Literature DB >> 18834306

Targeting proteins for destruction by the ubiquitin system: implications for human pathobiology.

Alan L Schwartz1, Aaron Ciechanover.   

Abstract

Cellular proteins are in a dynamic state maintained by synthesis and degradation. The ubiquitin proteolytic pathway is responsible for the degradation of the bulk of cellular proteins including short-lived, regulatory, and misfolded/denatured proteins. Ubiquitin-mediated proteolysis involves covalent attachment of multiple ubiquitin molecules to the protein substrate and degradation of the targeted protein by the 26S proteasome. Recent understanding of the molecular mechanisms involved provides a framework to understand a wide variety of human pathophysiological states as well as therapeutic interventions. This review focuses on the response to hypoxia, inflammatory diseases, neurodegenerative diseases, and muscle-wasting disorders, as well as human papillomaviruses, cervical cancer and other malignancies.

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Year:  2009        PMID: 18834306     DOI: 10.1146/annurev.pharmtox.051208.165340

Source DB:  PubMed          Journal:  Annu Rev Pharmacol Toxicol        ISSN: 0362-1642            Impact factor:   13.820


  193 in total

1.  Analysis of ubiquitinated proteome by quantitative mass spectrometry.

Authors:  Chan Hyun Na; Junmin Peng
Journal:  Methods Mol Biol       Date:  2012

2.  It takes two to tango: a new couple in the family of ubiquitin-editing complexes.

Authors:  Ingrid E Wertz
Journal:  Nat Immunol       Date:  2011-11-16       Impact factor: 25.606

3.  Blm10 protein promotes proteasomal substrate turnover by an active gating mechanism.

Authors:  Thomas Dange; David Smith; Tahel Noy; Philipp C Rommel; Lukas Jurzitza; Radames J B Cordero; Anne Legendre; Daniel Finley; Alfred L Goldberg; Marion Schmidt
Journal:  J Biol Chem       Date:  2011-10-24       Impact factor: 5.157

4.  Stable incorporation of ATPase subunits into 19 S regulatory particle of human proteasome requires nucleotide binding and C-terminal tails.

Authors:  Seung-Hoon Lee; Joo-Hong Moon; Sungjoo Kim Yoon; Jong-Bok Yoon
Journal:  J Biol Chem       Date:  2012-01-24       Impact factor: 5.157

Review 5.  Signaling to NF-kappaB: regulation by ubiquitination.

Authors:  Ingrid E Wertz; Vishva M Dixit
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-03       Impact factor: 10.005

6.  Osmotic stress inhibits proteasome by p38 MAPK-dependent phosphorylation.

Authors:  Seung-Hoon Lee; Yoon Park; Sungjoo Kim Yoon; Jong-Bok Yoon
Journal:  J Biol Chem       Date:  2010-11-02       Impact factor: 5.157

7.  Characterization of selective ubiquitin and ubiquitin-like protease inhibitors using a fluorescence-based multiplex assay format.

Authors:  Xufan Tian; Nigora S Isamiddinova; Raymond J Peroutka; Seth J Goldenberg; Michael R Mattern; Benjamin Nicholson; Craig Leach
Journal:  Assay Drug Dev Technol       Date:  2010-12-06       Impact factor: 1.738

8.  Promoter context determines the role of proteasome in ligand-dependent occupancy of retinoic acid responsive elements.

Authors:  Aliaa Higazi; Mahmoud Abed; Jihong Chen; Qiao Li
Journal:  Epigenetics       Date:  2011-02-01       Impact factor: 4.528

Review 9.  Advances in targeted therapy for malignant lymphoma.

Authors:  Li Wang; Wei Qin; Yu-Jia Huo; Xiao Li; Qing Shi; John E J Rasko; Anne Janin; Wei-Li Zhao
Journal:  Signal Transduct Target Ther       Date:  2020-03-06

Review 10.  Skeletal muscle atrophy and the E3 ubiquitin ligases MuRF1 and MAFbx/atrogin-1.

Authors:  Sue C Bodine; Leslie M Baehr
Journal:  Am J Physiol Endocrinol Metab       Date:  2014-08-05       Impact factor: 4.310

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