Regulation of the oncoprotein Smoothened by small molecules

被引:0
作者
Sharpe H.J. [1 ]
Wang W. [2 ]
Hannoush R.N. [3 ]
De Sauvage F.J. [1 ]
机构
[1] Department of Molecular Oncology, Genentech Inc., San Francisco, CA
[2] Department of Structural Biology, Genentech Inc., San Francisco, CA
[3] Department of Early Discovery Biochemistry, Genentech Inc., San Francisco, CA
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D O I
10.1038/nchembio.1776
中图分类号
学科分类号
摘要
The Hedgehog pathway is critical for animal development and has been implicated in multiple human malignancies. Despite great interest in targeting the pathway pharmacologically, many of the principles underlying the signal transduction cascade remain poorly understood. Hedgehog ligands are recognized by a unique receptor system that features the transporter-like protein Patched and the G protein-coupled receptor (GPCR)-like Smoothened (SMO). The biochemical interaction between these transmembrane proteins is the subject of intensive efforts. Recent structural and functional studies have provided great insight into the small-molecule regulation of SMO through identification of two distinct ligand-binding sites. In this Perspective, we review these recent findings and relate them to potential mechanisms for the endogenous regulation of SMO.
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页码:246 / 255
页数:9
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