磷酸化
激酶
三磷酸腺苷
细胞生物学
原癌基因酪氨酸蛋白激酶Src
化学
底物水平磷酸化
生物物理学
基质(水族馆)
酪氨酸蛋白激酶
SH3域
丝氨酸苏氨酸激酶
生物化学
腺苷
蛋白质磷酸化
酶
二磷酸腺苷
血浆蛋白结合
蛋白质结构
底物特异性
信号转导
生物
蛋白激酶A
核苷酸
酶激活剂
构象变化
作者
Yixin Cui,Rustam Ali,Mary C. Clay,P. Rossi,Aizhuo Liu,Darong Yang,Nancy R. Gough,Terrence L. Geiger,Charalampos G. Kalodimos
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-12-18
卷期号:390 (6779): eadw8310-eadw8310
被引量:1
标识
DOI:10.1126/science.adw8310
摘要
Processive phosphorylation by kinases enables the rapid multisite modification of signaling hubs, serving to integrate signals during time-sensitive cellular events. To achieve processivity, multiple catalytic cycles must occur before substrate dissociation, making rapid turnover rates essential. Src family kinases processively phosphorylate multisite substrates. Using nuclear magnetic resonance spectroscopy, we identified a transient intermediate state within the Src conformational ensemble, positioned between its active and inactive states. This intermediate state facilitates the rapid release of adenosine diphosphate following adenosine triphosphate hydrolysis, ensuring efficient catalytic turnover. Depletion of the intermediate state abrogated processive phosphorylation by Src, Lck, and Hck, impairing function. These findings reveal that the conformational ensemble of Src family kinases has evolved to incorporate a transient state that underpins their capacity for processive substrate phosphorylation.
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