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TitleMetabolic Modifier Screen Reveals Secondary Targets of Protein Kinase Inhibitors within Nucleotide Metabolism.
Journal, issue, pagesCell Chem Biol, Vol. 27, Page 197-, Year 2020
Publish dateMar 21, 2019 (structure data deposition date)
AuthorsAbt, E.R. / Rosser, E.W. / Durst, M.A. / Lok, V. / Poddar, S. / Le, T.M. / Cho, A. / Kim, W. / Wei, L. / Song, J. ...Abt, E.R. / Rosser, E.W. / Durst, M.A. / Lok, V. / Poddar, S. / Le, T.M. / Cho, A. / Kim, W. / Wei, L. / Song, J. / Capri, J.R. / Xu, S. / Wu, N. / Slavik, R. / Jung, M.E. / Damoiseaux, R. / Czernin, J. / Donahue, T.R. / Lavie, A. / Radu, C.G.
External linksCell Chem Biol / PubMed:31734178
MethodsX-ray diffraction
Resolution1.4 - 2.7 Å
Structure data

PDB-6oc0:
Crystal structure of human DHODH with OSU-03012
Method: X-RAY DIFFRACTION / Resolution: 1.4 Å

PDB-6oc1:
Crystal structure of human DHODH with TAK-632
Method: X-RAY DIFFRACTION / Resolution: 2.7 Å

Chemicals

ChemComp-ORO:
OROTIC ACID

ChemComp-FMN:
FLAVIN MONONUCLEOTIDE

ChemComp-SO4:
SULFATE ION

ChemComp-M4J:
N-{4-[5-(phenanthren-2-yl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}glycinamide / anticancer, Antimicrobial, inhibitor*YM

ChemComp-HOH:
WATER

ChemComp-PO4:
PHOSPHATE ION

ChemComp-1SU:
N-{7-cyano-6-[4-fluoro-3-({[3-(trifluoromethyl)phenyl]acetyl}amino)phenoxy]-1,3-benzothiazol-2-yl}cyclopropanecarboxamide

Source
  • homo sapiens (human)
KeywordsOXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR / DHODH / Inhibitor / OSU-03012 / OXIDOREDUCTASE / OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR complex / TAK-632

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