CLC chloride channels: correlating structure with function (Q34774321)

4 August 2017

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title

CLC chloride channels: correlating structure with function (English)

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4 August 2017

Thomas J Jentsch

2

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author name string

Raúl Estévez

series ordinal

1

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4 August 2017

publication date

1 August 2002

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Current Opinion in Structural Biology

4 August 2017

published in

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4 August 2017

volume

12

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4 August 2017

issue

4

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4 August 2017

page(s)

531-539

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Molecular structure and physiological function of chloride channels

4 August 2017

cites work

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Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

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Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion

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ClC-5 Cl- -channel disruption impairs endocytosis in a mouse model for Dent's disease.

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Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man

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A common molecular basis for three inherited kidney stone diseases

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Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

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Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene

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7 January 2021

X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity

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7 January 2021

Dimeric structure of single chloride channels from Torpedo electroplax

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Completely functional double-barreled chloride channel expressed from a single Torpedo cDNA

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Purification, reconstitution, and subunit composition of a voltage-gated chloride channel from Torpedo electroplax

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7 January 2021

Homodimeric architecture of a ClC-type chloride ion channel

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7 January 2021

Two physically distinct pores in the dimeric ClC-0 chloride channel.

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7 January 2021

Subunit stoichiometry of human muscle chloride channels

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7 January 2021

Projection structure of a ClC-type chloride channel at 6.5 A resolution

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7 January 2021

Heteromultimeric CLC chloride channels with novel properties

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7 January 2021

Pores Formed by Single Subunits in Mixed Dimers of Different CLC Chloride Channels

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Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes

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7 January 2021

The muscle chloride channel ClC-1 has a double-barreled appearance that is differentially affected in dominant and recessive myotonia

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7 January 2021

Steady-state coupling of ion-channel conformations to a transmembrane ion gradient

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7 January 2021

Gating of the voltage-dependent chloride channel CIC-0 by the permeant anion

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7 January 2021

Nonequilibrium gating and voltage dependence of the ClC-0 Cl- channel

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7 January 2021

Permeation and block of the skeletal muscle chloride channel, ClC-1, by foreign anions

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7 January 2021

Interaction of hydrophobic anions with the rat skeletal muscle chloride channel ClC-1: effects on permeation and gating

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7 January 2021

Transmembrane topology of a CLC chloride channel

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7 January 2021

Pore-forming segments in voltage-gated chloride channels

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7 January 2021

Pore stoichiometry of a voltage-gated chloride channel

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7 January 2021

Residues lining the inner pore vestibule of human muscle chloride channels

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7 January 2021

Reconstitution of Functional Voltage-gated Chloride Channels from Complementary Fragments of CLC-1

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7 January 2021

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

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7 January 2021

Structure of the light-driven chloride pump halorhodopsin at 1.8 A resolution

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7 January 2021

Chemistry of ion coordination and hydration revealed by a K+ channel-Fab complex at 2.0 A resolution

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7 January 2021

Identification of functionally important regions of the muscular chloride channel CIC-1 by analysis of recessive and dominant myotonic mutations

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7 January 2021

Functional and structural analysis of ClC-K chloride channels involved in renal disease

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7 January 2021

Mutational analysis demonstrates that ClC-4 and ClC-5 directly mediate plasma membrane currents.

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7 January 2021

Analysis of a protein region involved in permeation and gating of the voltage-gated Torpedo chloride channel ClC-0

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7 January 2021

Inward rectification in ClC-0 chloride channels caused by mutations in several protein regions

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7 January 2021

Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the CIC-1 chloride channel

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7 January 2021

Temperature dependence of fast and slow gating relaxations of ClC-0 chloride channels

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7 January 2021

Myotonia caused by mutations in the muscle chloride channel gene CLCN1.

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7 January 2021

Identification of three cysteines as targets for the Zn2+ blockade of the human skeletal muscle chloride channel

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7 January 2021

Elimination of the slow gating of ClC-0 chloride channel by a point mutation

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7 January 2021

Extracellular zinc ion inhibits ClC-0 chloride channels by facilitating slow gating

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7 January 2021

Determinants of slow gating in ClC-0, the voltage-gated chloride channel of Torpedo marmorata.

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7 January 2021

Formation of CLC-0 chloride channels from separated transmembrane and cytoplasmic domains

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7 January 2021

The CLC chloride channel family

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7 January 2021

An internalization signal in ClC-5, an endosomal Cl-channel mutated in dent's disease.

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7 January 2021

The structure of a domain common to archaebacteria and the homocystinuria disease protein

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7 January 2021

Structure and mechanism of inosine monophosphate dehydrogenase in complex with the immunosuppressant mycophenolic acid

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7 January 2021

Characteristics and crystal structure of bacterial inosine-5'-monophosphate dehydrogenase

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7 January 2021

Golgi localization and functionally important domains in the NH2 and COOH terminus of the yeast CLC putative chloride channel Gef1p

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7 January 2021

Domain architecture of the heme-independent yeast cystathionine beta-synthase provides insights into mechanisms of catalysis and regulation

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7 January 2021

Mutations in the regulatory domain of cystathionine beta synthase can functionally suppress patient-derived mutations in cis.

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7 January 2021

Relevance of the D13 region to the function of the skeletal muscle chloride channel, ClC-1.

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7 January 2021

High-level expression, functional reconstitution, and quaternary structure of a prokaryotic ClC-type chloride channel

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7 January 2021

Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice

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7 January 2021

Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa

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7 January 2021

Correction of disease-causing CBS mutations in yeast

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7 January 2021

Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

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7 January 2021

Identification of a gene responsible for familial Wolff-Parkinson-White syndrome

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7 January 2021

A mutation in PRKAG3 associated with excess glycogen content in pig skeletal muscle

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7 January 2021

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Identifiers

DOI

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release_3bqggn5fl5gw5osphivxlyqfge

4 August 2017

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https://api.fatcat.wiki/v0/release/3bqggn5fl5gw5osphivxlyqfge

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