(Q44631900)

4 December 2017

title

Molecular basis for Kv1.5 channel block: conservation of drug binding sites among voltage-gated K+ channels (English)

1 reference

4 December 2017

0 references

Karl-Heinz Baringhaus

5

object named as

Karl-Heinz Baringhaus

1 reference

4 December 2017

Niels Decher

1

1 reference

4 December 2017

Bernard Pirard

2

1 reference

4 December 2017

Florian Bundis

3

1 reference

4 December 2017

Stefan Peukert

4

1 reference

4 December 2017

Andreas E Busch

6

1 reference

4 December 2017

Klaus Steinmeyer

7

1 reference

4 December 2017

Michael C Sanguinetti

8

1 reference

4 December 2017

language of work or name

English

0 references

publication date

25 October 2003

1 reference

Journal of Biological Chemistry

4 December 2017

published in

1 reference

4 December 2017

volume

279

1 reference

4 December 2017

issue

1

1 reference

4 December 2017

page(s)

394-400

1 reference

Incidence and risks associated with atrial fibrillation

4 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Identity of a novel delayed rectifier current from human heart with a cloned K+ channel current.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

A rapidly activating and slowly inactivating potassium channel cloned from human heart. Functional analysis after stable mammalian cell culture expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Identification, synthesis, and activity of novel blockers of the voltage-gated potassium channel Kv1.5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Determinants of antiarrhythmic drug action. Electrostatic and hydrophobic components of block of the human cardiac hKv1.5 channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Molecular analysis of a binding site for quinidine in a human cardiac delayed rectifier K+ channel. Role of S6 in antiarrhythmic drug binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Molecular determinants of stereoselective bupivacaine block of hKv1.5 channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Stereoselective block of a human cardiac potassium channel (Kv1.5) by bupivacaine enantiomers

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Putative binding sites for benzocaine on a human cardiac cloned channel (Kv1.5).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

The internal quaternary ammonium receptor site of Shaker potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Two functionally distinct subsites for the binding of internal blockers to the pore of voltage-activated K+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Molecular determinants of high affinity phenylalkylamine block of L-type calcium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Construction of a high-affinity receptor site for dihydropyridine agonists and antagonists by single amino acid substitutions in a non-L-type Ca2+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Common molecular determinants of local anesthetic, antiarrhythmic, and anticonvulsant block of voltage-gated Na+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Analysis of the dihydropyridine receptor site of L-type calcium channels by alanine-scanning mutagenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

A structural basis for drug-induced long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Mutations affecting internal TEA blockade identify the probable pore-forming region of a K+ channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Interactions of the H5 pore region and hydroxylamine with N-type inactivation in the Shaker K+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Potassium channel receptor site for the inactivation gate and quaternary amine inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

External TEA block of shaker K+ channels is coupled to the movement of K+ ions within the selectivity filter

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

The open pore conformation of potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

X-ray structure of a voltage-dependent K+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Molecular determinants of KCNQ1 channel block by a benzodiazepine

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Binding of correolide to the K(v)1.3 potassium channel: characterization of the binding domain by site-directed mutagenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Characterization of TASK-4, a novel member of the pH-sensitive, two-pore domain potassium channel family

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Electrophysiological recording from Xenopus oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

QXP: powerful, rapid computer algorithms for structure-based drug design.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Position of aromatic residues in the S6 domain, not inactivation, dictates cisapride sensitivity of HERG and eag potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Molecular determinants of voltage-dependent human ether-a-go-go related gene (HERG) K+ channel block

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Sustained depolarization-induced outward current in human atrial myocytes. Evidence for a novel delayed rectifier K+ current similar to Kv1.5 cloned channel currents

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Blocker protection in the pore of a voltage-gated K+ channel and its structural implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Mechanism of flecainide's antiarrhythmic action in experimental atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Evidence for two components of delayed rectifier K+ current in human ventricular myocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

Open channel block of HERG K(+) channels by vesnarinone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M307411200

21 January 2018

Identifiers

DOI

10.1074/JBC.M307411200

1 reference

4 December 2017

1 reference