Aug 2026· Journal of Molecular Modeling· Vol 32· 0 citations· 42 references
Medicine
TL;DR
These findings provide a mechanistic explanation for entrectinib resistance at atomic resolution and illustrate how a single-point mutation can trigger long-range perturbations in protein dynamics and interdomain communication.
This study demonstrates that PKM2 mutations dynamically remodel the binding pocket and allosteric communication to facilitate shikonin recognition, highlighting the newly identified pocket as a promising therapeutic site for future PKM2 targeted drug design.
A number of lead candidates with strong EGFR inhibitory potential, promising pharmacokinetic profiles, and mutant selectivity were successfully identified by the integrated computational approach.
M. Kendre, S. S. Bhusari, Pravin S. Wakte· Journal of Pharmaceutical In...· 0 citations
Complementary strategies, including covalent stabilization and targeted degradation, further extend this framework, establishing mutation-encoded structural vulnerabilities as actionable therapeutic opportunities, in which oncogenic missense mutations can generate druggable neo-pockets.
Lin-Wan Song, Hua Wang· Medical Review· 0 citations
Background: Oncogenic alterations in KRAS are among the most frequent driver mutations in human cancers, particularly lung, colorectal, and pancreatic cancers. Mutant KRAS was historically considered an “undruggable” target because of its high affinity for guanosine triphosphate and guanosine diphosphate (GDP) and the...
V. Adhao, Sakshi N. Patil· INNOSC Theranostics and Phar...· 0 citations
This study analyzed two highly recalcitrant G1202R‐paired double mutations detected in EML4‐ALK variant 3 patients in cis following lorlatinib therapy and identified two compounds, CID 118002992 and CID 155425575, from virtual screening with better characteristics.
P. Bharath, Mohanraj Gopikrishnan, Magesh Ramasamy et al.· ChemistrySelect· 0 citations
A structure-based scaffold-hopping strategy to design kinase inhibitors with selectivity for mutant KIT/PDGFRA and the PDGFRA-G680R structure shows the molecular basis for targeting solvent-front mutations across oncogenic kinases.
T. Schulz, M. Beerbaum, A. Scrima et al.· Nature Communications· 0 citations
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