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4Q0E

Crystal structure of TS-DHFR from Cryptosporidium hominis in complex with NADPH, FdUMP and 2-amino-4-oxo-4,7-dihydro-pyrrolo[2,3-d]pyrimidine-methyl-phenyl-L-glutamic acid.

Summary for 4Q0E
Entry DOI10.2210/pdb4q0e/pdb
Related1QZF 2OIP 3DL5 3DL6 3HJ3 4KY8
DescriptorBifunctional dihydrofolate reductase-thymidylate synthase, NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, 5-FLUORO-2'-DEOXYURIDINE-5'-MONOPHOSPHATE, ... (5 entities in total)
Functional Keywordsbifunctional enzyme, transferase, oxidoreductase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceCryptosporidium hominis
Total number of polymer chains5
Total formula weight310804.40
Authors
Kumar, V.P.,Anderson, K.S. (deposition date: 2014-04-01, release date: 2014-10-15, Last modification date: 2023-09-20)
Primary citationKumar, V.P.,Cisneros, J.A.,Frey, K.M.,Castellanos-Gonzalez, A.,Wang, Y.,Gangjee, A.,White, A.C.,Jorgensen, W.L.,Anderson, K.S.
Structural studies provide clues for analog design of specific inhibitors of Cryptosporidium hominis thymidylate synthase-dihydrofolate reductase.
Bioorg.Med.Chem.Lett., 24:4158-4161, 2014
Cited by
PubMed: 25127103
DOI: 10.1016/j.bmcl.2014.07.049
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.78 Å)
Structure validation

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