7DD5
Structure of Calcium-Sensing Receptor in complex with NPS-2143
7DD5 の概要
エントリーDOI | 10.2210/pdb7dd5/pdb |
EMDBエントリー | 30644 |
分子名称 | Calcium-Sensing Receptor, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, CHLORIDE ION, ... (8 entities in total) |
機能のキーワード | calcium-sensing receptor, casr, nps-2143, membrane protein |
由来する生物種 | Gallus gallus |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 243190.99 |
構造登録者 | |
主引用文献 | Wen, T.,Wang, Z.,Chen, X.,Ren, Y.,Lu, X.,Xing, Y.,Lu, J.,Chang, S.,Zhang, X.,Shen, Y.,Yang, X. Structural basis for activation and allosteric modulation of full-length calcium-sensing receptor. Sci Adv, 7:-, 2021 Cited by PubMed Abstract: Calcium-sensing receptor (CaSR) is a class C G protein-coupled receptor (GPCR) that plays an important role in calcium homeostasis and parathyroid hormone secretion. Here, we present multiple cryo-electron microscopy structures of full-length CaSR in distinct ligand-bound states. Ligands (Ca and l-tryptophan) bind to the extracellular domain of CaSR and induce large-scale conformational changes, leading to the closure of two heptahelical transmembrane domains (7TMDs) for activation. The positive modulator (evocalcet) and the negative allosteric modulator (NPS-2143) occupy the similar binding pocket in 7TMD. The binding of NPS-2143 causes a considerable rearrangement of two 7TMDs, forming an inactivated TM6/TM6 interface. Moreover, a total of 305 disease-causing missense mutations of CaSR have been mapped to the structure in the active state, creating hotspot maps of five clinical endocrine disorders. Our results provide a structural framework for understanding the activation, allosteric modulation mechanism, and disease therapy for class C GPCRs. PubMed: 34088669DOI: 10.1126/sciadv.abg1483 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (3.2 Å) |
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