Pore stability and gating in voltage-activated calcium channels

scientific article

Pore stability and gating in voltage-activated calcium channels is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.4161/CHAN.2.2.5999
P932PMC publication ID3196840
P698PubMed publication ID18849656
P5875ResearchGate publication ID23313906

P2093author name stringH Robert Guy
Steffen Hering
Annette Hohaus
Eugen Timin
Michaela Kudrnac
Anna Stary
Stansilav Beyl
P2860cites workThe Structure of the Potassium Channel: Molecular Basis of K+ Conduction and SelectivityQ22337058
X-ray structure of a voltage-dependent K+ channelQ22337257
Chemistry of ion coordination and hydration revealed by a K+ channel-Fab complex at 2.0 A resolutionQ22337277
A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.Q24302179
Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neuronsQ24538702
Activation of Shaker potassium channels. III. An activation gating model for wild-type and V2 mutant channelsQ24642407
Atomic structure of a voltage-dependent K+ channel in a lipid membrane-like environmentQ27649044
The role of distal S6 hydrophobic residues in the voltage-dependent gating of CaV2.3 channelsQ27865194
Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autismQ28117072
Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraineQ28137616
Molecular physiology of low-voltage-activated t-type calcium channelsQ28200827
Currents related to movement of the gating particles of the sodium channelsQ28244673
Crystal structure of a mammalian voltage-dependent Shaker family K+ channelQ28260421
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kineticsQ28263620
Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effectsQ28284668
International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channelsQ28289138
Congenital stationary night blindness type 2 mutations S229P, G369D, L1068P, and W1440X alter channel gating or functional expression of Ca(v)1.4 L-type Ca2+ channelsQ28301295
The Ca2+ channel alpha2delta-1 subunit determines Ca2+ current kinetics in skeletal muscle but not targeting of alpha1S or excitation-contraction couplingQ28593153
Biodiversity of voltage sensor domain proteins.Q30360268
Familial hemiplegic migraineQ33280531
Voltage-dependent calcium channels: from structure to functionQ33715812
Voltage-gated ion channels and hereditary diseaseQ33744648
Isoform-specific regulation of mood behavior and pancreatic beta cell and cardiovascular function by L-type Ca 2+ channelsQ33784992
The voltage sensor in voltage-dependent ion channelsQ33881262
Role of S4 segments and the leucine heptad motif in the activation of an L-type calcium channelQ33915557
Critical role of conserved proline residues in the transmembrane segment 4 voltage sensor function and in the gating of L-type calcium channelsQ34990517
Voltage-gated K channelsQ35161667
Auxiliary subunits: essential components of the voltage-gated calcium channel complex.Q35172799
Cardiac calcium signallingQ35541340
L-type Ca2+ channels in Ca2+ channelopathiesQ35874336
Shaker potassium channel gating. III: Evaluation of kinetic models for activationQ36411441
Functional architecture of the inner pore of a voltage-gated Ca2+ channelQ36493546
The Timothy syndrome mutation differentially affects voltage- and calcium-dependent inactivation of CaV1.2 L-type calcium channelsQ36883128
Critical roles of the S3 segment and S3-S4 linker of repeat I in activation of L-type calcium channelsQ37558500
Structural determinants of L-type channel activation in segment IIS6 revealed by a retinal disorderQ38660530
Determinants of the differential gating properties of Cav3.1 and Cav3.3 T-type channels: a role of domain IV?Q40228543
Evidence for common structural determinants of activation and inactivation in T-type Ca2+ channelsQ40235133
Voltage gating of ion channelsQ40391780
Functional consequences of P/Q-type Ca2+ channel Cav2.1 missense mutations associated with episodic ataxia type 2 and progressive ataxiaQ40763673
Influence of L-type Ca channel alpha 2/delta-subunit on ionic and gating current in transiently transfected HEK 293 cellsQ41200281
Modulation of human neuronal alpha 1E-type calcium channel by alpha 2 delta-subunit.Q43977150
beta-Subunits: fine tuning of Ca(2+) channel blockQ44203164
Functional characterization of the L-type Ca2+ channel Cav1.4alpha1 from mouse retinaQ44743341
A gating hinge in Na+ channels; a molecular switch for electrical signalingQ44815981
Structures and functions of calcium channel beta subunitsQ46459475
Voltage sensor of Kv1.2: structural basis of electromechanical couplingQ46588794
Roles of molecular regions in determining differences between voltage dependence of activation of CaV3.1 and CaV1.2 calcium channelsQ47726373
Potentiation by the beta subunit of the ratio of the ionic current to the charge movement in the cardiac calcium channelQ49130329
Repeat I of the dihydropyridine receptor is critical in determining calcium channel activation kinetics.Q54075376
Energetics of pore opening in a voltage-gated K(+) channelQ78454007
P433issue2
P304page(s)61-69
P577publication date2008-03-14
P1433published inChannelsQ15764469
P1476titlePore stability and gating in voltage-activated calcium channels
P478volume2