ULK1
自噬
化学
蛋白激酶结构域
细胞生物学
激酶
药物靶点
药物发现
丝氨酸
蛋白激酶A
生物化学
细胞凋亡
磷酸化
生物
基因
安普克
突变体
作者
Lan Zhang,Liang Ouyang,Yongzhi Guo,Jin Zhang,Bo Liu
标识
DOI:10.1021/acs.jmedchem.7b01684
摘要
UNC-51-like kinase 1 (ULK1), known as an ortholog of the yeast Atg1, is the serine–threonine kinase and the autophagic initiator in mammals. Accumulating evidence has recently revealed the kinase domain structure of ULK1 and its post-translational modifications, as well as further elucidated its regulatory autophagic pathways and associations with diverse human diseases. Interestingly, a series of small molecules have been recently reported to target ULK1 or ULK1-modulating autophagy, which may provide a clue on exploiting them as novel candidate drugs. Taken together, this review discusses how ULK1 acts as an autophagic initiator for modulation of its intricate mechanisms, as well as how ULK1 becomes a multifunctional target for potential therapeutic applications.
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