GPCR

Naomi R Latorraca1, Matthieu Masureel2, Scott A Hollingsworth3

  • 1Department of Computer Science, Stanford University, Stanford, CA 94305, USA; Institute for Computational and Mathematical Engineering, Stanford University, Stanford, CA 94305, USA; Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, USA; Biophysics Program, Stanford University, Stanford, CA 94305, USA.

Cell
|December 9, 2020
PubMed
概括

不仅仅是酸盐的数量,GPCR酸化模式也决定了结合和构造的变化. 这揭示了 arrestin 的结构基础.

相关概念视频

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When a ligand binds to a cell-surface receptor, the receptor's intracellular domain changes shape, which may either activate its enzyme function or allow its binding to other molecules. The initial signal is amplified by most signal transduction pathways. This means that a single ligand molecule can activate multiple molecules of a downstream target. Proteins that relay a signal are most commonly phosphorylated at one or more sites, activating or inactivating the protein. Kinases catalyze...
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Assembly of Signaling Complexes

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IP3/DAG Signaling Pathway

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Activation and Inactivation of G Proteins01:22

Activation and Inactivation of G Proteins

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