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Structure paper

TitleStructural Connection between Activation Microswitch and Allosteric Sodium Site in GPCR Signaling.
Journal, issue, pagesStructure, Vol. 26, Page 259-269.e5, Year 2018
Publish dateJul 11, 2017 (structure data deposition date)
AuthorsWhite, K.L. / Eddy, M.T. / Gao, Z.G. / Han, G.W. / Lian, T. / Deary, A. / Patel, N. / Jacobson, K.A. / Katritch, V. / Stevens, R.C.
External linksStructure / PubMed:29395784
MethodsX-ray diffraction
Resolution2.6 - 2.9 Å
Structure data

PDB-5wf5:
Agonist bound human A2a adenosine receptor with D52N mutation at 2.60 A resolution
Method: X-RAY DIFFRACTION / Resolution: 2.6 Å

PDB-5wf6:
Agonist bound human A2a adenosine receptor with S91A mutation at 2.90 A resolution
Method: X-RAY DIFFRACTION / Resolution: 2.9 Å

Chemicals

ChemComp-UKA:
6-(2,2-diphenylethylamino)-9-[(2R,3R,4S,5S)-5-(ethylcarbamoyl)-3,4-dihydroxy-oxolan-2-yl]-N-[2-[(1-pyridin-2-ylpiperidin-4-yl)carbamoylamino]ethyl]purine-2-carboxamide / agonist*YM

ChemComp-OLC:
(2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
  • enterobacteria phage t4 (virus)
KeywordsMEMBRANE PROTEIN / human A2a adenosine receptor / D52N / GPCR-T4L chimera / LCP / agonist / UK432097 / Activation microswitch / allosteric Na-site mutant / GPCR signaling / S91A

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