ライフサイエンスコーパス: sense codon

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1 sults in the translation of UAG in vivo as a sense codon.

2 rokaryotes, which involves reassignment of a sense codon.

3 cognize the stop codons UAG and UAA, and ten sense codons.

4 plement, thereby orthogonalizing some of the sense codons.

5 ipts, there was no preference for CAG or UCG sense codons.

6 to efficiently discriminate between stop and sense codons.

7 tants with ribosomes programmed with stop or sense codons.

8 termination, serve an alternate function as sense codons.

9 ility of synthetic tRNAs to decode all of 61 sense codons.

10 via "recoding" of UGA from a stop codon to a sense codon, a process that requires specific secondary

11 is the ratio of non-synonymous codons to all sense codons accessible by one point mutation.

12 Replacing the tnaC UGA stop codon with a sense codon allows considerable expression, which is als

13 and an ATG initiation codon, followed by 19 sense codons and a stop codon.

14 arly all cases, the amber codon is used as a sense codon, and an orthogonal tRNA/aminoacyl-tRNA synth

15 last (3'-most) position and ensures that all sense codons are appropriately decoded.

16 eporters was constructed with nearly all the sense codons as the "takeoff site", each with its matche

17 e single most likely ancestral codon from 61 sense codons at each interior node.

18 this process, the stop codon is decoded as a sense codon by a near-cognate tRNA, which programs the r

19 eference for the stop codons UAG and UGA and sense codons CAG and UCG in vitro.

20 ow that several adjacent, arbitrarily chosen sense codons can be completely reassigned to various unn

21 ially enables the reassignment of at least 9 sense codons coding for Ser, Arg, Leu, Pro, Thr, and Gly

22 alanine and cysteine in response to stop and sense codons, depending on the identity element and anti

23 RF1 for ribosomes programmed with different sense codons does not correlate with the defects in pept

24 ent: a ribosome stalled inappropriately at a sense codon during translation elongation.

25 l components to convert TAG into a dedicated sense codon for sAAs.

26 enetic code by changing nonsense codons into sense codons for these amino acids.

27 pal termination codon has been replaced by a sense codon in the alphavirus genome.

28 ession of the tRNA corresponding to the last sense codon in the minigene.

29 modifiable analogs of amino acids at diverse sense codons in cells in rich media.

30 These results suggest that sense codons inhibit conformational changes necessary fo

31 Thus, discrimination against sense codons is achieved with both an increase in the di

32 However, dissociation of RF1 from sense codons is as much as 3 orders of magnitude faster

33 of eRF1 discrimination for stop codons over sense codons is not known.

34 he lysine residue at amino acid 472 to a non-sense codon (K472X).

35 etic recoding of genomes, to remove targeted sense codons, may facilitate the encoded cellular synthe

36 The last sense codon of tnaC, proline codon 24 (CCU), is translat

37 hanism of paromomycin inhibition on stop and sense codons, paired with correlated structural changes

38 of the UAG stop codon; however, reassigning sense codons poses a greater challenge because such codo

39 codons differing by one base change from the sense codons previously used.

40 aking the degeneracy of the genetic code via sense codon reassignment has emerged as a way to incorpo

41 stop codon to a UAA stop codon and to three sense codons that allow constitutive readthrough.

42 tem to simultaneously re-assign 35 of the 61 sense codons to 12 unnatural amino acid analogues.

43 m the sup45-2 strain do not show a defect in sense-codon translation at the non-permissive temperatur

44 mechanism of discrimination between stop and sense codons, we developed a new, pre-steady state kinet

45 hether A-site nuclease activity also cleaves sense codons, we induced ribosome pausing at each of the

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