3RIF
C. elegans glutamate-gated chloride channel (GluCl) in complex with Fab, ivermectin and glutamate.
3RIF の概要
エントリーDOI | 10.2210/pdb3rif/pdb |
関連するPDBエントリー | 3RHW 3RI5 3RIA |
分子名称 | Avermectin-sensitive glutamate-gated chloride channel GluCl alpha, UNDECANE, Mouse monoclonal Fab fragment, heavy chain, ... (10 entities in total) |
機能のキーワード | membrane protein, transport protein, cys-loop receptor, ligand-gated ion channel, neurotransmitter receptor, ivermectin, picrotoxin, glycosylation, transport protein-immune system complex, transport protein/immune system |
由来する生物種 | Caenorhabditis elegans (nematode) 詳細 |
タンパク質・核酸の鎖数 | 15 |
化学式量合計 | 438723.67 |
構造登録者 | |
主引用文献 | Hibbs, R.E.,Gouaux, E. Principles of activation and permeation in an anion-selective Cys-loop receptor. Nature, 474:54-60, 2011 Cited by PubMed Abstract: Fast inhibitory neurotransmission is essential for nervous system function and is mediated by binding of inhibitory neurotransmitters to receptors of the Cys-loop family embedded in the membranes of neurons. Neurotransmitter binding triggers a conformational change in the receptor, opening an intrinsic chloride channel and thereby dampening neuronal excitability. Here we present the first three-dimensional structure, to our knowledge, of an inhibitory anion-selective Cys-loop receptor, the homopentameric Caenorhabditis elegans glutamate-gated chloride channel α (GluCl), at 3.3 Å resolution. The X-ray structure of the GluCl-Fab complex was determined with the allosteric agonist ivermectin and in additional structures with the endogenous neurotransmitter L-glutamate and the open-channel blocker picrotoxin. Ivermectin, used to treat river blindness, binds in the transmembrane domain of the receptor and stabilizes an open-pore conformation. Glutamate binds in the classical agonist site at subunit interfaces, and picrotoxin directly occludes the pore near its cytosolic base. GluCl provides a framework for understanding mechanisms of fast inhibitory neurotransmission and allosteric modulation of Cys-loop receptors. PubMed: 21572436DOI: 10.1038/nature10139 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (3.345 Å) |
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