Protein targeting and degradation are coupled for elimination of mislocalized proteins

scientific article

Protein targeting and degradation are coupled for elimination of mislocalized proteins is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1040893323
P356DOI10.1038/NATURE10181
P932PMC publication ID3150218
P698PubMed publication ID21743475
P5875ResearchGate publication ID51481012

P50authorRamanujan Shankar HegdeQ24004353
P2093author name stringAjay Sharma
Malaiyalam Mariappan
Erik Gutierrez
Heather D Eshleman
Tara Hessa
P2860cites workMultilayered mechanism of CD4 downregulation by HIV-1 Vpu involving distinct ER retention and ERAD targeting stepsQ21131559
A ribosome-associating factor chaperones tail-anchored membrane proteinsQ24293683
Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III regionQ24301622
A ubiquitin ligase-associated chaperone holdase maintains polypeptides in soluble states for proteasome degradationQ24305231
The cytoplasmic Hsp70 chaperone machinery subjects misfolded and endoplasmic reticulum import-incompetent proteins to degradation via the ubiquitin-proteasome systemQ24676115
Protein translocation across the endoplasmic reticulum. I. Detection in the microsomal membrane of a receptor for the signal recognition particleQ24680984
Ubr1 and Ubr2 function in a quality control pathway for degradation of unfolded cytosolic proteinsQ27930363
Cytoplasmic protein quality control degradation mediated by parallel actions of the E3 ubiquitin ligases Ubr1 and San1Q27932129
Degradation of misfolded protein in the cytoplasm is mediated by the ubiquitin ligase Ubr1.Q27939178
Identification of a targeting factor for posttranslational membrane protein insertion into the ERQ28294726
BAG-6 is essential for selective elimination of defective proteasomal substratesQ28505838
Reduced translocation of nascent prion protein during ER stress contributes to neurodegenerationQ30483989
Conditions of endoplasmic reticulum stress favor the accumulation of cytosolic prion proteinQ33253898
Substrate-specific translocational attenuation during ER stress defines a pre-emptive quality control pathwayQ33264756
Functional depletion of mahogunin by cytosolically exposed prion protein contributes to neurodegenerationQ33289413
The efficiency of protein compartmentalization into the secretory pathwayQ33564834
Signal sequence insufficiency contributes to neurodegeneration caused by transmembrane prion proteinQ33689595
Enzymatic blockade of the ubiquitin-proteasome pathwayQ33863563
Cotranslational partitioning of nascent prion protein into multiple populations at the translocation channelQ34274103
The signal recognition particleQ34275497
Compartment-restricted biotinylation reveals novel features of prion protein metabolism in vivoQ34408461
In vitro dissection of protein translocation into the mammalian endoplasmic reticulumQ35065009
CHIP: a link between the chaperone and proteasome systemsQ35759085
Substrate-specific function of the translocon-associated protein complex during translocation across the ER membraneQ36325004
Retrotranslocation of prion proteins from the endoplasmic reticulum by preventing GPI signal transamidationQ36796856
A signal-anchor sequence stimulates signal recognition particle binding to ribosomes from inside the exit tunnelQ37068989
Photocrosslinking of the signal sequence of nascent preprolactin to the 54-kilodalton polypeptide of the signal recognition particleQ37407450
Delivering proteins for export from the cytosolQ37420386
Protection from cytosolic prion protein toxicity by modulation of protein translocationQ37671821
Protein quality control in the cytosol and the endoplasmic reticulum: brothers in arms.Q37802039
Bat3 promotes the membrane integration of tail-anchored proteinsQ41113412
Organelle pH studies using targeted avidin and fluorescein-biotinQ41724391
Signal sequences control gating of the protein translocation channel in a substrate-specific mannerQ42818885
Conversion of PrP to a self-perpetuating PrPSc-like conformation in the cytosolQ44184136
Neurotoxicity and neurodegeneration when PrP accumulates in the cytosolQ44184139
Mutant PrP is delayed in its exit from the endoplasmic reticulum, but neither wild-type nor mutant PrP undergoes retrotranslocation prior to proteasomal degradationQ44381518
A substrate-specific inhibitor of protein translocation into the endoplasmic reticulumQ46562004
Diffusional mobility of Golgi proteins in membranes of living cellsQ71160454
P433issue7356
P407language of work or nameEnglishQ1860
P304page(s)394-397
P577publication date2011-07-10
P1433published inNatureQ180445
P1476titleProtein targeting and degradation are coupled for elimination of mislocalized proteins
P478volume475

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