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5IPV

Cryo-EM structure of GluN1/GluN2B NMDA receptor in the DCKA/D-APV-bound conformation, state 1

Summary for 5IPV
Entry DOI10.2210/pdb5ipv/pdb
Related5IOU 5IOV 5IPQ 5IPR 5IPS 5IPT 5IPU
EMDB information8097 8098 8101 8102 8103 8104 8105 8106
DescriptorN-methyl-D-aspartate receptor subunit NR1-8a, Ionotropic glutamate receptor subunit NR2B (2 entities in total)
Functional Keywordsligand-gated ion channel, synaptic transmission, signaling protein
Biological sourceXenopus laevis (African clawed frog)
More
Total number of polymer chains4
Total formula weight371771.95
Authors
Zhu, S.,Stein, A.R.,Yoshioka, C.,Lee, C.H.,Goehring, A.,McHaourab, S.H.,Gouaux, E. (deposition date: 2016-03-10, release date: 2016-04-20, Last modification date: 2024-03-06)
Primary citationZhu, S.,Stein, R.A.,Yoshioka, C.,Lee, C.H.,Goehring, A.,Mchaourab, H.S.,Gouaux, E.
Mechanism of NMDA Receptor Inhibition and Activation.
Cell, 165:704-714, 2016
Cited by
PubMed Abstract: N-methyl-D-aspartate receptors (NMDARs) are glutamate-gated, calcium-permeable ion channels that mediate synaptic transmission and underpin learning and memory. NMDAR dysfunction is directly implicated in diseases ranging from seizure to ischemia. Despite its fundamental importance, little is known about how the NMDAR transitions between inactive and active states and how small molecules inhibit or activate ion channel gating. Here, we report electron cryo-microscopy structures of the GluN1-GluN2B NMDA receptor in an ensemble of competitive antagonist-bound states, an agonist-bound form, and a state bound with agonists and the allosteric inhibitor Ro25-6981. Together with double electron-electron resonance experiments, we show how competitive antagonists rupture the ligand binding domain (LBD) gating "ring," how agonists retain the ring in a dimer-of-dimers configuration, and how allosteric inhibitors, acting within the amino terminal domain, further stabilize the LBD layer. These studies illuminate how the LBD gating ring is fundamental to signal transduction and gating in NMDARs.
PubMed: 27062927
DOI: 10.1016/j.cell.2016.03.028
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (9.25 Å)
Structure validation

226707

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