自噬
磷脂酰肌醇
激酶
膜
细胞生物学
突变
化学
生物化学
生物
突变
细胞凋亡
基因
作者
Simon Miller,Brandon Tavshanjian,Arkadiusz Oleksy,Olga Perišić,Benjamin T. Houseman,Kevan M. Shokat,Roger Williams
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2010-03-25
卷期号:327 (5973): 1638-1642
被引量:280
标识
DOI:10.1126/science.1184429
摘要
Lipid Kinase Revealed The lipid kinase, Vps34, makes the key signaling lipid phosphatidylinositol 3-phosphate [PI(3)P] and has essential roles in autophagy, membrane trafficking, and cell signaling. It is a class III PI 3-kinase, a class against which there is currently no specific inhibitor. Miller et al. (p. 1638 ) now describe the crystal structure of Vps34. Modeling substrate binding and combining structural data with mutagenesis suggests a mechanism in which Vps34 is auto-inhibited in solution, but adopts a catalytically active conformation on membranes. Structures of Vps34 with existing inhibitors might allow for the generation of inhibitors with high affinity and specificity.
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