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A structurally guided dissection-then-evolution strategy for ligand optimization of smoothened receptor.

Lintao YeKang DingFei ZhaoXiaoyan LiuYiran WuYang LiuDongxiang XueFang ZhouXianjun ZhangRaymond C StevensFei XuSuwen ZhaoHouchao Tao
Published in: MedChemComm (2017)
We present herein a novel dissection-then-evolution strategy for ligand optimization. Using the co-crystal structure of the smoothened receptor (SMO) as a guide, we studied the modular contribution of LY2940680 by systematically "silencing" the specific interaction between the individual residue(s) and the fragment in the ligand. Following evolution by focusing on the benzoyl part finally yielded an improved ligand 21.
Keyphrases
  • binding protein