Varaico: Literature-Extracted Genetic Variants

Gene:CFTR
Variant:p.S737A
Back to variants list

CFTR

NM_000492.4:p.S737A

Associated Papers

A cluster of inhibitory residues in the regulatory domain prevents activation of the cystic fibrosis transmembrane conductance regulator.

Wu M et al.

The Journal of Biological Chemistry, 2025

Blue flash sheds light on the roles of individual phosphoserines in CFTR channel activation.

Csanády L

The Journal of General Physiology, 2023

Real-time observation of functional specialization among phosphorylation sites in CFTR.

Infield DT et al.

The Journal of General Physiology, 2023

A PI3Kγ mimetic peptide triggers CFTR gating, bronchodilation, and reduced inflammation in obstructive airway diseases.

Ghigo A et al.

Science Translational Medicine, 2022

Protein kinase A phosphorylation potentiates cystic fibrosis transmembrane conductance regulator gating by relieving autoinhibition on the stimulatory C terminus of the regulatory domain.

Chen JH

The Journal of Biological Chemistry, 2020

STRUCTURE, GATING, AND REGULATION OF THE CFTR ANION CHANNEL.

Csanády L et al.

Physiological Reviews, 2019

Trafficking and function of the cystic fibrosis transmembrane conductance regulator: a complex network of posttranslational modifications.

McClure ML et al.

American Journal of Physiology. Lung Cellular and Molecular Physiology, 2016

Molecular Basis for Fe(III)-Independent Curcumin Potentiation of Cystic Fibrosis Transmembrane Conductance Regulator Activity.

Wang G

Biochemistry, 2015

Sphingosine-1-Phosphate Is a Novel Regulator of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Activity.

Malik FA et al.

Plos One, 2015

LMTK2-mediated phosphorylation regulates CFTR endocytosis in human airway epithelial cells.

Luz S et al.

The Journal of Biological Chemistry, 2014

Role of tyrosine phosphorylation in the muscarinic activation of the cystic fibrosis transmembrane conductance regulator (CFTR).

Billet A et al.

The Journal of Biological Chemistry, 2013

Structural models of CFTR-AMPK and CFTR-PKA interactions: R-domain flexibility is a key factor in CFTR regulation.

Siwiak M et al.

Journal of Molecular Modeling, 2012

The inhibition mechanism of non-phosphorylated Ser768 in the regulatory domain of cystic fibrosis transmembrane conductance regulator.

Wang G

The Journal of Biological Chemistry, 2011

Effect of Annexin A5 on CFTR: regulated traffic or scaffolding?

Faria D et al.

Molecular Membrane Biology, 2011

State-dependent regulation of cystic fibrosis transmembrane conductance regulator (CFTR) gating by a high affinity Fe3+ bridge between the regulatory domain and cytoplasmic loop 3.

Wang G

The Journal of Biological Chemistry, 2010

Role of individual R domain phosphorylation sites in CFTR regulation by protein kinase A.

Hegedus T et al.

Biochimica Et Biophysica Acta, 2009

Mechanistic insight into control of CFTR by AMPK.

Kongsuphol P et al.

The Journal of Biological Chemistry, 2009

Cystic fibrosis transmembrane conductance regulator: a chloride channel gated by ATP binding and hydrolysis.

Bompadre SG et al.

Sheng Li Xue Bao : [acta Physiologica Sinica], 2007

Preferential phosphorylation of R-domain Serine 768 dampens activation of CFTR channels by PKA.

Csanády L et al.

The Journal of General Physiology, 2005

Capsaicin potentiates wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride-channel currents.

Ai T et al.

Molecular Pharmacology, 2004

Protein kinase A regulates ATP hydrolysis and dimerization by a CFTR (cystic fibrosis transmembrane conductance regulator) domain.

Howell LD et al.

The Biochemical Journal, 2004

Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by its R domain.

Ostedgaard LS et al.

The Journal of Biological Chemistry, 2001

Contribution of R domain phosphoserines to the function of CFTR studied in Fischer rat thyroid epithelia.

Baldursson O et al.

American Journal of Physiology. Lung Cellular and Molecular Physiology, 2000

Stimulatory and Inhibitory Functions of the R Domain on CFTR Chloride Channel.

Ma J

News in Physiological Sciences : an International Journal of Physiology Produced Jointly by the International Union of Physiological Sciences and the American Physiological Society, 2000

Structure and function of the CFTR chloride channel.

Sheppard DN et al.

Physiological Reviews, 1999

Stimulation of CFTR activity by its phosphorylated R domain.

Winter MC et al.

Nature, 1997

CFTR activation: additive effects of stimulatory and inhibitory phosphorylation sites in the R domain.

Wilkinson DJ et al.

The American Journal of Physiology, 1997

cAMP-dependent protein kinase-mediated phosphorylation of cystic fibrosis transmembrane conductance regulator residue Ser-753 and its role in channel activation.

Seibert FS et al.

The Journal of Biological Chemistry, 1995

Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by negative charge in the R domain.

Berger HA et al.

The Japanese Journal of Physiology, 1994

Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by negative charge in the R domain.

Rich DP et al.

The Journal of Biological Chemistry, 1993

Protein kinase A (PKA) still activates CFTR chloride channel after mutagenesis of all 10 PKA consensus phosphorylation sites.

Chang XB et al.

The Journal of Biological Chemistry, 1993

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

Cheng SH et al.

Cell, 1991

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."