The mechanism underlying cystic fibrosis transmembrane conductance regulator transport from the endoplasmic reticulum to the proteasome includes Sec61beta and a cytosolic, deglycosylated intermediary
about
Stress-associated endoplasmic reticulum protein 1 (SERP1)/Ribosome-associated membrane protein 4 (RAMP4) stabilizes membrane proteins during stress and facilitates subsequent glycosylationA membrane protein required for dislocation of misfolded proteins from the ERA glycosylated type I membrane protein becomes cytosolic when peptide: N-glycanase is compromised.The retrotranslocation protein Derlin-1 binds peptide:N-glycanase to the endoplasmic reticulumIdentification of proteins that interact with mammalian peptide:N-glycanase and implicate this hydrolase in the proteasome-dependent pathway for protein degradationPNG1, a yeast gene encoding a highly conserved peptide:N-glycanaseThe PEST sequence does not contribute to the stability of the cystic fibrosis transmembrane conductance regulatorA yeast phenomic model for the gene interaction network modulating CFTR-ΔF508 protein biogenesis.Traffic-independent function of the Sar1p/COPII machinery in proteasomal sorting of the cystic fibrosis transmembrane conductance regulatorExport from the endoplasmic reticulum represents the limiting step in the maturation and cell surface expression of the human delta opioid receptorMolecular characterization of a novel mammalian DnaJ-like Sec63p homologAggresomes: a cellular response to misfolded proteinsLuteinizing hormone receptor ectodomain splice variant misroutes the full-length receptor into a subcompartment of the endoplasmic reticulum.Inefficient maturation of the rat luteinizing hormone receptor. A putative way to regulate receptor numbers at the cell surfaceEndo-β-N-acetylglucosaminidase forms N-GlcNAc protein aggregates during ER-associated degradation in Ngly1-defective cellsThe cytoplasmic peptide:N-glycanase (NGLY1) - Structure, expression and cellular functionsRole of N-oligosaccharide endoplasmic reticulum processing reactions in glycoprotein folding and degradationApplications of proteomic technologies for understanding the premature proteolysis of CFTR.A synonymous single nucleotide polymorphism in DeltaF508 CFTR alters the secondary structure of the mRNA and the expression of the mutant protein.The cytoplasmic peptide:N-glycanase (Ngly1)-basic science encounters a human genetic disorder.The cytosolic tail of class I MHC heavy chain is required for its dislocation by the human cytomegalovirus US2 and US11 gene products5'-adenosine monophosphate mediated cooling treatment enhances ΔF508-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) stability in vivo.SEL1L, the homologue of yeast Hrd3p, is involved in protein dislocation from the mammalian ER.Sec61β controls sensitivity to platinum-containing chemotherapeutic agents through modulation of the copper-transporting ATPase ATP7AViral modulation of antigen presentation: manipulation of cellular targets in the ER and beyond.Hsp70 molecular chaperone facilitates endoplasmic reticulum-associated protein degradation of cystic fibrosis transmembrane conductance regulator in yeast.Ubiquitylation of ion channels.Cellular response to endoplasmic reticulum stress: a matter of life or death.A synonymous codon change alters the drug sensitivity of ΔF508 cystic fibrosis transmembrane conductance regulator.The Gp78 ubiquitin ligase: probing endoplasmic reticulum complexity.A novel quality control compartment derived from the endoplasmic reticulumFunctional stability of rescued delta F508 cystic fibrosis transmembrane conductance regulator in airway epithelial cells.Visualization of the ER-to-cytosol dislocation reaction of a type I membrane protein.ΔF508 CFTR surface stability is regulated by DAB2 and CHIP-mediated ubiquitination in post-endocytic compartmentsCystic fibrosis transmembrane conductance regulator degradation depends on the lectins Htm1p/EDEM and the Cdc48 protein complex in yeast.VCP/p97 AAA-ATPase does not interact with the endogenous wild-type cystic fibrosis transmembrane conductance regulator.Endoplasmic reticulum stress and the unfolded protein response regulate genomic cystic fibrosis transmembrane conductance regulator expression.Degradation of trafficking-defective long QT syndrome type II mutant channels by the ubiquitin-proteasome pathway.Reactive oxygen nitrogen species decrease cystic fibrosis transmembrane conductance regulator expression and cAMP-mediated Cl- secretion in airway epithelia.Pivotal role of calnexin and mannose trimming in regulating the endoplasmic reticulum-associated degradation of major histocompatibility complex class I heavy chain.
P2860
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P2860
The mechanism underlying cystic fibrosis transmembrane conductance regulator transport from the endoplasmic reticulum to the proteasome includes Sec61beta and a cytosolic, deglycosylated intermediary
description
1998 nî lūn-bûn
@nan
1998 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
The mechanism underlying cysti ...... c, deglycosylated intermediary
@ast
The mechanism underlying cysti ...... c, deglycosylated intermediary
@en
The mechanism underlying cysti ...... c, deglycosylated intermediary
@en-gb
The mechanism underlying cysti ...... c, deglycosylated intermediary
@nl
type
label
The mechanism underlying cysti ...... c, deglycosylated intermediary
@ast
The mechanism underlying cysti ...... c, deglycosylated intermediary
@en
The mechanism underlying cysti ...... c, deglycosylated intermediary
@en-gb
The mechanism underlying cysti ...... c, deglycosylated intermediary
@nl
prefLabel
The mechanism underlying cysti ...... c, deglycosylated intermediary
@ast
The mechanism underlying cysti ...... c, deglycosylated intermediary
@en
The mechanism underlying cysti ...... c, deglycosylated intermediary
@en-gb
The mechanism underlying cysti ...... c, deglycosylated intermediary
@nl
P2093
P921
P356
P1476
The mechanism underlying cysti ...... c, deglycosylated intermediary
@en
P2093
P304
P356
10.1074/JBC.273.45.29873
P407
P577
1998-11-06T00:00:00Z