Influence of phosphorylation by protein kinase A on CFTR at the cell surface and endoplasmic reticulum (Q33784420)

29 July 2017

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title

Influence of phosphorylation by protein kinase A on CFTR at the cell surface and endoplasmic reticulum (English)

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29 July 2017

main subject

endoplasmic reticulum

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F S Seibert

1

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29 July 2017

X B Chang

2

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29 July 2017

A A Aleksandrov

3

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29 July 2017

D M Clarke

4

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29 July 2017

J W Hanrahan

5

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29 July 2017

J R Riordan

6

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29 July 2017

language of work or name

English

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publication date

1 December 1999

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Biochimica et Biophysica Acta

29 July 2017

number of pages

9

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based on heuristic

inferred from page(s)

published in

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29 July 2017

volume

1461

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29 July 2017

issue

2

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29 July 2017

page(s)

275-283

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

29 July 2017

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Functionally distinct phospho-forms underlie incremental activation of protein kinase-regulated Cl- conductance in mammalian heart

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CFTR displays voltage dependence and two gating modes during stimulation

7 January 2021

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Effect of Deleting the R Domain on CFTR-Generated Chloride Channels

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

7 January 2021

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Phosphorylation by cAMP-dependent protein kinase causes a conformational change in the R domain of the cystic fibrosis transmembrane conductance regulator

7 January 2021

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Coupling of CFTR Cl- channel gating to an ATP hydrolysis cycle

7 January 2021

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ATPase activity of the cystic fibrosis transmembrane conductance regulator

7 January 2021

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Dibasic protein kinase A sites regulate bursting rate and nucleotide sensitivity of the cystic fibrosis transmembrane conductance regulator chloride channel.

7 January 2021

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7 January 2021

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7 January 2021

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Phosphatase inhibitors activate normal and defective CFTR chloride channels

7 January 2021

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Protein phosphatase 2C dephosphorylates and inactivates cystic fibrosis transmembrane conductance regulator

7 January 2021

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7 January 2021

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

7 January 2021

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

7 January 2021

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Degradation of CFTR by the ubiquitin-proteasome pathway

7 January 2021

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Mutant (delta F508) cystic fibrosis transmembrane conductance regulator Cl- channel is functional when retained in endoplasmic reticulum of mammalian cells.

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Regulation of plasma membrane recycling by CFTR.

7 January 2021

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Regulated endocytosis in a chloride secretory epithelial cell line

7 January 2021

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

7 January 2021

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cAMP-regulated trafficking of epitope-tagged CFTR.

7 January 2021

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10.1016/S0005-2736(99)00163-7

7 January 2021

Identifiers

DOI

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29 July 2017

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