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6CNA

GluN1-GluN2B NMDA receptors with exon 5

6CNA の概要
エントリーDOI10.2210/pdb6cna/pdb
EMDBエントリー7529
分子名称Glutamate receptor ionotropic, NMDA 1, Glutamate receptor ionotropic, NMDA 2B, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total)
機能のキーワードsplicing variant, membrane protein
由来する生物種Rattus norvegicus (Rat)
詳細
タンパク質・核酸の鎖数4
化学式量合計375990.61
構造登録者
Furukawa, H.,Grant, T.,Grigorieff, N. (登録日: 2018-03-07, 公開日: 2018-10-03, 最終更新日: 2025-05-14)
主引用文献Regan, M.C.,Grant, T.,McDaniel, M.J.,Karakas, E.,Zhang, J.,Traynelis, S.F.,Grigorieff, N.,Furukawa, H.
Structural Mechanism of Functional Modulation by Gene Splicing in NMDA Receptors.
Neuron, 98:521-529.e3, 2018
Cited by
PubMed Abstract: Alternative gene splicing gives rise to N-methyl-D-aspartate (NMDA) receptor ion channels with defined functional properties and unique contributions to calcium signaling in a given chemical environment in the mammalian brain. Splice variants possessing the exon-5-encoded motif at the amino-terminal domain (ATD) of the GluN1 subunit are known to display robustly altered deactivation rates and pH sensitivity, but the underlying mechanism for this functional modification is largely unknown. Here, we show through cryoelectron microscopy (cryo-EM) that the presence of the exon 5 motif in GluN1 alters the local architecture of heterotetrameric GluN1-GluN2 NMDA receptors and creates contacts with the ligand-binding domains (LBDs) of the GluN1 and GluN2 subunits, which are absent in NMDA receptors lacking the exon 5 motif. The unique interactions established by the exon 5 motif are essential to the stability of the ATD/LBD and LBD/LBD interfaces that are critically involved in controlling proton sensitivity and deactivation.
PubMed: 29656875
DOI: 10.1016/j.neuron.2018.03.034
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (4.6 Å)
構造検証レポート
Validation report summary of 6cna
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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