Literature DB >> 14573346

Proteasome degradation: enter the substrate.

Andreas Förster1, Christopher P Hill.   

Abstract

Cells depend upon the regulated destruction of their various proteins to maintain homeostasis and change their metabolic state. A key component of this process is the proteasome - a large multisubunit protease whose catalytic sites are sequestered within a central chamber. Entry of substrates into proteasomes is regulated by activators and is generally thought to proceed sequentially, starting from one end of the substrate polypeptide. This conventional view is expanded by a recent paper, which indicates that some unfolded substrates can open the entrance to the proteolytic chamber in the absence of an activator and can enter the proteasome in a hairpin conformation to allow limited proteolysis of internal segments.

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Year:  2003        PMID: 14573346     DOI: 10.1016/j.tcb.2003.09.001

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  16 in total

1.  The proteasome antechamber maintains substrates in an unfolded state.

Authors:  Amy M Ruschak; Tomasz L Religa; Sarah Breuer; Susanne Witt; Lewis E Kay
Journal:  Nature       Date:  2010-10-14       Impact factor: 49.962

2.  A mathematical model of protein degradation by the proteasome.

Authors:  Fabio Luciani; Can Keşmir; Michele Mishto; Michal Or-Guil; Rob J de Boer
Journal:  Biophys J       Date:  2005-01-21       Impact factor: 4.033

3.  Electrospray ionization mass spectrometry and ion mobility analysis of the 20S proteasome complex.

Authors:  Joseph A Loo; Beniam Berhane; Catherine S Kaddis; Kerry M Wooding; Yongming Xie; Stanley L Kaufman; Igor V Chernushevich
Journal:  J Am Soc Mass Spectrom       Date:  2005-07       Impact factor: 3.109

Review 4.  The proteasome: a central regulator of inflammation and macrophage function.

Authors:  Nilofer Qureshi; Stefanie N Vogel; Charles Van Way; Christopher J Papasian; Asaf A Qureshi; David C Morrison
Journal:  Immunol Res       Date:  2005       Impact factor: 2.829

5.  To misfold or to lose structure?: Detection and degradation of oxidized proteins by the 20S proteasome.

Authors:  Jasmina Kurepa; Jan A Smalle
Journal:  Plant Signal Behav       Date:  2008-06

Review 6.  Context-dependent resistance to proteolysis of intrinsically disordered proteins.

Authors:  Marcin J Suskiewicz; Joel L Sussman; Israel Silman; Yosef Shaul
Journal:  Protein Sci       Date:  2011-06-08       Impact factor: 6.725

7.  Hepatitis B virus large and middle glycoproteins are degraded by a proteasome pathway in glucosidase-inhibited cells but not in cells with functional glucosidase enzyme.

Authors:  Ender Simsek; Anand Mehta; Tianlun Zhou; Raymond A Dwek; Timothy Block
Journal:  J Virol       Date:  2005-10       Impact factor: 5.103

8.  Distinct palmitoylation events at the amino-terminal conserved cysteines of Env7 direct its stability, localization, and vacuolar fusion regulation in S. cerevisiae.

Authors:  Surya P Manandhar; Erika N Calle; Editte Gharakhanian
Journal:  J Biol Chem       Date:  2014-03-07       Impact factor: 5.157

9.  Genetic evidence linking age-dependent attenuation of the 26S proteasome with the aging process.

Authors:  Ayako Tonoki; Erina Kuranaga; Takeyasu Tomioka; Jun Hamazaki; Shigeo Murata; Keiji Tanaka; Masayuki Miura
Journal:  Mol Cell Biol       Date:  2008-12-15       Impact factor: 4.272

10.  Orthopoxviruses require a functional ubiquitin-proteasome system for productive replication.

Authors:  Alastair Teale; Stephanie Campbell; Nick Van Buuren; Wendy C Magee; Kelly Watmough; Brianne Couturier; Robyn Shipclark; Michele Barry
Journal:  J Virol       Date:  2008-12-24       Impact factor: 5.103

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