| タイトル | Two-Pronged Attack: Dual Inhibition of Plasmodium falciparum M1 and M17 Metalloaminopeptidases by a Novel Series of Hydroxamic Acid-Based Inhibitors. |
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| ジャーナル・号・ページ | J. Med. Chem., Vol. 57, Page 9168-9183, Year 2014 |
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| 掲載日 | 2014年8月22日 (構造データの登録日) |
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著者 | Mistry, S.N. / Drinkwater, N. / Ruggeri, C. / Sivaraman, K.K. / Loganathan, S. / Fletcher, S. / Drag, M. / Paiardini, A. / Avery, V.M. / Scammells, P.J. / McGowan, S. |
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リンク | J. Med. Chem. / PubMed:25299353 |
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| 手法 | X線回折 |
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| 解像度 | 1.85 - 2.85 Å |
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| 構造データ | PDB-4r5t: Structure of the m1 alanylaminopeptidase from malaria complexed with a hydroxamic acid-based inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.98 Å PDB-4r5v: Structure of the m1 alanylaminopeptidase from malaria complexed with a hydroxamic acid-based inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.1 Å PDB-4r5x: Structure of the m1 alanylaminopeptidase from malaria complexed with a hydroxamic acid-based inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.85 Å PDB-4r6t: Structure of the m17 leucyl aminopeptidase from malaria complexed with a hydroxamic acid-based inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.6 Å PDB-4r76: Structure of the m17 leucyl aminopeptidase from malaria complexed with a hydroxamic acid-based inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.5 Å PDB-4r7m: Structure of the m17 leucyl aminopeptidase from malaria complexed with a hydroxamic acid-based inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.85 Å |
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| 化合物 | ChemComp-R5T: tert-butyl {(1S)-2-(hydroxyamino)-2-oxo-1-[4-(1H-pyrazol-1-yl)phenyl]ethyl}carbamate
ChemComp-R5V: N-{(1R)-2-(hydroxyamino)-2-oxo-1-[4-(1H-pyrazol-1-yl)phenyl]ethyl}-2,2-dimethylpropanamide
ChemComp-R5X: 3-amino-N-{(1R)-2-(hydroxyamino)-2-oxo-1-[4-(1H-pyrazol-1-yl)phenyl]ethyl}benzamide
ChemComp-3MW: 4-amino-N-{(1R)-2-(hydroxyamino)-2-oxo-1-[4-(1H-pyrazol-1-yl)phenyl]ethyl}benzamide
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| 由来 |  plasmodium falciparum fcb1/columbia (マラリア病原虫) plasmodium falciparum 3d7 (マラリア病原虫)
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キーワード | HYDROLASE/HYDROLASE INHIBITOR / PROTEASE / HYDROLASE-HYDROLASE INHIBITOR complex |
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