Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Acceptor stem

Another hypothesis was provided by Mikio Shimitso (1982) on the basis of studies of steric effects in molecular models. It had been noted years previously that the fourth nucleotide at the 3 end of the tRNA molecules (referred to as the discrimination base) might have a recognition function. In the case of certain amino acids (i.e., their tRNA-amino acid complexes) this base pair, in combination with the anticodon of the tRNA molecule, can select the amino acid corresponding to the tRNA species in question this is done on the basis of the stereochemical properties of the molecule. Since the anticodon of a tRNA molecule and the fourth nucleotide of the acceptor stem are far apart in space, two tRNA molecules must complex in a head-to-tail manner. The pocket thus formed can then fit specifically to the corresponding amino acid. [Pg.218]

How, in turn, does the synthetase recognize its specific tRNA From extensive mutagenesis studies, it appears that the aminoacyl-tRNA synthetases recognize particular regions of the tRNA molecule, most often in their anticodon loops and/or in their acceptor stems. [Pg.73]

In order to allow for translocation of the tRNA-mRNA complex, the ribosome will have to undergo conformational changes as well. The contacts described above between the decoding center and the codon-anticodon helix as well as the base pairs between the SOS A and P loops and the tRNA acceptor stems will have... [Pg.370]

The first orthogonal E. coli tRNA-synthetase pair generated from archaeal bacteria was derived from the tyrosyl pair taken from Methanococcus janmschii In vitro experiments showed that the major recognition elements of M. jannaschii tRNA" include the discriminator base A73 and the first base pair, C1-G72, in the acceptor stem (Figure 2(a)). The anticodon triplet participates only weakly in identity determination. By contrast, E. coli uses A73, G1-C72, a long variable arm, and the anticodon as identity elements. The M. [Pg.590]

The suppressor tRNA developed by the Chamberlin lab for use in a rabbit reticulocyte lysate is based on an E. coli glycyl tRNA, which was initially chosen because glycyl-tRNA synthetases do not rely on a double-sieve editing mechanism for enzymatic hydrolysis of misacylated tRNAs [26]. Two base pair changes were made to the acceptor stem to allow incorporation of the optimal T7 RNA polymerase promoter into the DNA template for tRNA y-Con [27,28],... [Pg.84]

All tRNA molecules have the sequence -CCA at the 3 end. This three base sequence is termed the acceptor stem. The aminoacyl-tRNA synthetases catalyze the formation of an ester between the carboxyl group of the amino acid and the 3 -OH of the ribose of the terminal adenosine moiety ... [Pg.172]

The translation of the mRNA into proteins is the final step in the biological flow of information (see Fig. 6.1). Similar to other macromolecular polymerizations, protein synthesis can be divided into initiation, chain elongation, and termination. Critical players in this process are the aminoacyl transfer RNAs (tRNAs). These molecules form the interface between the mRNA and the growing polypeptide. Activation of tRNA involves the addition of an amino acid to its acceptor stem, a reaction catalyzed by an aminoacyl-tRNA synthetase. Each aminoacyl-tRNA synthetase is highly specific for one amino acid and its corresponding tRNA molecule. The anticodon loop of each aminoacyl-tRNA interacts... [Pg.71]

B) A similar spectrum for a 35-residue "minihelix" that contains the acceptor stem of the tRNAVal and seven fluorouracils. [Pg.270]

The results of these efforts show that no method of tRNA recognition is universal.2443 In some cases, e.g., for methionine- or valine-specific tRNAs, the synthetase does not aminoacylate a modified tRNA if the anticodon structure is incorrect. Although the anticodon is 7.5 ran away from the CCA end of the tRNA, the synthetases are large enzymes. Many of them are able to accommodate this large distance between a recognition site and the active site (Fig. 29-9A). For some other tRNAs the anticodon is not involved in recognition 245 For yeast tRNAphe residues in the stem of the dihydrouridine loop and at the upper end of the amino acid acceptor stem seem to be critical.241... [Pg.1695]


See other pages where Acceptor stem is mentioned: [Pg.256]    [Pg.256]    [Pg.386]    [Pg.387]    [Pg.388]    [Pg.191]    [Pg.219]    [Pg.365]    [Pg.370]    [Pg.383]    [Pg.383]    [Pg.388]    [Pg.388]    [Pg.389]    [Pg.389]    [Pg.390]    [Pg.390]    [Pg.391]    [Pg.392]    [Pg.392]    [Pg.392]    [Pg.395]    [Pg.396]    [Pg.402]    [Pg.407]    [Pg.410]    [Pg.414]    [Pg.84]    [Pg.85]    [Pg.320]    [Pg.161]    [Pg.169]    [Pg.4]    [Pg.266]    [Pg.232]    [Pg.233]    [Pg.266]    [Pg.1645]    [Pg.1651]    [Pg.1688]    [Pg.1688]    [Pg.1692]   
See also in sourсe #XX -- [ Pg.733 , Pg.734 , Pg.735 ]

See also in sourсe #XX -- [ Pg.601 , Pg.604 ]




SEARCH



Stability of tRNA-derived acceptor stem duplexes

© 2024 chempedia.info