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. 2019 Mar 20;24(6):1098. doi: 10.3390/molecules24061098

Table 1.

Summary of crystal structures for the 7TM domain of mGlu receptors.

Receptor PDB ID Method Resolution Description Reference
mGlu1 4OR2 X-ray diffraction 2.8 Å Crystal structure of 7TM domain of human mGlu1 bound to FITM (NAM). Soluble cytochrome b562 present for stabilization. [17]
mGlu5 4OO9 X-ray diffraction 2.6 Å Structure of the human 7TM domain of mGlu5 bound to mavoglurant (NAM). Lysozyme used for stabilization. [16]
5CGC X-ray diffraction 3.1 Å Structure of human 7TM domain of mGlu5 bound to 3-chloro-4-fluoro-5-[6-(1H-pyrazol-1-yl)pyrimidin-4-yl]benzonitrile (NAM). Endolysin present in the structure used for stabilization. [18]
5CGD X-ray diffraction 2.6 Å Structure of human 7TM of mGlu5 bound to HTL14242 (NAM). Endolysin present in the structure used for stabilization. [18]
6FFH X-ray diffraction 2.7 Å Crystal structure of 7TM domain of human mGlu5 bound to fenobam (NAM). Endolysin present in the structure for stabilization. [19]
6FFI X-ray diffraction 2.2 Å Crystal structure of 7TM domain of human mGlu5 bound to M-MPEP (NAM). Endolysin present for stabilization. [19]