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4G28

Calcium-calmodulin complexed with the calmodulin binding domain from a small conductance potassium channel splice variant and EBIO-1

4G28 の概要
エントリーDOI10.2210/pdb4g28/pdb
関連するPDBエントリー1G4Y 3SJQ 4G27
分子名称Small conductance calcium-activated potassium channel protein 2, Calmodulin, SULFATE ION, ... (7 entities in total)
機能のキーワードprotein-protein complex, ef hand, metal binding protein, metal transport-calcium binding protein complex, metal transport/calcium binding protein
由来する生物種Rattus norvegicus (rat)
詳細
細胞内の位置Membrane; Multi-pass membrane protein: P70604
タンパク質・核酸の鎖数2
化学式量合計29718.57
構造登録者
Zhang, M.,Pascal, J.M.,Zhang, J.-F. (登録日: 2012-07-11, 公開日: 2012-09-12, 最終更新日: 2024-02-28)
主引用文献Zhang, M.,Pascal, J.M.,Schumann, M.,Armen, R.S.,Zhang, J.F.
Identification of the functional binding pocket for compounds targeting small-conductance Ca(2+)-activated potassium channels.
Nat Commun, 3:1021-1021, 2012
Cited by
PubMed Abstract: Small- and intermediate-conductance Ca(2+)-activated potassium channels, activated by Ca(2+)-bound calmodulin, have an important role in regulating membrane excitability. These channels are also linked to clinical abnormalities. A tremendous amount of effort has been devoted to developing small molecule compounds targeting these channels. However, these compounds often suffer from low potency and lack of selectivity, hindering their potential for clinical use. A key contributing factor is the lack of knowledge of the binding site(s) for these compounds. Here we demonstrate by X-ray crystallography that the binding pocket for the compounds of the 1-ethyl-2-benzimidazolinone (1-EBIO) class is located at the calmodulin-channel interface. We show that, based on structure data and molecular docking, mutations of the channel can effectively change the potency of these compounds. Our results provide insight into the molecular nature of the binding pocket and its contribution to the potency and selectivity of the compounds of the 1-EBIO class.
PubMed: 22929778
DOI: 10.1038/ncomms2017
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.63 Å)
構造検証レポート
Validation report summary of 4g28
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2024-10-30に公開中

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