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TitleSynthesis, SAR, and X-ray structure of tricyclic compounds as potent FBPase inhibitors
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 19, Page 5909-5912, Year 2009
Publish dateMay 8, 2009 (structure data deposition date)
AuthorsTsukada, T. / Takahashi, M. / Takemoto, T. / Kanno, O. / Yamane, T. / Kawamura, S. / Nishi, T.
External linksBioorg. Med. Chem. Lett. / PubMed:19762234
MethodsX-ray diffraction
Resolution2.6 Å
Structure data

PDB-3a29:
Crystal structure of human liver FBPase in complex with tricyclic inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.6 Å

Chemicals

ChemComp-2T0:
2-amino-4,5-dihydronaphtho[1,2-d][1,3]thiazol-8-yl dihydrogen phosphate

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE / Allosteric enzyme / Carbohydrate metabolism / Disease mutation / Gluconeogenesis / Magnesium / Metal-binding / Polymorphism

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