ライフサイエンスコーパス: adenine residue

1 brium of the glycosidic bond in the modified adenine residue.

2 g bulge defects with up to five extrahelical adenine residues.

3 onors to the O2 of thymine residues or N3 of adenine residues.

4 rcinogen that preferentially modifies DNA in adenine residues.

5 irs along the major groove edges of opposing adenine residues.

6 ith a DNA oligomer containing a bulge of two adenine residues.

7 start site of transcription was mapped to an adenine residue 601 nt 5' of the translation initiation

8 sidues -889 and -885 and hypersensitivity of adenine residues -892 and -865 were observed.

9 the rRNA that involves the destacking of two adenine residues (A1492 and A1493 in Escherichia coli) a

10 orm is formed with three naturally occurring adenine residues, A21, A3 and A9, capping the top tetrad

11 emical features of the universally conserved adenine residue A2451 in 23S ribosomal RNA (Escherichia

12 f transcription by T7 RNA polymerase past an adenine residue adducted at the N6-position with (-)-ant

13 he proposed interaction, the loop 2 terminal adenine residue and two G.C pairs near the top of stem 1

14 D)-like sequence, a slippery sequence of six adenine residues and a guanine residue (A6G) and a 3' se

15 ad-to-head dimeric quadruplex involve single adenine residues and adds to our knowledge of chain reve

16 In vivo, modification of adenine residues appears to occur exclusively in the seq

17 During mutagenic homing, adenine residues are converted to random nucleotides in

18 s indicated a transcription start site at an adenine residue at 37 bases upstream of the translation

19 All 29 M. bovis isolates sequenced had an adenine residue at nucleotide 285, whereas all 76 other

20 side-induced reduction in the mobility of an adenine residue at position 1492 of the rRNA A-site is a

21 It was previously shown that inserting an adenine residue at position 751 or introducing the U2609

22 Simple insertion of an adenine residue at the stem 1-stem 2 junction (an essent

23 e rRNA A-site (centered around the conserved adenine residues at positions 1492 and 1493), which, in

24 ng dictated by the coupled destacking of the adenine residues at positions 1492 and 1493.

25 odiester modes can be assigned to individual adenine residues based on earlier NMR data.

26 CDE, to the exocyclic N(6)amino group of the adenine residue dA6, (designated (+)- trans-anti -(B[g]C

27 rved that reflect the structural contexts of adenine residues, disruption of A-form helical structure

28 ibitory activity by depurination of a single adenine residue from the 28S rRNA component of eukaryoti

29 activating protein, catalytically removes an adenine residue from the conserved alpha-sarcin loop of

30 slation by catalytically removing a specific adenine residue from the large rRNA of the 60S subunit o

31 slation by catalytically removing a specific adenine residue from the large rRNA of the 60S subunit o

32 slation by catalytically removing a specific adenine residue from the large rRNA of the 60S subunit o

33 sidase that catalytically removes a specific adenine residue from the stem loop of ribosomal RNA.

34 of DNA mutations by removing misincorporated adenine residues from 7, 8-dihydro-8-oxo-2'-deoxyguanosi

35 sociated with OG by removing misincorporated adenine residues from OG:A mismatches.

36 ER) glycosylase that removes misincorporated adenine residues from OG:A mispairs, as well as G:A and

37 TRIP released fewer amounts of adenine residues from ribosomal (Artemia sp. and rat rib

38 y denatured nucleic acids, randomly removing adenine residues from single-stranded regions and, to a

39 reactions being coupled to the destacking of adenine residues from the terminal G-tetrads.

40 ng A-tracts, runs of four or more contiguous adenine residues, has been assessed by capillary electro

41 Likewise, the second HTH interacts with an adenine residue in binding site 2.

42 olving general-acid catalysis by a conserved adenine residue in the active site.

43 somal inhibitory protein that depurinates an adenine residue in the alpha-sarcin loop of 25S rRNA and

44 NA N-glycosidases that depurinate a specific adenine residue in the conserved sarcin/ricin loop of 28

45 hyltransferase CcrM (M.CcrMI) methylates the adenine residue in the sequence GANTC.

46 of the Bordetella phage DGR is primed by an adenine residue in TR RNA and is dependent on the DGR-en

47 ch in Escherichia coli dimethylates adjacent adenine residues in a stem-loop of the 16S rRNA.

48 We have found that both guanine and adenine residues in codons 12, 13, and 61 of the H-ras g

49 ned and exploited to assign the H2 proton of adenine residues in DNA oligonucleotides.

50 These react predominantly with adenine residues in DNA to produce the stereoisomeric 1R

51 These can react with adenine residues in DNA, to produce the stereoisomeric 1

52 mismatches between 8-oxoguanine (8-oxoG) and adenine residues in DNA.

53 Most of the adenine residues in GATC sequences in the Escherichia co

54 essential DNA methylase, Mox, which modifies adenine residues in occurrences of XhoI and PstI recogni

55 OG) in DNA by the removal of misincorporated adenine residues in OG:A mispairs.

56 leotide deletion in a track of 9 consecutive adenine residues in pstS, encoding a component of a high

57 ozoan TETRAHYMENA: Approximately 0.8% of the adenine residues in the macronuclear DNA of Tetrahymena

58 Approximately 0.8% of the adenine residues in the macronuclear DNA of the ciliated

59 , the bend angle conferred by a tract of six adenine residues increases from about 7 degrees in the a

60 , [d(CGCGAATTCGCG)](2), in which each of the adenine residues, individually or jointly, was replaced

61 For D5 that has all of its adenine residues labeled with (13)C and (15)N and utiliz

62 lls was shown to occur predominantly from an adenine residue located 39 base pairs downstream of a co

63 ermutation in a short homopolymeric tract of adenine residues located in the N-terminal coding region

64 5-nucleotide repeat, AGATT, and a string of adenine residues mark this locus.

65 otide deletion/insertion in a short tract of adenine residues near the 5' end of the mature Vaa codin

66 ary structure motif in which two consecutive adenine residues occupy the strand opposite a single uri

67 age at Ap sites in duplex DNA can react with adenine residues on the opposing strand to generate a co

68 covalent adduct with the N(6)-amino group of adenine residues on the opposing strand.

69 chia coli MutY DNA glycosylase (MYH) cleaves adenine residues paired with either oxidized or non-modi

70 We found that the P4 helix and flanking adenine residues play crucial and unexpected roles in co

71 etermine the effect of a carcinogen-modified adenine residue, positioned site-specifically within a r

72 Further, four adenine residues stack in pairs at one end, H-bonding th

73 Overhang adenine residues stack within the duplexes with C3'-endo

74 s inhibited by premethylation of guanine and adenine residues, suggesting that binding does not requi

75 Sequences of four to six adenine residues, termed A-tracts, have been shown to pr

76 rd and the fourth G-quartets consists of two adenine residues that are flipped out to facilitate cons

77 artite target sequence, but one in which the adenine residues that are the substrates for methylation

78 As well as being smaller than for other adenine residues, the 1H T2 values exhibited a magnetic

79 of Ile9 braces the sugar moieties of the two adenine residues, thereby decreasing the roll and tilt a

80 eferential binding of isomiRs ending with 3' adenine residues to AGO1 and 3' uridine residues to AGO2

81 Deletions in the string of adenine residues were associated with both a decreased-p

82 usative mutation is an insertion of an extra adenine residue within a tract of nine A's in exon 21 of