Human XTP3-B forms an endoplasmic reticulum quality control scaffold with the HRD1-SEL1L ubiquitin ligase complex and BiP
about
A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machineryDefining human ERAD networks through an integrative mapping strategySEL1L protein critically determines the stability of the HRD1-SEL1L endoplasmic reticulum-associated degradation (ERAD) complex to optimize the degradation kinetics of ERAD substratesMalectin forms a complex with ribophorin I for enhanced association with misfolded glycoproteinsMannose trimming is required for delivery of a glycoprotein from EDEM1 to XTP3-B and to late endoplasmic reticulum-associated degradation stepsA luminal flavoprotein in endoplasmic reticulum-associated degradationHuman OS-9, a lectin required for glycoprotein endoplasmic reticulum-associated degradation, recognizes mannose-trimmed N-glycansEDEM1 recognition and delivery of misfolded proteins to the SEL1L-containing ERAD complexOne step at a time: endoplasmic reticulum-associated degradationProtein folding and quality control in the ERRecent technical developments in the study of ER-associated degradationRoad to ruin: targeting proteins for degradation in the endoplasmic reticulumThe delicate balance between secreted protein folding and endoplasmic reticulum-associated degradation in human physiologyHow Polyomaviruses Exploit the ERAD Machinery to Cause InfectionFive Questions (with their Answers) on ER-Associated DegradationAssociation of the SEL1L protein transmembrane domain with HRD1 ubiquitin ligase regulates ERAD-LCyclosporine A-sensitive, cyclophilin B-dependent endoplasmic reticulum-associated degradationEDEM1 accelerates the trimming of alpha1,2-linked mannose on the C branch of N-glycansDeficiency of suppressor enhancer Lin12 1 like (SEL1L) in mice leads to systemic endoplasmic reticulum stress and embryonic lethalityDerlin-1 deficiency is embryonic lethal, Derlin-3 deficiency appears normal, and Herp deficiency is intolerant to glucose load and ischemia in miceLive cell imaging of protein dislocation from the endoplasmic reticulum.EDEM2 and OS-9 are required for ER-associated degradation of non-glycosylated sonic hedgehog.SEL1L deficiency impairs growth and differentiation of pancreatic epithelial cells.Stringent requirement for HRD1, SEL1L, and OS-9/XTP3-B for disposal of ERAD-LS substrates.Modularity of the Hrd1 ERAD complex underlies its diverse client range.The endoplasmic reticulum-associated degradation of the epithelial sodium channel requires a unique complement of molecular chaperones.Novel thioredoxin-related transmembrane protein TMX4 has reductase activity.Identification of FBXL4 as a Metastasis Associated Gene in Prostate Cancer.Protein homeostasis of a metastable subproteome associated with Alzheimer's disease.OS-9 facilitates turnover of nonnative GRP94 marked by hyperglycosylation.Retroviral Rem protein requires processing by signal peptidase and retrotranslocation for nuclear functionQuality and quantity control at the endoplasmic reticulum.The ubiquitin-selective segregase VCP/p97 orchestrates the response to DNA double-strand breaks.Deglycosylation-dependent fluorescent proteins provide unique tools for the study of ER-associated degradation.Forcible destruction of severely misfolded mammalian glycoproteins by the non-glycoprotein ERAD pathwayProcessing and turnover of the Hedgehog protein in the endoplasmic reticulum.Analysis of the sperm head protein profiles in fertile men: consistency across time in the levels of expression of heat shock proteins and peroxiredoxins.Characterization of early EDEM1 protein maturation events and their functional implications.Protein folding and quality control in the endoplasmic reticulum: Recent lessons from yeast and mammalian cell systems.Retroviral vectors elevate coexpressed protein levels in trans through cap-dependent translation.
P2860
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P2860
Human XTP3-B forms an endoplasmic reticulum quality control scaffold with the HRD1-SEL1L ubiquitin ligase complex and BiP
description
2008 nî lūn-bûn
@nan
2008 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2008年の論文
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2008年学术文章
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2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
name
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@ast
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@en
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@en-gb
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@nl
type
label
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@ast
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@en
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@en-gb
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@nl
prefLabel
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@ast
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@en
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@en-gb
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@nl
P2093
P2860
P921
P3181
P356
P1476
Human XTP3-B forms an endoplas ...... iquitin ligase complex and BiP
@en
P2093
Katsuya Okawa
Kazuhiro Nagata
Koji Nagasawa
Nobuko Hosokawa
P2860
P304
P3181
P356
10.1074/JBC.M709336200
P407
P577
2008-07-25T00:00:00Z