Plasmodium falciparum 20S proteasome bound to an inhibitor
收藏Protein Data Bank Japan2025-05-28 更新2026-04-25 收录
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Plasmodium falciparum 20S proteasome bound to an inhibitor Descriptor: (3S)-1-[(2-fluoroethoxy)acetyl]-N-{[(4P)-4-(6-methylpyridin-3-yl)-1,3-thiazol-2-yl]methyl}piperidine-3-carboxamide, Proteasome endopeptidase complex, Proteasome subunit alpha type, ... Authors: Han, Y, Deng, X, Ray, S, Chen, Z, Phillips, M. Deposit date: 2024-02-20 Release date: 2024-07-31 Last modified: 2025-05-28 Method: ELECTRON MICROSCOPY (3.1 Å) Cite: Identification of potent and reversible piperidine carboxamides that are species-selective orally active proteasome inhibitors to treat malaria. Cell Chem Biol, 31, 2024
创建时间：
2024-02-20
