Pubmed abstracts for Protein-Protein Interaction search result :


Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
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Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
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Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
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Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
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Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
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Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
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Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
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Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
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Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.54292879
Although calnexin binds nascent CFTR via its oligosaccharide chains in the ER lumen and Hsp 70 binds CFTR cytoplasmic domains , perturbation of these interactions alone is without major influence on maturation or degradation . 0.54292879^^^
Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.75368423
Csp induced band B CFTR was found adjacent to the nucleus , co localizing with calnexin , and it remained detergent soluble . 0.75368423^^^
Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
Synthesis of a molecular mimic of the Glc1Man9 oligoside as potential inhibitor of calnexin binding to DeltaF 508 CFTR protein . ^^^
Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
Although the bulk of wild type and delta F 508 CFTRs were present initially in complexes containing calnexin , only wild type CFTR was able to escape from this association and exit the ER . ^^^ Calnexin retains misfolded or incompletely assembled proteins in the ER and thus is likely to contribute to the mislocalization of mutant CFTR . . ^^^ Participation of the endoplasmic reticulum chaperone calnexin ( p 88 , IP 90 ) in the biogenesis of the cystic fibrosis transmembrane conductance regulator . ^^^
Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
Conversely , calnexin and binding protein ( BiP ) , which are required for the proteolysis of ER lumenal proteins in both yeast and mammals , are dispensable for the degradation of CFTR , suggesting unique mechanisms for the disposal of at least some soluble and integral membrane ERAD substrates in yeast . . ^^^
Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
In Calu 3 airway cells , immunofluorescence colocalized Csp with calnexin in the endoplasmic reticulum and with CFTR at the apical membrane domain . ^^^
Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
In immortalized human CF cell lines expressing Delta F 508 CFTR , a halide efflux assay showed that calnexin Delta 185 520 partially restored CFTR function . ^^^ We show that calnexin Delta 185 520 but not calnexin can partially reverse the mislocalization of Delta F 508 CFTR . ^^^ Calnexin Delta 185 520 interacted with CFTR directly , and was secreted into the extracellular compartment over time . ^^^ Forty eight hours after transfection into CHO cells , calnexin Delta 185 520 increased the conversion of immature Delta F 508 CFTR into mature Delta F 508 CFTR . ^^^ These data indicate that calnexin Delta 185 520 may give a clue to develop the therapeutic way of cystic fibrosis with Delta F 508 CFTR . . ^^^
Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
Delta F 508 CFTR pool in the endoplasmic reticulum is increased by calnexin overexpression . ^^^ Because the prolonged interaction of Delta F 508 CFTR with calnexin , an ER chaperone , results in the ERAD of Delta F 508 CFTR , calnexin seems to lead it to the ERAD pathway . ^^^ In this study , we found that calnexin overexpression partially attenuated the ERAD of Delta F 508 CFTR . ^^^ We observed the formation of concentric membranous bodies in the ER upon calnexin overexpression and that the Delta F 508 CFTR but not the wild type CFTR was retained in the concentric membranous bodies . ^^^ Furthermore , we observed that calnexin overexpression moderately inhibited the formation of aggresomes accumulating the ubiquitinated Delta F 508 CFTR . ^^^
Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
Some knowledge is emerging on CFTR membrane folding and on the role of this process of molecular chaperones , such as Hsp70 / Hdj 1 and calnexin . ^^^
Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
Most F508del CFTR is targeted to degradation at an early folding checkpoint and independently of calnexin . ^^^ Our data show that the major degradation pathway of the cystic fibrosis transmembrane conductance regulator ( CFTR ) with F508del ( the most frequent mutation found in patients with the genetic disease cystic fibrosis ) from the ER is independent of calnexin . ^^^ Together , our data support a novel model by which wt and F508del CFTR undergo ERAD from two distinct checkpoints , the mutant being disposed of independently of N glycosidic residues and calnexin , probably by the Hsc70 / Hsp70 machinery , and wt CFTR undergoing glycan mediated ERAD . . ^^^
Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
We also used Baby Hamster Kidney cells , heterologously expressing deltaF 508 CFTR , to determine if SERCA inhibitors could interfere with the interaction between calnexin and CFTR and thereby correct the deltaF 508 CFTR misfolding defect . ^^^
Interacting proteins: P27824 and P13569 Pubmed SVM Score :0.0
The isocyanide ligand forms complexes with ruthenium ( 2 ) bis bipyridine of the type [ Ru ( bpy ) ( 2 ) ( CNx ) Cl ] ( CF ( 3 ) SO ( 3 ) ) ( 1 ) , [ Ru ( bpy ) ( 2 ) ( CNx ) ( py ) ] ( PF ( 6 ) ) ( 2 ) ( 2 ) , and [ Ru ( bpy ) ( 2 ) ( CNx ) ( 2 ) ] ( PF ( 6 ) ) ( 2 ) ( 3 ) ( bpy = 2 , 2 ' bipyridine , py = pyridine , and CNx = 2 , 6 dimethylphenylisocyanide ) . ^^^