7MF4
Crystal structure of Trypanosoma cruzi cytosolic Malic Enzyme
7MF4 の概要
エントリーDOI | 10.2210/pdb7mf4/pdb |
関連するPDBエントリー | 6W29 6W2N 6W49 6W53 6W56 6W57 6W59 |
分子名称 | Malic enzyme, CITRIC ACID, 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, ... (4 entities in total) |
機能のキーワード | cytosol, oxidoreductase |
由来する生物種 | Trypanosoma cruzi (strain CL Brener) |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 62040.84 |
構造登録者 | |
主引用文献 | Mercaldi, G.F.,Eufrasio, A.G.,Ranzani, A.T.,do Nascimento Faria, J.,Mota, S.G.R.,Fagundes, M.,Bruder, M.,Cordeiro, A.T. Trypanosoma cruzi Malic Enzyme Is the Target for Sulfonamide Hits from the GSK Chagas Box. Acs Infect Dis., 7:2455-2471, 2021 Cited by PubMed Abstract: Chagas disease, an infectious condition caused by , lacks treatment with drugs with desired efficacy and safety profiles. To address this unmet medical need, a set of trypanocidal compounds were identified through a large multicenter phenotypic-screening initiative and assembled in the GSK Chagas Box. In the present work, we report the screening of the Chagas Box against malic enzymes (MEs) and the identification of three potent inhibitors of its cytosolic isoform (TcMEc). One of these compounds, TCMDC-143108 (), came out as a nanomolar inhibitor of TcMEc, and 14 new derivatives were synthesized and tested for target inhibition and efficacy against the parasite. Moreover, we determined the crystallographic structures of TcMEc in complex with TCMDC-143108 () and six derivatives, revealing the allosteric inhibition site and the determinants of specificity. Our findings connect phenotypic hits from the Chagas Box to a relevant metabolic target in the parasite, providing data to foster new structure-activity guided hit optimization initiatives. PubMed: 34279922DOI: 10.1021/acsinfecdis.1c00231 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.55 Å) |
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