IUPHAR/BPS Guide to Pharmacology CITE
https://doi.org/10.2218/gtopdb/F82/2019.4
Voltage-gated sodium channels (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database
William A. Catterall1,
Alan L. Goldin2 and
Stephen G. Waxman3
- University of Washington, USA
- University of California, USA
- Yale University, USA
Abstract
Sodium channels are voltage-gated sodium-selective ion channels present in the membrane of most excitable cells. Sodium channels comprise of one pore-forming α subunit, which may be associated with either one or two β subunits [176]. α-Subunits consist of four homologous domains (I–IV), each containing six transmembrane segments (S1–S6) and a pore-forming loop. The positively charged fourth transmembrane segment (S4) acts as a voltage sensor and is involved in channel gating. The crystal structure of the bacterial NavAb channel has revealed a number of novel structural features compared to earlier potassium channel structures including a short selectivity filter with ion selectivity determined by interactions with glutamate side chains [268]. Interestingly, the pore region is penetrated by fatty acyl chains that extend into the central cavity which may allow the entry of small, hydrophobic pore-blocking drugs [268]. Auxiliary β1, β2, β3 and β4 subunits consist of a large extracellular N-terminal domain, a single transmembrane segment and a shorter cytoplasmic domain.
The nomenclature for sodium channels was proposed by Goldin et al., (2000) [143] and approved by the NC-IUPHAR Subcommittee on sodium channels (Catterall et al., 2005, [51]).
Contents
This is a citation summary for Voltage-gated sodium channels in the
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Database links
Voltage-gated sodium channels
http://www.guidetopharmacology.org/GRAC/FamilyDisplayForward?familyId=82
Introduction to Voltage-gated sodium channels
http://www.guidetopharmacology.org/GRAC/FamilyIntroductionForward?familyId=82
Channels and Subunits
Nav1.1
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=578
Nav1.2
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=579
Nav1.3
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=580
Nav1.4
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=581
Nav1.5
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=582
Nav1.6
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=583
Nav1.7
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=584
Nav1.8
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=585
Nav1.9
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=586
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