| Literature DB >> 33466288 |
Abstract
Riboswitches reside in the untranslated region of RNA and regulate genes involved in the biosynthesis of essential metabolites through binding of small molecules. Since their discovery at the beginning of this century, riboswitches have been regarded as potential antibacterial targets. Using fragment screening, high-throughput screening and rational ligand design guided by X-ray crystallography, lead compounds against various riboswitches have been identified. Here, we review the current status and suitability of the thiamine pyrophosphate (TPP), flavin mononucleotide (FMN), glmS, guanine, and other riboswitches as antibacterial targets and discuss them in a biological context. Further, we highlight challenges in riboswitch drug discovery and emphasis the need to develop riboswitch specific high-throughput screening methods.Entities:
Keywords: antibacterial drug target; fragment screening; high-throughput screening; riboswitch; structure-based drug design
Year: 2021 PMID: 33466288 PMCID: PMC7824784 DOI: 10.3390/antibiotics10010045
Source DB: PubMed Journal: Antibiotics (Basel) ISSN: 2079-6382