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Colocalization Strategy Unveils an Underside Binding Site in the Transmembrane Domain of Smoothened Receptor.

Fang ZhouKang DingYiqing ZhouYang LiuXiaoyan LiuFei ZhaoYiran WuXianjun ZhangQiwen TanFei XuWenfu TanYouli XiaoSuwen ZhaoHouchao Tao
Published in: Journal of medicinal chemistry (2019)
We unveiled an underside binding site on smoothened receptor (SMO) by a colocalization strategy using two structurally complementary photoaffinity probes derived from a known ligand Allo-1. Docking study and structural dissection identified key interactions within the site, including hydrogen bonding, π-π interactions, and hydrophobic interactions between Allo-1 and its contacting residues. Taken together, our results reveal the molecular base of Allo-1 binding and provide a basis for the design of new-generation ligands to overcome drug resistance.
Keyphrases
  • small molecule
  • binding protein
  • molecular dynamics
  • single molecule
  • molecular dynamics simulations
  • protein protein
  • ionic liquid
  • single cell