A fully atomistic model of the Cx32 connexon (Q28473231)

April 2022 Public Data File from Crossref

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Three-dimensional structure of a human connexin26 gap junction channel reveals a plug in the vestibule

7 April 2017

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Molecular modeling and mutagenesis of gap junction channels

29 September 2017

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The role of phosphorylation on the structure and dynamics of phospholamban: a model from molecular simulations

29 September 2017

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29 September 2017

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Molecular simulations and lipid-protein interactions: potassium channels and other membrane proteins

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Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions

29 September 2017

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Structural organization of gap junction channels

29 September 2017

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Conformational sampling and dynamics of membrane proteins from 10-nanosecond computer simulations.

29 September 2017

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29 September 2017

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29 September 2017

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Single-channel SCAM identifies pore-lining residues in the first extracellular loop and first transmembrane domains of Cx46 hemichannels

29 September 2017

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29 September 2017

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Identification of amino acid residues lining the pore of a gap junction channel

29 September 2017

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Conformational changes in surface structures of isolated connexin 26 gap junctions.

29 September 2017

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Connexin genes in the mouse and human genome

29 September 2017

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29 September 2017

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Functional alterations in gap junction channels formed by mutant forms of connexin 32: evidence for loss of function as a pathogenic mechanism in the X-linked form of Charcot-Marie-Tooth disease

29 September 2017

1 reference

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Transmembrane alpha-helices in the gap junction membrane channel: systematic search of packing models based on the pair potential function.

29 September 2017

1 reference

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Cx26 deafness: mutation analysis and clinical variability

29 September 2017

1 reference

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The role of a conserved proline residue in mediating conformational changes associated with voltage gating of Cx32 gap junctions

29 September 2017

1 reference

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Three-dimensional structure of a recombinant gap junction membrane channel

29 September 2017

1 reference

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Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss

29 September 2017

1 reference

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Rapid refinement of protein interfaces incorporating solvation: application to the docking problem

29 September 2017

1 reference

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The pattern of disulfide linkages in the extracellular loop regions of connexin 32 suggests a model for the docking interface of gap junctions

29 September 2017

1 reference

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Changes in permeability caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Identification of a pore lining segment in gap junction hemichannels.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Connexins, connexons, and intercellular communication

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Structure of gap junction intercellular channels

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

The gap junction communication channel

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Do salt bridges stabilize proteins? A continuum electrostatic analysis.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Modelling mutations and homologous proteins

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Topology of the 32-kd liver gap junction protein determined by site-directed antibody localizations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Roles of Met-34, Cys-64, and Arg-75 in the assembly of human connexin 26. Implication for key amino acid residues for channel formation and function.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Structure of the amino terminus of a gap junction protein

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Physical Characterization of Gap Junction Membrane Connexons (Hemi-channels) Isolated from Rat Liver

2 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Size selectivity between gap junction channels composed of different connexins

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Lipid rafts prepared by different methods contain different connexin channels, but gap junctions are not lipid rafts

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Connexin26 mutations associated with nonsyndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Connexin 26 mutations in cases of sensorineural deafness in eastern Austria

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Loss of function mutations of the GJB2 gene detected in patients with DFNB1-associated hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

A Second Generation Force Field for the Simulation of Proteins, Nucleic Acids, and Organic Molecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Numerical integration of the cartesian equations of motion of a system with constraints: molecular dynamics of n-alkanes

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Particle mesh Ewald: An N⋅log(N) method for Ewald sums in large systems

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

A Cα Model for the Transmembrane α Helices of Gap Junction Intercellular Channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

The Structural Context of Disease-causing Mutations in Gap Junctions

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Molecular dynamics with coupling to an external bath

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Mechanism of the defect in gap-junctional communication by expression of a connexin 26 mutant associated with dominant deafness

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease show two distinct behaviors: loss of function and altered gating properties.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Novel mutations in the connexin 32 gene associated with X-linked Charcot-Marie tooth disease

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481295

Selective defects in channel permeability associated with Cx32 mutations causing X-linked Charcot–Marie–Tooth disease

27 November 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002614

Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)

21 January 2018

1 reference

12 December 2020

Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritance

1 reference

12 December 2020

Theory and applications of the generalized Born solvation model in macromolecular simulations

1 reference

12 December 2020

Molecular dynamics simulations on HIV-1 Tat

1 reference

12 December 2020

Analysis of the relationship between side-chain conformation and secondary structure in globular proteins

1 reference

12 December 2020

Potassium and sodium binding to the outer mouth of the K+ channel

1 reference

12 December 2020

Unitary permeability of gap junction channels to second messengers measured by FRET microscopy

1 reference

12 December 2020

Mutation analysis of the connexin 32 (Cx32) gene in Charcot-Marie-Tooth neuropathy type 1: identification of five new mutations

1 reference

12 December 2020