Although the RBD engages KRAS through a conserved mechanism, the BRAF(CRD) adopts a hinge-like displacement away from KRAS, forming fewer contacts and contributing less to binding than CRAF(CRD).
D. Bonsor, Suzanne I. Sandin Lawrence, Timothy H. Tran et al.· Structure· 0 citations
Direct targeting of KRAS through the Switch-II pocket is an effective therapeutic strategy, but acquired resistance limits clinical benefit. We examine clinically observed resistance mutations (R68S, H95Q, Y96C, Y96D and Q99L) arising during KRAS G12C inhibitor therapy using biochemical, structural, computational and c...
M. J. Whitley, M. Dyba, Mayukh Chakrabarti et al.· Nature Communications· 0 citations
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