Literature DB >> 30309741

Structural and Druggability Landscape of Frizzled G Protein-Coupled Receptors.

Xianjun Zhang1, Shaowei Dong1, Fei Xu2.   

Abstract

Class Frizzled G protein-coupled receptors (GPCRs), which includes the Smoothened receptor (SMO) and 10 Frizzled receptors (FZDs), are responsible for mediating fundamental signaling in embryonic development and tissue homeostasis. Dysregulation of these receptors can lead to cancer. Structural understanding of these molecules has provided insight to their function and signaling, and guided drug discovery. To date, the structures of the multi- and individual domains of SMO, 14 FZD extracellular domains, and the transmembrane domain (TMD) of FZD4, have been reported. Here, we review all reported frizzled family structures and diverse signalosome models, with an emphasis on the different ligand binding sites and lipid binding grooves, aiming to uncover the druggability landscape of the frizzled GPCR family.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  class Frizzled receptors; ligand binding site; lipid binding groove; structure

Mesh:

Substances:

Year:  2018        PMID: 30309741     DOI: 10.1016/j.tibs.2018.09.002

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


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