(Q40485134)

20 September 2017

Effects of the delta F508 mutation on the structure, function, and folding of the first nucleotide-binding domain of CFTR. (English)

1 reference

20 September 2017

P J Thomas

1

1 reference

PubMed ID

7680027

20 September 2017

P L Pedersen

series ordinal

2

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20 September 2017

1 February 1993

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Journal of Bioenergetics and Biomembranes

20 September 2017

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20 September 2017

25

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20 September 2017

11-19

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20 September 2017

1

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00768063

20 September 2017

0 references

cites work

Evidence for an ancestral core structure in nucleotide-binding proteins with the type A motif.

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12 December 2020

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

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12 December 2020

Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

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12 December 2020

Benign missense variations in the cystic fibrosis gene

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12 December 2020

A program for prediction of protein secondary structure from nucleotide sequence data: application to histocompatibility antigens

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12 December 2020

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

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12 December 2020

Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance

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12 December 2020

Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel

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12 December 2020

The cystic fibrosis transmembrane conductance regulator. Effects of the most common cystic fibrosis-causing mutation on the secondary structure and stability of a synthetic peptide

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12 December 2020

Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity

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12 December 2020

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12 December 2020

Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells

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12 December 2020

Cystic Fibrosis Transmembrane Conductance Regulator: Nucleotide Binding to a Synthetic Peptide

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12 December 2020

Nucleoside triphosphates are required to open the CFTR chloride channel.

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12 December 2020

Phosphorylation fails to activate chloride channels from cystic fibrosis airway cells

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12 December 2020

Analysis of the accuracy and implications of simple methods for predicting the secondary structure of globular proteins

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12 December 2020

Structural model of the nucleotide-binding conserved component of periplasmic permeases

1 reference

12 December 2020

Structural details of the binding of guanosine diphosphate to elongation factor Tu from E. coli as studied by X-ray crystallography

1 reference

12 December 2020

Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer

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12 December 2020

Structure of the recA protein–ADP complex

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12 December 2020

A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein

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12 December 2020

Cl- channels in CF: lack of activation by protein kinase C and cAMP-dependent protein kinase

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12 December 2020

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

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12 December 2020

Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)

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12 December 2020

Structure of the GDP domain of EF-Tu and location of the amino acids homologous to ras oncogene proteins

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12 December 2020

Generation of cAMP-Activated Chloride Currents by Expression of CFTR

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12 December 2020

Peptide-binding specificity of the molecular chaperone BiP

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12 December 2020

Chemical probes of the mitochondrial ATP synthesis and translocation

1 reference

12 December 2020

Structure-function analysis of the histidine permease and comparison with cystic fibrosis mutations

1 reference

12 December 2020

Structural and functional relationships in the adenylate kinase family

1 reference

12 December 2020

Screening for non-delta F508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy.

1 reference

12 December 2020

Cyclic AMP-dependent protein kinase opens chloride channels in normal but not cystic fibrosis airway epithelium

1 reference

12 December 2020

Recombinant synthesis, purification, and nucleotide binding characteristics of the first nucleotide binding domain of the cystic fibrosis gene product

1 reference

12 December 2020

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene

1 reference

12 December 2020

Prediction of the Secondary Structure of Proteins from their Amino Acid Sequence

1 reference

12 December 2020

Intrinsic anion channel activity of the recombinant first nucleotide binding fold domain of the cystic fibrosis transmembrane regulator protein

1 reference

12 December 2020

Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00768063

1 reference

20 September 2017

1 reference

PubMed ID

7680027