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iLMS, Computational Identification of Lysine-Malonylation Sites by Combining Multiple Sequence Features: Identification of lysine-malonylation sites

机译:通过组合多序列特征,赖氨酸 - 丙二酰基化位点的ILMS,鉴定赖氨酸 - 丙二酰基化位点的鉴定

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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.
机译:赖氨酸丙二酰基化是一种新发现的蛋白质后翻译后修饰,其在调节许多细胞功能方面发挥着重要作用。然而,有几种方法可用于鉴定丙基化蛋白及其丙二酰基化位点;丙二酰位点的实验鉴定通常是艰苦的且昂贵的。因此,需要在体外​​实验之前识别潜在的丙基化位点。本文通过支持矢量机分类器组合主要序列和进化特征,开发了一种新的计算方案ILMS(鉴定赖氨酸 - 丙基化位点)。最终的ILMS方案在人类和鼠标数据集中实现了跨验证测试的强大性能。对于鼠标数据,ILMS预测器优于其他现有实现。 ILMS是预测丙基化位点的有希望的计算方案。

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