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Ribosome tetramer

Upon release of the two types of chain, a folding of the polypeptides occurs to obtain a stable physicochemical configuration. The assembly of an ajS unit rather than an 2 or 2 dimer is also based on favorable steric arrangements. There is evidence that the heme-globin association occurs after the release of the completed chain from the ribosomes and probably after the formation of the dimer. The formation of a stable tetramer follows soon after the heme-protein association has taken place. [Pg.168]

Figure 19.10 Functional cycle of EF-Tli. The cycle is driven by GDP to GTP exchange which is catalyzed by EF-Ts and GTPase, stimulated by programmed ribosome with A-site bound aminoacyl-tRNA. EF-Tli EF-Ts complex occurs in vitro as (EF-Tu EF-Ts>2 tetramer. This fact is not indicated in the figure. Figure 19.10 Functional cycle of EF-Tli. The cycle is driven by GDP to GTP exchange which is catalyzed by EF-Ts and GTPase, stimulated by programmed ribosome with A-site bound aminoacyl-tRNA. EF-Tli EF-Ts complex occurs in vitro as (EF-Tu EF-Ts>2 tetramer. This fact is not indicated in the figure.
The taxonomic assignation can be made by the search for targeted markers, already sequenced in numerous species, like 16S ribosomal RNA (16S-rRNA), and their comparison with databases, by a statistical analysis of the reads (e.g. tetramers frequency) or by comparison to all of the already known sequences. The interest and the difficulty of metagenomics is that a large part of the sequences obtained come fi om species that have never been previously observed, and are not cultivable [SHA 14],... [Pg.178]

The main variation of EM that has been reported is cryo-electron microscopy (GEM). Of the reports on the use of GEM during this review period the most-studied structure is the ribosome (from various organisms) and its associated machinery. There have also been a number of studies on various viruses. Other studies that have been reported include ribonucleoproteins, the RNA guide surveillance complex from E.coli, a p53 tetramer bound to a DNA-encoding transcription factor response element, human RXR/VDR nuclear receptor in complex with its DR3 target DNA, a complex (UPF-EJG) from eukaryotic nonsense-mediated mRNA decay,and of a DNA origami structure. ... [Pg.196]


See other pages where Ribosome tetramer is mentioned: [Pg.200]    [Pg.82]    [Pg.22]    [Pg.494]    [Pg.471]    [Pg.474]    [Pg.200]    [Pg.233]    [Pg.488]    [Pg.200]    [Pg.267]    [Pg.422]    [Pg.553]    [Pg.65]    [Pg.215]   
See also in sourсe #XX -- [ Pg.16 ]




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