4X3H
CRYSTAL STRUCTURE OF ARC N-LOBE COMPLEXED WITH STARGAZIN PEPTIDE
4X3H の概要
エントリーDOI | 10.2210/pdb4x3h/pdb |
関連するPDBエントリー | 4X3I 4X3X |
分子名称 | Activity-regulated cytoskeleton-associated protein, VOLTAGE-DEPENDENT CALCIUM CHANNEL GAMMA-2 SUBUNIT (3 entities in total) |
機能のキーワード | endocytosis mediator, signaling protein |
由来する生物種 | Rattus norvegicus (Rat) 詳細 |
細胞内の位置 | Cytoplasm, cytoskeleton: Q63053 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 10622.80 |
構造登録者 | |
主引用文献 | Zhang, W.,Wu, J.,Ward, M.D.,Yang, S.,Chuang, Y.A.,Xiao, M.,Li, R.,Leahy, D.J.,Worley, P.F. Structural basis of arc binding to synaptic proteins: implications for cognitive disease. Neuron, 86:490-500, 2015 Cited by PubMed Abstract: Arc is a cellular immediate-early gene (IEG) that functions at excitatory synapses and is required for learning and memory. We report crystal structures of Arc subdomains that form a bi-lobar architecture remarkably similar to the capsid domain of human immunodeficiency virus (HIV) gag protein. Analysis indicates Arc originated from the Ty3/Gypsy retrotransposon family and was "domesticated" in higher vertebrates for synaptic functions. The Arc N-terminal lobe evolved a unique hydrophobic pocket that mediates intermolecular binding with synaptic proteins as resolved in complexes with TARPγ2 (Stargazin) and CaMKII peptides and is essential for Arc's synaptic function. A consensus sequence for Arc binding identifies several additional partners that include genes implicated in schizophrenia. Arc N-lobe binding is inhibited by small chemicals suggesting Arc's synaptic action may be druggable. These studies reveal the remarkable evolutionary origin of Arc and provide a structural basis for understanding Arc's contribution to neural plasticity and disease. PubMed: 25864631DOI: 10.1016/j.neuron.2015.03.030 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.401 Å) |
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