蛋白激酶B
磷酸化
细胞生物学
信号转导
激酶
蛋白激酶A
MAPK/ERK通路
ASK1
蛋白激酶结构域
化学
生物
丝裂原活化蛋白激酶激酶
癌症研究
生物化学
基因
突变体
作者
Sven Zimmermann,Karin Moelling
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1999-11-26
卷期号:286 (5445): 1741-1744
被引量:1078
标识
DOI:10.1126/science.286.5445.1741
摘要
Activation of the protein kinase Raf can lead to opposing cellular responses such as proliferation, growth arrest, apoptosis, or differentiation. Akt (protein kinase B), a member of a different signaling pathway that also regulates these responses, interacted with Raf and phosphorylated this protein at a highly conserved serine residue in its regulatory domain in vivo. This phosphorylation of Raf by Akt inhibited activation of the Raf-MEK-ERK signaling pathway and shifted the cellular response in a human breast cancer cell line from cell cycle arrest to proliferation. These observations provide a molecular basis for cross talk between two signaling pathways at the level of Raf and Akt.
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