scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1040893323 |
P356 | DOI | 10.1038/NATURE10181 |
P932 | PMC publication ID | 3150218 |
P698 | PubMed publication ID | 21743475 |
P5875 | ResearchGate publication ID | 51481012 |
P50 | author | Ramanujan Shankar Hegde | Q24004353 |
P2093 | author name string | Ajay Sharma | |
Malaiyalam Mariappan | |||
Erik Gutierrez | |||
Heather D Eshleman | |||
Tara Hessa | |||
P2860 | cites work | Multilayered mechanism of CD4 downregulation by HIV-1 Vpu involving distinct ER retention and ERAD targeting steps | Q21131559 |
A ribosome-associating factor chaperones tail-anchored membrane proteins | Q24293683 | ||
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 region | Q24301622 | ||
A ubiquitin ligase-associated chaperone holdase maintains polypeptides in soluble states for proteasome degradation | Q24305231 | ||
The cytoplasmic Hsp70 chaperone machinery subjects misfolded and endoplasmic reticulum import-incompetent proteins to degradation via the ubiquitin-proteasome system | Q24676115 | ||
Protein translocation across the endoplasmic reticulum. I. Detection in the microsomal membrane of a receptor for the signal recognition particle | Q24680984 | ||
Ubr1 and Ubr2 function in a quality control pathway for degradation of unfolded cytosolic proteins | Q27930363 | ||
Cytoplasmic protein quality control degradation mediated by parallel actions of the E3 ubiquitin ligases Ubr1 and San1 | Q27932129 | ||
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 ER | Q28294726 | ||
BAG-6 is essential for selective elimination of defective proteasomal substrates | Q28505838 | ||
Reduced translocation of nascent prion protein during ER stress contributes to neurodegeneration | Q30483989 | ||
Conditions of endoplasmic reticulum stress favor the accumulation of cytosolic prion protein | Q33253898 | ||
Substrate-specific translocational attenuation during ER stress defines a pre-emptive quality control pathway | Q33264756 | ||
Functional depletion of mahogunin by cytosolically exposed prion protein contributes to neurodegeneration | Q33289413 | ||
The efficiency of protein compartmentalization into the secretory pathway | Q33564834 | ||
Signal sequence insufficiency contributes to neurodegeneration caused by transmembrane prion protein | Q33689595 | ||
Enzymatic blockade of the ubiquitin-proteasome pathway | Q33863563 | ||
Cotranslational partitioning of nascent prion protein into multiple populations at the translocation channel | Q34274103 | ||
The signal recognition particle | Q34275497 | ||
Compartment-restricted biotinylation reveals novel features of prion protein metabolism in vivo | Q34408461 | ||
In vitro dissection of protein translocation into the mammalian endoplasmic reticulum | Q35065009 | ||
CHIP: a link between the chaperone and proteasome systems | Q35759085 | ||
Substrate-specific function of the translocon-associated protein complex during translocation across the ER membrane | Q36325004 | ||
Retrotranslocation of prion proteins from the endoplasmic reticulum by preventing GPI signal transamidation | Q36796856 | ||
A signal-anchor sequence stimulates signal recognition particle binding to ribosomes from inside the exit tunnel | Q37068989 | ||
Photocrosslinking of the signal sequence of nascent preprolactin to the 54-kilodalton polypeptide of the signal recognition particle | Q37407450 | ||
Delivering proteins for export from the cytosol | Q37420386 | ||
Protection from cytosolic prion protein toxicity by modulation of protein translocation | Q37671821 | ||
Protein quality control in the cytosol and the endoplasmic reticulum: brothers in arms. | Q37802039 | ||
Bat3 promotes the membrane integration of tail-anchored proteins | Q41113412 | ||
Organelle pH studies using targeted avidin and fluorescein-biotin | Q41724391 | ||
Signal sequences control gating of the protein translocation channel in a substrate-specific manner | Q42818885 | ||
Conversion of PrP to a self-perpetuating PrPSc-like conformation in the cytosol | Q44184136 | ||
Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol | Q44184139 | ||
Mutant PrP is delayed in its exit from the endoplasmic reticulum, but neither wild-type nor mutant PrP undergoes retrotranslocation prior to proteasomal degradation | Q44381518 | ||
A substrate-specific inhibitor of protein translocation into the endoplasmic reticulum | Q46562004 | ||
Diffusional mobility of Golgi proteins in membranes of living cells | Q71160454 | ||
P433 | issue | 7356 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 394-397 | |
P577 | publication date | 2011-07-10 | |
P1433 | published in | Nature | Q180445 |
P1476 | title | Protein targeting and degradation are coupled for elimination of mislocalized proteins | |
P478 | volume | 475 |
Q35751874 | A calmodulin-dependent translocation pathway for small secretory proteins |
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Q34256996 | A novel BAT3 sequence generated by alternative RNA splicing of exon 11B displays cell type-specific expression and impacts on subcellular localization |
Q38040951 | A portrait of the GET pathway as a surprisingly complicated young man. |
Q24305231 | A ubiquitin ligase-associated chaperone holdase maintains polypeptides in soluble states for proteasome degradation |
Q36947746 | A ubiquitin-like domain recruits an oligomeric chaperone to a retrotranslocation complex in endoplasmic reticulum-associated degradation |
Q38093231 | All roads lead to Rome (but some may be harder to travel): SRP-independent translocation into the endoplasmic reticulum |
Q46325087 | Assembly and Function of Heterotypic Ubiquitin Chains in Cell-Cycle and Protein Quality Control |
Q38168708 | BAG-6, a jack of all trades in health and disease |
Q84597133 | BAG6 'mops up' mislocalized proteins |
Q92479518 | BAG6 contributes to glucose uptake by supporting the cell surface translocation of the glucose transporter GLUT4 |
Q92270950 | BAG6 deficiency induces mis-distribution of mitochondrial clusters under depolarization |
Q41482461 | BAG6 regulates the quality control of a polytopic ERAD substrate |
Q38070391 | BAG6/BAT3: emerging roles in quality control for nascent polypeptides |
Q100157394 | BAG6:GET4:UBL4A binds mislocalized membrane protein:SGTA and ASNA1:ATP |
Q34103187 | BAT3 guides misfolded glycoproteins out of the endoplasmic reticulum |
Q24311324 | Bag6 complex contains a minimal tail-anchor-targeting module and a mock BAG domain |
Q38082449 | Bag6/Bat3/Scythe: a novel chaperone activity with diverse regulatory functions in protein biogenesis and degradation. |
Q43240834 | Binding of SGTA to Rpn13 selectively modulates protein quality control |
Q38664342 | Charged residues next to transmembrane regions revisited: "Positive-inside rule" is complemented by the "negative inside depletion/outside enrichment rule" |
Q38864129 | Comparative Haploid Genetic Screens Reveal Divergent Pathways in the Biogenesis and Trafficking of Glycophosphatidylinositol-Anchored Proteins. |
Q33628850 | Control of mitochondrial biogenesis and function by the ubiquitin-proteasome system |
Q51830754 | Cotransin induces accumulation of a cytotoxic clusterin variant that cotranslationally rerouted to the cytosol. |
Q64104486 | Cytoplasmic control of Rab family small GTPases through BAG6 |
Q24300029 | Cytosolic quality control of mislocalized proteins requires RNF126 recruitment to Bag6 |
Q52424984 | Distinct types of protease systems are involved in homeostasis regulation of mitochondrial morphology via balanced fusion and fission. |
Q36091833 | Efficient secretion of small proteins in mammalian cells relies on Sec62-dependent posttranslational translocation |
Q34294233 | Elevation of proteasomal substrate levels sensitizes cells to apoptosis induced by inhibition of proteasomal deubiquitinases |
Q44897873 | Elimination of a signal sequence-uncleaved form of defective HLA protein through BAG6. |
Q26866138 | Endoplasmic reticulum targeting and insertion of tail-anchored membrane proteins by the GET pathway |
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Q40209893 | HLA-B-associated transcript 3 (Bat3/Scythe) negatively regulates Smad phosphorylation in BMP signaling |
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Q47255663 | In vitro reconstitution of translational arrest pathways |
Q41558826 | Inhibition of protein translocation at the endoplasmic reticulum promotes activation of the unfolded protein response |
Q38864831 | Involvement of Bag6 and the TRC pathway in proteasome assembly |
Q28675845 | Listerin-dependent nascent protein ubiquitination relies on ribosome subunit dissociation |
Q58583775 | Lost in Translation: Ribosome-Associated mRNA and Protein Quality Controls |
Q55044914 | MARCH6 and TRC8 facilitate the quality control of cytosolic and tail-anchored proteins. |
Q46465153 | Mechanisms of Tail-Anchored Membrane Protein Targeting and Insertion. |
Q42292851 | Mechanistic basis for a molecular triage reaction |
Q34179638 | Membrane protein insertion at the endoplasmic reticulum |
Q34095072 | Metabolism of minor isoforms of prion proteins: Cytosolic prion protein and transmembrane prion protein |
Q39612063 | Mice lacking WRB reveal differential biogenesis requirements of tail-anchored proteins in vivo |
Q64290441 | Misfolded GPI-anchored proteins are escorted through the secretory pathway by ER-derived factors |
Q26828990 | Molecular chaperones in targeting misfolded proteins for ubiquitin-dependent degradation |
Q55114046 | Molecular mechanism of ER stress-induced pre-emptive quality control involving association of the translocon, Derlin-1, and HRD1. |
Q34343289 | Msp1/ATAD1 maintains mitochondrial function by facilitating the degradation of mislocalized tail-anchored proteins |
Q41869462 | Msp1: patrolling mitochondria for lost proteins |
Q47108141 | Multiple pathways facilitate the biogenesis of mammalian tail-anchored proteins |
Q40778656 | Multiple selection filters ensure accurate tail-anchored membrane protein targeting |
Q98878656 | Multiplexed measurement of variant abundance and activity reveals VKOR topology, active site and human variant impact |
Q37297662 | Nodular lymphocyte predominant hodgkin lymphoma and T cell/histiocyte rich large B cell lymphoma--endpoints of a spectrum of one disease? |
Q46703828 | Novel characterization of the HSPA2-stabilizing protein BAG6 in human spermatozoa |
Q42224037 | Overexpression of BAT3 alleviates prion protein fragment PrP106-126-induced neuronal apoptosis. |
Q28306492 | Perilous journey: a tour of the ubiquitin-proteasome system |
Q37047936 | Peroxin-dependent targeting of a lipid-droplet-destined membrane protein to ER subdomains |
Q38900355 | Porcine reproductive and respiratory syndrome virus nonstructural protein 2 (nsp2) topology and selective isoform integration in artificial membranes |
Q47305042 | Positive charge in the n-region of the signal peptide contributes to efficient post-translational translocation of small secretory preproteins |
Q46498597 | PrP-containing aggresomes are cytosolic components of an ER quality control mechanism. |
Q33743186 | Predicting the targeting of tail-anchored proteins to subcellular compartments in mammalian cells. |
Q36224548 | Proteasomal degradation of preemptive quality control (pQC) substrates is mediated by an AIRAPL-p97 complex |
Q37953004 | Protein quality control in the ER: balancing the ubiquitin checkbook |
Q38954697 | Proteome complexity and the forces that drive proteome imbalance. |
Q90740558 | Quality Control of Orphaned Proteins |
Q34244144 | Reconstitution of a minimal ribosome-associated ubiquitination pathway with purified factors |
Q39430414 | Repair or destruction-an intimate liaison between ubiquitin ligases and molecular chaperones in proteostasis |
Q39185522 | Rescue of impaired NK cell activity in hodgkin lymphoma with bispecific antibodies in vitro and in patients |
Q90864188 | Ribosomal mistranslation leads to silencing of the unfolded protein response and increased mitochondrial biogenesis |
Q28596609 | SGTA antagonizes BAG6-mediated protein triage |
Q90678120 | SGTA associates with nascent membrane protein precursors |
Q42371745 | SGTA interacts with the proteasomal ubiquitin receptor Rpn13 via a carboxylate clamp mechanism. |
Q24306367 | SGTA recognizes a noncanonical ubiquitin-like domain in the Bag6-Ubl4A-Trc35 complex to promote endoplasmic reticulum-associated degradation |
Q42186480 | SGTA regulates the cytosolic quality control of hydrophobic substrates |
Q37374069 | Secretory protein profiling reveals TNF-α inactivation by selective and promiscuous Sec61 modulators |
Q24338887 | Signal-peptide-mediated translocation is regulated by a p97-AIRAPL complex |
Q28545114 | Solution structure of the SGTA dimerisation domain and investigation of its interactions with the ubiquitin-like domains of BAG6 and UBL4A |
Q42111753 | Spatial control of lipid droplet proteins by the ERAD ubiquitin ligase Doa10. |
Q51036230 | Specific inhibition of hamster prion protein translocation by the dodecadepsipeptide valinomycin. |
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Q42011073 | Structural and functional insights into the E3 ligase, RNF126. |
Q46122220 | Structural basis for regulation of the nucleo-cytoplasmic distribution of Bag6 by TRC35. |
Q39582237 | Structural features within the nascent chain regulate alternative targeting of secretory proteins to mitochondria |
Q42700283 | Structure and Interactions of the TPR Domain of Sgt2 with Yeast Chaperones and Ybr137wp |
Q35064391 | Structure and assembly pathway of the ribosome quality control complex |
Q39474998 | Structure of a BAG6 (Bcl-2-associated athanogene 6)-Ubl4a (ubiquitin-like protein 4a) complex reveals a novel binding interface that functions in tail-anchored protein biogenesis |
Q27675050 | Structures of the Sgt2/SGTA Dimerization Domain with the Get5/UBL4A UBL Domain Reveal an Interaction that Forms a Conserved Dynamic Interface |
Q41176440 | Structures of the scanning and engaged states of the mammalian SRP-ribosome complex |
Q35915784 | Subcellular Fractionation Analysis of the Extraction of Ubiquitinated Polytopic Membrane Substrate during ER-Associated Degradation |
Q36242781 | TRC40 can deliver short secretory proteins to the Sec61 translocon |
Q36655456 | Tail-anchored PEX26 targets peroxisomes via a PEX19-dependent and TRC40-independent class I pathway |
Q37140792 | Tail-anchored membrane protein insertion into the endoplasmic reticulum |
Q47292355 | The ER membrane protein complex is a transmembrane domain insertase |
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Q36824020 | The Vpu-interacting Protein SGTA Regulates Expression of a Non-glycosylated Tetherin Species |
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Q34637885 | The association of BAG6 with SGTA and tail-anchored proteins |
Q35110985 | The chaperone BAG6 captures dislocated glycoproteins in the cytosol. |
Q35986793 | The complex process of GETting tail-anchored membrane proteins to the ER. |
Q38419066 | The emerging role of calcium-modulating cyclophilin ligand in posttranslational insertion of tail-anchored proteins into the endoplasmic reticulum membrane |
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Q34029353 | Towards a systems understanding of MHC class I and MHC class II antigen presentation. |
Q55235796 | Transmembrane E3 ligase RNF183 mediates ER stress-induced apoptosis by degrading Bcl-xL. |
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