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4X3H

CRYSTAL STRUCTURE OF ARC N-LOBE COMPLEXED WITH STARGAZIN PEPTIDE

4X3H の概要
エントリーDOI10.2210/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
zhang, W.,ward, m.,leahy, d.,worley, p. (登録日: 2014-11-30, 公開日: 2015-06-03, 最終更新日: 2024-02-28)
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: 25864631
DOI: 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)
構造検証レポート
Validation report summary of 4x3h
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-11-06に公開中

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