人支原体基因组分析鉴定推定治疗靶点。

IF 2 Q3 PHARMACOLOGY & PHARMACY Drug Target Insights Pub Date : 2014-12-09 eCollection Date: 2014-01-01 DOI:10.4137/DTI.S19728
Md Masud Parvege, Monzilur Rahman, Mohammad Shahnoor Hossain
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引用次数: 8

摘要

病原菌对抗生素耐药性的倾向日益增加,这就要求开发新的治疗药物来控制这一严重问题。生物信息学、基因组学和蛋白质组学领域的进步通过快速识别新的药物靶点,极大地促进了替代药物的发现。在本研究中,我们采用比较基因组学和代谢途径分析,目的是确定人支原体的治疗靶点。我们的研究揭示了40条注释的代谢途径,其中包括5条独特的人原分枝杆菌代谢途径。我们的研究还鉴定了179种必需蛋白质,其中59种蛋白质与人类蛋白质没有相似性。通过分子量、亚细胞定位、功能分析和蛋白质网络相互作用进一步筛选,我们确定了57种可能的候选药物,可以开发新药。对每个确定的靶点进行药物性分析,优先选择16种适合潜在药物开发的蛋白质。
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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Genome-wide Analysis of Mycoplasma hominis for the Identification of Putative Therapeutic Targets.

Ever increasing propensity of antibiotic resistance among pathogenic bacteria raises the demand for the development of novel therapeutic agents to control this grave problem. Advances in the field of bioinformatics, genomics, and proteomics have greatly facilitated the discovery of alternative drugs by swift identification of new drug targets. In the present study, we employed comparative genomics and metabolic pathway analysis with an aim of identifying therapeutic targets in Mycoplasma hominis. Our study has revealed 40 annotated metabolic pathways, including five unique pathways of M. hominis. Our study also identified 179 essential proteins, including 59 proteins having no similarity with human proteins. Further filtering by molecular weight, subcellular localization, functional analysis, and protein network interaction, we identified 57 putative candidates for which new drugs can be developed. Druggability analysis for each of the identified targets has prioritized 16 proteins as suitable for potential drug development.

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来源期刊
Drug Target Insights
Drug Target Insights PHARMACOLOGY & PHARMACY-
CiteScore
2.70
自引率
0.00%
发文量
5
审稿时长
8 weeks
期刊最新文献
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