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8PF5

Crystal structure of Trypanosoma brucei trypanothione reductase in complex with 1-(3,4-dichlorobenzyl)-4-(((5-((4-fluorophenethyl)carbamoyl)furan-2-yl)methyl)carbamoyl)-1-(3-phenylpropyl)piperazin-1-ium

Summary for 8PF5
Entry DOI10.2210/pdb8pf5/pdb
Related8PF3 8PF4
DescriptorTrypanothione reductase, FLAVIN-ADENINE DINUCLEOTIDE, 4-[(3,4-dichlorophenyl)methyl]-~{N}-[[5-[2-(4-fluorophenyl)ethylcarbamoyl]furan-2-yl]methyl]-4-(3-phenylpropyl)-1,4$l^{4}-diazinane-1-carboxamide, ... (8 entities in total)
Functional Keywordsoxidoreductase activity, nucleotide binding, flavoenzyme, inhibitor binding, oxidoreductase
Biological sourceTrypanosoma brucei
More
Total number of polymer chains4
Total formula weight220269.17
Authors
Exertier, C.,Antonelli, L.,Fiorillo, A.,Ilari, A. (deposition date: 2023-06-15, release date: 2024-04-03)
Primary citationExertier, C.,Salerno, A.,Antonelli, L.,Fiorillo, A.,Ocello, R.,Seghetti, F.,Caciolla, J.,Uliassi, E.,Masetti, M.,Fiorentino, E.,Orsini, S.,Di Muccio, T.,Ilari, A.,Bolognesi, M.L.
Fragment Merging, Growing, and Linking Identify New Trypanothione Reductase Inhibitors for Leishmaniasis.
J.Med.Chem., 67:402-419, 2024
Cited by
PubMed: 38164929
DOI: 10.1021/acs.jmedchem.3c01439
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.42 Å)
Structure validation

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PDB entries from 2024-05-01

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