A novel quality control compartment derived from the endoplasmic reticulum
about
Endoplasmic reticulum (ER) mannosidase I is compartmentalized and required for N-glycan trimming to Man5-6GlcNAc2 in glycoprotein ER-associated degradationA complex between peptide:N-glycanase and two proteasome-linked proteins suggests a mechanism for the degradation of misfolded glycoproteinsMannose trimming is required for delivery of a glycoprotein from EDEM1 to XTP3-B and to late endoplasmic reticulum-associated degradation stepsAnkyrin facilitates intracellular trafficking of alpha1-Na+-K+-ATPase in polarized cells.An endoplasmic reticulum (ER) membrane complex composed of SPFH1 and SPFH2 mediates the ER-associated degradation of inositol 1,4,5-trisphosphate receptorsLocalization of a highly active pool of type II phosphatidylinositol 4-kinase in a p97/valosin-containing-protein-rich fraction of the endoplasmic reticulumThe retrotranslocation protein Derlin-1 binds peptide:N-glycanase to the endoplasmic reticulumA subset of chaperones and folding enzymes form multiprotein complexes in endoplasmic reticulum to bind nascent proteins.Misfolded proteins partition between two distinct quality control compartmentsEDEM1 reveals a quality control vesicular transport pathway out of the endoplasmic reticulum not involving the COPII exit sitesSorting out the trash: the spatial nature of eukaryotic protein quality controlRole of the asialoglycoprotein receptor in binding and entry of hepatitis C virus structural proteins in cultured human hepatocytes.An HRD/DER-independent ER quality control mechanism involves Rsp5p-dependent ubiquitination and ER-Golgi transportTraffic-independent function of the Sar1p/COPII machinery in proteasomal sorting of the cystic fibrosis transmembrane conductance regulatorN-Glycan-based ER Molecular Chaperone and Protein Quality Control System: The Calnexin Binding CycleHeterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with AnemiaPresence of tissue transglutaminase in granular endoplasmic reticulum is characteristic of melanized neurons in Parkinson's disease brainOrganizing principles of mammalian nonsense-mediated mRNA decayThe oxidoreductase ERp57 efficiently reduces partially folded in preference to fully folded MHC class I moleculesLuteinizing hormone receptor ectodomain splice variant misroutes the full-length receptor into a subcompartment of the endoplasmic reticulum.Bap31 enhances the endoplasmic reticulum export and quality control of human class I MHC moleculesBap31 is an itinerant protein that moves between the peripheral endoplasmic reticulum (ER) and a juxtanuclear compartment related to ER-associated Degradation.Distinct partitioning of ALS associated TDP-43, FUS and SOD1 mutants into cellular inclusionsRab2A is a pivotal switch protein that promotes either secretion or ER-associated degradation of (pro)insulin in insulin-secreting cells.Probing for membrane domains in the endoplasmic reticulum: retention and degradation of unassembled MHC class I molecules.The role of UDP-Glc:glycoprotein glucosyltransferase 1 in the maturation of an obligate substrate prosaposin.Ricin A chain without its partner B chain is degraded after retrotranslocation from the endoplasmic reticulum to the cytosol in plant cells.Quality and quantity control at the endoplasmic reticulum.Mixed-disulfide folding intermediates between thyroglobulin and endoplasmic reticulum resident oxidoreductases ERp57 and protein disulfide isomerase.The association of Shiga-like toxin with detergent-resistant membranes is modulated by glucosylceramide and is an essential requirement in the endoplasmic reticulum for a cytotoxic effectSelective re-routing of prion protein to proteasomes and alteration of its vesicular secretion prevent PrP(Sc) formation.A novel carboxyl-terminal heptapeptide initiates the regulated secretion of LH from unique sub-domains of the ER.Mammalian ER mannosidase I resides in quality control vesicles, where it encounters its glycoprotein substrates.Trafficking-deficient hERG K⁺ channels linked to long QT syndrome are regulated by a microtubule-dependent quality control compartment in the ER.Role of calnexin in the glycan-independent quality control of proteolipid protein.Golgi localization of ERManI defines spatial separation of the mammalian glycoprotein quality control system.Proteasomal dysfunction and endoplasmic reticulum stress enhance trafficking of prion protein aggregates through the secretory pathway and increase accumulation of pathologic prion proteinThe annotation of the asparagine N-linked glycosylation pathway in the Reactome database.Quality control in the endoplasmic reticulum protein factory.Constant serum levels of secreted asialoglycoprotein receptor sH2a and decrease with cirrhosis
P2860
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P2860
A novel quality control compartment derived from the endoplasmic reticulum
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
A novel quality control compartment derived from the endoplasmic reticulum
@en
type
label
A novel quality control compartment derived from the endoplasmic reticulum
@en
prefLabel
A novel quality control compartment derived from the endoplasmic reticulum
@en
P2093
P2860
P921
P356
P1476
A novel quality control compartment derived from the endoplasmic reticulum
@en
P2093
Kamhi-Nesher S
Lederkremer GZ
Shenkman M
Tolchinsky S
P2860
P304
P356
10.1091/MBC.12.6.1711
P577
2001-06-01T00:00:00Z