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Journal Abstract Search

213 related items for PubMed ID: 27448207

  • 21. Inhibiting K63 polyubiquitination abolishes no-go type stalled translation surveillance in Saccharomyces cerevisiae.
    Saito K, Horikawa W, Ito K.
    PLoS Genet; 2015 Apr; 11(4):e1005197. PubMed ID: 25909477
    [Abstract] [Full Text] [Related]

  • 22. The protein quality control machinery regulates its misassembled proteasome subunits.
    Peters LZ, Karmon O, David-Kadoch G, Hazan R, Yu T, Glickman MH, Ben-Aroya S.
    PLoS Genet; 2015 Apr; 11(4):e1005178. PubMed ID: 25919710
    [Abstract] [Full Text] [Related]

  • 23. Hul5 ubiquitin ligase: good riddance to bad proteins.
    Fang NN, Mayor T.
    Prion; 2012 Jul 01; 6(3):240-4. PubMed ID: 22561164
    [Abstract] [Full Text] [Related]

  • 24. Dysfunction of Avo3, an essential component of target of rapamycin complex 2, induces ubiquitin-proteasome-dependent downregulation of Avo2 in Saccharomyces cerevisiae.
    Chen PK, Chang YJ, Chou YW, Chen MY.
    Biochem Biophys Res Commun; 2024 Jul 12; 717():150045. PubMed ID: 38718572
    [Abstract] [Full Text] [Related]

  • 25. LRSAM1 E3 ubiquitin ligase: molecular neurobiological perspectives linked with brain diseases.
    Mishra R, Upadhyay A, Prajapati VK, Dhiman R, Poluri KM, Jana NR, Mishra A.
    Cell Mol Life Sci; 2019 Jun 12; 76(11):2093-2110. PubMed ID: 30826859
    [Abstract] [Full Text] [Related]

  • 26. Yeast chaperones and ubiquitin ligases contribute to proteostasis during arsenite stress by preventing or clearing protein aggregates.
    Rodrigues JI, Lorentzon E, Hua S, Boucher A, Tamás MJ.
    FEBS Lett; 2023 Jul 12; 597(13):1733-1747. PubMed ID: 37191881
    [Abstract] [Full Text] [Related]

  • 27. False start: cotranslational protein ubiquitination and cytosolic protein quality control.
    Comyn SA, Chan GT, Mayor T.
    J Proteomics; 2014 Apr 04; 100():92-101. PubMed ID: 23954725
    [Abstract] [Full Text] [Related]

  • 28. Substrate recognition in nuclear protein quality control degradation is governed by exposed hydrophobicity that correlates with aggregation and insolubility.
    Fredrickson EK, Gallagher PS, Clowes Candadai SV, Gardner RG.
    J Biol Chem; 2013 Mar 01; 288(9):6130-9. PubMed ID: 23335508
    [Abstract] [Full Text] [Related]

  • 29. Most mutations that cause spinocerebellar ataxia autosomal recessive type 16 (SCAR16) destabilize the protein quality-control E3 ligase CHIP.
    Kanack AJ, Newsom OJ, Scaglione KM.
    J Biol Chem; 2018 Feb 23; 293(8):2735-2743. PubMed ID: 29317501
    [Abstract] [Full Text] [Related]

  • 30. Hul5 HECT ubiquitin ligase plays a major role in the ubiquitylation and turnover of cytosolic misfolded proteins.
    Fang NN, Ng AH, Measday V, Mayor T.
    Nat Cell Biol; 2011 Oct 09; 13(11):1344-52. PubMed ID: 21983566
    [Abstract] [Full Text] [Related]

  • 31. CHIP: a co-chaperone for degradation by the proteasome.
    Edkins AL.
    Subcell Biochem; 2015 Oct 09; 78():219-42. PubMed ID: 25487024
    [Abstract] [Full Text] [Related]

  • 32. HUWE1 ubiquitinates MyoD and targets it for proteasomal degradation.
    Noy T, Suad O, Taglicht D, Ciechanover A.
    Biochem Biophys Res Commun; 2012 Feb 10; 418(2):408-13. PubMed ID: 22277673
    [Abstract] [Full Text] [Related]

  • 33. Ubiquitin ligase ITCH recruitment suppresses the aggregation and cellular toxicity of cytoplasmic misfolded proteins.
    Chhangani D, Upadhyay A, Amanullah A, Joshi V, Mishra A.
    Sci Rep; 2014 May 28; 4():5077. PubMed ID: 24865853
    [Abstract] [Full Text] [Related]

  • 34. Cytosolic splice isoform of Hsp70 nucleotide exchange factor Fes1 is required for the degradation of misfolded proteins in yeast.
    Gowda NK, Kaimal JM, Masser AE, Kang W, Friedländer MR, Andréasson C.
    Mol Biol Cell; 2016 Apr 15; 27(8):1210-9. PubMed ID: 26912797
    [Abstract] [Full Text] [Related]

  • 35. Absence of the Yeast Hsp31 Chaperones of the DJ-1 Superfamily Perturbs Cytoplasmic Protein Quality Control in Late Growth Phase.
    Amm I, Norell D, Wolf DH.
    PLoS One; 2015 Apr 15; 10(10):e0140363. PubMed ID: 26466368
    [Abstract] [Full Text] [Related]

  • 36. Protein quality control systems associated with no-go and nonstop mRNA surveillance in yeast.
    Matsuda R, Ikeuchi K, Nomura S, Inada T.
    Genes Cells; 2014 Jan 15; 19(1):1-12. PubMed ID: 24261871
    [Abstract] [Full Text] [Related]

  • 37. The yeast ubr1 ubiquitin ligase participates in a prominent pathway that targets cytosolic thermosensitive mutants for degradation.
    Khosrow-Khavar F, Fang NN, Ng AH, Winget JM, Comyn SA, Mayor T.
    G3 (Bethesda); 2012 May 15; 2(5):619-28. PubMed ID: 22670231
    [Abstract] [Full Text] [Related]

  • 38. N-Myristoylation of the Rpt2 subunit of the yeast 26S proteasome is implicated in the subcellular compartment-specific protein quality control system.
    Kimura A, Kurata Y, Nakabayashi J, Kagawa H, Hirano H.
    J Proteomics; 2016 Jan 01; 130():33-41. PubMed ID: 26344132
    [Abstract] [Full Text] [Related]

  • 39. A ubiquitin ligase-associated chaperone holdase maintains polypeptides in soluble states for proteasome degradation.
    Wang Q, Liu Y, Soetandyo N, Baek K, Hegde R, Ye Y.
    Mol Cell; 2011 Jun 24; 42(6):758-70. PubMed ID: 21636303
    [Abstract] [Full Text] [Related]

  • 40. In vivo action of the HRD ubiquitin ligase complex: mechanisms of endoplasmic reticulum quality control and sterol regulation.
    Gardner RG, Shearer AG, Hampton RY.
    Mol Cell Biol; 2001 Jul 24; 21(13):4276-91. PubMed ID: 11390656
    [Abstract] [Full Text] [Related]

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