8OFI
Ivabradine bound to HCN4 channel
8OFI の概要
| エントリーDOI | 10.2210/pdb8ofi/pdb |
| EMDBエントリー | 16860 |
| 分子名称 | Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4, Ivabradine (2 entities in total) |
| 機能のキーワード | hcn channels, ivabradine, ion transport, membrane protein, drug, hearth, hcn4 |
| 由来する生物種 | Oryctolagus cuniculus (rabbit) |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 394559.49 |
| 構造登録者 | Saponaro, A.,Chaves-Sanjuan, A.,Sharifzadeh, A.S.,Clarke, O.B.,Marabelli, C.,Bolognesi, M.,Thiel, G.,Moroni, A. (登録日: 2023-03-15, 公開日: 2024-08-14) |
| 主引用文献 | Saponaro, A.,Krumbach, J.H.,Chaves-Sanjuan, A.,Sharifzadeh, A.S.,Porro, A.,Castelli, R.,Hamacher, K.,Bolognesi, M.,DiFrancesco, D.,Clarke, O.B.,Thiel, G.,Moroni, A. Structural determinants of ivabradine block of the open pore of HCN4. Proc.Natl.Acad.Sci.USA, 121:e2402259121-e2402259121, 2024 Cited by PubMed Abstract: HCN1-4 channels are the molecular determinants of the I/I current that crucially regulates cardiac and neuronal cell excitability. HCN dysfunctions lead to sinoatrial block (HCN4), epilepsy (HCN1), and chronic pain (HCN2), widespread medical conditions awaiting subtype-specific treatments. Here, we address the problem by solving the cryo-EM structure of HCN4 in complex with ivabradine, to date the only HCN-specific drug on the market. Our data show ivabradine bound inside the open pore at 3 Å resolution. The structure unambiguously proves that Y507 and I511 on S6 are the molecular determinants of ivabradine binding to the inner cavity, while F510, pointing outside the pore, indirectly contributes to the block by controlling Y507. Cysteine 479, unique to the HCN selectivity filter (SF), accelerates the kinetics of block. Molecular dynamics simulations further reveal that ivabradine blocks the permeating ion inside the SF by electrostatic repulsion, a mechanism previously proposed for quaternary ammonium ions. PubMed: 38917012DOI: 10.1073/pnas.2402259121 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.6 Å) |
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