Phenylalanine identity of yeast tRNAPhe is governed by five nucleotides including residues A73, G20, and the three anticodon nucleotides (Sampson et al., 1989, Science 243, 1363-1366). Analysis of in vitro transcripts derived from yeast tRNAPhe and Escherichia coli tRNAAla bearing these recognition elements shows that phenylalanyl-tRNA synthetase is sensitive to additional nucleotides within the acceptor stem. Insertion of G2-C71 has dramatic negative effects in both tRNA frameworks. These effects become compensated by a second-site mutation, the insertion of the wobble G3-U70 pair, which by itself has no effect on phenylalanylation. From a mechanistic point of view, the G2-C71/G3-U70 combination is not a "classical" recognition element sin...
High-resolution X-ray structures for the tRNA/aminoacyl-tRNA synthetase complexes between Escherichi...
International audienceCrystallographic studies of the aspartyl-tRNA synthetase-tRNAAsp complex from ...
Although the anticodon is the primary element in Escherichia coli tRNAVal for recognition by valyl-t...
Arginylation of tRNA transcripts by yeast arginyl-tRNA synthetase can be triggered by two alternate ...
Residue G-1 and discriminator base C73 are the major histidine identity elements in prokaryotes. Her...
Identity determinants are essential for the accurate recognition of transfer RNAs by aminoacyl-tRNA ...
AbstractBackground: The attachment of specific amino acids to the 3′-end of cognate transfer RNAs (t...
Non-protein amino acids, particularly isomers of the proteinogenic amino acids, present a threat to ...
The nucleotides crucial for the specific aminoacylation of yeast tRNA(Asp) by its cognate synthetase...
A method for synthesizing yeast tRNA$\sp{\rm Phe}$ mutants having nucleotide substitutions at any de...
Non-protein amino acids, particularly isomers of the proteinogenic amino acids, present a threat to ...
A method for synthesizing yeast tRNA$\sp{\rm Phe}$ mutants having nucleotide substitutions at any de...
AbstractIn this study, we identified nucleotides that specify aminoacylation of tRNAThr by Thermus t...
AbstractPrimary structures of phage T5- and Escherichia coli-encoded tRNAPhe are distinct at four ou...
The specificity of transfer RNA aminoacylation by cognate aminoacyl-tRNA synthetase is a crucial ste...
High-resolution X-ray structures for the tRNA/aminoacyl-tRNA synthetase complexes between Escherichi...
International audienceCrystallographic studies of the aspartyl-tRNA synthetase-tRNAAsp complex from ...
Although the anticodon is the primary element in Escherichia coli tRNAVal for recognition by valyl-t...
Arginylation of tRNA transcripts by yeast arginyl-tRNA synthetase can be triggered by two alternate ...
Residue G-1 and discriminator base C73 are the major histidine identity elements in prokaryotes. Her...
Identity determinants are essential for the accurate recognition of transfer RNAs by aminoacyl-tRNA ...
AbstractBackground: The attachment of specific amino acids to the 3′-end of cognate transfer RNAs (t...
Non-protein amino acids, particularly isomers of the proteinogenic amino acids, present a threat to ...
The nucleotides crucial for the specific aminoacylation of yeast tRNA(Asp) by its cognate synthetase...
A method for synthesizing yeast tRNA$\sp{\rm Phe}$ mutants having nucleotide substitutions at any de...
Non-protein amino acids, particularly isomers of the proteinogenic amino acids, present a threat to ...
A method for synthesizing yeast tRNA$\sp{\rm Phe}$ mutants having nucleotide substitutions at any de...
AbstractIn this study, we identified nucleotides that specify aminoacylation of tRNAThr by Thermus t...
AbstractPrimary structures of phage T5- and Escherichia coli-encoded tRNAPhe are distinct at four ou...
The specificity of transfer RNA aminoacylation by cognate aminoacyl-tRNA synthetase is a crucial ste...
High-resolution X-ray structures for the tRNA/aminoacyl-tRNA synthetase complexes between Escherichi...
International audienceCrystallographic studies of the aspartyl-tRNA synthetase-tRNAAsp complex from ...
Although the anticodon is the primary element in Escherichia coli tRNAVal for recognition by valyl-t...