| Literature DB >> 9016680 |
H Y Mei1, M Cui, S T Sutton, H N Truong, F Z Chung, A W Czarnik.
Abstract
High-throughput screening assays have been developed to rapidly identify small molecule inhibitors targeting catalytic group I introns. Biochemical reactions catalyzed by a self-splicing group I intron derived from Pneumocystis carinii or from bacteriophage T4 have been investigated. In vitro biochemical assays amenable to high-throughput screening have been established. Small molecules that inhibit the functions of group I introns have been identified. These inhibitors should be useful in better understanding ribozyme catalysis or in therapeutic intervention of group I intron-containing microorganisms.Entities:
Mesh:
Substances:
Year: 1996 PMID: 9016680 PMCID: PMC146325 DOI: 10.1093/nar/24.24.5051
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 16.971