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人类激酶调控图谱。

An atlas of human kinase regulation.

作者信息

Ochoa David, Jonikas Mindaugas, Lawrence Robert T, El Debs Bachir, Selkrig Joel, Typas Athanasios, Villén Judit, Santos Silvia Dm, Beltrao Pedro

机构信息

European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.

Quantitative Cell Biology Group, MRC Clinical Sciences Centre, Imperial College, London, UK.

出版信息

Mol Syst Biol. 2016 Dec 1;12(12):888. doi: 10.15252/msb.20167295.

Abstract

The coordinated regulation of protein kinases is a rapid mechanism that integrates diverse cues and swiftly determines appropriate cellular responses. However, our understanding of cellular decision-making has been limited by the small number of simultaneously monitored phospho-regulatory events. Here, we have estimated changes in activity in 215 human kinases in 399 conditions derived from a large compilation of phosphopeptide quantifications. This atlas identifies commonly regulated kinases as those that are central in the signaling network and defines the logic relationships between kinase pairs. Co-regulation along the conditions predicts kinase-complex and kinase-substrate associations. Additionally, the kinase regulation profile acts as a molecular fingerprint to identify related and opposing signaling states. Using this atlas, we identified essential mediators of stem cell differentiation, modulators of Salmonella infection, and new targets of AKT1. This provides a global view of human phosphorylation-based signaling and the necessary context to better understand kinase-driven decision-making.

摘要

蛋白激酶的协调调控是一种快速机制,它整合各种信号并迅速确定适当的细胞反应。然而,我们对细胞决策的理解一直受到同时监测的磷酸化调节事件数量较少的限制。在这里,我们根据大量磷酸肽定量数据,估计了399种条件下215种人类激酶的活性变化。该图谱将共同调节的激酶识别为信号网络中的核心激酶,并定义了激酶对之间的逻辑关系。沿这些条件的共同调节可预测激酶复合物和激酶-底物关联。此外,激酶调节谱可作为分子指纹来识别相关和相反的信号状态。利用该图谱,我们鉴定了干细胞分化的关键介质、沙门氏菌感染的调节因子以及AKT1的新靶点。这提供了基于人类磷酸化的信号传导的全局视图以及更好理解激酶驱动决策的必要背景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5350/5199121/d8806f27a6d9/MSB-12-888-g003.jpg

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