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5K5T

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

Summary for 5K5T
Entry DOI10.2210/pdb5k5t/pdb
DescriptorExtracellular calcium-sensing receptor, CALCIUM ION, SULFATE ION, ... (5 entities in total)
Functional Keywordsvenus flytrap module, cysteine rich domain, homodimer, signaling protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight71104.34
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 (3.1 Å)
Structure validation

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건을2024-11-06부터공개중

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