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TitleOptimization of Benzoxazole-Based Inhibitors of Cryptosporidium parvum Inosine 5'-Monophosphate Dehydrogenase.
Journal, issue, pagesJ. Med. Chem., Vol. 56, Page 4028-4043, Year 2013
Publish dateJan 25, 2013 (structure data deposition date)
AuthorsGorla, S.K. / Kavitha, M. / Zhang, M. / Chin, J.E. / Liu, X. / Striepen, B. / Makowska-Grzyska, M. / Kim, Y. / Joachimiak, A. / Hedstrom, L. / Cuny, G.D.
External linksJ. Med. Chem. / PubMed:23668331
MethodsX-ray diffraction
Resolution2.105 Å
Structure data

PDB-4ixh:
Crystal Structure of the Catalytic Domain of the Inosine Monophosphate Dehydrogenase from Cryptosporidium parvum
Method: X-RAY DIFFRACTION / Resolution: 2.105 Å

Chemicals

ChemComp-IMP:
INOSINIC ACID

ChemComp-EDO:
1,2-ETHANEDIOL

ChemComp-Q21:
(2S)-2-(naphthalen-1-yloxy)-N-[2-(pyridin-4-yl)-1,3-benzoxazol-5-yl]propanamide

ChemComp-HOH:
WATER

Source
  • cryptosporidium parvum (eukaryote)
KeywordsOXIDOREDUCTASE / Structural Genomics / NIAID / National Institute of Allergy and Infectious Diseases / Center for Structural Genomics of Infectious Diseases / CSGID / alpha-beta fold / TIM barrel

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