Literature DB >> 16608998

What's Ub chain linkage got to do with it?

Ikjin Kim1, Hai Rao.   

Abstract

Ubiquitination-the covalent conjugation of ubiquitin (Ub) to other cellular proteins-regulates a wide range of cellular processes. Often, multiple Ub molecules are added to the substrate to form a Ub chain. Distinct outcomes have been observed for substrates modified with multi-Ub chains linked through particular lysine residues. However, recent studies suggest that Ub chain linkages may not be the key determinant for substrate fate. Here, we review evidence suggesting that Ub-binding proteins play a pivotal role in determining the outcome of substrate ubiquitination. In fulfilling their functions in proteasome-mediated proteolysis or signaling, Ub receptors link ubiquitinated proteins to downstream molecules through protein-protein interactions. Studies of Ub-binding factors may therefore hold the key to understanding the diverse functions of the Ub molecule.

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Year:  2006        PMID: 16608998     DOI: 10.1126/stke.3302006pe18

Source DB:  PubMed          Journal:  Sci STKE        ISSN: 1525-8882


  13 in total

Review 1.  Protein targeting to ATP-dependent proteases.

Authors:  Tomonao Inobe; Andreas Matouschek
Journal:  Curr Opin Struct Biol       Date:  2008-02-13       Impact factor: 6.809

2.  Ubiquitination-mediated internalization and degradation of the astroglial glutamate transporter, GLT-1.

Authors:  Amanda L Sheldon; Marco I González; Elizabeth N Krizman-Genda; Bala T S Susarla; Michael B Robinson
Journal:  Neurochem Int       Date:  2008-08-29       Impact factor: 3.921

3.  Tripartite motif ligases catalyze polyubiquitin chain formation through a cooperative allosteric mechanism.

Authors:  Frederick C Streich; Virginia P Ronchi; J Patrick Connick; Arthur L Haas
Journal:  J Biol Chem       Date:  2013-02-13       Impact factor: 5.157

Review 4.  The cellular response to DNA damage: a focus on MDC1 and its interacting proteins.

Authors:  Gideon Coster; Michal Goldberg
Journal:  Nucleus       Date:  2009-12-29       Impact factor: 4.197

5.  Structural and functional characterization of the monomeric U-box domain from E4B.

Authors:  Kyle A Nordquist; Yoana N Dimitrova; Peter S Brzovic; Whitney B Ridenour; Kim A Munro; Sarah E Soss; Richard M Caprioli; Rachel E Klevit; Walter J Chazin
Journal:  Biochemistry       Date:  2010-01-19       Impact factor: 3.162

6.  Linkage-specific avidity defines the lysine 63-linked polyubiquitin-binding preference of rap80.

Authors:  Joshua J Sims; Robert E Cohen
Journal:  Mol Cell       Date:  2009-03-27       Impact factor: 17.970

Review 7.  Polyubiquitin chains: functions, structures, and mechanisms.

Authors:  W Li; Y Ye
Journal:  Cell Mol Life Sci       Date:  2008-08       Impact factor: 9.261

8.  A genome-wide synthetic dosage lethality screen reveals multiple pathways that require the functioning of ubiquitin-binding proteins Rad23 and Dsk2.

Authors:  Chang Liu; Dewald van Dyk; Yue Li; Brenda Andrews; Hai Rao
Journal:  BMC Biol       Date:  2009-11-12       Impact factor: 7.431

9.  Avid interactions underlie the Lys63-linked polyubiquitin binding specificities observed for UBA domains.

Authors:  Joshua J Sims; Aydin Haririnia; Bryan C Dickinson; David Fushman; Robert E Cohen
Journal:  Nat Struct Mol Biol       Date:  2009-07-20       Impact factor: 15.369

10.  Rad4 regulates protein turnover at a postubiquitylation step.

Authors:  Yue Li; Jing Yan; Ikjin Kim; Chang Liu; Keke Huo; Hai Rao
Journal:  Mol Biol Cell       Date:  2009-11-04       Impact factor: 4.138

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