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Prediction of kinase-specific phosphorylation sites with sequence features by a log-odds ratio approach
被引:47
作者:
Li, Tingting
[1
,2
]
Li, Fei
[1
,2
]
Zhang, Xuegong
[1
,2
]
机构:
[1] Tsinghua Univ, Bioinformat Div, TNLIST, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Dept Automat, Beijing 100084, Peoples R China
关键词:
phosphorylation;
protein kinase;
substrate specificity;
computational prediction;
D O I:
10.1002/prot.21563
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Protein phosphorylation plays important roles in a variety of cellular processes. Detecting possible phosphorylation sites and their corresponding protein kinases is crucial for studying the function of many proteins. This article presents a new prediction system, called PhoScan, to predict phosphorylation sites in a kinase-family-specific way. Common phosphorylation features and kinase-specific features are extracted from substrate sequences of different protein kinases based on the analysis of published experiments, and a scoring system is developed for evaluating the possibility that a peptide can be phosphorylated by the protein kinase at the specific site in its sequence context. PhoScan can achieve a specificity of above 90% with sensitivity around 90% at kinase-family level on the data experimented. The system is applied on a set of human proteins collected from Swiss-Prot and sets of putative phosphorylation sites are predicted for protein kinase A, cyclin-dependent kinase, and casein kinase 2 families. PhoScan is available at http://bioinfo. au. tsinghua.edu.cn/phoscan/.
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页码:404 / 414
页数:11
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