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Titlebook: G Protein-Coupled Receptor Kinases; Vsevolod V. Gurevich,Eugenia V. Gurevich,John J.G. Book 2016 Springer Science+Business Media New York

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樓主: T-cell
51#
發(fā)表于 2025-3-30 11:06:08 | 只看該作者
G Protein-Coupled Receptor Kinases (GRKs) History: Evolution and DiscoveryPCR field. The existence of GRKs and arrestins revealed the primary mechanism for termination of GPCR signaling. GRKs appeared in evolution long before animals, and it remains to be elucidated whether their first substrates were GPCRs or other proteins. It is also unclear whether and how GRKs are ac
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發(fā)表于 2025-3-30 14:59:59 | 只看該作者
53#
發(fā)表于 2025-3-30 17:52:58 | 只看該作者
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發(fā)表于 2025-3-30 21:57:58 | 只看該作者
Molecular Basis for Targeting, Inhibition, and Receptor Phosphorylation in the G Protein-Coupled Recignals during stress. The seven human GRKs belong to three subfamilies with distinct structural features and membrane targeting mechanisms. Although crystal structures representing each subfamily have now been reported, a recent series of GRK4 subfamily structures provide new information about how t
55#
發(fā)表于 2025-3-31 02:58:19 | 只看該作者
“Barcode” and Differential Effects of GPCR Phosphorylation by Different GRKster of modern medicine. Multiple site phosphorylation of GPCRs by G protein-coupled receptor kinases (GRKs) plays an essential role in the regulation of various functions and signaling cascades of a receptor. Research in recent years has elucidated a common mechanism by which different ligand-bound
56#
發(fā)表于 2025-3-31 07:58:44 | 只看該作者
Cell-Type Specific GRK2 Interactomes: Pathophysiological Implicationsreceptors, GRK2 can phosphorylate and/or functionally interact with a complex network of cellular proteins in a cell-type and physiological context-dependent way. A combination of such canonical and noncanonical interactions underlies the participation of this kinase in the control of cell migration
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