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Structure paper

TitleHDX-MS reveals structural determinants for ROR gamma hyperactivation by synthetic agonists.
Journal, issue, pagesElife, Vol. 8, Year 2019
Publish dateFeb 7, 2019 (structure data deposition date)
AuthorsStrutzenberg, T.S. / Garcia-Ordonez, R.D. / Novick, S.J. / Park, H. / Chang, M.R. / Doebellin, C. / He, Y. / Patouret, R. / Kamenecka, T.M. / Griffin, P.R.
External linksElife / PubMed:31172947
MethodsX-ray diffraction
Resolution2.35 - 3.2 Å
Structure data

PDB-6nws:
RORgamma Ligand Binding Domain
Method: X-RAY DIFFRACTION / Resolution: 2.44 Å

PDB-6nwt:
RORgamma Ligand Binding Domain
Method: X-RAY DIFFRACTION / Resolution: 2.35 Å

PDB-6nwu:
RORgamma Ligand Binding Domain
Method: X-RAY DIFFRACTION / Resolution: 3.2 Å

Chemicals

ChemComp-L77:
2-chloro-6-fluoro-N-(1-{[3-(trifluoromethyl)phenyl]sulfonyl}-2,3-dihydro-1H-indol-6-yl)benzamide

ChemComp-HOH:
WATER

ChemComp-L7P:
1,1,1,3,3,3-hexafluoro-2-[2-fluoro-4'-({4-[(pyridin-4-yl)methyl]piperazin-1-yl}methyl)[1,1'-biphenyl]-4-yl]propan-2-ol

ChemComp-L7J:
6-[(3,5-dichloropyridin-4-yl)methoxy]-1-{[3-(trifluoromethyl)phenyl]sulfonyl}-2,3-dihydro-1H-indole

Source
  • homo sapiens (human)
KeywordsNUCLEAR PROTEIN / Orphan Nuclear Receptor / synthetic modulator / chemical probe

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