5EK0

Human Nav1.7-VSD4-NavAb in complex with GX-936.

5EK0 の概要

• エントリーDOI: 10.2210/pdb5ek0/pdb
• 分子名称: Chimera of bacterial Ion transport protein and human Sodium channel protein type 9 subunit alpha, 1,2-DIMYRISTOYL-SN-GLYCERO-3-PHOSPHOCHOLINE, 3-cyano-4-[2-[2-(1-ethylazetidin-3-yl)pyrazol-3-yl]-4-(trifluoromethyl)phenoxy]-~{N}-(1,2,4-thiadiazol-5-yl)benzenesulfonamide (3 entities in total)
• 機能のキーワード: membrane protein, ion channel, voltage-gated sodium channel, small molecule antagonist, metal transport
• 由来する生物種: Arcobacter butzleri, Homo sapiens
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 155032.46

構造登録者

Ahuja, S.,Mukund, S.,Starovasnik, M.A.,Koth, C.M.,Payandeh, J. (登録日: 2015-11-03, 公開日: 2015-12-23, 最終更新日: 2023-09-27)

主引用文献

Ahuja, S.,Mukund, S.,Deng, L.,Khakh, K.,Chang, E.,Ho, H.,Shriver, S.,Young, C.,Lin, S.,Johnson, J.P.,Wu, P.,Li, J.,Coons, M.,Tam, C.,Brillantes, B.,Sampang, H.,Mortara, K.,Bowman, K.K.,Clark, K.R.,Estevez, A.,Xie, Z.,Verschoof, H.,Grimwood, M.,Dehnhardt, C.,Andrez, J.C.,Focken, T.,Sutherlin, D.P.,Safina, B.S.,Starovasnik, M.A.,Ortwine, D.F.,Franke, Y.,Cohen, C.J.,Hackos, D.H.,Koth, C.M.,Payandeh, J.
Structural basis of Nav1.7 inhibition by an isoform-selective small-molecule antagonist.
Science, 350:aac5464-aac5464, 2015

PubMed Abstract: Voltage-gated sodium (Nav) channels propagate action potentials in excitable cells. Accordingly, Nav channels are therapeutic targets for many cardiovascular and neurological disorders. Selective inhibitors have been challenging to design because the nine mammalian Nav channel isoforms share high sequence identity and remain recalcitrant to high-resolution structural studies. Targeting the human Nav1.7 channel involved in pain perception, we present a protein-engineering strategy that has allowed us to determine crystal structures of a novel receptor site in complex with isoform-selective antagonists. GX-936 and related inhibitors bind to the activated state of voltage-sensor domain IV (VSD4), where their anionic aryl sulfonamide warhead engages the fourth arginine gating charge on the S4 helix. By opposing VSD4 deactivation, these compounds inhibit Nav1.7 through a voltage-sensor trapping mechanism, likely by stabilizing inactivated states of the channel. Residues from the S2 and S3 helices are key determinants of isoform selectivity, and bound phospholipids implicate the membrane as a modulator of channel function and pharmacology. Our results help to elucidate the molecular basis of voltage sensing and establish structural blueprints to design selective Nav channel antagonists.

PubMed: 26680203
DOI: 10.1126/science.aac5464

実験手法

X-RAY DIFFRACTION (3.53 Å)