GTP-Dependent K-Ras Dimerization.

GTP-Dependent K-Ras Dimerization.
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DOI:
10.1016/j.str.2015.04.019
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发表时间:
2015-07-07
期刊:
影响因子:
5.7
通讯作者:
Nussinov, Ruth
Nussinov, Ruth
中科院分区:
生物学2区
文献类型:
--
作者:
Muratcioglu, Serena;Chavan, Tanmay S.;Freed, Benjamin C.;Jang, Hyunbum;Khavrutskii, Lyuba;Freed, R. Natasha;Dyba, Marzena A.;Stefanisko, Karen;Tarasov, Sergey G.;Gursoy, Attila;Keskin, Ozlem;Tarasova, Nadya I.;Gaponenko, Vadim;Nussinov, Ruth

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Ras proteins recruit and activate effectors, including Raf, that transmit receptor-initiated signals. Monomeric Ras can bind Raf; however, activation of Raf requires its dimerization. It has been suspected that dimeric Ras may promote dimerization and activation of Raf. Here we show that the GTP-bound catalytic domain of K-Ras4B, a highly oncogenic splice variant of the K-Ras isoform, forms stable homodimers. We observe two major dimer interfaces. The first, highly populated β-sheet dimer interface is at the Switch I and effector binding regions, overlapping Raf’s, PI3K’s, RalGDS’ and additional effectors’ binding surfaces. This interface has to be inhibitory to such effectors. The second, helical interface also overlaps some effectors’ binding sites. This interface may promote Raf‘s activation. Our data reveal how Ras self-association can regulate effector binding and activity, and suggest that disruption of the helical dimer interface by drugs may abate Raf’s signaling in cancer.
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