Protein Phosphatase 2A and Neutral Sphingomyelinase 2 Regulate IRAK-1 Protein Ubiquitination and Degradation in Response to Interleukin-1β
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference75 articles.
1. Pathogen Recognition: TLRs Throw Us a Curve
2. The Toll/interleukin-1 receptor domain: a molecular switch for inflammation and host defence
3. MyD88: An Adapter That Recruits IRAK to the IL-1 Receptor Complex
4. Mass Spectrometric Analysis of the Endogenous Type I Interleukin-1 (IL-1) Receptor Signaling Complex Formed after IL-1 Binding Identifies IL-1RAcP, MyD88, and IRAK-4 as the Stable Components
5. The death domain of IRAK-1: An oligomerization domain mediating interactions with MyD88, Tollip, IRAK-1, and IRAK-4
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2. Regulated translocation of neutral sphingomyelinase-2 to the plasma membrane drives insulin resistance in steatotic hepatocytes;Journal of Lipid Research;2023-10
3. Elimination of negative feedback in TLR signalling allows rapid and hypersensitive detection of microbial contaminants;Scientific Reports;2021-12
4. Protein phosphatases in TLR signaling;Cell Communication and Signaling;2021-04-21
5. Diverse Facets of Sphingolipid Involvement in Bacterial Infections;Frontiers in Cell and Developmental Biology;2019-09-19
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