The Cullin 4A/B-DDB1-Cereblon E3 Ubiquitin Ligase Complex Mediates the Degradation of CLC-1 Chloride Channels (Q35662832)

9 August 2017

The Cullin 4A/B-DDB1-Cereblon E3 Ubiquitin Ligase Complex Mediates the Degradation of CLC-1 Chloride Channels (English)

1 reference

9 August 2017

3

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12 June 2020

June-Tai Wu

6

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12 June 2020

Chih-Yung Tang

8

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12 June 2020

author name string

Yi-An Chen

1

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12 June 2020

Yi-Jheng Peng

2

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12 June 2020

Jing-Jia Huang

4

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12 June 2020

Yun-Chia Chien

5

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12 June 2020

Tsung-Yu Chen

7

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12 June 2020

language of work or name

English

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publication date

29 May 2015

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9 August 2017

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12 June 2020

volume

5

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12 June 2020

page(s)

10667

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Creative Commons Attribution 4.0 International

12 June 2020

copyright license

start time

29 May 2015

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

ImageJ

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4448132/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

exact match

https://scigraph.springernature.com/pub.10.1038/srep10667

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cites work

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Myotonia congenita mutation enhances the degradation of human CLC-1 chloride channels

12 July 2018

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Cell surface expression of human ether-a-go-go-related gene (hERG) channels is regulated by caveolin-3 protein via the ubiquitin ligase Nedd4-2

12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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Protein quality control in the ER: balancing the ubiquitin checkbook

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Damage-specific DNA binding protein 1 (DDB1): a protein with a wide range of functions

12 July 2018

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The NEDD8 Conjugation Pathway and Its Relevance in Cancer Biology and Therapy

12 July 2018

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The cullin protein family

12 July 2018

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Nedd4-2-dependent ubiquitylation and regulation of the cardiac potassium channel hERG1

12 July 2018

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Structural regulation of cullin-RING ubiquitin ligase complexes

12 July 2018

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Functional modulation of AMP-activated protein kinase by cereblon

12 July 2018

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Structural assembly of cullin-RING ubiquitin ligase complexes

12 July 2018

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Protein homeostasis and aging in neurodegeneration

12 July 2018

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Identification of a primary target of thalidomide teratogenicity

12 July 2018

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Substrate-assisted inhibition of ubiquitin-like protein-activating enzymes: the NEDD8 E1 inhibitor MLN4924 forms a NEDD8-AMP mimetic in situ

12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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Cereblon is expressed in the retina and binds to voltage-gated chloride channels

12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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DDB1 functions as a linker to recruit receptor WD40 proteins to CUL4-ROC1 ubiquitin ligases

12 July 2018

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CUL4-DDB1 ubiquitin ligase interacts with multiple WD40-repeat proteins and regulates histone methylation

12 July 2018

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Molecular architecture and assembly of the DDB1-CUL4A ubiquitin ligase machinery

12 July 2018

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A family of diverse Cul4-Ddb1-interacting proteins includes Cdt2, which is required for S phase destruction of the replication factor Cdt1

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Identification of substrates for F-box proteins

12 July 2018

1 reference

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Ubiquitylation of ion channels

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Identification and functional characterization of cereblon as a binding protein for large-conductance calcium-activated potassium channel in rat brain

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Phenotypic variability in myotonia congenita

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

The Keap1-BTB protein is an adaptor that bridges Nrf2 to a Cul3-based E3 ligase: oxidative stress sensing by a Cul3-Keap1 ligase

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Proteasome-mediated degradation of p21 via N-terminal ubiquitinylation.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Involvement of helices at the dimer interface in ClC-1 common gating

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Skeletal muscle channelopathies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Novel CLCN1 mutations with unique clinical and electrophysiological consequences.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Traffic jams II: an update of diseases of intracellular transport

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Traffic jam: a compendium of human diseases that affect intracellular transport processes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Founder mutations and the high prevalence of myotonia congenita in northern Finland

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Integration of endoplasmic reticulum signaling in health and disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

ClC-1 chloride channel mutations in myotonia congenita: variable penetrance of mutations shifting the voltage dependence.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Chloride conductance in normal and myotonic muscle fibres and the action of monocarboxylic aromatic acids

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

12 July 2018

Muscle chloride channels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Distribution of potassium and chloride permeability over the surface and T-tubule membranes of mammalian skeletal muscle

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Hsp90 prevents interaction between CHIP and HERG proteins to facilitate maturation of wild-type and mutant HERG proteins.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

F413C and A531V but not R894X myotonia congenita mutations cause defective endoplasmic reticulum export of the muscle-specific chloride channel CLC-1.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Chemical and genetic strategies for manipulating polyubiquitin chain structure

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Ubiquitin ligase component Cul4 associates with Clr4 histone methyltransferase to assemble heterochromatin.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4448132

Disease-causing mutations C277R and C277Y modify gating of human ClC-1 chloride channels in myotonia congenita

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26021757

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26021757

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/SREP10667

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26021757%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26021757%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26021757%20AND%20SRC:MED&resulttype=core&format=json