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Insights into the Structural Aspects of the mGlu Receptor Orthosteric Binding Site.
Hao, Junliang; Chen, Qi.
Affiliation
  • Hao J; Discovery Chemistry Research and Technologies, Lilly Research Laboratory, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, United States.
  • Chen Q; Discovery Chemistry Research and Technologies, Lilly Research Laboratory, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, United States.
Curr Top Med Chem ; 19(26): 2421-2446, 2019.
Article in En | MEDLINE | ID: mdl-31660833
ABSTRACT
The amino terminal domain (ATD) of the metabotropic glutamate (mGlu) receptors contains the orthosteric glutamate recognition site, which is highly conserved across the eight mGlu receptor subtypes. In total, 29 X-ray crystal structures of the mGlu ATD proteins have been reported to date. These structures span across 3 subgroups and 6 subtypes, and include apo, agonist- and antagonist-bound structures. We will discuss the insights gained from the analysis of these structures with the focus on the interactions contributing to the observed group and subtype selectivity for select agonists. Furthermore, we will define the full expanded orthosteric ligand binding pocket (LBP) of the mGlu receptors, and discuss the macroscopic features of the mGlu ATD proteins.
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Full text: 1 Database: MEDLINE Main subject: Receptors, Metabotropic Glutamate Limits: Animals / Humans Language: En Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: Receptors, Metabotropic Glutamate Limits: Animals / Humans Language: En Year: 2019 Type: Article