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

机译:MusiteDeep:用于蛋白质翻译后修饰位点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(PTM)位点预测的计算方法在蛋白质功能研究和实验设计中起着重要作用。现有的大多数方法都是基于特征提取的,这可能会导致特征不完整或存在偏差。深度学习作为最先进的机器学习方法,具有从原始序列中自动发现PTM模式的复杂表示的能力,因此它为改进翻译后修饰位点预测提供了强大的工具。在我们之前的工作中,我们提出了MusiteDeep,这是第一个用于预测磷酸化的深度学习框架,它是经过充分研究的PTM之一。先前的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。与基准数据上的其他知名工具相比,它在一般磷酸化位点预测中的精确召回曲线下的面积提高了50%以上,并且在激酶特异性预测中获得了竞争性结果。在这项工作中,我们扩展了探索更多类型的PTM的方法,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,以提高性能。将来将开发用于PTM站点预测和复杂图案可视化的Web服务器。

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