دورية أكاديمية

Structure Based Virtual Screening Studies to Identify Novel Potential Compounds for GPR142 and Their Relative Dynamic Analysis for Study of Type 2 Diabetes

التفاصيل البيبلوغرافية
العنوان: Structure Based Virtual Screening Studies to Identify Novel Potential Compounds for GPR142 and Their Relative Dynamic Analysis for Study of Type 2 Diabetes
المؤلفون: Aman C. Kaushik, Sanjay Kumar, Dong Q. Wei, Shakti Sahi
المصدر: Frontiers in Chemistry, Vol 6 (2018)
بيانات النشر: Frontiers Media S.A., 2018.
سنة النشر: 2018
المجموعة: LCC:Chemistry
مصطلحات موضوعية: GPR142, virtual screening, pharmacophore hypothesis, VSW, IFD, systems biology, Chemistry, QD1-999
الوصف: GPR142 (G protein receptor 142) is a novel orphan GPCR (G protein coupled receptor) belonging to “Class A” of GPCR family and expressed in β cells of pancreas. In this study, we reported the structure based virtual screening to identify the hit compounds which can be developed as leads for potential agonists. The results were validated through induced fit docking, pharmacophore modeling, and system biology approaches. Since, there is no solved crystal structure of GPR142, we attempted to predict the 3D structure followed by validation and then identification of active site using threading and ab initio methods. Also, structure based virtual screening was performed against a total of 1171519 compounds from different libraries and only top 20 best hit compounds were screened and analyzed. Moreover, the biochemical pathway of GPR142 complex with screened compound2 was also designed and compared with experimental data. Interestingly, compound2 showed an increase in insulin production via Gq mediated signaling pathway suggesting the possible role of novel GPR142 agonists in therapy against type 2 diabetes.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2296-2646
Relation: http://journal.frontiersin.org/article/10.3389/fchem.2018.00023/full; https://doaj.org/toc/2296-2646
DOI: 10.3389/fchem.2018.00023
URL الوصول: https://doaj.org/article/01fb754a473b48af93c106f2922c6770
رقم الأكسشن: edsdoj.01fb754a473b48af93c106f2922c6770
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:22962646
DOI:10.3389/fchem.2018.00023