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

被引:178
作者
Xue, Y
Li, A
Wang, LR
Feng, HQ
Yao, XB [1 ]
机构
[1] Univ Sci & Technol China, Sch Life Sci, Hefei 230027, Anhui, Peoples R China
[2] Univ Sci & Technol China, Dept Elect Sci & Technol, Hefei 230027, Anhui, Peoples R China
[3] Morehouse Sch Med, Dept Physiol, Atlanta, GA 30310 USA
关键词
D O I
10.1186/1471-2105-7-163
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 similar to 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.
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页数:11
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