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8F0S

Structure of VSD4-NaV1.7-NaVPas channel chimera bound to the hybrid inhibitor GNE-9296

Summary for 8F0S
Entry DOI10.2210/pdb8f0s/pdb
EMDB information28779
DescriptorSodium channel protein PaFPC1,Sodium channel protein type 9 subunit alpha chimera, Beta-diguetoxin-Dc1a, beta-D-mannopyranose-(1-3)-[beta-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-3)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-3)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (8 entities in total)
Functional Keywordsion channel, small molecule, inhibitor, membrane protein-inhibitor complex, membrane protein/inhibitor
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight196743.09
Authors
Primary citationKschonsak, M.,Jao, C.C.,Arthur, C.P.,Rohou, A.L.,Bergeron, P.,Ortwine, D.F.,McKerrall, S.J.,Hackos, D.H.,Deng, L.,Chen, J.,Li, T.,Dragovich, P.S.,Volgraf, M.,Wright, M.R.,Payandeh, J.,Ciferri, C.,Tellis, J.C.
Cryo-EM reveals an unprecedented binding site for Na V 1.7 inhibitors enabling rational design of potent hybrid inhibitors.
Elife, 12:-, 2023
Cited by
PubMed: 36975198
DOI: 10.7554/eLife.84151
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.1 Å)
Structure validation

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