病毒蛋白亚细胞定位的综合预测和解释

Xiyu Liu
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引用次数: 0

摘要

确定病毒蛋白的亚细胞定位是了解病毒活性和推断病毒蛋白功能的必要条件。虽然之前关于预测病毒蛋白亚细胞定位的研究已经发展起来,但它们往往存在以下缺点:(i)只关注一个物种的一部分蛋白质(ii)没有考虑多位置蛋白质的存在(iii)缺乏结果的可解释性。为了解决这些问题,本文首先在UniProtKB中预测了整个病毒蛋白质组的所有亚细胞定位,并对结果进行了解释。本文给出了FUEL-mLoc预测器对单位点和多位点病毒蛋白具有较高的预测精度。更重要的是,我们对所有病毒蛋白的亚细胞定位进行了深入的分析和解释。最后,我们发现了一些基本的氧化石墨烯术语,这些术语可以解释结果,并且在预测病毒蛋白的亚细胞定位方面具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive Prediction and Interpretation of Viral Protein Subcellular Localization
Determining the subcellular localization of viral proteins is indispensable for understanding the activity of the virus and inferring viral protein functions. Although previous studies about predicting viral protein subcellular localization have been developed, they often have the following disadvantages: (i) only focusing on a part of proteins of a species (ii) not considering the presence of multi-location proteins and (iii) lacking interpretability for the results. To address these problems, this paper is firstly predicting all the subcellular localization of the whole viral proteome in the UniProtKB and is interpretable for the results. This paper gives high prediction accuracy for the single-location and multi-location viral proteins by the FUEL-mLoc predictor. More importantly, we did deeply analysis and interpretation of the subcellular localization of all viral proteins. Finally, we have found some essential GO terms which are interpretable for the results and are significant in predicting the subcellular localization of the viral proteins.
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