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6GDP

Trypanosoma brucei PTR1 in complex with inhibitor 4l (F162)

Summary for 6GDP
Entry DOI10.2210/pdb6gdp/pdb
Related6GCK 6GCL 6GCP 6GCQ 6GD0 6GD4 6GDO
DescriptorPteridine reductase, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, 2-azanyl-~{N}-(diphenylmethyl)-1,3-benzothiazole-6-carboxamide, ... (6 entities in total)
Functional Keywordstrypanosoma brucei, pteridine reductase, ptr1, tbptr1, benzothiazole, oxidoreductase
Biological sourceTrypanosoma brucei brucei
Total number of polymer chains4
Total formula weight127309.67
Authors
Pozzi, C.,Landi, G.,Mangani, S. (deposition date: 2018-04-24, release date: 2019-04-03, Last modification date: 2024-01-17)
Primary citationLinciano, P.,Pozzi, C.,Iacono, L.D.,di Pisa, F.,Landi, G.,Bonucci, A.,Gul, S.,Kuzikov, M.,Ellinger, B.,Witt, G.,Santarem, N.,Baptista, C.,Franco, C.,Moraes, C.B.,Muller, W.,Wittig, U.,Luciani, R.,Sesenna, A.,Quotadamo, A.,Ferrari, S.,Pohner, I.,Cordeiro-da-Silva, A.,Mangani, S.,Costantino, L.,Costi, M.P.
Enhancement of Benzothiazoles as Pteridine Reductase-1 Inhibitors for the Treatment of Trypanosomatidic Infections.
J.Med.Chem., 62:3989-4012, 2019
Cited by
PubMed: 30908048
DOI: 10.1021/acs.jmedchem.8b02021
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.52 Å)
Structure validation

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