Structural analysis on mutations related to Alzheimer’s disease

A. Avramouli, Eleftheria Polychronidou, P. Vlamos
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Abstract

Proteins have a significant role in all biological processes. The functional properties of proteins rely upon their three-dimensional structures. Over the last twenty years substantial advances in genomic technologies have enhanced our knowledge of the genetics of Alzheimer’s disease. To that end the identification of mutations pathogenicity is still of vital importance. The methodology of the present research work focuses on the structural analysis of proteins related to Alzheimer’s disease and the comparative study to create groups with clear structural similarity and pathogenicity. To achieve that, three-dimensional descriptors (fpfh, rsd and 3dsc) were applied along with supervised machine learning classification methods. In total, 62 APP, 286 PSEN1, 68 PSEN2 and 25 MAPT variants were evaluated in our study.The output of the methodology characterized thirty mutations that were unclear at the point of the data collection.
阿尔茨海默病相关突变的结构分析
蛋白质在所有生物过程中都起着重要的作用。蛋白质的功能特性依赖于它们的三维结构。在过去的二十年中,基因组技术的巨大进步增强了我们对阿尔茨海默病遗传学的认识。为此目的,鉴定突变的致病性仍然至关重要。本研究工作的方法学侧重于对阿尔茨海默病相关蛋白的结构分析和比较研究,以创建具有明确结构相似性和致病性的群体。为了实现这一目标,三维描述符(fpfh, rsd和3dsc)与监督机器学习分类方法一起应用。在我们的研究中,总共评估了62个APP, 286个PSEN1, 68个PSEN2和25个MAPT变体。该方法的输出表征了在数据收集时尚不清楚的30个突变。
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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