicted, thus this work might be helpful in the direction of the treatment of this disease.
结核分枝杆菌H37Rv Rv0378基因的重要特征用计算方法揭示PE_PGRS样特性
Rv0378是结核分枝杆菌H37Rv (M. tuberculosis H37Rv)的保守假设基因。据预测,该基因具有一些类似PE_PGRS的特征。结核分枝杆菌H37Rv含有一组PE_PGRS特性,具有各种已识别的基序,编码具有丰富甘氨酸和丙氨酸的紧密相关蛋白。这些基因在其他毒力菌株中缺失的证据被预测为该细菌致病机制的关键调节因子之一。本文指出了假设蛋白Rv0378作为PE_PGRS蛋白的一些最有价值的方面。本研究的主要见解包括相互作用研究,使用I-TASSER建模,通过RAMPAGE分析验证模型以及使用Insilico方法预测金属结合位点。研究表明,该基因主要为卷曲结构,长度很短,与其他已证实的PE_PGRS蛋白具有相似性。该结构通过生物信息学方法进行了验证。STRING的相互作用研究表明,该蛋白与邻近的伴侣蛋白和转运蛋白secE2蛋白相互作用。配体结合位点的预测证实了该基因与钙、镁的结合具有非常高的亲和力,这使我们朝着该基因作为PE_PGRS蛋白和发病机制所必需的方向迈进了一步。本研究对该领域的实验设计工作有一定的帮助,如果实验结果如预测的那样正确,本研究可能对该疾病的治疗方向有一定的帮助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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