Database of articles cited by EMDB/PDB/SASBDB data

Keywords
Structure methods	All X-ray diffraction NMR electron microscopy small angle scattering neutron diffraction fiber diffraction powder diffraction infrared spectroscopy EPR fluorescence transfer theoretical model Hybrid
Author
Journal
IF	>30 >20 >10 >5 all

Title	Landscape of activating cancer mutations in FGFR kinases and their differential responses to inhibitors in clinical use.
Journal, issue, pages	Oncotarget, Vol. 7, Page 24252-24268, Year 2016
Publish date	Nov 20, 2015 (structure data deposition date)
Authors	Patani, H. / Bunney, T.D. / Thiyagarajan, N. / Norman, R.A. / Ogg, D. / Breed, J. / Ashford, P. / Potterton, A. / Edwards, M. / Williams, S.V. ...Patani, H. / Bunney, T.D. / Thiyagarajan, N. / Norman, R.A. / Ogg, D. / Breed, J. / Ashford, P. / Potterton, A. / Edwards, M. / Williams, S.V. / Thomson, G.S. / Pang, C.S. / Knowles, M.A. / Breeze, A.L. / Orengo, C. / Phillips, C. / Katan, M.
External links	Oncotarget / PubMed:26992226
Methods	X-ray diffraction
Resolution	1.63 - 2.58 Å
Structure data	PDB-5ew8: FIBROBLAST GROWTH FACTOR RECEPTOR 1 IN COMPLEX WITH JNJ-4275693 Method: X-RAY DIFFRACTION / Resolution: 1.63 Å PDB-5flf: DISEASE LINKED MUTATION IN FGFR Method: X-RAY DIFFRACTION / Resolution: 2.58 Å
Chemicals	ChemComp-SO4: SULFATE ION ChemComp-5SF: ~{N}'-(3,5-dimethoxyphenyl)-~{N}'-[3-(1-methylpyrazol-4-yl)quinoxalin-6-yl]-~{N}-propan-2-yl-ethane-1,2-diamine / medication, anticancer, inhibitorYM ChemComp-HOH: WATER ChemComp-ACT: ACETATE ION ChemComp-CL: Unknown entry ChemComp-PGE*: TRIETHYLENE GLYCOL
Source	homo sapiens (human)
Keywords	TRANSFERASE / FGFR1 KINASE INHIBITOR COMPLEX / KINASE / AUTO-ACTIVATING / CANCER / GROWTH FACTOR / RECEPTOR / MUTATION;