4EF9
Crystal structure of dihydroorotate dehydrogenase from Leishmania major in complex with 4-Nitrophenyl isothiocyanate
Summary for 4EF9
Entry DOI | 10.2210/pdb4ef9/pdb |
Related | 4EF8 |
Descriptor | Dihydroorotate dehydrogenase, N-(4-nitrophenyl)thioformamide, FLAVIN MONONUCLEOTIDE, ... (6 entities in total) |
Functional Keywords | leishmania major, dihydroorotate dehydrogenase, 4-nitrophenyl isothiocyanate, pyrd, oxidoreductase, oxidoreductase-oxidoreductase inhibitor complex, oxidoreductase/oxidoreductase inhibitor |
Biological source | Leishmania major |
Total number of polymer chains | 2 |
Total formula weight | 78452.77 |
Authors | Pinheiro, M.P.,Emery, F.S.,Nonato, M.C. (deposition date: 2012-03-29, release date: 2012-12-12, Last modification date: 2024-10-16) |
Primary citation | Pinheiro, M.P.,Emery, F.S.,Nonato, M.C. Target sites for the design of anti-trypanosomatid drugs based on the structure of dihydroorotate dehydrogenase. Curr.Pharm.Des., 19:2615-2627, 2013 Cited by PubMed Abstract: Trypanosomatids consist of a large group of flagellated parasitic protozoa, including parasites from the genera Leishmania and Trypanosoma, responsible for causing infections in millions of humans worldwide and for which currently no appropriate therapy is available. The significance of pyrimidines in cellular metabolism makes their de novo and salvage pathways ideal druggable targets for pharmacological intervention and open an opportunity for pharmaceutical innovation. In the current review, we discuss the merits in targeting the enzyme dihydroorotate dehydrogenase (DHODH), a flavin-dependent enzyme that catalyzes the fourth and only redox step in pyrimidine de novo biosynthesis, as a strategy for the development of efficient therapeutic strategies for trypanosomatid-related diseases.We also describe the advances and perspectives from the structural biology point of view in order to unravel the structure-function relationship of trypanosomatid DHODHs, and to identify and validate target sites for drug development. PubMed: 23116399PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.6 Å) |
Structure validation
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