磷酸化
磷酸化级联
丝氨酸
雌激素受体
雌激素受体
激酶
雌激素受体α
细胞生物学
蛋白激酶A
蛋白质磷酸化
生物
化学
生物化学
遗传学
癌症
乳腺癌
出处
期刊:Steroids
[Elsevier]
日期:2002-12-11
卷期号:68 (1): 1-9
被引量:473
标识
DOI:10.1016/s0039-128x(02)00110-1
摘要
Estrogen receptor alpha (ERalpha) is phosphorylated on multiple amino acid residues. For example, in response to estradiol binding, human ERalpha is predominately phosphorylated on Ser-118 and to a lesser extent on Ser-104 and Ser-106. In response to activation of the mitogen-activated protein kinase pathway, phosphorylation occurs on Ser-118 and Ser-167. These serine residues are all located within the activation function 1 region of the N-terminal domain of ERalpha. In contrast, activation of protein kinase A increases the phosphorylation of Ser-236, which is located in the DNA-binding domain. The in vivo phosphorylation status of Tyr-537, located in the ligand-binding domain, remains controversial. In this review, I present evidence that these phosphorylations occur, and identify the kinases thought to be responsible. Additionally, the functional importance of ERalpha phosphorylation is discussed.
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