Structural Dynamics of Rho GTPases

被引:0
作者
Lin, Yuan [1 ]
Zheng, Yi [1 ,2 ]
机构
[1] Cincinnati Childrenss Hosp, Med Ctr, Canc & Blood Dis Inst, Div Expt Hematol & Canc Biol, Cincinnati, OH USA
[2] Univ Cincinnati, Coll Med, Cincinnati, OH USA
关键词
Rho GTPase; conformation dynamics; oncogenic mutation; atomic structures; molecular dynamics; ACCELERATED MOLECULAR-DYNAMICS; CONFORMATIONAL STATES; BINDING DOMAIN; K-RAS; ONCOGENIC MUTATIONS; CRYSTAL-STRUCTURE; POLYBASIC REGION; RATIONAL DESIGN; GTP; CDC42;
D O I
10.1016/j.jmb.2024.168919
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
Rho family GTPases are a part of the Ras superfamily and are signaling hubs for many cellular processes. While the detailed understanding of Ras structure and function has led to tremendous progress in oncogenic Ras-targeted drug discovery, studies of the related Rho GTPases are still catching up as the recurrent cancer-related Rho GTPase mutations have only been discovered in the last decade. Like that of Ras, an in-depth understanding of the structural basis of how Rho GTPases and their mutants behave as key oncogenic drivers benefits the development of clinically effective therapies. Recent studies of structure dynamics in Rho GTPase structure-function relationship have added new twists to the conventional wisdom of Rho GTPase signaling mechanism. (c) 2024 Elsevier Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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页数:13
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