ライフサイエンスコーパス: DNA-dependent ATPase

1 nother double helix is passed, and acts as a DNA dependent ATPase.

2 ATP-dependent helicase and a single-stranded DNA-dependent ATPase.

3 neity from yeast cells and show that it is a DNA-dependent ATPase.

4 f ATP-dependent, in vitro reactions and is a DNA-dependent ATPase.

5 sphohydrolase I (NPH I) is a single-stranded DNA-dependent ATPase.

6 ts subunits, the RecB and RecD proteins, are DNA-dependent ATPases.

7 is a member of the SWI/SNF protein family of DNA-dependent ATPases.

8 family members and less potent toward other DNA-dependent ATPases.

9 hanisms to specifically target this class of DNA-dependent ATPases.

10 activated DNA polymerase V (pol V Mut), is a DNA-dependent ATPase; (2) bound ATP is required for DNA

11 tifunctional enzyme with 5'-3' DNA helicase, DNA-dependent ATPase, 3' exo/endonuclease, and 5' exo/en

12 ds inhibit the ATPase activity of the active DNA-dependent ATPase A domain (ADAAD) by competing with

13 n (HARP) protein (also known as SMARCAL1 and DNA-dependent ATPase A) is an annealing helicase that re

14 ytic function of an SWI2/SNF2 family member: DNA-dependent ATPase A.

15 RadA is a DNA-dependent ATPase, a DNA-binding protein and can stim

16 ein exhibits defects in its DNA helicase and DNA-dependent ATPase activities and was unable to suppor

17 Although strand passage and DNA-dependent ATPase activities are affected in these mu

18 inhibited the helicase, the primase and the DNA-dependent ATPase activities of the enzyme with IC50

19 The DNA helicase and DNA-dependent ATPase activities of UL9 protein were stim

20 hat Rad51-K342E displays DNA-independent and DNA-dependent ATPase activities, owing to its ability to

21 5'-3' endonuclease, the 5'-3' helicase, and DNA-dependent ATPase activities.

22 r interaction, which in turn activates their DNA-dependent ATPase activity (intermolecular mode).

23 Mutations in motifs III-VI decrease DNA-dependent ATPase activity 3-6-fold.

24 The protein has a weak DNA-dependent ATPase activity and binds both single-stra

25 The UL52-UL8 complex lacked detectable DNA-dependent ATPase activity and could not synthesize p

26 The purified protein has a DNA-dependent ATPase activity and is a 3'-5' DNA helicas

27 single- and double-stranded DNA, possesses a DNA-dependent ATPase activity and promotes intermolecula

28 The mutant enzyme, however, is impaired in DNA-dependent ATPase activity and single-stranded DNA bi

29 ified Pfh1 protein displayed single-stranded DNA-dependent ATPase activity as well as 5' to 3' DNA he

30 RgyB has a DNA-dependent ATPase activity at high temperature (80 de

31 RuvB proteins showed strong double-stranded DNA-dependent ATPase activity at their temperature optim

32 binding activity, DNA helicase activity, and DNA-dependent ATPase activity consistent with the proper

33 e sequence dependency, while DNA binding and DNA-dependent ATPase activity did not.

34 1 protein, a component of SWI-SNF that has a DNA-dependent ATPase activity essential for SWI-SNF func

35 MgsA DNA-dependent ATPase activity is inhibited by single-str

36 in filament whose k(cat) for single-stranded DNA-dependent ATPase activity is reduced approximately 3

37 ther to dramatically stimulate the intrinsic DNA-dependent ATPase activity of DnaA via a process term

38 Analysis of the Ssl2 and DNA-dependent ATPase activity of TFIIH suggests that Ssl

39 The DNA-dependent ATPase activity of the Escherichia coli Re

40 it enhances the catalytic specificity of the DNA-dependent ATPase activity of the helicase-like subun

41 ICP8 specifically stimulated the DNA-dependent ATPase activity of the UL9 protein with DN

42 The DNA-dependent ATPase activity of UL9C111A protein is res

43 The DNA-dependent ATPase activity of UvrB is required to sup

44 Like SWI/SNF, RSC exhibits a DNA-dependent ATPase activity stimulated by both free an

45 Factor 2 demonstrated a strong DNA-dependent ATPase activity that correlated with its t

46 CSB also has a DNA-dependent ATPase activity that may play a role in re

47 an factor displayed a strong double-stranded DNA-dependent ATPase activity that was inhibited by sing

48 DnaBbetagamma had a DNA-dependent ATPase activity that was kinetically compa

49 ve for DNA replication, was found to possess DNA-dependent ATPase activity that was not responsive to

50 The hHcsA protein had a strong DNA-dependent ATPase activity that was stimulated >/=5-f

51 omplex, like the five-subunit RFC, contained DNA-dependent ATPase activity that was stimulated by PCN

52 in its strong inhibition of single-stranded DNA-dependent ATPase activity when uncoupled from the DN

53 The recombinant enzyme had DNA-dependent ATPase activity with an estimated kcat of

54 eSRS2-encodedproteinhasasingle-stranded (ss) DNA-dependent ATPase activity, a DNA helicase activity,

55 Rad51 protein has a DNA-dependent ATPase activity, and it catalyzes ATP-depe

56 at Rad54 protein possesses a double-stranded DNA-dependent ATPase activity, and that it interacts wit

57 of the N and C termini affect differentially DNA-dependent ATPase activity, and whereas a C-terminal

58 RP/SMARCAL1 protein exhibits single-stranded DNA-dependent ATPase activity, consistent with it being

59 olase active site of the AdnB subunit ablate DNA-dependent ATPase activity, DSB end resection, and AT

60 The protein has single-stranded DNA-dependent ATPase activity, includes seven helicase m

61 opose that factor X, which has an associated DNA-dependent ATPase activity, mediates the requirement

62 The mutants also show altered DNA-dependent ATPase activity, suggesting that the latch

63 i2 protein family, and it possesses a robust DNA-dependent ATPase activity, uses free energy from ATP

64 lthough the afRFC complex showed significant DNA-dependent ATPase activity, which could be further st

65 ut 9% of wild type levels of single-stranded DNA-dependent ATPase activity.

66 dation, DNA and RNA helicase activities, and DNA-dependent ATPase activity.

67 ase II transcript release factor, exhibits a DNA-dependent ATPase activity.

68 three subunits (p40, p37, and p36) contained DNA-dependent ATPase activity.

69 otifs I and II exhibit profound decreases in DNA-dependent ATPase activity.

70 -stranded DNA, and possesses single-stranded DNA-dependent ATPase activity.

71 higher KM for single-stranded DNA and lower DNA-dependent ATPase activity.

72 d DNA and decreased Kcat for single-stranded DNA-dependent ATPase activity.

73 substrates by perturbing its DNA binding and DNA-dependent ATPase activity.

74 direction and unwind duplex DNA utilizing a DNA-dependent ATPase activity.

75 ant protein when expressed in E. coli showed DNA-dependent ATPase activity.

76 POLQ further exhibited a single-stranded DNA-dependent ATPase activity.

77 All fragments exhibit DNA-dependent ATPase activity.

78 ee to which the G-quadruplex DNA can support DNA-dependent ATPase activity.

79 dicating that SUMOylation might regulate its DNA-dependent ATPase activity.

80 hRad51 protein possesses DNA-dependent ATPase activity; however, the role of this

81 Here, we show that BACH1 is both a DNA-dependent ATPase and a 5'-to-3' DNA helicase.

82 Mycobacterial UvrD1 is a DNA-dependent ATPase and a Ku-dependent 3' to 5' DNA hel

83 Therefore, (i) a prototypical DNA-dependent ATPase and ATP-stimulated DNA-binding prot

84 This enzyme is a double-stranded DNA-dependent ATPase and chromatin remodeller and was fo

85 nificantly attenuated DNA binding as well as DNA-dependent ATPase and DNA helicase activities, indica

86 Recombinant hDna2 has single-stranded DNA-dependent ATPase and DNA helicase activity.

87 HEL308 is a single-stranded DNA-dependent ATPase and DNA helicase.

88 t yeast DNA topoisomerase II exhibits robust DNA-dependent ATPase and DNA transport activities.

89 ected trinucleotide-repeating sequences, the DNA-dependent ATPase and DNA-binding activities of RecA

90 Purified WRNp has DNA-dependent ATPase and helicase activities consistent

91 l residues from RecQ severely diminishes its DNA-dependent ATPase and helicase activities, but does n

92 cells and demonstrated that hChlR1 possesses DNA-dependent ATPase and helicase activities.

93 ed levels of DNA binding and single-stranded DNA-dependent ATPase and helicase activities.

94 with and regulates the activity of DDX11, a DNA-dependent ATPase and helicase involved in DNA replic

95 RecA is a DNA-dependent ATPase and mediates homologous recombinati

96 he interaction between a particular class of DNA-dependent ATPase and their DNA effectors.

97 As a RecQ helicase family member, WRN is a DNA-dependent ATPase and unwinding enzyme, but also poss

98 s: (i) an ATP-dependent DNA helicase, (ii) a DNA-dependent ATPase, and (iii) a kinase with specificit

99 type of DNA synthesis which requires Rad5, a DNA-dependent ATPase, and also PCNA and Poldelta.

100 examined their role(s) in hexamer formation, DNA-dependent ATPase, and DNA helicase activities.

101 RNp, defective in WS, has helicase function, DNA-dependent ATPase, and exonuclease activity.

102 We find that the RFC(3/4) complex is a DNA-dependent ATPase, and we use this activity to determ

103 mon feature of fork remodeling, SNF2-family, DNA-dependent ATPases, and our study provides further me

104 Nuclear histone acetyltransferases, DNA-dependent ATPases, and transcriptional intermediary

105 ant hydrolyzes ATP rapidly, establishing the DNA-dependent ATPase as an intrinsic property of pol V M

106 in filaments, (ii) RadA is a single-stranded DNA-dependent ATPase at elevated temperatures, and (iii)

107 4/6/7 heterotrimer possessed single stranded DNA-dependent ATPase, ATP-dependent single stranded DNA

108 emodeling complexes based on the alternative DNA-dependent ATPases, Brg1 and Brm, plays essential rol

109 UvrD1 per se is a vigorous DNA-dependent ATPase but a feeble DNA helicase.

110 RecA is a DNA-dependent ATPase, but ATP hydrolysis is not required

111 We show that SftH is a monomeric DNA-dependent ATPase/dATPase that translocates 3' to 5'

112 We show that RqlH is a DNA-dependent ATPase/dATPase that translocates 3'-5' on

113 ciated with multiple biochemical activities: DNA-dependent ATPase, DNA helicase, and DNA nuclease.

114 erase II transcription factor that possesses DNA-dependent ATPase, DNA helicase, and protein kinase a

115 Mutation of lysine residue 798 in the DNA-dependent ATPase domain of BRG1 significantly reduce

116 by the catalytic subunit Snf2, containing a DNA-dependent ATPase domain.

117 ession, and provisional evidence for altered DNA-dependent ATPase expression in suicide only.

118 rand exchange protein: The RadA protein is a DNA-dependent ATPase, forms a nucleoprotein filament on

119 ight ( approximately 1.17 MDa) species, is a DNA-dependent ATPase, has 3'-->5' DNA helicase activity,

120 The heterotrimeric enzyme has DNA-dependent ATPase, helicase, and primase activities.

121 Rad5, a PCNA polyubiquitin ligase and DNA-dependent ATPase in yeast, is orthologous to putativ

122 ) and is a member of the SWI2/SNF2 family of DNA-dependent ATPases involved in chromatin remodeling.

123 Pontin/RUVBL1 and Reptin/RUVBL2 are DNA-dependent ATPases involved in numerous cellular proc

124 ease sensitivity of Ori(s) and single-strand DNA-dependent ATPase measurements of the UL9 protein ind

125 karos and Aiolos proteins associate with the DNA-dependent ATPase Mi-2 and histone deacetylases, in a

126 ap 2'-O-methyltransferase; A18 DNA helicase; DNA-dependent ATPase NPH-I; and DNA topoisomerase.

127 osphate phosphohydrolase-I), a virus-encoded DNA-dependent ATPase of the DExH-box family.

128 This screen identified BRM/SMARCA2, a DNA-dependent ATPase of the mammalian SWI/SNF (mSWI/SNF)

129 The lack of DNA-dependent ATPase of the mutant may indicate that bin

130 We demonstrate that it is feasible to target DNA-dependent ATPases of a particular type without affec

131 hTid-1 had no effect on the DNA-dependent ATPase or helicase activities associated w

132 ex lacked any detectable catalytic activity (DNA-dependent ATPase, primase, or RNA polymerase using a

133 he direct association of RAP94 with NPH I, a DNA-dependent ATPase required for transcription terminat

134 is a single-stranded DNA endonuclease and a DNA-dependent ATPase, suggesting that both of these acti

135 Rad26, a DNA dependent ATPase that is homologous to human CSB, ha

136 We show that topo IIbeta is a DNA-dependent ATPase that appears to fit Michaelis-Mente

137 Rad54 (SsoRad54) protein is a double-strand DNA-dependent ATPase that can alter the topology of dupl

138 We find that Cdc6 is an ORC- and origin DNA-dependent ATPase that functions at a step preceding

139 triphosphate phosphohydrolase I (NPH-I) is a DNA-dependent ATPase that serves as a transcription term

140 III tau and gamma subunits are single-strand DNA-dependent ATPases (the latter requires the delta and

141 ation factor (VTF), NPH I, a single stranded DNA-dependent ATPase, the virion form of RNA polymerase

142 erved motifs that are present in a family of DNA-dependent ATPases, the SWI2/SNF2-like proteins.

143 Within the superfamily of DNA-dependent ATPases, these compounds are most potent t

144 The SNF2/Brahma proteins are a class of DNA-dependent ATPases which activate gene expression by

145 and Rad26 belong to the Swi2/Snf2 family of DNA-dependent ATPases, which change DNA accessibility to

146 udied CS gene, CSB, codes for a Swi/Snf-like DNA-dependent ATPase, whose yeast homologue is called Ra

147 Mycobacterial UvrD2 is a DNA-dependent ATPase with 3' to 5' helicase activity.