Table 1.
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] |