Literature DB >> 32120017

Structural and mechanistic insights into the Keap1-Nrf2 system as a route to drug discovery.

Sarah K Madden1, Laura S Itzhaki2.   

Abstract

The proteins Keap1 and Nrf2 together act as a cytoprotective mechanism that enables cells to overcome electrophilic and oxidative stress. Research has shown that manipulating this system by modulating the Keap1-Nrf2 interaction either through inhibition at the binding interface or via the covalent modification of Keap1 could provide a powerful therapeutic strategy for a range of diseases. However, despite intensive investigation of the system and significant progress in the development of inhibitory small molecules, there is still much to learn about the pathways associated with the Keap1-Nrf2 system and the structural details underpinning its mechanism of action. In this review, we discuss how a deeper understanding could prove revolutionary in the development of new inhibitors and activators as well as guiding how to best harness Keap1 for targeted protein degradation.
Copyright © 2020. Published by Elsevier B.V.

Entities:  

Keywords:  Covalent inhibitors; Cul3; E3 ubiquitin ligase; Keap1; Nrf2; PROTACs; Protein-protein interactions

Year:  2020        PMID: 32120017     DOI: 10.1016/j.bbapap.2020.140405

Source DB:  PubMed          Journal:  Biochim Biophys Acta Proteins Proteom        ISSN: 1570-9639            Impact factor:   3.036


  13 in total

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7.  Exploring the binding of rationally engineered tandem-repeat proteins to E3 ubiquitin ligase Keap1.

Authors:  Sarah K Madden; Laura S Itzhaki
Journal:  Protein Eng Des Sel       Date:  2021-02-15       Impact factor: 1.650

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Review 10.  Preventing Oxidative Stress in the Liver: An Opportunity for GLP-1 and/or PASK.

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