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Musite a Tool for Global Prediction of General and Kinase-specific Phosphorylation Sites

机译:Musite一种用于一般和激酶特异性磷酸化位点全球预测的工具

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摘要

Reversible protein phosphorylation is one of the most pervasive post-translational modifications, regulating diverse cellular processes in various organisms. High throughput experimental studies using mass spectrometry have identified many phosphorylation sites, primarily from eukaryotes. However, the vast majority of phosphorylation sites remain undiscovered, even in well studied systems. Because mass spectrometry-based experimental approaches for identifying phosphorylation events are costly, time-consuming, and biased toward abundant proteins and proteotypic peptides, in silico prediction of phosphorylation sites is potentially a useful alternative strategy for whole proteome annotation. Because of various limitations, current phosphorylation site prediction tools were not well designed for comprehensive assessment of proteomes. Here, we present a novel software tool, Musite, specifically designed for large scale predictions of both general and kinase-specific phosphorylation sites. We collected phosphoproteomics data in multiple organisms from several reliable sources and used them to train prediction models by a comprehensive machine-learning approach that integrates local sequence similarities to known phosphorylation sites, protein disorder scores, and amino acid frequencies. Application of Musite on several proteomes yielded tens of thousands of phosphorylation site predictions at a high stringency level. Cross-validation tests show that Musite achieves some improvement over existing tools in predicting general phosphorylation sites, and it is at least comparable with those for predicting kinase-specific phosphorylation sites. In Musite V1.0, we have trained general prediction models for six organisms and kinase-specific prediction models for 13 kinases or kinase families. Although the current pretrained models were not correlated with any particular cellular conditions, Musite provides a unique functionality for training customized prediction models (including condition-specific models) from users' own data. In addition, with its easily extensible open source application programming interface, Musite is aimed at being an open platform for community-based development of machine learning-based phosphorylation site prediction applications. Musite is available at .
机译:可逆蛋白的磷酸化是最普遍的翻译后修饰之一,可调节各种生物体中的各种细胞过程。使用质谱的高通量实验研究已经鉴定出许多磷酸化位点,主要来自真核生物。但是,即使在经过充分研究的系统中,绝大多数的磷酸化位点仍未被发现。由于用于鉴定磷酸化事件的基于质谱的实验方法成本高昂,耗时且偏向于丰富的蛋白质和蛋白质型肽,因此对磷酸化位点进行计算机模拟预测可能是整个蛋白质组注释的一种有用的替代策略。由于各种限制,当前的磷酸化位点预测工具设计不佳,无法对蛋白质组进行全面评估。在这里,我们介绍了一种新颖的软件工具Musite,该工具专门设计用于一般和激酶特异性磷酸化位点的大规模预测。我们从几个可靠的来源收集了多种生物的磷酸化蛋白质组学数据,并使用它们通过全面的机器学习方法来训练预测模型,该方法整合了与已知磷酸化位点的局部序列相似性,蛋白质失调评分和氨基酸频率。 Musite在几种蛋白质组上的应用在高严格性水平下产生了数以万计的磷酸化位点预测。交叉验证测试表明,Musite在预测一般磷酸化位点方面比现有工具取得了一些进步,并且至少与预测激酶特异性磷酸化位点的可比性相当。在Musite V1.0中,我们训练了6种生物的一般预测模型和13种激酶或激酶家族的激酶特异性预测模型。尽管当前的预训练模型与任何特定的细胞状况均不相关,但Musite提供了独特的功能,可根据用户自己的数据训练定制的预测模型(包括特定于条件的模型)。此外,凭借其易于扩展的开源应用程序编程接口,Musite的目标是成为一个基于社区的基于机器学习的磷酸化位点预测应用程序开发的开放平台。可从那里购买Musite。

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