基诺美
变构调节
蛋白激酶结构域
激酶
酪氨酸激酶
生物
化学
细胞生物学
生物化学
信号转导
受体
突变体
基因
作者
Xiaoyun Lu,Jeff B. Smaill,Ke Ding
标识
DOI:10.1002/anie.201914525
摘要
Drugs that function through allosteric inhibition of kinase signaling represent a promising approach for the targeted discovery of therapeutics. The majority of developed allosteric kinase inhibitors are characterized as type III and IV inhibitors that show good kinome selectivity but generally lack the subtype selectivity of same kinase family. Recently allosteric inhibitors have been developed that bind outside the catalytic kinase domain with high selectivity for specific kinase subtypes. Allosteric inhibitors that bind to the pseudokinase domain of pseudokinase or the extracellular domain of receptor tyrosine kinases are reviewed. We also review recent developments in the field of allosteric kinase inhibitors including examples of proteolysis targeting chimeras, and highlight the unique binding modes for each type of inhibitors and address future opportunities in this area.
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