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MusiteDeep: A deep-learning framework for protein post-translational modification site prediction

机译:Musitedeep:蛋白质翻译后修改现场预测的深度学习框架

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Computational methods for post-translational modification (PTM) site prediction play important roles in protein function studies and experimental design. Most existing methods are based on feature extraction, which may result in incomplete or biased features. Deep learning as the cutting-edge machine learning method has the ability to automatically discover complex representations of PTM patterns from the raw sequences, and hence it provides a powerful tool for improvement of post-translational modification site prediction. In our previous work, we proposed MusiteDeep, the first deep-learning framework for predicting the phosphorylation, one of the well-studied PTMs. The previous MusiteDeep takes protein raw sequence as the input and uses convolutional neural networks with a two-dimensional attention mechanism. It achieved over a 50% improvement in the area under the precision-recall curve in general phosphorylation site prediction and obtains competitive results in kinase-specific prediction compared to other well-known tools on the benchmark data. In this work, we extended to explore more types of PTMs, including acetylation, methylation and glycosylation. New deep-learning architecture and new training strategy are proposed for better performance. Web server for more PTM site predictions and complex motif visualization will be developed in the future.
机译:翻译后修饰的计算方法(PTM)现场预测在蛋白质函数研究和实验设计中起重要作用。大多数现有方法都基于特征提取,这可能导致不完整或偏置的功能。随着尖端机器学习方法的深度学习能够自动发现从原始序列中的PTM模式的复杂表示,因此它提供了改进翻译后修改站点预测的强大工具。在我们以前的工作中,我们提出了MusitedeeP,这是一种预测磷酸化的第一个深度学习框架,其中一个研究的PTMS之一。以前的Musitedeep将蛋白质原始序列作为输入,并使用具有二维注意力机制的卷积神经网络。它在一般磷酸化站点预测中的精密召回曲线下的该区域的改善超过了50 %的改善,并且与基准数据上的其他众所周知的工具相比,获得了基酶特定预测中的竞争结果。在这项工作中,我们扩展以探索更多类型的PTM,包括乙酰化,甲基化和糖基化。提出了新的深度学习架构和新的培训策略,以实现更好的表现。 Web服务器对于更多PTM站点预测和复杂的图案可视化将在未来开发。

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