9F0P
VIM-2 in complex with GKV61 (5c) - dynamically chiral phosphonic acid-type metallo-beta-lactamase inhibitors
これはPDB形式変換不可エントリーです。
9F0P の概要
| エントリーDOI | 10.2210/pdb9f0p/pdb |
| 分子名称 | Metallo-beta-lactamase type 2, FORMIC ACID, [(S)-(1-benzothiophen-2-ylcarbonylamino)-(2-hydroxyphenyl)methyl]phosphonic acid, ... (6 entities in total) |
| 機能のキーワード | beta-lactamase, metallo-beta-lactamase, inhibitor, antibiotic |
| 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 | 56369.13 |
| 構造登録者 | Bartels, K.,Prester, A.,Bosman, R.,Gulyas, K.V.,Erdelyi, M.,Schulz, E.C. (登録日: 2024-04-17, 公開日: 2025-04-30, 最終更新日: 2025-05-07) |
| 主引用文献 | Gulyas, K.V.,Zhou, L.,Salamonsen, D.,Prester, A.,Bartels, K.,Bosman, R.,Haffke, P.,Li, J.,Tamasi, V.,Deufel, F.,Thoma, J.,Andersson Rasmussen, A.,Csala, M.,Schroder Leiros, H.K.,Xu, Z.,Widersten, M.,Rohde, H.,Schulz, E.C.,Zhu, W.,Erdelyi, M. Dynamically chiral phosphonic acid-type metallo-beta-lactamase inhibitors. Commun Chem, 8:119-119, 2025 Cited by PubMed Abstract: Antibiotic resistance is a growing global health threat that risks the lives of millions. Among the resistance mechanisms, that mediated by metallo-β-lactamases is of particular concern as these bacterial enzymes dismantle most β-lactam antibiotics, which are our widest applied and cheapest to produce antibiotic agents. So far, no clinically applicable metallo-β-lactamase inhibitors are available. Aiming to adapt to structural variations, we introduce the inhibitor concept: dynamically chiral phosphonic acids. We demonstrate that they are straightforward to synthesize, penetrate bacterial membranes, inhibit the metallo-β-lactamase enzymes NDM-1, VIM-2 and GIM-1, and are non-toxic to human cells. Mimicking the transition state of β-lactam hydrolysis, they target the Zn ions of the metallo-β-lactamase active site. As a unique feature, both of their stereoisomers bind metallo-β-lactamases, which provides them unparalleled adaptability to the structural diversity of these enzymes, and may allow them to hamper bacteria's ability for resistance development. PubMed: 40253435DOI: 10.1038/s42004-025-01510-5 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.34 Å) |
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