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TitleIdentification of PARP14 inhibitors using novel methods for detecting auto-ribosylation.
Journal, issue, pagesBiochem. Biophys. Res. Commun., Vol. 486, Page 626-631, Year 2017
Publish dateMar 20, 2017 (structure data deposition date)
AuthorsYoneyama-Hirozane, M. / Matsumoto, S.I. / Toyoda, Y. / Saikatendu, K.S. / Zama, Y. / Yonemori, K. / Oonishi, M. / Ishii, T. / Kawamoto, T.
External linksBiochem. Biophys. Res. Commun. / PubMed:28315326
MethodsX-ray diffraction
Resolution2.3 - 2.65 Å
Structure data

PDB-5v7t:
crystal structure of PARP14 bound to N-{4-[4-(diphenylmethoxy)piperidin-1-yl]butyl}[1,2,4]triazolo[4,3-b]pyridazin-6-amine inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.3 Å

PDB-5v7w:
Crystal structure of human PARP14 bound to 2-{[(1-methylpiperidin-4-yl)methyl]amino}-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4(3H)-one inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.65 Å

Chemicals

ChemComp-91V:
N-{4-[4-(diphenylmethoxy)piperidin-1-yl]butyl}[1,2,4]triazolo[4,3-b]pyridazin-6-amine

ChemComp-HOH:
WATER

ChemComp-91J:
2-{[(1-methylpiperidin-4-yl)methyl]amino}-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4(3H)-one

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / human parp14 / TRANSFERASE-TRANSFERASE INHIBITOR complex

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