「ｔｒｎａ」の共起表現一覧(1語右で並び替え)
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| selection for optimizing translation process by | tRNA abundance), %G+C composition (reflecting horizo |
| They catalyze their own excision from mRNA, | tRNA and rRNA precursors in a wide range of organism |
| factor EF-G catalyzes the translocation of the | tRNA and mRNA down the ribosome at the end of each r |
| rease the fidelity of binding the right pair of | tRNA and amino-acid. |
| cture of the whole ribosome in complex with its | tRNA and mRNA ligands. |
| yotic EF-G, catalyzing the translocation of the | tRNA and mRNA down the ribosome at the end of each r |
| IF2 binds to an initator | tRNA and controls the entry of that tRNA into the ri |
| IF2 binds to an initiator | tRNA and controls the entry of that tRNA into the ri |
| -tRNA and protein, whereas its two products are | tRNA and L-leucyl-protein. |
| sphatidylglycerol, whereas its two products are | tRNA and 3-phosphatidyl-1'-(3'-O-L-lysyl)glycerol. |
| -tRNA and protein, whereas its two products are | tRNA and L-arginyl-protein. |
| D is found in | tRNA and rRNA molecules as a nucleoside; the corresp |
| tochondria genomes contain 37 genes, 2 rRNA, 22 | tRNA and 13 mRNA. |
| Stringent factors take uncharged | tRNA and converts it to an alarmone. |
| trates of this enzyme are [[2'-phospho-[ligated | tRNA]]] and NAD+, whereas its 4 products are mature |
| thetase enzyme that specifically recognizes the | tRNA anticodon. |
| It is commonly found in | tRNA, associated with thymidine and cytosine in the |
| However, | tRNA binding involves an alpha-helical structure tha |
| element in the genomes of retroviruses to which | tRNA binds to initiate reverse transcription. |
| es of this enzyme are S-adenosyl methionine and | tRNA containing uridine at position 54, whereas its |
| this enzyme are 5,10-methylenetetrahydrofolate, | tRNA containing uridine at position 54, and FADH2, w |
| roups worldwide for solving the 3D structure of | tRNA during the sixties and early seventies. |
| Homologous to EF-Tu + | tRNA, EF-G also binds to the ribosome in its GTP-bou |
| Organisms with T-loop lacking | tRNA exhibit a much lower level of aminoacylation an |
| ors IF2-GTP, IF1, IF3, as well as the initiator | tRNA fMet-tRNA(fmet) are recruited to the ribosome. |
| The transfer RNA ( | tRNA) for histidine is unique among eukaryotic tRNAs |
| tRNA-like structures mimic some | tRNA function, such as aminoacylation. |
| The nonsense suppressor is a | tRNA gene (from Escherichia coli) which has a mutate |
| ntent of ribosomal RNA (rRNA) and transfer RNA ( | tRNA) genes in hyperthermophiles shows a strong corr |
| nsfer ribonucleate guanine 1-methyltransferase, | tRNA guanine 1-methyltransferase, and S-adenosyl-L-m |
| tRNA guanosine-2'-O-methyltransferase | |
| c acids where it is present in the anticodon of | tRNA in the form of its nucleoside inosine. |
| les ; It is known to add the 3' CCA sequence to | tRNA in prokaryotic tRNA processing. |
| t-tRNAf binds to the IF2 then IF2 transfers the | tRNA into the partial P site. |
| tic EF-Tu, mediating the entry of the aminoacyl | tRNA into a free site of the ribosome. |
| In the HIV virus, the | tRNA is tRNA(3)(Lys) although it can use other tRNAs |
| This is because a separate | tRNA is used for initiation. |
| ctive amino-acids - the enzyme that charges the | tRNA is called aminoacyl tRNA synthetase. |
| tRNA is the only RNA species that contains the nucle | |
| ch lack the 3' termini lack complete or partial | tRNA mimicry. |
| Klug's group not realizing that there were two | tRNA models in the US: the MIT model (produced by Ri |
| Sup35p protein and then takes on the shape of a | tRNA molecule so that it can safety incorporate itse |
| me to fold into an unusual structure before the | tRNA molecule has time to add another amino acid. |
| f the first radiochemically pure precursor to a | tRNA molecule enabled me to get a job as an assistan |
| T-arm or T-loop is a specialized region on the | tRNA molecule which acts as a special recognition si |
| comes activated when an uncharged transfer RNA ( | tRNA) molecule enters the A site of the ribosome, du |
| tion step in protein synthesis (movement of two | tRNA molecules and mRNA in relation to the ribosome) |
| off an extra, or precursor, sequence of RNA on | tRNA molecules . |
| Transfer RNA ( | tRNA) molecules contain a particularly large number |
| A nonsense suppressor is a | tRNA mutation that suppresses the protein truncation |
| , in the formation of creatine, carnitine, DNA, | tRNA, norepinephrine, and other compounds, it is tra |
| In enzymology, a | tRNA nucleotidyltransferase (EC 2.7.7.56) is an enzy |
| tRNA of organisms that grow at low temperatures (psy | |
| The RNA molecules (rRNA and | tRNA) played an important role in the catalytic acti |
| ect the composition of their respective genomic | tRNA pool. |
| rRNA, whereas endolytic cleavage corresponds to | tRNA precursors. |
| it associates with the A site, EF-G causes the | tRNA previously occupying that site to occupy an int |
| RNA genome, specific removal of the (-)-strand | tRNA primer, and removal of the (+)-strand PPT prime |
| nt in archaea and bacteria, that is involved in | tRNA processing. |
| This study also identified several partial | tRNA sequences within the cDNA libraries which corre |
| It is has been suggested that these partial | tRNA stall protein synthesis however, further studie |
| e facilitates binding and cleavage of precursor | tRNA substrates. |
| In enzymology, a | tRNA sulfurtransferase (EC 2.8.1.4) |
| For the enzyme aaRS, see Aminoacyl | tRNA synthetase. |
| hen there is a deficiency of the charged leucyl | tRNA the ribosome translating the leader peptide sta |
| ces, which have a similar tertiary structure to | tRNA; they frequently contain a pseudoknot close to |
| auses a conformation change that forces the A/P | tRNA to fully occupy the P site, the P/E tRNA to ful |
| rapid codon-anticodon pairing for the initiator | tRNA to bind quickly to. |
| The systematic name of this enzyme class is [ | tRNA]-guanine:queuine tRNA-D-ribosyltransferase. Oth |
| imary and secondary structure of selenocysteine | tRNA, tRNA(Sec), differ from those of standard tRNAs |
| -D-alanyl-D-alanine, whereas its 3 products are | tRNA, UDP-N-acetylmuramoyl-L-alanyl-D-glutamyl-N6-(L |
| thyltransferase, transfer RNA uracil methylase, | tRNA uracil 5-methyltransferase, m5U-methyltransfera |
| of this enzyme are S-adenosyl-L-methionine and | tRNA uridine, whereas its two products are 5'-methyl |
| es of this enzyme are S-adenosyl methionine and | tRNA, whereas its two products are S-adenosylhomocys |
| s of this enzyme are L-cysteine and 'activated' | tRNA, whereas its two products are L-serine and tRNA |
| es of this enzyme are S-adenosyl methionine and | tRNA, whereas its two products are S-adenosylhomocys |
| elenocysteine synthesis occurs on a specialized | tRNA, which also functions to incorporate it into na |
| acyl group is coupled to the 2'-hydroxyl of the | tRNA, while, in class II reactions, the 3'-hydroxyl |
| When | tRNA with compete CCA sequence at its acceptor stem |
| ey Altman discovered the existence of precursor | tRNA with flanking sequences and was the first to ch |
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