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Molecular Cell|April 1, 2004
Yeast adapt to near-freezing temperatures by STRE/Msn2,4-dependent induction of trehalose synthesis and certain molecular chaperonesOlga Kandror, Nancy Bretschneider, Evgeniy Kreydin, et al.Biomolecules|June 2, 2021
Mechanisms That Activate 26S Proteasomes and Enhance Protein DegradationAlfred L Goldberg, Hyoung Tae Kim, Donghoon Lee, et al.The EMBO Journal|May 29, 2002
Properties of the hybrid form of the 26S proteasome containing both 19S and PA28 complexesPaolo Cascio, Matthew Call, Benjamin M Petre, et al.Cell|February 22, 2011
ATP binds to proteasomal ATPases in pairs with distinct functional effects, implying an ordered reaction cycleDavid M Smith, Hugo Fraga, Christian Reis, et al.The Journal of Cell Biology|February 26, 2014
Trim32 reduces PI3K-Akt-FoxO signaling in muscle atrophy by promoting plakoglobin-PI3K dissociationShenhav Cohen, Donghoon Lee, Bo Zhai, et al.Apoptosis : an International Journal on Programmed Cell Death|December 7, 2007
The COP9 signalosome-mediated deneddylation is stimulated by caspases during apoptosisBettina K J Hetfeld, Andreas Peth, Xiao-Ming Sun, et al.Journal of Immunology (Baltimore, Md. : 1950)|July 20, 2006
Tripeptidyl peptidase II is the major peptidase needed to trim long antigenic precursors, but is not required for most MHC class I antigen presentationIan A York, Nidhi Bhutani, Sophia Zendzian, et al.Trends in Immunology|February 26, 2014
Re-examining class-I presentation and the DRiP hypothesisKenneth L Rock, Diego J Farfán-Arribas, Jeff D Colbert, et al.Molecular Cell|December 13, 2005
ATP binding to PAN or the 26S ATPases causes association with the 20S proteasome, gate opening, and translocation of unfolded proteinsDavid M Smith, Galit Kafri, Yifan Cheng, et al.Cell|March 5, 2013
Immuno- and constitutive proteasomes do not differ in their abilities to degrade ubiquitinated proteinsJames A Nathan, Valentina Spinnenhirn, Gunter Schmidtke, et al.Pageof 15