Tight coupling of rubidium conductance and inactivation in human KCNQ1 potassium channels (Q48820160)

15 February 2018

title

Tight coupling of rubidium conductance and inactivation in human KCNQ1 potassium channels (English)

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15 February 2018

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3

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15 February 2018

author name string

Guiscard Seebohm

series ordinal

1

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15 February 2018

Michael C Sanguinetti

series ordinal

2

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15 February 2018

language of work or name

English

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publication date

1 October 2003

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15 February 2018

published in

Journal of Physiology

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15 February 2018

volume

552

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15 February 2018

issue

Pt 2

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15 February 2018

page(s)

369-378

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15 February 2018

The principle of gating charge movement in a voltage-dependent K channel

cites work

1 reference

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X-ray structure of a voltage-dependent K channel

26 August 2018

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KCNE5 induces time- and voltage-dependent modulation of the KCNQ1 current

26 August 2018

1 reference

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The voltage-gated potassium channels and their relatives

26 August 2018

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

26 August 2018

1 reference

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Energetic optimization of ion conduction rate by the K selectivity filter

26 August 2018

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Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K channel

26 August 2018

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KcsA: it's a potassium channel

26 August 2018

1 reference

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Dynamic interaction of S5 and S6 during voltage-controlled gating in a potassium channel

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Location and orientation of minK within the I(Ks) potassium channel complex

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Two open states and rate-limiting gating steps revealed by intracellular Na block of human KCNQ1 and KCNQ1/KCNE1 K channels

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Identification of specific pore residues mediating KCNQ1 inactivation. A novel mechanism for long QT syndrome

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

A constitutively open potassium channel formed by KCNQ1 and KCNE3

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Gating and flickery block differentially affected by rubidium in homomeric KCNQ1 and heteromeric KCNQ1/KCNE1 potassium channels

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K channels causes epilepsy

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Single-channel properties of IKs potassium channels

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Single-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Increase of the single-channel conductance of KvLQT1 potassium channels induced by the association with minK.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Electrophysiologic recordings from Xenopus oocytes

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Activation and inactivation of homomeric KvLQT1 potassium channels.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Voltage-dependent inactivation of the human K channel KvLQT1 is eliminated by association with minimal K channel (minK) subunits

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

A side chain in S6 influences both open-state stability and ion permeation in a voltage-gated K channel

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

A potassium channel mutation in neonatal human epilepsy

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Dominant-Negative KvLQT1 Mutations Underlie the LQT1 Form of Long QT Syndrome

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Mutations in the K channel signature sequence

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Cloning of a membrane protein that induces a slow voltage-gated potassium current

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343369

Molecular genetics of the long QT syndrome: Two novel mutations of the KVLQT1 gene and phenotypic expression of the mutant gene in a large kindred

26 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/14561821

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1113/JPHYSIOL.2003.046490

1 reference

15 February 2018

PMC publication ID

2343369

0 references

1 reference

15 February 2018