ライフサイエンスコーパス: exonuclease I

1 These ends are susceptible to degradation by exonuclease I.

2 the 5'-to-3' activity of MutSalpha-activated exonuclease I.

3 NA results in protection from degradation by exonuclease I.

4 recently determined structure of the E. coli Exonuclease I.

5 ereas SCE-associated events are sensitive to exonuclease I.

6 ilar to the processive exonucleases RecJ and exonuclease I.

7 Phage T5 exonuclease is a 5'-->3'exodeoxyribonuclease that also e

8 Lambda exonuclease is a highly processive 5'-->3' exonuclease t

9 Bacteriophage T5 5'-->3' exonuclease is a member of a family of sequence related

10 T5 5'-3' exonuclease is a member of a homologous group of 5' nucl

11 lambda Exonuclease is a toroidal homotrimeric molecule and this

12 Dictyostelium cells disrupted in exonuclease I, a critical factor for HR, are sensitive t

13 We found that the Ape1 exonuclease is active at both mismatched and correctly m

14 ly identified SSB-Ct binding site on E. coli exonuclease I, although the SSB binding domains in the t

15 The lambda exonuclease is an ATP-independent enzyme that binds to d

16 Free primers are removed by exonuclease I and a poly(A) tail is added to the 3' end

17 etected the activities of two model enzymes, exonuclease I and uracil DNA glycosylase with high sensi

18 A 3' ends from resection by Escherichia coli exonucleases I and III and from end-healing by T4 polynu

19 ading strand bias was lost in the absence of exonucleases I and VII, suggesting that it results from

20 s dramatically stimulated by inactivation of exonucleases I and VII, which degrade single-strand DNA

21 the UV sensitivity of a strain lacking RecJ, exonuclease I, and exonuclease VII.

22 ngle-strand DNA-specific exonucleases, RecJ, exonuclease I, and exonuclease VII.

23 mplicated RecJ exonuclease, exonuclease VII, exonuclease I, and exonuclease X in Escherichia coli met

24 bsence of RecJ exonuclease, exonuclease VII, exonuclease I, and exonuclease X.

25 : SSB (single-stranded DNA-binding protein), exonuclease I, and RecJ exonuclease.

26 Electrical force applied to individual ssDNA-exonuclease I complexes pulls the two molecules apart, w

27 Previously, we demonstrated that exonuclease I-deficient strains of Escherichia coli accu

28 WRN exonuclease is distinguished from known mammalian DNA nu

29 The availability of any one exonuclease is enough to support full mismatch correctio

30 ing subunit of the replisome, the varepsilon exonuclease, is essential for high-fidelity DNA replicat

31 tif, which, by analogy to other proofreading exonucleases, is essential for the catalytic activity.

32 to CCC DNA conversion, two 3' exonucleases, exonuclease I (Exo I) and Exo III, were used in combinat

33 plementary strands of aptamer (CSs) complex, exonuclease I (Exo I) and gold electrode.

34 escent probe system that shows resistance to exonuclease I (Exo I) digestion upon binding to ATP mole

35 elective detection of streptomycin, based on exonuclease I (Exo I), complimentary strand of aptamer (

36 This exonuclease, referred to as exonuclease I (Exo I), has been purified more than 300-f

37 pe structure on the surface of electrode and exonuclease I (Exo I).

38 f aptamer (CS) conjugate, gold electrode and exonuclease I (Exo I).

39 lepsilon mutants that in combination with an exonuclease I (exo1) mutation could cause a synergistic

40 A crystal structure of Escherichia coli exonuclease I (ExoI) bound to a peptide comprising the E

41 Escherichia coli Exonuclease I (ExoI) digests single-stranded DNA (ssDNA)

42 a peptide comprising the SSB-Ct element and exonuclease I (ExoI) from Escherichia coli.

43 exes formed between Escherichia coli SSB and Exonuclease I (ExoI), a well-studied SSB-interacting enz

44 xperiments have implicated RecJ exonuclease, Exonuclease I (ExoI), and Exonuclease VII (ExoVII) in th

45 ific exonucleases in Escherichia coli: RecJ, exonuclease I (ExoI), and exonuclease VII (ExoVII).

46 a coli SSB stimulates hydrolysis of ssDNA by Exonuclease I (ExoI).

47 randed DNA (ssDNA) exonuclease, which can be exonuclease I, exonuclease VII, or SbcCD.

48 pose a model in which processivity of lambda exonuclease is expressed as the net result of competitio

49 recombinant MP90 and recombinant RNA editing exonuclease I from L. major, and recombinant RNA editing

50 of DNA polymerase-associated proofreading 3'-exonucleases is generally enhanced in less stable DNA re

51 nt in RecJ exonuclease, exonuclease VII, and exonuclease I, grow poorly in the presence of the base a

52 Human exonuclease I (hExoI) is a member of a family of conserv

53 exonuclease X is capable of substituting for exonuclease I in UV repair.

54 Progression of the WRN exonuclease is inhibited by the action of WRN helicase c

55 ition between elongating pol II and the Xrn2 exonuclease is integral to termination of transcription

56 We conclude that the 5'-exonuclease is intrinsic to ARTEMIS, making it relevant

57 no major defect in meiosis, suggesting that exonuclease I is unlikely to be the primary activity tha

58 coli there are 14 DNA exonucleases including exonucleases I-IX (including the two DNA polymerase I ex

59 The 5'-3' exonuclease is known to be a structure-specific nuclease

60 berberine, is digested upon the addition of exonuclease I, leading to the release of berberine into

61 Thus, in adapted cells, Mre11 exonuclease is mainly present in the cytoplasm, rather t

62 servation suggests that RecJ exonuclease and exonuclease I may enhance recombination by degrading the

63 In addition, our data indicate that exonuclease I may have a minor role in the correction of

64 The WRN helicase/exonuclease is mutated in Werner syndrome of genomic ins

65 randed DNA and 5'-overhangs, because this 5'-exonuclease is not dependent upon DNA-PKcs.

66 The mechanism of the PHP-exonuclease is not known.

67 in those instances where the proofreading 3'-exonuclease is not part of the polymerase polypeptide.

68 the 3' exonuclease of DNA polymerase III and exonuclease I on deletion via these mechanisms in vivo.

69 ; bacteriophage T4 dexA and Escherichia coli exonuclease I, processive 3'-->5' exodeoxyribonucleases

70 sed to measure the degradation of DNA by DNA exonuclease I, providing data that would not be availabl

71 ally, lowering deamination density increases exonuclease I recruitment and single-stranded DNA at the

72 The H. pylori AddAB helicase-exonuclease is required for DNA repair and efficient sto

73 First, each of these exonucleases is required for the processing of distinct

74 Our analysis reveals that the exonuclease is sandwiched between the polymerase and cla

75 Here, we show that this exonuclease is strongly upregulated in human psoriasis,

76 n different biological matrices show that 5'-exonuclease is the most prevalent nuclease activity in e

77 , encoding the major mammalian 3' --> 5' DNA exonuclease, is the AGS1 gene, and AGS-causing mutations

78 port heterogeneity in the time necessary for Exonuclease I to hydrolyze identical DNA fragments.

79 d measured the time required by molecules of Exonuclease I to hydrolyze single-stranded DNA that was

80 hole observed in the crystal structure of T5 exonuclease is too small to permit the passage of double

81 The single-stranded DNA produced by lambda exonuclease is utilized by homologous pairing proteins t

82 Exonuclease I was originally identified as a 5' --> 3' d