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Title6-(Hetero)Arylpurine nucleotides as inhibitors of the oncogenic target DNPH1: Synthesis, structural studies and cytotoxic activities.
Journal, issue, pagesEur. J. Med. Chem., Vol. 85C, Page 418-437, Year 2014
Publish dateMar 16, 2014 (structure data deposition date)
AuthorsAmiable, C. / Paoletti, J. / Haouz, A. / Padilla, A. / Labesse, G. / Kaminski, P.A. / Pochet, S.
External linksEur. J. Med. Chem. / PubMed:25108359
MethodsX-ray diffraction
Resolution1.35 - 2.11 Å
Structure data

PDB-4p5d:
CRYSTAL STRUCTURE OF RAT DNPH1 (RCL) WITH 6-NAPHTHYL-PURINE-RIBOSIDE-MONOPHOSPHATE
Method: X-RAY DIFFRACTION / Resolution: 2.11 Å

PDB-4p5e:
CRYSTAL STRUCTURE OF HUMAN DNPH1 (RCL) WITH 6-NAPHTHYL-PURINE-RIBOSIDE-MONOPHOSPHATE
Method: X-RAY DIFFRACTION / Resolution: 1.35 Å

Chemicals

ChemComp-N6P:
6-(naphthalen-2-yl)-9-(5-O-phosphono-beta-D-ribofuranosyl)-9H-purine

ChemComp-SO4:
SULFATE ION

ChemComp-HOH:
WATER

ChemComp-CA:
Unknown entry

Source
  • rattus norvegicus (Norway rat)
  • homo sapiens (human)
KeywordsHYDROLASE / N-GLYCOSIDASE / INHIBITOR / RCL / DNPH1 / Rossmann Fold

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