(Q48610642)

English

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

scientific article published in October 1997

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scholarly article

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

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

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

transmembrane protein

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cystic fibrosis

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molecular chaperones

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author name string

Strickland E

1

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

Qu BH

2

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

Millen L

3

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

Thomas PJ

4

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

language of work or name

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publication date

1 October 1997

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

Journal of Biological Chemistry

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Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

272

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Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

25421-25424

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Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

41

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

Defective protein folding as a basis of human disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Molecular chaperones in cellular protein folding

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Different conformations for the same polypeptide bound to chaperones DnaK and GroEL.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Analysis of three DnaK mutant proteins suggests that progression through the ATPase cycle requires conformational changes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

ATP-induced protein-Hsp70 complex dissociation requires K+ but not ATP hydrolysis.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Kinetics of molecular chaperone action

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https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

The ubiquitin-proteasome proteolytic pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Alteration of the cystic fibrosis transmembrane conductance regulator folding pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Degradation of CFTR by the ubiquitin-proteasome pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Interaction of Hsp 70 with newly synthesized proteins: implications for protein folding and assembly.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

hsp70 binds specifically to a peptide derived from the highly conserved domain (I) region of p53.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Assessment of the ATP binding properties of Hsp90.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.41.25421

21 January 2018

Identifiers

10.1074/JBC.272.41.25421

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9325249

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