Background: The CHIP E3 ligase regulates Hsp70 pro-degradation activities. Results: The P269A CHIP U-box mutation induces CHIP oligomerization and modulates nucleotide- and substrate-dependent interactions between the TPR domain and Hsp70 C terminus. Conclusion: The U-box domain plays a key role in CHIP recruitment to Hsp70-client complexes, possibly by controlling oligomerization. Significance: Hsp70-CHIP substrate triage is governed by complex allosteric interactions between multiple domains in both proteins. © 2013 by The American Society for Biochemistry and Molecular Biology, Inc. Published in the U.S.A.
CITATION STYLE
Matsumura, Y., Sakai, J., & Skach, W. R. (2013). Endoplasmic reticulum protein quality control is determined by cooperative interactions between Hsp/c70 protein and the CHIP E3 ligase. Journal of Biological Chemistry, 288(43), 31069–31079. https://doi.org/10.1074/jbc.M113.479345
Mendeley helps you to discover research relevant for your work.