AbstractAminoglycoside antibiotics inhibit protein biosynthesis and various ribozymes. Structural electrostatic complementarity can explain the inhibition mechanism of the hammerhead ribozyme: positively charged ammonium groups match the negatively charged metalion-binding pockets created by the RNA fold's electrostatic field
AbstractUnderstanding the basic principles that govern RNA binding by aminoglycosides is important f...
AbstractElectrostatic interactions often play key roles in the recognition of small molecules by nuc...
SummaryWe have solved the crystal structure of an all-RNA hammerhead ribozyme having a single 2′-O-m...
AbstractAminoglycoside antibiotics inhibit protein biosynthesis and various ribozymes. Structural el...
A variety of drugs inhibit biological key processes by binding to a speci®c RNA component. We focus ...
Abstract: Among saccharides, the antibiotics of the aminoglycoside family are the best-studied class...
AbstractBackground: Aminoglycoside antibiotics bind to the A-site of the decoding region of 16S RNA ...
AbstractBackground: Aminoglycoside antibiotics interfere with ribosomal protein synthesis and with i...
AbstractBackground: Aminoglycoside antibiotics bind to the A-site of the decoding region of 16S RNA ...
Abstract Aminoglycoside antibiotics are protein synthesis inhibitors applied to treat infections cau...
AbstractBackground: Aminoglycoside antibiotics can target RNA folds with micromolar affinity and inh...
AbstractBackground: Aminoglycoside antibiotics interfere with translation in both gram-positive and ...
AbstractAminoglycoside antibiotics target the decoding aminoacyl site (A site) on the 16S ribosomal ...
AbstractBackground: Aminoglycoside antibiotics interfere with ribosomal protein synthesis and with i...
Abstract: RNA is increasingly recognized for its signifi cant functions in biological systems and ha...
AbstractUnderstanding the basic principles that govern RNA binding by aminoglycosides is important f...
AbstractElectrostatic interactions often play key roles in the recognition of small molecules by nuc...
SummaryWe have solved the crystal structure of an all-RNA hammerhead ribozyme having a single 2′-O-m...
AbstractAminoglycoside antibiotics inhibit protein biosynthesis and various ribozymes. Structural el...
A variety of drugs inhibit biological key processes by binding to a speci®c RNA component. We focus ...
Abstract: Among saccharides, the antibiotics of the aminoglycoside family are the best-studied class...
AbstractBackground: Aminoglycoside antibiotics bind to the A-site of the decoding region of 16S RNA ...
AbstractBackground: Aminoglycoside antibiotics interfere with ribosomal protein synthesis and with i...
AbstractBackground: Aminoglycoside antibiotics bind to the A-site of the decoding region of 16S RNA ...
Abstract Aminoglycoside antibiotics are protein synthesis inhibitors applied to treat infections cau...
AbstractBackground: Aminoglycoside antibiotics can target RNA folds with micromolar affinity and inh...
AbstractBackground: Aminoglycoside antibiotics interfere with translation in both gram-positive and ...
AbstractAminoglycoside antibiotics target the decoding aminoacyl site (A site) on the 16S ribosomal ...
AbstractBackground: Aminoglycoside antibiotics interfere with ribosomal protein synthesis and with i...
Abstract: RNA is increasingly recognized for its signifi cant functions in biological systems and ha...
AbstractUnderstanding the basic principles that govern RNA binding by aminoglycosides is important f...
AbstractElectrostatic interactions often play key roles in the recognition of small molecules by nuc...
SummaryWe have solved the crystal structure of an all-RNA hammerhead ribozyme having a single 2′-O-m...