(Q34131032)

31 July 2017

title

Cysteine string protein interacts with and modulates the maturation of the cystic fibrosis transmembrane conductance regulator (English)

1 reference

31 July 2017

main subject

transmembrane protein

0 references

0 references

Jochen Lang

5

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author name string

Hui Zhang

1

1 reference

31 July 2017

Kathryn W Peters

2

1 reference

31 July 2017

Fei Sun

3

1 reference

31 July 2017

Christopher R Marino

4

1 reference

31 July 2017

Robert D Burgoyne

6

1 reference

31 July 2017

Raymond A Frizzell

7

1 reference

31 July 2017

language of work or name

English

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publication date

30 May 2002

1 reference

Journal of Biological Chemistry

31 July 2017

published in

1 reference

31 July 2017

volume

277

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31 July 2017

issue

32

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31 July 2017

page(s)

28948-28958

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Role of CFTR in airway disease

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Cystic fibrosis: a disease of altered protein folding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Defects in processing and trafficking of the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Multiple proteolytic systems, including the proteasome, contribute to CFTR processing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Degradation of CFTR by the ubiquitin-proteasome pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Regulation of plasma membrane recycling by CFTR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Syntaxin 1A inhibits CFTR chloride channels by means of domain-specific protein-protein interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Syntaxin 1A is expressed in airway epithelial cells, where it modulates CFTR Cl(-) currents

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

The carboxyl terminus of the cystic fibrosis transmembrane conductance regulator binds to AP-2 clathrin adaptors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Protein kinase A associates with cystic fibrosis transmembrane conductance regulator via an interaction with ezrin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

E3KARP mediates the association of ezrin and protein kinase A with the cystic fibrosis transmembrane conductance regulator in airway cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

PKA holoenzyme is functionally coupled to CFTR by AKAPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

A cysteine-string protein is expressed in retina and brain of Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Cysteine string proteins: a potential link between synaptic vesicles and presynaptic Ca2+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Widespread expression of human cysteine string proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Cysteine-string protein: the chaperone at the synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Paralysis and early death in cysteine string protein mutants of Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Cysteine string protein (CSP) is an insulin secretory granule-associated protein regulating beta-cell exocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Presynaptic dysfunction in Drosophila csp mutants

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Analysis of regulated exocytosis in adrenal chromaffin cells: insights into NSF/SNAP/SNARE function

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Chaperone-mediated protein folding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Identification of a novel cysteine string protein variant and expression of cysteine string proteins in non-neuronal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

A Xenopus cysteine string protein with a cysteine residue in the J domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Non-coordinate regulation of endogenous epithelial sodium channel (ENaC) subunit expression at the apical membrane of A6 cells in response to various transporting conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

The first C2 domain of synaptotagmin is required for exocytosis of insulin from pancreatic beta-cells: action of synaptotagmin at low micromolar calcium.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Interaction of syntaxins with the amiloride-sensitive epithelial sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

The Hsc70 co-chaperone CHIP targets immature CFTR for proteasomal degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

CFTR-dependent membrane insertion is linked to stimulation of the CFTR chloride conductance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Intrinsic membrane association of Drosophila cysteine string proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Model systems for investigating mucin gene expression in airway diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Reverse transcription-polymerase chain reaction (RT-PCR) phenotypic analysis of cell cultures of human tracheal epithelium, tracheobronchial glands, and lung carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Mucous granule exocytosis and CFTR expression in gallbladder epithelium

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Cysteine-string proteins: a cycle of acylation and deacylation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

The molecular chaperone function of the secretory vesicle cysteine string proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

The cysteine-string domain of the secretory vesicle cysteine-string protein is required for membrane targeting

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Capacitance measurements reveal different pathways for the activation of CFTR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

The Hdj-2/Hsc70 chaperone pair facilitates early steps in CFTR biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

The molecular chaperone Hsc70 assists the in vitro folding of the N-terminal nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

The cysteine string secretory vesicle protein activates Hsc70 ATPase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Apoprotein B degradation is promoted by the molecular chaperones hsp90 and hsp70.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Traffic pattern of cystic fibrosis transmembrane regulator through the early exocytic pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

Non-conventional trafficking of the cystic fibrosis transmembrane conductance regulator through the early secretory pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111706200

21 January 2018

Identifiers

DOI

10.1074/JBC.M111706200

1 reference

release_gzhyigodx5dxzg77plpmcav5ha

31 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/gzhyigodx5dxzg77plpmcav5ha

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference