From Phosphosites to Kinases

磷酸蛋白质组学 磷酸化 激酶 计算生物学 蛋白质组学 背景(考古学) 生物 蛋白质磷酸化 生物信息学 细胞生物学 生物化学 蛋白激酶A 基因 古生物学
作者
Stephanie Munk,Jan C. Refsgaard,Jesper V. Olsen,Lars Juhl Jensen
出处
期刊:Methods in molecular biology 卷期号:: 307-321 被引量:22
标识
DOI:10.1007/978-1-4939-3049-4_21
摘要

Kinases play a pivotal role in propagating the phosphorylation-mediated signaling networks in living cells. With the overwhelming quantities of phosphoproteomics data being generated, the number of identified phosphorylation sites (phosphosites) is ever increasing. Often, proteomics investigations aim to understand the global signaling modulation that takes place in different biological conditions investigated. For phosphoproteomics data, identifying the kinases central to mediating this response is key. This has prompted several efforts to catalogue the immense amounts of phosphorylation data and known or predicted kinases responsible for the modifications. However, barely 20 % of the known phosphosites are assigned to a kinase, initiating various bioinformatics efforts that attempt to predict the responsible kinases. These algorithms employ different approaches to predict kinase consensus sequence motifs, mostly based on large scale in vivo and in vitro experiments. The context of the kinase and the phosphorylated proteins in a biological system is equally important for predicting association between the enzymes and substrates, an aspect that is also being tackled with available bioinformatics tools. This chapter summarizes the use of the larger phosphorylation databases, and approaches that can be applied to predict kinases that phosphorylate individual sites or that are globally modulated in phosphoproteomics datasets.
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