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Journal Abstract Search

221 related items for PubMed ID: 20008553

  • 1. The ubiquitin ligase Hul5 promotes proteasomal processivity.
    Aviram S, Kornitzer D.
    Mol Cell Biol; 2010 Feb; 30(4):985-94. PubMed ID: 20008553
    [Abstract] [Full Text] [Related]

  • 2. Ubiquitin chains are remodeled at the proteasome by opposing ubiquitin ligase and deubiquitinating activities.
    Crosas B, Hanna J, Kirkpatrick DS, Zhang DP, Tone Y, Hathaway NA, Buecker C, Leggett DS, Schmidt M, King RW, Gygi SP, Finley D.
    Cell; 2006 Dec 29; 127(7):1401-13. PubMed ID: 17190603
    [Abstract] [Full Text] [Related]

  • 3. Ubiquitin ligase Hul5 is required for fragment-specific substrate degradation in endoplasmic reticulum-associated degradation.
    Kohlmann S, Schäfer A, Wolf DH.
    J Biol Chem; 2008 Jun 13; 283(24):16374-83. PubMed ID: 18436532
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Functional characterization of rpn3 uncovers a distinct 19S proteasomal subunit requirement for ubiquitin-dependent proteolysis of cell cycle regulatory proteins in budding yeast.
    Bailly E, Reed SI.
    Mol Cell Biol; 1999 Oct 01; 19(10):6872-90. PubMed ID: 10490625
    [Abstract] [Full Text] [Related]

  • 6. Ubiquitinated proteins promote the association of proteasomes with the deubiquitinating enzyme Usp14 and the ubiquitin ligase Ube3c.
    Kuo CL, Goldberg AL.
    Proc Natl Acad Sci U S A; 2017 Apr 25; 114(17):E3404-E3413. PubMed ID: 28396413
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Inherent asymmetry in the 26S proteasome is defined by the ubiquitin receptor RPN13.
    Berko D, Herkon O, Braunstein I, Isakov E, David Y, Ziv T, Navon A, Stanhill A.
    J Biol Chem; 2014 Feb 28; 289(9):5609-18. PubMed ID: 24429290
    [Abstract] [Full Text] [Related]

  • 9. Vms1 and ANKZF1 peptidyl-tRNA hydrolases release nascent chains from stalled ribosomes.
    Verma R, Reichermeier KM, Burroughs AM, Oania RS, Reitsma JM, Aravind L, Deshaies RJ.
    Nature; 2018 May 28; 557(7705):446-451. PubMed ID: 29632312
    [Abstract] [Full Text] [Related]

  • 10. To degrade or release: ubiquitin-chain remodeling.
    Kraut DA, Prakash S, Matouschek A.
    Trends Cell Biol; 2007 Sep 28; 17(9):419-21. PubMed ID: 17900906
    [Abstract] [Full Text] [Related]

  • 11. Conserved proline residues in the coiled coil-OB domain linkers of Rpt proteins facilitate eukaryotic proteasome base assembly.
    Cheng CL, Wong MK, Li Y, Hochstrasser M.
    J Biol Chem; 2021 Sep 28; 296():100660. PubMed ID: 33862083
    [Abstract] [Full Text] [Related]

  • 12. A cryptic protease couples deubiquitination and degradation by the proteasome.
    Yao T, Cohen RE.
    Nature; 2002 Sep 26; 419(6905):403-7. PubMed ID: 12353037
    [Abstract] [Full Text] [Related]

  • 13. Degradation of misfolded protein in the cytoplasm is mediated by the ubiquitin ligase Ubr1.
    Eisele F, Wolf DH.
    FEBS Lett; 2008 Dec 24; 582(30):4143-6. PubMed ID: 19041308
    [Abstract] [Full Text] [Related]

  • 14. Structural defects in the regulatory particle-core particle interface of the proteasome induce a novel proteasome stress response.
    Park S, Kim W, Tian G, Gygi SP, Finley D.
    J Biol Chem; 2011 Oct 21; 286(42):36652-66. PubMed ID: 21878652
    [Abstract] [Full Text] [Related]

  • 15. Rqc1 and Ltn1 Prevent C-terminal Alanine-Threonine Tail (CAT-tail)-induced Protein Aggregation by Efficient Recruitment of Cdc48 on Stalled 60S Subunits.
    Defenouillère Q, Zhang E, Namane A, Mouaikel J, Jacquier A, Fromont-Racine M.
    J Biol Chem; 2016 Jun 03; 291(23):12245-53. PubMed ID: 27129255
    [Abstract] [Full Text] [Related]

  • 16. UFD4 lacking the proteasome-binding region catalyses ubiquitination but is impaired in proteolysis.
    Xie Y, Varshavsky A.
    Nat Cell Biol; 2002 Dec 03; 4(12):1003-7. PubMed ID: 12447385
    [Abstract] [Full Text] [Related]

  • 17. Timer-based proteomic profiling of the ubiquitin-proteasome system reveals a substrate receptor of the GID ubiquitin ligase.
    Kong KE, Fischer B, Meurer M, Kats I, Li Z, Rühle F, Barry JD, Kirrmaier D, Chevyreva V, San Luis BJ, Costanzo M, Huber W, Andrews BJ, Boone C, Knop M, Khmelinskii A.
    Mol Cell; 2021 Jun 03; 81(11):2460-2476.e11. PubMed ID: 33974913
    [Abstract] [Full Text] [Related]

  • 18. Translocation of polyubiquitinated protein substrates by the hexameric Cdc48 ATPase.
    Ji Z, Li H, Peterle D, Paulo JA, Ficarro SB, Wales TE, Marto JA, Gygi SP, Engen JR, Rapoport TA.
    Mol Cell; 2022 Feb 03; 82(3):570-584.e8. PubMed ID: 34951965
    [Abstract] [Full Text] [Related]

  • 19. Proteasome-associated HECT-type ubiquitin ligase activity is required for plant immunity.
    Furniss JJ, Grey H, Wang Z, Nomoto M, Jackson L, Tada Y, Spoel SH.
    PLoS Pathog; 2018 Nov 03; 14(11):e1007447. PubMed ID: 30458055
    [Abstract] [Full Text] [Related]

  • 20. Lysine 63-linked polyubiquitin chain may serve as a targeting signal for the 26S proteasome.
    Saeki Y, Kudo T, Sone T, Kikuchi Y, Yokosawa H, Toh-e A, Tanaka K.
    EMBO J; 2009 Feb 18; 28(4):359-71. PubMed ID: 19153599
    [Abstract] [Full Text] [Related]

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