Cargando…
Identification of key phosphorylation sites in PTH1R that determine arrestin3 binding and fine-tune receptor signaling
The parathyroid hormone receptor 1 (PTH1R) is a member of family B of G-protein-coupled receptors (GPCRs), predominantly expressed in bone and kidney where it modulates extracellular Ca(2+) homeostasis and bone turnover. It is well established that phosphorylation of GPCRs constitutes a key event in...
Autores principales: | Zindel, Diana, Engel, Sandra, Bottrill, Andrew R., Pin, Jean-Philippe, Prézeau, Laurent, Tobin, Andrew B., Bünemann, Moritz, Krasel, Cornelius, Butcher, Adrian J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103873/ https://www.ncbi.nlm.nih.gov/pubmed/27623777 http://dx.doi.org/10.1042/BCJ20160740 |
Ejemplares similares
-
The Effect of Cell Surface Expression and Linker Sequence on the Recruitment of Arrestin to the GIP Receptor
por: Al-Sabah, Suleiman, et al.
Publicado: (2020) -
Disentangling bias between G(q), GRK2, and arrestin3 recruitment to the M(3) muscarinic acetylcholine receptor
por: Flöser, Anja, et al.
Publicado: (2021) -
The GIP Receptor Displays Higher Basal Activity than the GLP-1 Receptor but Does Not Recruit GRK2 or Arrestin3 Effectively
por: Al-Sabah, Suleiman, et al.
Publicado: (2014) -
Selective phosphorylation of threonine residues defines GPR84–arrestin interactions of biased ligands
por: Marsango, Sara, et al.
Publicado: (2022) -
β-arrestin1 and 2 exhibit distinct phosphorylation-dependent conformations when coupling to the same GPCR in living cells
por: Haider, Raphael S., et al.
Publicado: (2022)