| Literature DB >> 15571810 |
Kylie J Walters1, Amanda M Goh, Qinghua Wang, Gerhard Wagner, Peter M Howley.
Abstract
Many biological processes rely on targeted protein degradation, the dysregulation of which contributes to the pathogenesis of various diseases. Ubiquitin plays a well-established role in this process, in which the covalent attachment of polyubiquitin chains to protein substrates culminates in their degradation via the proteasome. The three-dimensional structural topology of ubiquitin is highly conserved as a domain found in a variety of proteins of diverse biological function. Some of these so-called "ubiquitin family proteins" have recently been shown to bind components of the 26S proteasome via their ubiquitin-like domains, thus implicating proteasome activity in pathways other than protein degradation. In this chapter, we provide a structural perspective of how the ubiquitin family of proteins interacts with the proteasome.Mesh:
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Year: 2004 PMID: 15571810 DOI: 10.1016/j.bbamcr.2004.10.005
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002