9RFG
Crystal structure of the metallo-beta-lactamase VIM-1 with 1476
This is a non-PDB format compatible entry.
Summary for 9RFG
| Entry DOI | 10.2210/pdb9rfg/pdb |
| Descriptor | Beta-lactamase VIM-1, GLYCEROL, 3-[3,5-bis(chloranyl)phenyl]-4-ethyl-5-phenyl-1~{H}-pyrrole-2-carboxylic acid, ... (5 entities in total) |
| Functional Keywords | inhibitor, complex, lactamase, hydrolase |
| Biological source | Pseudomonas aeruginosa |
| Total number of polymer chains | 1 |
| Total formula weight | 26017.27 |
| Authors | Wilson, L.A.,Singha, M.,Farley, A.J.M.,Schofield, C.J. (deposition date: 2025-06-04, release date: 2026-05-27, Last modification date: 2026-06-03) |
| Primary citation | Singha, M.,Wilson, L.A.,C M Moura, E.C.,Trush, M.M.,Calvopina, K.,Kaur, G.,Zaborskyte, G.,Kalnins, T.,Panduwawala, T.,Bowen, M.J.,Beech, M.J.,Brem, J.,McHugh, P.J.,Suna, E.,Walsh, T.R.,Schofield, C.J.,Farley, A.J.M. Development of Water-Trapping Pyrrole-2-carboxylic Acids as Broad-Spectrum Metallo-beta-lactamase Inhibitors. J.Med.Chem., 69:11961-11984, 2026 Cited by PubMed Abstract: Use of the clinically vital β-lactam antibiotics is increasingly compromised by resistance, commonly mediated by β-lactamases. While clinically used serine-β-lactamase (SBL) inhibitors have long been available, metallo-β-lactamase (MBL) inhibitors are not yet approved for clinical use. We report the structure-guided development of pyrrole-2-carboxylic acid derivatives as potent inhibitors of the clinically important di-Zn(II) ion containing B1 MBLs (NDM-1, VIM-1, VIM-2, IMP-1). Crystallographic studies reveal the pyrrole-2-carboxylic acids inhibit B1 MBLs via active site Zn(II)-coordination of the inhibitor carboxylate and trapping of the di-Zn(II) ion bridging hydroxide, the latter of which reacts with the substrate β-lactam ring during hydrolysis. Appropriately derivatized pyrrole-2-carboxylic acids enhance the activity of carbapenems against MBL producing Gram-negative clinical isolates. The results support further development of metalloenzyme inhibitors that exploit binding to structural or catalytically important water molecules, an approach which may help in achieving selectivity over other metalloenzymes compared to metal-chelation based approaches. PubMed: 42133983DOI: 10.1021/acs.jmedchem.5c03534 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.15 Å) |
Structure validation
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