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Page "Ribosome" ¶ 32
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ribosome and then
Eukaryotic mRNA that has been processed and transported to the cytoplasm ( i. e., mature mRNA ) can then be translated by the ribosome.
Most organisms then process the pre-mRNA ( also known as a primary transcript ) using various forms of Post-transcriptional modification to form the mature mRNA, which is then used as a template for protein synthesis by the ribosome.
The attached amino acids are then linked together by another part of the ribosome.
The newly produced polypeptide chains are inserted directly into the ER by the ribosome undertaking vectorial synthesis and are then transported to their destinations, through the secretory pathway.
Amino acids are then chained together by the ribosome according to order of triplets in the coding region.
If ribozymes were the first molecular machines used by early life, then today's remaining ribozymes — such as the ribosome machinery — could be considered living fossils of a life based primarily on nucleic acids.
The tRNA bound in the E / E site then leaves the ribosome.
This complex is then recognized by other translation initiation machinery including the ribosome.
The initiation complex scans along the mRNA strand until it reaches a start codon, and then the large subunit of the ribosome attaches to the small subunit and translation of a protein begins.
Also, if the oncoming ribosome pauses because of a knot in the RNA, then the polypeptide can have time to fold into an unusual structure before the tRNA molecule has time to add another amino acid.

ribosome and contains
For example, the region of the hepatitis C virus genome that encodes the core protein is highly conserved, because it contains an RNA structure involved in an internal ribosome entry site.
In addition to this nucleoid, there are two other membrane-separated compartments ; the pirellulosome or riboplasm, which contains the ribosome and related proteins, and the ribosome-free paryphoplasm.
Expression of the antisense ncRNA prevents splicing of an intron that contains a ribosome entry site necessary for efficient expression of the Zeb2 protein.
In prokaryotes, the 5 ' UTR usually contains a ribosome binding site ( RBS ), also known as the Shine Dalgarno sequence ( AGGAGGU ).
The matrix of N. ovalis hydrogenosomes contains ribosome-like particles of the same size as a numerous type of ribosome ( 70s ) of the endosymbiotic methanogenic archaea.
* In Bacteria, the 50S ( 23S component ) ribosome subunit contains the peptidyl transferase component and acts as a ribozyme.
* In eukaryotic cells, the 60S ( 28S component ) ribosome subunit contains the peptidyl transferase component and acts as the ribozyme.

ribosome and three
In ribosome biogenesis, two of the three eukaryotic RNA polymerases ( pol I and III ) are required, and these function in a coordinated manner.
The mRNA is loaded onto the ribosome and is read three nucleotides at a time by matching each codon to its base pairing anticodon located on a transfer RNA molecule, which carries the amino acid corresponding to the codon it recognizes.
The ribosome has three sites for tRNA to bind.
The ribosome has three binding sites for tRNA molecules that span the space between the two ribosomal subunits: the A ( aminoacyl ), P ( peptidyl ), and E ( exit ) sites.

ribosome and RNA
A few RNA molecules called ribozymes also catalyze reactions, with an important example being some parts of the ribosome.
RNA is transcription ( genetics ) | transcribed in the cell nucleus | nucleus ; processed, it is transported to the cytoplasm and Translation ( genetics ) | translated by the ribosome.
During genome replication the circularization acts to enhance genome replication speeds, cycling viral RNA dependent RNA polymerase much the same as the ribosome is hypothesized to cycle.
Ribosomal RNA is a major component of the ribosome, and catalyzes peptide bond formation.
In higher eukaryotes and plants, the situation is more complex, for the 5S DNA sequence lies outside the NOR and is transcribed by RNA pol III in the nucleoplasm, after which it finds its way into the nucleolus to participate in the ribosome assembly.
RNA is transcription ( genetics ) | transcribed in the cell nucleus | nucleus ; once completely processed, it is transported to the cytoplasm and Translation ( genetics ) | translated by the ribosome ( not shown ).
This whole complex of processes is carried out by the ribosome, formed of two main chains of RNA, called ribosomal RNA ( rRNA ), and more than 50 different proteins.
This process uses transfer RNA ( tRNA ) molecules to deliver amino acids to the ribosome, where ribosomal RNA ( rRNA ) links amino acids together to form proteins.
For instance, determination of the structure of the ribosomean enzyme that catalyzes peptide bond formation — revealed that its active site is composed entirely of RNA.
Messenger RNA ( mRNA ) is the RNA that carries information from DNA to the ribosome, the sites of protein synthesis ( translation ) in the cell.
Certain RNAs are able to catalyse chemical reactions such as cutting and ligating other RNA molecules, and the catalysis of peptide bond formation in the ribosome ; these are known as ribozymes.
In the cytoplasm, ribosomal RNA and protein combine to form a nucleoprotein called a ribosome.
The RNA world would have eventually been replaced by the DNA, RNA and protein world of today, likely through an intermediate stage of RNP enzymes such as the ribosome and ribozymes, since proteins large enough to self-fold and have useful activities would only have come about after RNA was available to catalyze peptide ligation or amino acid polymerization.
The ribosome assembles polymeric protein molecules whose sequence is controlled by the sequence of messenger RNA molecules.
The ribosome ( from ribonucleic acid and the Greek soma, meaning " body ") is a large complex of RNA and protein which catalyzes protein translation, the formation of proteins from individual amino acids using messenger RNA as a template.
Amino acids are selected, collected and carried to the ribosome by transfer RNA ( tRNA molecules ), which enter one part of the ribosome and bind to the messenger RNA chain.

ribosome and binding
Unique triplets promoted the binding of specific tRNAs to the ribosome.
The N-RNAP complex is stabilized by subsequent binding of several host Nus ( N utilisation substance ) proteins ( which include transcription termination / antitermination factors and, bizarrely, a ribosome subunit ).
Macrolide antibiotics do so by binding reversibly to the P site on the subunit 50S of the bacterial ribosome.
Initiation involves the small subunit of the ribosome binding to 5 ' end of mRNA with the help of initiation factors ( IF ), other proteins that assist the process.
Affinity label for the tRNA binding sites on the E. coli ribosome allowed the identification of A and P site proteins most likely associated with the peptidyltransferase activity ; labelled proteins are L27, L14, L15, L16, L2 ; at least L27 is located at the donor site, as shown by E. Collatz and A. P.
Both a promoter and a ribosome binding site ( Shine-Dalgarno sequence ) are present upstream of the gene.
Another bacterial ncRNA, OxyS RNA represses translation by binding to Shine-Dalgarno sequences thereby occluding ribosome binding.
The ribosome facilitates decoding by inducing the binding of tRNAs with complementary anticodon sequences to that of the mRNA.
Initiation involves the small subunit of the ribosome binding to the 5 ' end of mRNA with the help of initiation factors ( IF ).
Instead, the stop codon induces the binding of a release factor protein that prompts the disassembly of the entire ribosome / mRNA complex.
For example, basic transcription of a gene can be represented by the following single-step reaction ( RNAP is the RNA polymerase, RBS is the RNA ribosome binding site, and Pro < sub > i </ sub > is the promoter region of gene i ):
In addition, the ribosome has two other sites for tRNA binding that are used during mRNA decoding or during the initiation of protein synthesis.
In this experiment, using a ribosome binding assay, various combinations of mRNA were passed through a filter which contained ribosomes.
Unique triplets promoted the binding of specific tRNAs to the ribosome.
This is due to strong, irreversible binding to the ribosome, and remains intracellular long after plasma levels drop.
The antibacterial properties of aminoglycosides were believed to result from inhibition of bacterial protein synthesis through irreversible binding to the 30S bacterial ribosome.
The 5 ' UTR has a ribosome binding site ( IRES — Internal ribosome entry site ) that starts the translation of a very long protein containing about 3, 000 amino acids.
At low temperatures, the PrfA transcript is not translated due to structural elements near the ribosome binding site.
The small subunit of the ribosome usually starts by binding to one end of the mRNA and is joined there by various other eukaryotic initiation factors, forming the initiation complex.

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