8B20
NDM-1 metallo-beta-lactamase in complex with triazole-based inhibitor CP57
8B20 の概要
| エントリーDOI | 10.2210/pdb8b20/pdb |
| 関連するPDBエントリー | 8B1W 8B1Z |
| 分子名称 | Beta-lactamase NDM-1, ZINC ION, CALCIUM ION, ... (7 entities in total) |
| 機能のキーワード | beta-lactamase, antibiotic resistance, beta-lactamase inhibitor, hydrolase |
| 由来する生物種 | Pseudomonas aeruginosa |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 52462.37 |
| 構造登録者 | Vascon, F.,Lazzarato, L.,Bersani, M.,Gianquinto, E.,Docquier, J.D.,Spyrakis, F.,Tondi, D.,Cendron, L. (登録日: 2022-09-12, 公開日: 2023-12-27, 最終更新日: 2024-03-20) |
| 主引用文献 | Bersani, M.,Failla, M.,Vascon, F.,Gianquinto, E.,Bertarini, L.,Baroni, M.,Cruciani, G.,Verdirosa, F.,Sannio, F.,Docquier, J.D.,Cendron, L.,Spyrakis, F.,Lazzarato, L.,Tondi, D. Structure-Based Optimization of 1,2,4-Triazole-3-Thione Derivatives: Improving Inhibition of NDM-/VIM-Type Metallo-beta-Lactamases and Synergistic Activity on Resistant Bacteria. Pharmaceuticals, 16:-, 2023 Cited by PubMed Abstract: The worldwide emergence and dissemination of Gram-negative bacteria expressing metallo-β-lactamases (MBLs) menace the efficacy of all β-lactam antibiotics, including carbapenems, a last-line treatment usually restricted to severe pneumonia and urinary tract infections. Nonetheless, no MBL inhibitor is yet available in therapy. We previously identified a series of 1,2,4-triazole-3-thione derivatives acting as micromolar inhibitors of MBLs in vitro, but devoid of synergistic activity in microbiological assays. Here, via a multidisciplinary approach, including molecular modelling, synthesis, enzymology, microbiology, and X-ray crystallography, we optimized this series of compounds and identified low micromolar inhibitors active against clinically relevant MBLs (NDM-1- and VIM-type). The best inhibitors increased, to a certain extent, the susceptibility of NDM-1- and VIM-4-producing clinical isolates to meropenem. X-ray structures of three selected inhibitors in complex with NDM-1 elucidated molecular recognition at the base of potency improvement, confirmed in silico predicted orientation, and will guide further development steps. PubMed: 38139809DOI: 10.3390/ph16121682 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.78 Å) |
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