Background: Mutation in the B RAF at V600E has been well implicated in the carcinogenesis that makes
it as an attractive therapeutictarget. In the present study, we sought to identify the basis of V600E mutation at functional
and structural grounds. The study also endeavors in identification of small molecule as a potential candidate
with considerable pharmacological profile than available BRAF inhibitors through computational approaches.
Methods: The functional effects of V600E mutation was predicted using SIFT and Polyphen servers. Protein structural
alterations werepredicted using SDM server and RMSD calculations. Virtual screening was performed considering
existing BRAF inhibitors viz., Vemurafenib, Sorafenib, Dabrfenib, Trametinibthat formed query compounds
for shape similarity search by Tanimoto similarity indices with a threshold of 95%. Compound with high affinity as
similar to query compound was retrieved and screened for its ADMET properties.
Results: The SNP was shown to be highly vulnerable to malfunction and have damaging effects. Mutated protein
showed that the secondary structure was irregular and side chain hydrogen bonds were unsaturated. The superimposition
of wild onto mutated V600E BRAF revealed helix-coil transition occurring wherein residues Val 502, Leu
505, Arg506, Lys 507 assumed coiled conformation in the mutated BRAF. Virtual screening led to identification of
SCHEMBL298689 akin to Vemurafenib as high affinity B-Raf inhibitors; with least toxicity and optimal bioactivity.
Conclusion: In the present investigation, we put forth the structural and functional basis of B RAF V600E mutation
showing helix coil transitions. In addition identified high affinity compound targeting V600E B RAF through virtual