Exploring the conformational landscape of protein kinases

被引:2
|
作者
Gough, Nancy R. [1 ]
Kalodimos, Charalampos G. [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Struct Biol, Memphis, TN 38105 USA
关键词
ALLOSTERIC REGULATION; CATALYTIC SUBUNIT; ACTIVATION; DYNAMICS; PREDICTION; INHIBITORS; COMPLEX;
D O I
10.1016/j.sbi.2024.102890
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein kinases are dynamic enzymes that display complex regulatory mechanisms. Although they possess a structurally conserved catalytic domain, significant conformational dynamics are evident both within a single kinase and across different kinases in the kinome. Here, we highlight methods for exploring this conformational space and its dynamics using kinase domains from ABL1 (Abelson kinase), PKA (protein kinase A), AurA (Aurora A), and PYK2 (proline-rich tyrosine bined with AI-driven methods, such as AlphaFold, will yield discoveries about kinase regulation, the catalytic process, substrate specificity, the effect of disease-associated mutations, as well as new opportunities for structure-based drug design.
引用
收藏
页数:8
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