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5K5S

Crystal structure of the active form of human calcium-sensing receptor extracellular domain

Summary for 5K5S
Entry DOI10.2210/pdb5k5s/pdb
Related5K5T
DescriptorExtracellular calcium-sensing receptor, TRYPTOPHAN, PHOSPHATE ION, ... (6 entities in total)
Functional Keywordsvenus flytrap module, cysteine-rich domain, homodimer, signaling protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight140698.29
Authors
Primary citationGeng, Y.,Mosyak, L.,Kurinov, I.,Zuo, H.,Sturchler, E.,Cheng, T.C.,Subramanyam, P.,Brown, A.P.,Brennan, S.C.,Mun, H.C.,Bush, M.,Chen, Y.,Nguyen, T.X.,Cao, B.,Chang, D.D.,Quick, M.,Conigrave, A.D.,Colecraft, H.M.,McDonald, P.,Fan, Q.R.
Structural mechanism of ligand activation in human calcium-sensing receptor.
Elife, 5:-, 2016
Cited by
PubMed Abstract: Human calcium-sensing receptor (CaSR) is a G-protein-coupled receptor (GPCR) that maintains extracellular Ca(2+) homeostasis through the regulation of parathyroid hormone secretion. It functions as a disulfide-tethered homodimer composed of three main domains, the Venus Flytrap module, cysteine-rich domain, and seven-helix transmembrane region. Here, we present the crystal structures of the entire extracellular domain of CaSR in the resting and active conformations. We provide direct evidence that L-amino acids are agonists of the receptor. In the active structure, L-Trp occupies the orthosteric agonist-binding site at the interdomain cleft and is primarily responsible for inducing extracellular domain closure to initiate receptor activation. Our structures reveal multiple binding sites for Ca(2+) and PO4(3-) ions. Both ions are crucial for structural integrity of the receptor. While Ca(2+) ions stabilize the active state, PO4(3-) ions reinforce the inactive conformation. The activation mechanism of CaSR involves the formation of a novel dimer interface between subunits.
PubMed: 27434672
DOI: 10.7554/eLife.13662
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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数据于2024-11-06公开中

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