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Structure paper

TitleHigh-resolution crystal structure of human protease-activated receptor 1
Journal, issue, pagesNature, Vol. 492, Page 387-392, Year 2012
Publish dateAug 7, 2012 (structure data deposition date)
AuthorsZhang, C. / Srinivasan, Y. / Arlow, D.H. / Fung, J.J. / Palmer, D. / Zheng, Y. / Green, H.F. / Pandey, A. / Dror, R.O. / Shaw, D.E. ...Zhang, C. / Srinivasan, Y. / Arlow, D.H. / Fung, J.J. / Palmer, D. / Zheng, Y. / Green, H.F. / Pandey, A. / Dror, R.O. / Shaw, D.E. / Weis, W.I. / Coughlin, S.R. / Kobilka, B.K.
External linksNature / PubMed:23222541
MethodsX-ray diffraction
Resolution2.2 Å
Structure data

PDB-3vw7:
Crystal structure of human protease-activated receptor 1 (PAR1) bound with antagonist vorapaxar at 2.2 angstrom
Method: X-RAY DIFFRACTION / Resolution: 2.2 Å

Chemicals

ChemComp-VPX:
ethyl / antagonist*YM

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

ChemComp-CL:
Unknown entry

ChemComp-NA:
Unknown entry

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
  • enterobacteria phage t4 (virus)
KeywordsSignaling protein/antagonist / High resolution structure / protease-activated receptor 1 / inactive conformation / antagonist vorapaxar / G protein-coupled receptor / signaling protein / membrane protein / thrombin receptor-antagonist complex / Signaling protein-antagonist complex

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