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GPS 2.1: enhanced prediction of kinase-specific phosphorylation sites with an algorithm of motif length selection

机译:GPS 2.1:通过选择基序长度的算法增强对激酶特异性磷酸化位点的预测

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摘要

As the most important post-translational modification of proteins, phosphorylation plays essential roles in all aspects of biological processes. Besides experimental approaches, computational prediction of phosphorylated proteins with their kinase-specific phosphorylation sites has also emerged as a popular strategy, for its low-cost, fast-speed and convenience. In this work, we developed a kinase-specific phosphorylation sites predictor of GPS 2.1 (Group-based Prediction System), with a novel but simple approach of motif length selection (MLS). By this approach, the robustness of the prediction system was greatly improved. All algorithms in GPS old versions were also reserved and integrated in GPS 2.1. The online service and local packages of GPS 2.1 were implemented in JAVA 1.5 (J2SE 5.0) and freely available for academic researches at: http://gps.biocuckoo.org.
机译:作为蛋白质最重要的翻译后修饰,磷酸化在生物过程的各个方面都起着至关重要的作用。除实验方法外,由于其低成本,快速和便捷的优点,磷酸化蛋白及其激酶特异性磷酸化位点的计算预测也已成为一种流行的策略。在这项工作中,我们开发了一种GPS 2.1(基于群组的预测系统)的激酶特异性磷酸化位点预测器,采用了新颖但简单的基序长度选择(MLS)方法。通过这种方法,大大提高了预测系统的鲁棒性。 GPS旧版本中的所有算法也都保留并集成到GPS 2.1中。 GPS 2.1的在线服务和本地软件包已在JAVA 1.5(J2SE 5.0)中实现,可从以下网址免费进行学术研究:http://gps.biocuckoo.org。

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  • 来源
    《Protein Engineering, Design and Selection》 |2011年第3期|p.255-260|共6页
  • 作者

    Jian Ren;

  • 作者单位

    Huazhong University of Science and Technology, @%@, University of Science & Technology of China, @%@ @%@, Sun Yat-sen University (SYSU), @%@To whom correspondence should be addressed. E-mail: @%@ (X.Y.)/;

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