6W6O
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![BU of 6w6o by Molmil](/molmil-images/mine/6w6o) | NaChBac-Nav1.7VSDII chimera and HWTX-IV complex | 分子名称: | (2S)-3-(hexadecanoyloxy)-2-[(9Z)-octadec-9-enoyloxy]propyl 2-(trimethylammonio)ethyl phosphate, Huwentoxin-IV, NaChBac-Nav1.7VSDII chimera | 著者 | Yan, N, Gao, S. | 登録日 | 2020-03-17 | 公開日 | 2020-06-24 | 最終更新日 | 2021-01-13 | 実験手法 | ELECTRON MICROSCOPY (3.2 Å) | 主引用文献 | Employing NaChBac for cryo-EM analysis of toxin action on voltage-gated Na + channels in nanodisc. Proc.Natl.Acad.Sci.USA, 117, 2020
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7K48
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![BU of 7k48 by Molmil](/molmil-images/mine/7k48) | Structure of NavAb/Nav1.7-VS2A chimera trapped in the resting state by tarantula toxin m3-Huwentoxin-IV | 分子名称: | Maltose/maltodextrin-binding periplasmic protein,Ion transport protein,Sodium channel protein type 9 subunit alpha chimera, Mu-theraphotoxin-Hs2a | 著者 | Wisedchaisri, G, Tonggu, L, Gamal El-Din, T.M, McCord, E, Zheng, N, Catterall, W.A. | 登録日 | 2020-09-15 | 公開日 | 2020-12-02 | 最終更新日 | 2021-01-20 | 実験手法 | ELECTRON MICROSCOPY (3.6 Å) | 主引用文献 | Structural Basis for High-Affinity Trapping of the Na V 1.7 Channel in Its Resting State by Tarantula Toxin. Mol.Cell, 81, 2021
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1MB6
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2M50
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![BU of 2m50 by Molmil](/molmil-images/mine/2m50) | Analysis of the structural and molecular basis of voltage-sensitive sodium channel inhibition by the spider toxin, Huwentoxin-IV (-TRTX-Hh2a). | 分子名称: | Mu-theraphotoxin-Hh2a | 著者 | Gibbs, A, Minassian, N, Flinspach, M, Wickenden, A. | 登録日 | 2013-02-12 | 公開日 | 2013-06-19 | 最終更新日 | 2023-11-29 | 実験手法 | SOLUTION NMR | 主引用文献 | Analysis of the Structural and Molecular Basis of Voltage-sensitive Sodium Channel Inhibition by the Spider Toxin Huwentoxin-IV ( mu-TRTX-Hh2a). J.Biol.Chem., 288, 2013
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2M4X
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2M4Z
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5T3M
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5TLR
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![BU of 5tlr by Molmil](/molmil-images/mine/5tlr) | Solution NMR structure of gHwTx-IV | 分子名称: | Mu-theraphotoxin-Hs2a | 著者 | Agwa, A.J, Schroeder, C.I. | 登録日 | 2016-10-11 | 公開日 | 2017-02-22 | 最終更新日 | 2023-06-14 | 実験手法 | SOLUTION NMR | 主引用文献 | Spider peptide toxin HwTx-IV engineered to bind to lipid membranes has an increased inhibitory potency at human voltage-gated sodium channel hNaV1.7. Biochim. Biophys. Acta, 1859, 2017
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