5OJM
Structure of a chimaeric beta3-alpha5 GABAA receptor in complex with nanobody Nb25
5OJM の概要
| エントリーDOI | 10.2210/pdb5ojm/pdb |
| 分子名称 | Human GABAA receptor chimera beta3-alpha5,Gamma-aminobutyric acid receptor subunit beta-3,Gamma-aminobutyric acid receptor subunit alpha-5, Nanobody Nb25, alpha-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (5 entities in total) |
| 機能のキーワード | gabaa receptor, nanobody complex, neurosteroid, ion channel, membrane protein |
| 由来する生物種 | synthetic construct 詳細 |
| タンパク質・核酸の鎖数 | 10 |
| 化学式量合計 | 296516.39 |
| 構造登録者 | Miller, P.S.,Scott, S.,Masiulis, S.,De Colibus, L.,Pardon, E.,Steyaert, J.,Aricescu, A.R. (登録日: 2017-07-21, 公開日: 2017-10-04, 最終更新日: 2024-10-16) |
| 主引用文献 | Miller, P.S.,Scott, S.,Masiulis, S.,De Colibus, L.,Pardon, E.,Steyaert, J.,Aricescu, A.R. Structural basis for GABAA receptor potentiation by neurosteroids. Nat. Struct. Mol. Biol., 24:986-992, 2017 Cited by PubMed Abstract: Type A γ-aminobutyric acid receptors (GABARs) are the principal mediators of inhibitory neurotransmission in the human brain. Endogenous neurosteroids interact with GABARs to regulate acute and chronic anxiety and are potent sedative, analgesic, anticonvulsant and anesthetic agents. Their mode of binding and mechanism of receptor potentiation, however, remain unknown. Here we report crystal structures of a chimeric GABAR construct in apo and pregnanolone-bound states. The neurosteroid-binding site is mechanically coupled to the helices lining the ion channel pore and modulates the desensitization-gate conformation. We demonstrate that the equivalent site is responsible for physiological, heteromeric GABAR potentiation and explain the contrasting modulatory properties of 3a versus 3b neurosteroid epimers. These results illustrate how peripheral lipid ligands can regulate the desensitization gate of GABARs, a process of broad relevance to pentameric ligand-gated ion channels. PubMed: 28991263DOI: 10.1038/nsmb.3484 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (3.3 Å) |
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