5EBK

Trypanothione reductase in complex with 6-(sec-butoxy)-2-((3-chlorophenyl)thio)pyrimidin-4-amine

5EBK の概要

• エントリーDOI: 10.2210/pdb5ebk/pdb
• 関連するPDBエントリー: 2jk6
• 分子名称: Trypanothione reductase, FLAVIN-ADENINE DINUCLEOTIDE, 6-sec-Butoxy-2-[(3-chlorophenyl)sulfanyl]-4-pyrimidinamine, ... (4 entities in total)
• 機能のキーワード: oxidoreductase
• 由来する生物種: Leishmania infantum
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 114350.96

構造登録者

Ilari, A.,Angiulli, G. (登録日: 2015-10-19, 公開日: 2016-10-26, 最終更新日: 2024-10-23)

主引用文献

Saccoliti, F.,Angiulli, G.,Pupo, G.,Pescatori, L.,Madia, V.N.,Messore, A.,Colotti, G.,Fiorillo, A.,Scipione, L.,Gramiccia, M.,Di Muccio, T.,Di Santo, R.,Costi, R.,Ilari, A.
Inhibition of Leishmania infantum trypanothione reductase by diaryl sulfide derivatives.
J Enzyme Inhib Med Chem, 32:304-310, 2017

PubMed Abstract: The study presented here aimed at identifying a new class of compounds acting against Leishmania parasites, the causative agent of Leishmaniasis. For this purpose, the thioether derivatives of our in-house library have been evaluated in whole-cell screening assays in order to determine their in vitro activity against Leishmania protozoan. Among them, promising results have been achieved with compound RDS 777 (6-(sec-butoxy)-2-((3-chlorophenyl)thio)pyrimidin-4-amine) (IC=29.43 µM), which is able to impair the mechanism of the parasite defence against the reactive oxygen species by inhibiting the trypanothione reductase (TR) with high efficiency (K 0.25 ± 0.18 µM). The X-ray structure of L. infantum TR in complex with RDS 777 disclosed the mechanism of action of this compound that binds to the catalytic site and engages in hydrogen bonds the residues more involved in the catalysis, namely Glu466', Cys57 and Cys52, thereby inhibiting the trypanothione binding and avoiding its reduction.

PubMed: 28098499
DOI: 10.1080/14756366.2016.1250755

実験手法

X-RAY DIFFRACTION (3.51 Å)