Literature DB >> 10797484

Ubiquitin-mediated proteolysis: biological regulation via destruction.

A Ciechanover1, A Orian, A L Schwartz.   

Abstract

The ubiquitin proteolytic system plays an important role in a broad array of basic cellular processes. Among these are regulation of cell cycle, modulation of the immune and inflammatory responses, control of signal transduction pathways, development and differentiation. These complex processes are controlled via specific degradation of a single or a subset of proteins. Degradation of a protein by the ubiquitin system involves two successive steps, conjugation of multiple moieties of ubiquitin and degradation of the tagged protein by the 26S proteasome. An important question concerns the identity of the mechanisms that underlie the high degree of specificity of the system. Substrate recognition is governed by a large family ubiquitin ligases that recognize the substrates, bind them and catalyze/facilitate their interaction with ubiquitin.

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Year:  2000        PMID: 10797484     DOI: 10.1002/(SICI)1521-1878(200005)22:5<442::AID-BIES6>3.0.CO;2-Q

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  257 in total

1.  Ubiquitin is part of the retrovirus budding machinery.

Authors:  A Patnaik; V Chau; J W Wills
Journal:  Proc Natl Acad Sci U S A       Date:  2000-11-21       Impact factor: 11.205

2.  A protein-protein interaction map of the Caenorhabditis elegans 26S proteasome.

Authors:  A Davy; P Bello; N Thierry-Mieg; P Vaglio; J Hitti; L Doucette-Stamm; D Thierry-Mieg; J Reboul; S Boulton; A J Walhout; O Coux; M Vidal
Journal:  EMBO Rep       Date:  2001-09       Impact factor: 8.807

3.  The NMR structure of the class I human ubiquitin-conjugating enzyme 2b.

Authors:  Takaaki Miura; Werner Klaus; Alfred Ross; Peter Güntert; Hans Senn
Journal:  J Biomol NMR       Date:  2002-01       Impact factor: 2.835

4.  Nucleocytoplasmic shuttling and mCRY-dependent inhibition of ubiquitylation of the mPER2 clock protein.

Authors:  Kazuhiro Yagita; Filippo Tamanini; Maya Yasuda; Jan H J Hoeijmakers; Gijsbertus T J van der Horst; Hitoshi Okamura
Journal:  EMBO J       Date:  2002-03-15       Impact factor: 11.598

5.  Rapid degradation of auxin/indoleacetic acid proteins requires conserved amino acids of domain II and is proteasome dependent.

Authors:  J A Ramos; N Zenser; O Leyser; J Callis
Journal:  Plant Cell       Date:  2001-10       Impact factor: 11.277

6.  Auxin modulates the degradation rate of Aux/IAA proteins.

Authors:  N Zenser; A Ellsmore; C Leasure; J Callis
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-25       Impact factor: 11.205

7.  Proteasome-dependent, ubiquitin-independent degradation of the Rb family of tumor suppressors by the human cytomegalovirus pp71 protein.

Authors:  Robert F Kalejta; Thomas Shenk
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-07       Impact factor: 11.205

8.  The COOH-terminal domain of wild-type Cot regulates its stability and kinase specific activity.

Authors:  Maria Luisa Gándara; Pilar López; Raquel Hernando; José G Castaño; Susana Alemany
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

9.  Two ubiquitin-conjugating enzymes, UbcP1/Ubc4 and UbcP4/Ubc11, have distinct functions for ubiquitination of mitotic cyclin.

Authors:  Hiroaki Seino; Tsutomu Kishi; Hideo Nishitani; Fumiaki Yamao
Journal:  Mol Cell Biol       Date:  2003-05       Impact factor: 4.272

10.  T-cell regulator RNF125/TRAC-1 belongs to a novel family of ubiquitin ligases with zinc fingers and a ubiquitin-binding domain.

Authors:  Ana Lucia Giannini; Yifang Gao; Marie-José Bijlmakers
Journal:  Biochem J       Date:  2008-02-15       Impact factor: 3.857

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