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7E27

Structure of PfFNT in complex with MMV007839

7E27 の概要
エントリーDOI10.2210/pdb7e27/pdb
EMDBエントリー30953
分子名称Formate-nitrite transporter, (Z)-4,4,5,5,5-pentakis(fluoranyl)-1-(4-methoxy-2-oxidanyl-phenyl)-3-oxidanyl-pent-2-en-1-one (3 entities in total)
機能のキーワードlactate transporter, transport protein
由来する生物種Plasmodium falciparum 3D7
タンパク質・核酸の鎖数5
化学式量合計174022.35
構造登録者
Yan, C.Y.,Jiang, X.,Deng, D.,Peng, X.,Wang, N.,Zhu, A.,Xu, H.,Li, J. (登録日: 2021-02-04, 公開日: 2021-08-18, 最終更新日: 2024-06-05)
主引用文献Peng, X.,Wang, N.,Zhu, A.,Xu, H.,Li, J.,Zhou, Y.,Wang, C.,Xiao, Q.,Guo, L.,Liu, F.,Jia, Z.J.,Duan, H.,Hu, J.,Yuan, W.,Geng, J.,Yan, C.,Jiang, X.,Deng, D.
Structural characterization of the Plasmodium falciparum lactate transporter PfFNT alone and in complex with antimalarial compound MMV007839 reveals its inhibition mechanism.
Plos Biol., 19:e3001386-e3001386, 2021
Cited by
PubMed Abstract: Plasmodium falciparum, the deadliest causal agent of malaria, caused more than half of the 229 million malaria cases worldwide in 2019. The emergence and spreading of frontline drug-resistant Plasmodium strains are challenging to overcome in the battle against malaria and raise urgent demands for novel antimalarial agents. The P. falciparum formate-nitrite transporter (PfFNT) is a potential drug target due to its housekeeping role in lactate efflux during the intraerythrocytic stage. Targeting PfFNT, MMV007839 was identified as a lead compound that kills parasites at submicromolar concentrations. Here, we present 2 cryogenic-electron microscopy (cryo-EM) structures of PfFNT, one with the protein in its apo form and one with it in complex with MMV007839, both at 2.3 Å resolution. Benefiting from the high-resolution structures, our study provides the molecular basis for both the lactate transport of PfFNT and the inhibition mechanism of MMV007839, which facilitates further antimalarial drug design.
PubMed: 34499638
DOI: 10.1371/journal.pbio.3001386
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.29 Å)
構造検証レポート
Validation report summary of 7e27
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-01-28に公開中

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