By S. Cusack, C. Berthet-Colominas, V. Biou, F. Borel, M. Fujinaga, M. Hartlein (auth.), Knud H. Nierhaus, François Franceschi, Alap R. Subramanian, Volker A. Erdmann, Brigitte Wittmann-Liebold (eds.)
tRNA and AminoacyltRNA Synthetases: Charging of RNA Microhelices and deciphering Genetic info; P. Schimmel.rRNA and mRNA: Regulation,Processing, and Assembly: Genetic ways to the research of Eukaryotic Ribosomes; J.R. Warner, et al.Translational Initiation andTermination: Mechanisms of Translational Initiation and Repression in Prokaryotes; D.E. Draper.The Elongation strategy: websites, Factors,Nascent Chain: The Allosteric ThreeSite version and the Mechanism of motion of either Elongation components EFTu and EFG; K.H. Nierhaus, et al.Accuracy in Translation: Mutants of tRNA, Ribosomes, and mRNA Affecting Frameshifting, Hopping, or cease Codon Read-Through; J.F.Atkins, et al.Quaternary constitution, useful facilities, and Domainsin the Ribosome. Translation in cellphone Organelles. The TranslationalApparatus and Evolution. sixty four extra articles. Index.
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Additional info for The Translational Apparatus: Structure, Function, Regulation, Evolution
Figure 4. In vivo assay systems for mu~ted imt or emt genes. In separate strains of S288C genetic background, the four IMT or EMT genes have been disrupted by a functional TRP1 gene. The viability of the strains are main~ined by having a wild type IMT or EMT gene on a URA3 based vector. By using a LEU2 vector a second IMT or EMT gene, mutated or wild type, can be introduced into the strains. Thus, a strain that habors both a wild type gene (URA3 vector) and a mutated gene (LEU2 vector) can be obtained.
USA 76:3289. 45 SPECIFICITY IN RNA:PROTEIN INTERACfIONS; THE RECOGNITION OF ESCHERICHIA COLI GLUTAMINE tRNA M. John Rogers, Ivana Weygand-Durasevic, Etienne Schwob. Joyce M. Sherman, Kelley C. -Ulrich Thomann, Lee A. Sylvers, Martina Jahn, Hachiro Inokuchi,t Eiko Ohtsuka,2 and Dieter SolI Department of Molecular Biophysics and Biochemistry Yale University New Haven, cr 06511 USA IDepartment of Biophysics Kyoto University Kyoto,606 Japan 2Paculty of Pharmaceutical Sciences Hokkaido University Sapporo, 060 Japan INTRODUCTION A major element ensuring the accuracy of translation of the genetic code is the recognition of tRNA by its cognate aminoacyl-tRNA synthetase.
1991). Nucleosides are circled and numbers within circles represent the following modifications: 1, 1Methylguanosine (miG); 2, N2 - Methylguanosine (m 2G); 3, Dihydrouridine (D); 4, N2,N2 Dimethylguanosine (m22G); 5, N-(N-(9-B-D-Ribofuranosylpurin-6-yl)carbamoyl)threonine (t6 A); 6,7Methylguanosine (m7G); 7, 5-Methylcytidine (m5C); 8, I-Methyladenosine (mlA); 9, 2'-1 "-B-(5"phosphoryl)-ribosyl-adenosine; 10, Pseudouridine (Y); 11, 5-Methyluridine (m5U). Base pair 3-70, 12-23, 30-40 and 31-39 are G-C base pairs almost conserved among all initiator tRNA species.