(Q37280509)

English

The external pore loop interacts with S6 and S3-S4 linker in domain 4 to assume an essential role in gating control and anticonvulsant action in the Na(+) channel

scientific article published on August 2009

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scholarly article

1 reference

Europe PubMed Central

19 August 2017

The external pore loop interacts with S6 and S3-S4 linker in domain 4 to assume an essential role in gating control and anticonvulsant action in the Na(+) channel (English)

1 reference

Europe PubMed Central

19 August 2017

author name string

Ya-Chin Yang

1

1 reference

Europe PubMed Central

19 August 2017

Jui-Yi Hsieh

2

1 reference

Europe PubMed Central

19 August 2017

Chung-Chin Kuo

3

1 reference

Europe PubMed Central

19 August 2017

publication date

1 August 2009

1 reference

Europe PubMed Central

19 August 2017

The Journal of General Physiology

1 reference

Europe PubMed Central

19 August 2017

134

1 reference

Europe PubMed Central

19 August 2017

2

1 reference

Europe PubMed Central

19 August 2017

95-113

1 reference

Europe PubMed Central

19 August 2017

Role of aromatic side chains in the folding and thermodynamic stability of integral membrane proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

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Tetracaine-membrane interactions: effects of lipid composition and phase on drug partitioning, location, and ionization

1 reference

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6 September 2017

Crystal structure of a mammalian voltage-dependent Shaker family K+ channel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

6 September 2017

An inactivation stabilizer of the Na+ channel acts as an opportunistic pore blocker modulated by external Na+.

1 reference

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Block of tetrodotoxin-resistant Na+ channel pore by multivalent cations: gating modification and Na+ flow dependence.

1 reference

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The Na+ channel inactivation gate is a molecular complex: a novel role of the COOH-terminal domain.

1 reference

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6 September 2017

Selective aromatic interactions in beta-hairpin peptides

1 reference

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S4 charges move close to residues in the pore domain during activation in a K channel

1 reference

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Structural and gating changes of the sodium channel induced by mutation of a residue in the upper third of IVS6, creating an external access path for local anesthetics.

1 reference

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How proteins adapt to a membrane-water interface

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6 September 2017

Localization and molecular determinants of the Hanatoxin receptors on the voltage-sensing domains of a K(+) channel

1 reference

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6 September 2017

Rapid and slow voltage-dependent conformational changes in segment IVS6 of voltage-gated Na(+) channels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

6 September 2017

Movement of voltage sensor S4 in domain 4 is tightly coupled to sodium channel fast inactivation and gating charge immobilization

1 reference

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The Na channel voltage sensor associated with inactivation is localized to the external charged residues of domain IV, S4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

6 September 2017

Batrachotoxin-resistant Na+ channels derived from point mutations in transmembrane segment D4-S6

1 reference

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6 September 2017

Interaction between the pore and a fast gate of the cardiac sodium channel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

6 September 2017

Imipramine inhibition of transient K+ current: an external open channel blocker preventing fast inactivation

1 reference

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Interaction of batrachotoxin with the local anesthetic receptor site in transmembrane segment IVS6 of the voltage-gated sodium channel

1 reference

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6 September 2017

Characterization of lamotrigine inhibition of Na+ channels in rat hippocampal neurones

1 reference

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6 September 2017

Altered ionic selectivity of the sodium channel revealed by cysteine mutations within the pore

1 reference

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6 September 2017

A unique role for the S4 segment of domain 4 in the inactivation of sodium channels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

6 September 2017

Role of an S4-S5 linker in sodium channel inactivation probed by mutagenesis and a peptide blocker

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

6 September 2017

Experimentally determined hydrophobicity scale for proteins at membrane interfaces

1 reference

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6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

6 September 2017

Adjacent pore-lining residues within sodium channels identified by paired cysteine mutagenesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

6 September 2017

Molecular determinants of high affinity binding of alpha-scorpion toxin and sea anemone toxin in the S3-S4 extracellular loop in domain IV of the Na+ channel alpha subunit

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

6 September 2017

Molecular determinants of drug access to the receptor site for antiarrhythmic drugs in the cardiac Na+ channel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

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Transcainide causes two modes of open-channel block with different voltage sensitivities in batrachotoxin-activated sodium channels

1 reference

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6 September 2017

A mutation in the pore of the sodium channel alters gating

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

6 September 2017

Nitrendipine block of cardiac calcium channels: high-affinity binding to the inactivated state

1 reference

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Diphenylhydantoin Inhibition of Sodium Conductance in Squid Giant Axon

1 reference

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6 September 2017

Site of covalent attachment of alpha-scorpion toxin derivatives in domain I of the sodium channel alpha subunit

1 reference

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6 September 2017

Localization of the receptor site for alpha-scorpion toxins by antibody mapping: implications for sodium channel topology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

6 September 2017

Molecular mechanisms of local anesthesia: a review

1 reference

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Aromatic-aromatic interactions and protein stability. Investigation by double-mutant cycles

1 reference

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6 September 2017

A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

6 September 2017

Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction

1 reference

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6 September 2017

Charge at the lidocaine binding site residue Phe-1759 affects permeation in human cardiac voltage-gated sodium channels

1 reference

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Recognition of transmembrane helices by the endoplasmic reticulum translocon.

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Accessibility of mid-segment domain IV S6 residues of the voltage-gated Na+ channel to methanethiosulfonate reagents

1 reference

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A specific interaction between the cardiac sodium channel and site-3 toxin anthopleurin B.

1 reference

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A common local anesthetic receptor for benzocaine and etidocaine in voltage-gated mu1 Na+ channels

1 reference

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28 September 2017

The rates of interaction of local anesthetics with sodium channels in nerve.

1 reference

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28 September 2017

Phenytoin and carbamazepine: potential- and frequency-dependent block of Na currents in mammalian myelinated nerve fibers

1 reference

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28 September 2017

State-dependent access to the batrachotoxin receptor on the sodium channel

1 reference

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A critical role for the S4-S5 intracellular loop in domain IV of the sodium channel alpha-subunit in fast inactivation

1 reference

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Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

1 reference

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Interaction of the antiepileptic drug lamotrigine with recombinant rat brain type IIA Na+ channels and with native Na+ channels in rat hippocampal neurones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

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Lidocaine block of cardiac sodium channels

1 reference

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Sodium channels: ionic model of slow inactivation and state-dependent drug binding

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A novel drug binding site on voltage-gated sodium channels in rat brain

1 reference

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Voltage sensor of Kv1.2: structural basis of electromechanical coupling

1 reference

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3 September 2018

A multifunctional aromatic residue in the external pore vestibule of Na+ channels contributes to the local anesthetic receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

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Cooperative effect of S4-S5 loops in domains D3 and D4 on fast inactivation of the Na+ channel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

3 September 2018

The orientation and molecular movement of a k(+) channel voltage-sensing domain.

1 reference

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3 September 2018

Atomic proximity between S4 segment and pore domain in Shaker potassium channels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

3 September 2018

The position of the fourth segment of domain 4 determines status of the inactivation gate in Na+ channels.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

3 September 2018

Inhibition of Na(+) current by imipramine and related compounds: different binding kinetics as an inactivation stabilizer and as an open channel blocker

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

3 September 2018

Role of amino acid residues in transmembrane segments IS6 and IIS6 of the Na+ channel alpha subunit in voltage-dependent gating and drug block.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

3 September 2018

Cardiac-specific external paths for lidocaine, defined by isoform-specific residues, accelerate recovery from use-dependent block.

1 reference

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3 September 2018

The selectivity filter of the voltage-gated sodium channel is involved in channel activation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

3 September 2018

Molecular determinants of voltage-dependent gating and binding of pore-blocking drugs in transmembrane segment IIIS6 of the Na(+) channel alpha subunit.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

3 September 2018

Inhibition of Na(+) current by diphenhydramine and other diphenyl compounds: molecular determinants of selective binding to the inactivated channels.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

3 September 2018

Carbamazepine inhibition of neuronal Na+ currents: quantitative distinction from phenytoin and possible therapeutic implications.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

3 September 2018

Molecular determinants of state-dependent block of Na+ channels by local anesthetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

3 September 2018

Slow binding of phenytoin to inactivated sodium channels in rat hippocampal neurons.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717694

3 September 2018

Structural parts involved in activation and inactivation of the sodium channel

1 reference

https://api.crossref.org/works/10.1085%2FJGP.200810158

21 January 2018

Lamotrigine, phenytoin and carbamazepine interactions on the sodium current present in N4TG1 mouse neuroblastoma cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/19635852

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A critical role for transmembrane segment IVS6 of the sodium channel alpha subunit in fast inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19635852

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Guidelines for protein design: the energetics of beta sheet side chain interactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/19635852

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the block of sodium channels by phenytoin in mouse neuroblastoma cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/19635852

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of double mutants to detect structural changes in the active site of the tyrosyl-tRNA synthetase (Bacillus stearothermophilus)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19635852

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Voltage clamp analysis of the inhibitory actions of diphenylhydantoin and carbamazepine on voltage-sensitive sodium channels in neuroblastoma cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/19635852

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common anticonvulsant binding site for phenytoin, carbamazepine, and lamotrigine in neuronal Na+ channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/19635852

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1085/JGP.200810158

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

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