结合多个序列特征的赖氨酸丙二醛化位点的计算鉴定

M. Hasan, H. Kurata
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引用次数: 6

摘要

赖氨酸丙二醛酰化是一种新发现的蛋白质翻译后修饰,在调节许多细胞功能中起着重要作用。然而,有几种方法可用于鉴定丙二醛化蛋白及其丙二醛化位点;丙二醛化位点的实验鉴定通常是费力和昂贵的。因此,在体外实验之前,需要计算方案来确定潜在的丙二醛化位点。本文通过支持向量机分类器将初级序列和进化特征相结合,提出了一种新的计算方案iLMS(赖氨酸-丙二酰化位点识别)。最终的iLMS方案在人类和小鼠数据集的交叉验证测试中都取得了稳健的性能。对于鼠标数据,iLMS预测器优于其他现有实现。iLMS是预测丙二醛化位点的一种很有前途的计算方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
iLMS, Computational Identification of Lysine-Malonylation Sites by Combining Multiple Sequence Features
Lysine malonylation is a newly discovered post-translational modification of proteins, which plays an important role in regulating many cellular functions. Several approaches are available to identify malonylation proteins and its malonylation sites, however; experimental identification of malonylation sites is often laborious and costly. Therefore, computational schemes are needed to identify potential malonylation sites prior to in vitro experimentation. In this paper, a novel computational scheme iLMS (Identification of Lysine-Malonylation Sites) has been developed by combining primary sequences and evolutionary features via a support vector machine classifier. The final iLMS scheme achieved a robust performance in cross-validation test in both human and mouse datasets. For the mouse data, the iLMS predictor outperformed other existing implementations. The iLMS is a promising computational scheme for the prediction of malonylation sites.
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