基于二面角数据挖掘的次相似度匹配。

Q4 Pharmacology, Toxicology and Pharmaceutics
Egemen Berki Cimen, Fatih Akin, R Murat Demirer
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引用次数: 0

摘要

蛋白质亚相似性匹配在很大程度上仍然是未知的,尽管它正在成为药物和疫苗设计生物信息学中最重要的开放问题之一。人类对疫苗的免疫反应的变化,因此反应失败。提出了一种基于聚类和最长公共子序列(LCS)技术的蛋白质匹配与比对方法。聚类后,我们发现候选蛋白和每个候选脑膜炎外膜抗原之间存在LCS。对每个相似度进行评分,并用统计方法确定最接近的相似度。我们在总共50个人类免疫系统蛋白中找到了三个紧密匹配的蛋白。此外,我们从其中一种情况中选择了HIV-1相关蛋白,因为它揭示了HIV和脑膜炎患者之间的关系。我们还发现,CA、C和N原子的Ω主链扭转角是确定脑膜炎抗原与免疫蛋白之间亚相似性的最佳角度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sub-similarity matching based on data mining with dihedral angles.

Protein sub-similarity matching remains largely unknown even though it is becoming one of the most important open problems in bioinformatics for drug and vaccine design. Variations in human immune responses to vaccines are, and thus responses, fail. We propose a new matching and protein alignment method based on clustering and Longest Common Subsequence (LCS) techniques. After clustering, we found LCS between a candidate protein and meningitis outer membrane antigen for each candidate. Each similarity was scored, and closest similarities were determined with statistical methods. We located three closely matching proteins among a total of 50 human immune system proteins. Moreover, we selected a HIV-1 related protein from one of scenarios, because it revealed a relationship between HIV and meningitis patients. We also found that Ω main chain torsion angle for atoms CA, C and N is the best angle for determining sub-similarities between meningitis antigen and immune proteins.

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来源期刊
International Journal of Computational Biology and Drug Design
International Journal of Computational Biology and Drug Design Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
1.00
自引率
0.00%
发文量
8
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