4BFQ
Assembly of a triple pi-stack of ligands in the binding site of Aplysia californica acetylcholine binding protein (AChBP)
4BFQ の概要
| エントリーDOI | 10.2210/pdb4bfq/pdb |
| 分子名称 | SOLUBLE ACETYLCHOLINE RECEPTOR, 4,6-dimethyl-N'-(3-pyridin-2-ylisoquinolin-1-yl)pyrimidine-2-carboximidamide, GLYCEROL, ... (4 entities in total) |
| 機能のキーワード | receptor, acetylcholine binding protein, nicotinic acetylcholine receptor, cys-loop receptor, nachr, ion channel, pi-stacking, triple ligand binding, drug design |
| 由来する生物種 | APLYSIA CALIFORNICA (CALIFORNIA SEA HARE) |
| タンパク質・核酸の鎖数 | 5 |
| 化学式量合計 | 128496.70 |
| 構造登録者 | Stornaiuolo, M.,De Kloe, G.E.,Rucktooa, P.,Fish, A.,van Elk, R.,Edink, E.S.,Bertrand, D.,Smit, A.B.,de Esch, I.J.P.,Sixma, T.K. (登録日: 2013-03-21, 公開日: 2013-05-22, 最終更新日: 2024-11-06) |
| 主引用文献 | Stornaiuolo, M.,De Kloe, G.E.,Rucktooa, P.,Fish, A.,van Elk, R.,Edink, E.S.,Bertrand, D.,Smit, A.B.,de Esch, I.J.P.,Sixma, T.K. Assembly of a Pi-Pi Stack of Ligands in the Binding Site of an Acetylcholine Binding Protein Nat.Commun., 4:1875-, 2013 Cited by PubMed Abstract: Acetylcholine-binding protein is a water-soluble homologue of the extracellular ligand-binding domain of cys-loop receptors. It is used as a structurally accessible prototype for studying ligand binding to these pharmaceutically important pentameric ion channels, in particular to nicotinic acetylcholine receptors, due to conserved binding site residues present at the interface between two subunits. Here we report that an aromatic conjugated small molecule binds acetylcholine-binding protein in an ordered π-π stack of three identical molecules per binding site, two parallel and one antiparallel. Acetylcholine-binding protein stabilizes the assembly of the stack by aromatic contacts. Thanks to the plasticity of its ligand-binding site, acetylcholine-binding protein can accommodate the formation of aromatic stacks of different size by simple loop repositioning and minimal adjustment of the interactions. This type of supramolecular binding provides a novel paradigm in drug design. PubMed: 23695669DOI: 10.1038/NCOMMS2900 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.4 Å) |
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