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挖掘人类基因组中的新型嘌呤能P2Y受体:一种序列分析和分子建模方法。

Mining human genome for novel purinergic P2Y receptors: a sequence analysis and molecular modeling approach.

作者信息

Bhatnagar Sonika, Mishra Shubhi, Pathak Ravi

机构信息

Division of Biotechnology, Netaji Subhas Institute of Technology, New Delhi, India.

出版信息

J Recept Signal Transduct Res. 2011 Feb;31(1):75-84. doi: 10.3109/10799893.2010.529578. Epub 2010 Dec 13.

Abstract

The purinergic P2Y receptors are G-protein coupled receptors (GPCRs) that control many physiological processes by mediating cellular responses to purines, pyrimidines and their analogues. They can be used as potential therapeutic targets in a variety of disease conditions. Therefore, it is critical to identify new members of this family of receptors from the human genome and characterize them for their role in health and disease. In the present work, molecular modeling was carried out for the 21 known P2Y receptors. Binding site analysis was done on the basis of docking and site-directed mutagenesis data. Thus, conserved features of P2Y receptors could be formulated. These features can be used to determine the purinergic nature of potential P2Y receptors in the human genome. We applied this knowledge to human genome GPCR sequences found by sensitive sequence search techniques and identified two orphan receptors, namely GPR34 and GP171 that have all the necessary conserved features of P2Y receptors.

摘要

嘌呤能P2Y受体是G蛋白偶联受体(GPCRs),通过介导细胞对嘌呤、嘧啶及其类似物的反应来控制许多生理过程。它们可作为多种疾病状态下的潜在治疗靶点。因此,从人类基因组中识别该受体家族的新成员并表征它们在健康和疾病中的作用至关重要。在本研究中,对21种已知的P2Y受体进行了分子建模。基于对接和定点诱变数据进行了结合位点分析。由此,可以总结出P2Y受体的保守特征。这些特征可用于确定人类基因组中潜在P2Y受体的嘌呤能性质。我们将这一知识应用于通过灵敏序列搜索技术发现的人类基因组GPCR序列,并鉴定出两个孤儿受体,即GPR34和GP171,它们具有P2Y受体所有必要的保守特征。

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