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首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >STRUCTURAL COMPARISON OF PROKARYOTIC AND EUKARYOTIC FOLATE TRANSPORTERS BY COMPUTATIONAL APPROACH
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STRUCTURAL COMPARISON OF PROKARYOTIC AND EUKARYOTIC FOLATE TRANSPORTERS BY COMPUTATIONAL APPROACH

机译:计算方法对原核和真核叶酸转运蛋白的结构比较

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Objective: In silico approach has particularly drawn attention in providing a realistic representation needed to understand the fundamental molecular structure of a transporter. The importance of folate metabolism and role in the internalization of antifolates in eukaryotes have been studied extensively, but the structural study of folate transporters in Homo sapiens (HFT), Plasmodium falciparum (PFT), and Streptococcus sp. (SFT) is still lacking. This study was conducted to study and compare the structures of prokaryotic and eukaryotic folate transporters. Methods: HFT, PFT, and SFT were queried using blast and sequences were retrieved using National Center for Biotechnology and Information (NCBI) databases. This was superseded by structural and functional prediction of transporters. The structure has been generated using Swiss model which was visualized using PyMol and validated by Procheck and ERRAT analysis along with the values of different secondary structures mapping to diverse sections of the Ramachandran plot. The structural and functional comparison was performed by PROSO, ProFunc, TM Score, Porewalker, TMHMM, and Protscale. Result: All the parameters for structural comparison suggest that H. sapiens folate transporter is 16.67% and 17.72% identical to Plasmodium and Streptococcus whereas Plasmodium is 21.59% identical to Streptococcus . The evaluation of transmembrane helices and hydrophobicity resulted in the presence of 1, 4, and 12 membrane-spanning segments with predicted US, UDUD, and UDS as pore shape in Plasmodium , Streptococcus , and humans. Conclusion: Such folate receptors are the main targets for the specific conveyance of antifolates. The differences found between these species may offer possibilities for the development of new drugs in future.
机译:目的:计算机模拟方法在提供一种了解转运蛋白基本分子结构所需的逼真的表示方式时特别引起关注。叶酸代谢的重要性及其在真核生物中抗叶酸内在化中的作用已得到广泛研究,但是智人(HFT),恶性疟原虫(PFT)和链球菌sp中叶酸转运蛋白的结构研究。 (SFT)仍然缺乏。进行这项研究以研究和比较原核和真核叶酸转运蛋白的结构。方法:使用blast查询HFT,PFT和SFT,并使用美国国家生物技术和信息中心(NCBI)数据库检索序列。这被转运蛋白的结构和功能预测所取代。结构是使用Swiss模型生成的,该模型使用PyMol进行了可视化,并通过Procheck和ERRAT分析以及映射到Ramachandran图的不同部分的不同二级结构的值进行了验证。通过PROSO,ProFunc,TM Score,Porewalker,TMHMM和Protscale进行结构和功能比较。结果:所有用于结构比较的参数表明,智人叶酸转运蛋白与疟原虫和链球菌相同,分别为16.67%和17.72%,而疟原虫与链球菌相同,为21.59%。跨膜螺旋和疏水性的评估导致存在1、4和12个跨膜节段,这些节段具有预期的US,UDUD和UDS,它们分别作为疟原虫,链球菌和人类的孔形状。结论:此类叶酸受体是抗叶酸特异性转运的主要靶标。这些物种之间的差异可能为将来开发新药提供可能。

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