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Prediction of Protein Acetylation Sites using Kernel Naive Bayes Classifier Based on Protein Sequences Profiling

机译:基于蛋白质序列分析的朴素贝叶斯分类器预测蛋白质乙酰化位点

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摘要

Lysine acetylation is one of the decisive categories of protein post-translational modification (PTM), it is convoluted in many significant cellular developments and severe diseases in the biological system. The experimental identification of protein-acetylated sites is painstaking, time-consuming and expensive. Hence, there is significant interest in the development of computational approaches for consistent prediction of acetylation sites using protein sequences. Features selection from protein sequences plays a significant role for acetylation sites prediction. We describe an improved feature selection approach for acetylation sites prediction based on kernel naive Bayes classifier (KNBC). We have shown that KNBC generated from selected features by a new feature selection method outperforms than the existing methods for identification of acetylation sites. The sensitivity, specificity, ACC (Accuracy), MCC (Matthews Correlation Coefficient) and AUC (Area under Curve of ROC) in our proposed method are as follows 80.71%, 93.39%, 76.73%, 41.37% and 83.0% with the optimum window size is 47. Thus the kernel naive Bayes classifier finds application in acetylation site prediction.
机译:赖氨酸乙酰化是蛋白质翻译后修饰(PTM)的决定性类别之一,在许多重要的细胞发育和生物系统中的严重疾病中令人费解。蛋白质乙酰化位点的实验鉴定费力,费时且昂贵。因此,人们对使用蛋白质序列一致预测乙酰化位点的计算方法的开发非常感兴趣。从蛋白质序列中选择特征对于乙酰化位点的预测起着重要作用。我们描述了一种基于内核朴素贝叶斯分类器(KNBC)的乙酰化位点预测的改进的特征选择方法。我们已经表明,通过一种新的特征选择方法从选定特征生成的KNBC优于现有的用于识别乙酰化位点的方法。我们提出的方法的灵敏度,特异性,ACC(准确度),MCC(马修斯相关系数)和AUC(ROC曲线下面积)分别为80.71%,93.39%,76.73%,41.37%和83.0%,且具有最佳窗口大小为47。因此,朴素的朴素贝叶斯分类器可用于乙酰化位点预测。

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