| Literature DB >> 31699241 |
Ieva Sutkeviciute1, Lisa J Clark2, Alex D White3, Thomas J Gardella4, Jean-Pierre Vilardaga5.
Abstract
The parathyroid hormone (PTH) type 1 receptor (PTHR) is the canonical G protein-coupled receptor (GPCR) for PTH and PTH-related protein (PTHrP) and the key regulator of calcium homeostasis and bone turnover. PTHR function is critical for human health to maintain homeostatic control of ionized serum Ca2+ levels and has several unusual signaling features, such as endosomal cAMP signaling, that are well-studied but not structurally understood. In this review, we discuss how recently solved high resolution near-atomic structures of hormone-bound PTHR in its inactive and active signaling states and discovery of extracellular Ca2+ allosterism shed light on the structural basis for PTHR signaling and function.Entities:
Keywords: G protein-coupled receptor; allostery; cAMP; cryo-EM structure; endosomes; parathyroid hormone
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Year: 2019 PMID: 31699241 PMCID: PMC6857722 DOI: 10.1016/j.tem.2019.07.011
Source DB: PubMed Journal: Trends Endocrinol Metab ISSN: 1043-2760 Impact factor: 12.015