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Characterization and Identification of Lysine Succinylation Sites based on Deep Learning Method

机译:基于深度学习方法的赖氨酸琥珀酸位点的表征与鉴定

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Succinylation is a type of protein post-translational modification (PTM), which can play important roles in a variety of cellular processes. Due to an increasing number of site-specific succinylated peptides obtained from high-throughput mass spectrometry (MS), various tools have been developed for computationally identifying succinylated sites on proteins. However, most of these tools predict succinylation sites based on traditional machine learning methods. Hence, this work aimed to carry out the succinylation site prediction based on a deep learning model. The abundance of MS-verified succinylated peptides enabled the investigation of substrate site specificity of succinylation sites through sequence-based attributes, such as position-specific amino acid composition, the composition of k-spaced amino acid pairs (CKSAAP), and position-specific scoring matrix (PSSM). Additionally, the maximal dependence decomposition (MDD) was adopted to detect the substrate signatures of lysine succinylation sites by dividing all succinylated sequences into several groups with conserved substrate motifs. According to the results of ten-fold cross-validation, the deep learning model trained using PSSM and informative CKSAAP attributes can reach the best predictive performance and also perform better than traditional machine-learning methods. Moreover, an independent testing dataset that truly did not exist in the training dataset was used to compare the proposed method with six existing prediction tools. The testing dataset comprised of 218 positive and 2621 negative instances, and the proposed model could yield a promising performance with 84.40% sensitivity, 86.99% specificity, 86.79% accuracy, and an MCC value of 0.489. Finally, the proposed method has been implemented as a web-based prediction tool (CNN-SuccSite), which is now freely accessible at http://csb.cse.yzu.edu.tw/CNN-SuccSite/ .
机译:琥珀酰化是一种翻译后修饰(PTM)的蛋白质类型,其可以在各种细胞过程中起重要作用。由于从高通量质谱(MS)获得的位点特异性琥珀酰化肽的数量越来越多,已经开发了各种工具,用于计算蛋白质上的琥珀酰化位点。然而,这些工具中的大多数是基于传统机器学习方法的琥珀酰化站点预测。因此,这项工作旨在基于深度学习模型进行琥珀酰化站点预测。 MS-验证的琥珀酰化肽的丰度使琥珀酰化位点的底物位点特异性通过序列的属性进行研究,例如特异性氨基酸组合物,K-间隔氨基酸对(CKSAAP)的组成,以及特异性特异性的评分矩阵(PSSM)。另外,采用最大依赖性分解(MDD)来检测赖氨酸琥珀酰化位点的底物签名通过将所有琥珀酰化的序列除以具有保守基板基序的几组。根据十倍交叉验证的结果,使用PSSM和信息性CKSAAP属性培训的深度学习模型可以达到最佳预测性能,并且也比传统的机器学习方法更好。此外,使用训练数据集中真正不存在的独立测试数据集用于比较具有六个现有预测工具的提出方法。测试数据集由218个阳性和2621个负实例组成,所提出的模型可以产生有希望的性能,灵敏度为84.40%,特异性86.99%,精度为86.79%,MCC值为0.489。最后,该方法已经实现为基于Web的预测工具(CNN-SuccSite),现在可以在http://csb.cse.yzu.edu.tw/cnn-succsite/上自由访问。

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