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	The Design, Synthesis, and Biological Evaluation of Pim Kinase Inhibitors.
Journal, issue, pages	Bioorg. Med. Chem. Lett., Vol. 22, Page 3732-, Year 2012
Publish date	Mar 5, 2012 (structure data deposition date)
Authors	Tsuhako, A.L. / Brown, D.S. / Koltun, E.S. / Aay, N. / Arcalas, A. / Chan, V. / Du, H. / Engst, S. / Franzini, M. / Galan, A. ...Tsuhako, A.L. / Brown, D.S. / Koltun, E.S. / Aay, N. / Arcalas, A. / Chan, V. / Du, H. / Engst, S. / Franzini, M. / Galan, A. / Huang, P. / Johnston, S. / Kane, B. / Kim, M.H. / Laird, A.D. / Lin, R. / Mock, L. / Ngan, I. / Pack, M. / Stott, G. / Stout, T.J. / Yu, P. / Zaharia, C. / Zhang, W. / Zhou, P. / Nuss, J.M. / Kearney, P.C. / Xu, W.
External links	Bioorg. Med. Chem. Lett. / PubMed:22542012
Methods	X-ray diffraction
Resolution	1.92 - 2.6 Å
Structure data	PDB-4alu: Benzofuropyrimidinone Inhibitors of Pim-1 Method: X-RAY DIFFRACTION / Resolution: 2.6 Å PDB-4alv: Benzofuropyrimidinone Inhibitors of Pim-1 Method: X-RAY DIFFRACTION / Resolution: 2.59 Å PDB-4alw: Benzofuropyrimidinone Inhibitors of Pim-1 Method: X-RAY DIFFRACTION / Resolution: 1.92 Å
Chemicals	ChemComp-IMD: IMIDAZOLE ChemComp-79O: 8-bromo-2-(2-chlorophenyl)[1]benzofuro[3,2-d]pyrimidin-4(3H)-one ChemComp-HOH: WATER ChemComp-R9P: 8-bromo-2-{2-chloro-4-[(piperidin-4-ylmethyl)amino]phenyl}[1]benzofuro[3,2-d]pyrimidin-4(3H)-one ChemComp-HY7: 8-BROMANYL-2-[(4-METHYLPIPERAZIN-1-YL)METHYL]-3H-[1]BENZOFURO[3,2-D]PYRIMIDIN-4-ONE
Source	homo sapiens (human)
Keywords	TRANSFERASE / PROTO-ONCOGENE / PROTO-ONCOGENE SERINE/THREONINE-PROTEIN KINASE PIM-1