Literature DB >> 12646216

U-box proteins as a new family of ubiquitin ligases.

Shigetsugu Hatakeyama1, Kei-ichi I Nakayama.   

Abstract

Ubiquitin-protein ligases (E3s) determine the substrate specificity of ubiquitylation and, until recently, had been classified into two families, the HECT and RING-finger families. The U-box is a domain of approximately 70 amino acids that is present in proteins from yeast to humans. The prototype U-box protein, yeast Ufd2, was identified as a ubiquitin chain assembly factor (E4) that cooperates with a ubiquitin-activating enzyme (E1), a ubiquitin-conjugating enzyme (E2), and an E3 to catalyze the formation of a ubiquitin chain on artificial substrates. We recently showed that mammalian U-box proteins, in conjunction with an E1 and an E2, mediate polyubiquitylation in the absence of a HECT type or RING-finger type E3. U-box proteins have thus been defined as a third family of E3s. We here review recent progress in the characterization of U-box proteins and of their role in the quality control system that underlies the cellular stress response to the intracellular accumulation of abnormal proteins.

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Year:  2003        PMID: 12646216     DOI: 10.1016/s0006-291x(03)00245-6

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  87 in total

1.  A large complement of the predicted Arabidopsis ARM repeat proteins are members of the U-box E3 ubiquitin ligase family.

Authors:  Yashwanti Mudgil; Shin-Han Shiu; Sophia L Stone; Jennifer N Salt; Daphne R Goring
Journal:  Plant Physiol       Date:  2003-12-04       Impact factor: 8.340

Review 2.  Getting into position: the catalytic mechanisms of protein ubiquitylation.

Authors:  Lori A Passmore; David Barford
Journal:  Biochem J       Date:  2004-05-01       Impact factor: 3.857

3.  E3 ubiquitin ligase activity and targeting of BAT3 by multiple Legionella pneumophila translocated substrates.

Authors:  Alexander W Ensminger; Ralph R Isberg
Journal:  Infect Immun       Date:  2010-06-14       Impact factor: 3.441

4.  Working on a chain: E3s ganging up for ubiquitylation.

Authors:  Meredith B Metzger; Allan M Weissman
Journal:  Nat Cell Biol       Date:  2010-12       Impact factor: 28.824

Review 5.  The ubiquitin-proteasome pathway and plant development.

Authors:  Jennifer Moon; Geraint Parry; Mark Estelle
Journal:  Plant Cell       Date:  2004-12       Impact factor: 11.277

6.  The Prp19 U-box crystal structure suggests a common dimeric architecture for a class of oligomeric E3 ubiquitin ligases.

Authors:  Craig W Vander Kooi; Melanie D Ohi; Joshua A Rosenberg; Michael L Oldham; Marcia E Newcomer; Kathleen L Gould; Walter J Chazin
Journal:  Biochemistry       Date:  2006-01-10       Impact factor: 3.162

Review 7.  Ubiquitin and ubiquitin-like modifications of the p53 family.

Authors:  Ian R Watson; Meredith S Irwin
Journal:  Neoplasia       Date:  2006-08       Impact factor: 5.715

8.  The ETS protein MEF is regulated by phosphorylation-dependent proteolysis via the protein-ubiquitin ligase SCFSkp2.

Authors:  Yan Liu; Cyrus V Hedvat; Shifeng Mao; Xin-Hua Zhu; Jinjuan Yao; Hoang Nguyen; Andrew Koff; Stephen D Nimer
Journal:  Mol Cell Biol       Date:  2006-04       Impact factor: 4.272

9.  The Spen homolog Msx2-interacting nuclear target protein interacts with the E2 ubiquitin-conjugating enzyme UbcH8.

Authors:  Junfeng Li; Jishu Wang; Xi Yang; Junlin Li; Hongyan Qin; Xiao Dong; Yangting Zhu; Liang Liang; Yingmin Liang; Hua Han
Journal:  Mol Cell Biochem       Date:  2006-04-01       Impact factor: 3.396

10.  Arabidopsis PUB22 and PUB23 are homologous U-Box E3 ubiquitin ligases that play combinatory roles in response to drought stress.

Authors:  Seok Keun Cho; Moon Young Ryu; Charlotte Song; June M Kwak; Woo Taek Kim
Journal:  Plant Cell       Date:  2008-07-29       Impact factor: 11.277

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