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8TAO

Quis and CDPPB bound active mGlu5

Summary for 8TAO
Entry DOI10.2210/pdb8tao/pdb
EMDB information41139 41789 41793 41796
DescriptorMetabotropic glutamate receptor 5, Nb43, (S)-2-AMINO-3-(3,5-DIOXO-[1,2,4]OXADIAZOLIDIN-2-YL)-PROPIONIC ACID, ... (4 entities in total)
Functional Keywordsgpcr, signaling protein
Biological sourceHomo sapiens (human)
More
Total number of polymer chains4
Total formula weight225188.59
Authors
Krishna Kumar, K.,Wang, H.,Kobilka, B.K. (deposition date: 2023-06-27, release date: 2023-10-11, Last modification date: 2024-11-20)
Primary citationKrishna Kumar, K.,Wang, H.,Habrian, C.,Latorraca, N.R.,Xu, J.,O'Brien, E.S.,Zhang, C.,Montabana, E.,Koehl, A.,Marqusee, S.,Isacoff, E.Y.,Kobilka, B.K.
Stepwise activation of a metabotropic glutamate receptor.
Nature, 629:951-956, 2024
Cited by
PubMed Abstract: Metabotropic glutamate receptors belong to a family of G protein-coupled receptors that are obligate dimers and possess a large extracellular ligand-binding domain that is linked via a cysteine-rich domain to their 7-transmembrane domain. Upon activation, these receptors undergo a large conformational change to transmit the ligand binding signal from the extracellular ligand-binding domain to the G protein-coupling 7-transmembrane domain. In this manuscript, we propose a model for a sequential, multistep activation mechanism of metabotropic glutamate receptor subtype 5. We present a series of structures in lipid nanodiscs, from inactive to fully active, including agonist-bound intermediate states. Further, using bulk and single-molecule fluorescence imaging, we reveal distinct receptor conformations upon allosteric modulator and G protein binding.
PubMed: 38632403
DOI: 10.1038/s41586-024-07327-x
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.9 Å)
Structure validation

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