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Tethered agonist activated ADGRF1 structure reveals molecular preference for Gαq signalling
Daniel T. D. Jones, Andrew N. Dates, Shaun D. Rawson, Maggie M. Burruss, Colin H. Lipper, Stephen C. Blacklow
doi: https://doi.org/10.1101/2022.09.09.507336
Daniel T. D. Jones
1Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA
Andrew N. Dates
1Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA
Shaun D. Rawson
1Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA
Maggie M. Burruss
1Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA
Colin H. Lipper
1Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA
Stephen C. Blacklow
1Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA
2Department of Cancer Biology, Dana Farber Cancer Institute, Boston, MA 02215, USA

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Posted September 10, 2022.
Tethered agonist activated ADGRF1 structure reveals molecular preference for Gαq signalling
Daniel T. D. Jones, Andrew N. Dates, Shaun D. Rawson, Maggie M. Burruss, Colin H. Lipper, Stephen C. Blacklow
bioRxiv 2022.09.09.507336; doi: https://doi.org/10.1101/2022.09.09.507336
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