Pages that link to "Q43023020"

The following pages link to Computational studies reveal phosphorylation-dependent changes in the unstructured R domain of CFTR. (Q43023020):

Displaying 28 items.

• Intrinsic Disorder in Transmembrane Proteins: Roles in Signaling and Topology Prediction (Q33292127) (← links)
• An electrostatic interaction at the tetrahelix bundle promotes phosphorylation-dependent cystic fibrosis transmembrane conductance regulator (CFTR) channel opening (Q34430936) (← links)
• Interaction with the 5D3 monoclonal antibody is regulated by intramolecular rearrangements but not by covalent dimer formation of the human ABCG2 multidrug transporter (Q35674430) (← links)
• Regulation of the cystic fibrosis transmembrane conductance regulator anion channel by tyrosine phosphorylation (Q35997983) (← links)
• CFTR–SLC26 transporter interactions in epithelia (Q36015274) (← links)
• Development and characterization of synthetic antibodies binding to the cystic fibrosis conductance regulator (Q36019421) (← links)
• Molecular modelling and molecular dynamics of CFTR. (Q36158194) (← links)
• The CFTR ion channel: gating, regulation, and anion permeation (Q36488258) (← links)
• Channel Gating Regulation by the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) First Cytosolic Loop (Q36489303) (← links)
• Long-range coupling between the extracellular gates and the intracellular ATP binding domains of multidrug resistance protein pumps and cystic fibrosis transmembrane conductance regulator channels (Q36570921) (← links)
• Restoration of NBD1 thermal stability is necessary and sufficient to correct ∆F508 CFTR folding and assembly (Q36591437) (← links)
• Dynamics intrinsic to cystic fibrosis transmembrane conductance regulator function and stability (Q36629079) (← links)
• Cooperative assembly and misfolding of CFTR domains in vivo. (Q37146655) (← links)
• Review. ATP hydrolysis-driven gating in cystic fibrosis transmembrane conductance regulator. (Q37310608) (← links)
• Regulation of ABC Transporter Function Via Phosphorylation by Protein Kinases (Q37813724) (← links)
• Insights into the mechanisms underlying CFTR channel activity, the molecular basis for cystic fibrosis and strategies for therapy (Q37941759) (← links)
• Functional Rescue of F508del-CFTR Using Small Molecule Correctors (Q38051325) (← links)
• Structural changes of CFTR R region upon phosphorylation: a plastic platform for intramolecular and intermolecular interactions (Q38119262) (← links)
• Structural models of CFTR-AMPK and CFTR-PKA interactions: R-domain flexibility is a key factor in CFTR regulation (Q40098219) (← links)
• Phosphorylation-dependent changes in nucleotide binding, conformation, and dynamics of the first nucleotide binding domain (NBD1) of the sulfonylurea receptor 2B (SUR2B). (Q40710861) (← links)
• Graphlet kernels for prediction of functional residues in protein structures (Q42272603) (← links)
• Molecular models of the open and closed states of the whole human CFTR protein (Q42631749) (← links)
• A SAXS-based ensemble model of the native and phosphorylated regulatory domain of the CFTR. (Q46491265) (← links)
• Intrinsic protein disorder reduces small-scale gene duplicability (Q47171932) (← links)
• Protein disorder in the centrosome correlates with complexity in cell types number (Q47250514) (← links)
• Modeling Mutations in Proteins Using Medusa and Discrete Molecule Dynamics (Q57829204) (← links)
• Graph-Theoretic Models of Mutations in the Nucleotide Binding Domain 1 of the Cystic Fibrosis Transmembrane Conductance Regulator (Q58920296) (← links)
• Changes in the R-region interactions depend on phosphorylation and contribute to PKA and PKC regulation of the cystic fibrosis transmembrane conductance regulator chloride channel (Q89985615) (← links)