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PPSP: prediction of PK-specific phosphorylation site with Bayesian decision theory

机译:PPSP:使用贝叶斯决策理论预测PK特异性磷酸化位点

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Background As a reversible and dynamic post-translational modification (PTM) of proteins, phosphorylation plays essential regulatory roles in a broad spectrum of the biological processes. Although many studies have been contributed on the molecular mechanism of phosphorylation dynamics, the intrinsic feature of substrates specificity is still elusive and remains to be delineated. Results In this work, we present a novel, versatile and comprehensive program, PPSP (Prediction of PK-specific Phosphorylation site), deployed with approach of Bayesian decision theory (BDT). PPSP could predict the potential phosphorylation sites accurately for ~70 PK (Protein Kinase) groups. Compared with four existing tools Scansite, NetPhosK, KinasePhos and GPS, PPSP is more accurate and powerful than these tools. Moreover, PPSP also provides the prediction for many novel PKs, say, TRK, mTOR, SyK and MET/RON, etc. The accuracy of these novel PKs are also satisfying. Conclusion Taken together, we propose that PPSP could be a potentially powerful tool for the experimentalists who are focusing on phosphorylation substrates with their PK-specific sites identification. Moreover, the BDT strategy could also be a ubiquitous approach for PTMs, such as sumoylation and ubiquitination, etc.
机译:背景技术作为蛋白质的可逆和动态翻译后修饰(PTM),磷酸化在广泛的生物学过程中起着重要的调节作用。尽管已经对磷酸化动力学的分子机理进行了许多研究,但是底物特异性的内在特征仍然难以捉摸,尚待描述。结果在这项工作中,我们提出了一种新颖,通用和全面的程序PPSP(PK特异性磷酸化位点的预测),并采用了贝叶斯决策理论(BDT)的方法进行了部署。 PPSP可以准确预测〜70 PK(蛋白激酶)组的潜在磷酸化位点。与现有的四个工具Scansite,NetPhosK,KinasePhos和GPS相比,PPSP比这些工具更为准确和强大。而且,PPSP还提供了许多新颖PK的预测,例如TRK,mTOR,SyK和MET / RON等。这些新颖PK的准确性也令人满意。结论综上所述,我们认为PPSP对于潜在的研究者来说是一种潜在的强大工具,他们专注于通过PK特异性位点鉴定来研究磷酸化底物。此外,BDT策略也可能是PTM的普遍方法,例如SUMO化和泛素化等。

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