Cargando…
An siRNA library screen identifies CYLD and USP34 as deubiquitinases that regulate GPCR-p38 MAPK signaling and distinct inflammatory responses
G protein–coupled receptors (GPCRs) are highly druggable and implicated in numerous diseases, including vascular inflammation. GPCR signals are transduced from the plasma membrane as well as from endosomes and controlled by posttranslational modifications. The thrombin-activated GPCR protease-activa...
Autores principales: | Cheng, Norton, Trejo, JoAnn |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10694601/ https://www.ncbi.nlm.nih.gov/pubmed/37865315 http://dx.doi.org/10.1016/j.jbc.2023.105370 |
Ejemplares similares
-
Mutual regulation between deubiquitinase CYLD and retroviral oncoprotein Tax
por: Wu, Xuefeng, et al.
Publicado: (2011) -
The deubiquitinase USP38 affects cellular functions through interacting with LSD1
por: Liu, Wenbin, et al.
Publicado: (2018) -
CaMKII Mediates Recruitment and Activation of the Deubiquitinase CYLD at the Postsynaptic Density
por: Thein, Soe, et al.
Publicado: (2014) -
The deubiquitinase CYLD is a specific checkpoint of the STING antiviral signaling pathway
por: Zhang, Lele, et al.
Publicado: (2018) -
Inhibition of PDE4B suppresses inflammation by increasing expression of the deubiquitinase CYLD
por: Komatsu, Kensei, et al.
Publicado: (2013)