8FK2
The N-terminal VicR from Streptococcus mutans
8FK2 の概要
| エントリーDOI | 10.2210/pdb8fk2/pdb |
| 分子名称 | Putative response regulator CovR VicR-like protein (2 entities in total) |
| 機能のキーワード | gene regulator, gene regulation |
| 由来する生物種 | Streptococcus mutans UA159 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 27583.67 |
| 構造登録者 | |
| 主引用文献 | Liu, C.,Zhang, H.,Peng, X.,Blackledge, M.S.,Furlani, R.E.,Li, H.,Su, Z.,Melander, R.J.,Melander, C.,Michalek, S.,Wu, H. Small Molecule Attenuates Bacterial Virulence by Targeting Conserved Response Regulator. Mbio, 14:e0013723-e0013723, 2023 Cited by PubMed Abstract: Antibiotic tolerance within a biofilm community presents a serious public health challenge. Here, we report the identification of a 2-aminoimidazole derivative that inhibits biofilm formation by two pathogenic Gram-positive bacteria, Streptococcus mutans and Staphylococcus aureus. In S. mutans, the compound binds to VicR, a key response regulator, at the N-terminal receiver domain, and concurrently inhibits expression of and VicR-regulated genes, including the genes that encode the key biofilm matrix producing enzymes, Gtfs. The compound inhibits S. aureus biofilm formation via binding to a Staphylococcal VicR homolog. In addition, the inhibitor effectively attenuates S. mutans virulence in a rat model of dental caries. As the compound targets bacterial biofilms and virulence through a conserved transcriptional factor, it represents a promising new class of anti-infective agents that can be explored to prevent or treat a host of bacterial infections. Antibiotic resistance is a major public health issue due to the growing lack of effective anti-infective therapeutics. New alternatives to treat and prevent biofilm-driven microbial infections, which exhibit high tolerance to clinically available antibiotics, are urgently needed. We report the identification of a small molecule that inhibits biofilm formation by two important pathogenic Gram-positive bacteria, Streptococcus mutans and Staphylococcus aureus. The small molecule selectively targets a transcriptional regulator leading to attenuation of a biofilm regulatory cascade and concurrent reduction of bacterial virulence . As the regulator is highly conserved, the finding has broad implication for the development of antivirulence therapeutics that selectively target biofilms. PubMed: 37074183DOI: 10.1128/mbio.00137-23 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.29 Å) |
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