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1 nother double helix is passed, and acts as a DNA dependent ATPase.
2 re-specific nuclease, 5'-to-3' helicase, and DNA-dependent ATPase.
3 ATP-dependent helicase and a single-stranded DNA-dependent ATPase.
4 neity from yeast cells and show that it is a DNA-dependent ATPase.
5 f ATP-dependent, in vitro reactions and is a DNA-dependent ATPase.
6 sphohydrolase I (NPH I) is a single-stranded DNA-dependent ATPase.
7 hanisms to specifically target this class of DNA-dependent ATPases.
8 ts subunits, the RecB and RecD proteins, are DNA-dependent ATPases.
9 is a member of the SWI/SNF protein family of DNA-dependent ATPases.
10  family members and less potent toward other DNA-dependent ATPases.
11 activated DNA polymerase V (pol V Mut), is a DNA-dependent ATPase; (2) bound ATP is required for DNA
12 tifunctional enzyme with 5'-3' DNA helicase, DNA-dependent ATPase, 3' exo/endonuclease, and 5' exo/en
13 ds inhibit the ATPase activity of the active DNA-dependent ATPase A domain (ADAAD) by competing with
14 n (HARP) protein (also known as SMARCAL1 and DNA-dependent ATPase A) is an annealing helicase that re
15 ytic function of an SWI2/SNF2 family member: DNA-dependent ATPase A.
16                                    RadA is a DNA-dependent ATPase, a DNA-binding protein and can stim
17 ein exhibits defects in its DNA helicase and DNA-dependent ATPase activities and was unable to suppor
18                  Although strand passage and DNA-dependent ATPase activities are affected in these mu
19  inhibited the helicase, the primase and the DNA-dependent ATPase activities of the enzyme with IC50
20                         The DNA helicase and DNA-dependent ATPase activities of UL9 protein were stim
21 hat Rad51-K342E displays DNA-independent and DNA-dependent ATPase activities, owing to its ability to
22  5'-3' endonuclease, the 5'-3' helicase, and DNA-dependent ATPase activities.
23 r interaction, which in turn activates their DNA-dependent ATPase activity (intermolecular mode).
24          Mutations in motifs III-VI decrease DNA-dependent ATPase activity 3-6-fold.
25                       The protein has a weak DNA-dependent ATPase activity and binds both single-stra
26       The UL52-UL8 complex lacked detectable DNA-dependent ATPase activity and could not synthesize p
27                   The purified protein has a DNA-dependent ATPase activity and is a 3'-5' DNA helicas
28 single- and double-stranded DNA, possesses a DNA-dependent ATPase activity and promotes intermolecula
29   The mutant enzyme, however, is impaired in DNA-dependent ATPase activity and single-stranded DNA bi
30 ified Pfh1 protein displayed single-stranded DNA-dependent ATPase activity as well as 5' to 3' DNA he
31                                   RgyB has a DNA-dependent ATPase activity at high temperature (80 de
32  RuvB proteins showed strong double-stranded DNA-dependent ATPase activity at their temperature optim
33 1 characterized originally displays vigorous DNA-dependent ATPase activity but only feeble helicase a
34 binding activity, DNA helicase activity, and DNA-dependent ATPase activity consistent with the proper
35 e sequence dependency, while DNA binding and DNA-dependent ATPase activity did not.
36 1 protein, a component of SWI-SNF that has a DNA-dependent ATPase activity essential for SWI-SNF func
37                                         MgsA DNA-dependent ATPase activity is inhibited by single-str
38 in filament whose k(cat) for single-stranded DNA-dependent ATPase activity is reduced approximately 3
39 ther to dramatically stimulate the intrinsic DNA-dependent ATPase activity of DnaA via a process term
40                     Analysis of the Ssl2 and DNA-dependent ATPase activity of TFIIH suggests that Ssl
41                                          The DNA-dependent ATPase activity of the Escherichia coli Re
42 it enhances the catalytic specificity of the DNA-dependent ATPase activity of the helicase-like subun
43                               Inhibiting the DNA-dependent ATPase activity of the TFIIH complex subun
44             ICP8 specifically stimulated the DNA-dependent ATPase activity of the UL9 protein with DN
45                                          The DNA-dependent ATPase activity of UL9C111A protein is res
46                                          The DNA-dependent ATPase activity of UvrB is required to sup
47                 Like SWI/SNF, RSC exhibits a DNA-dependent ATPase activity stimulated by both free an
48               Factor 2 demonstrated a strong DNA-dependent ATPase activity that correlated with its t
49                               CSB also has a DNA-dependent ATPase activity that may play a role in re
50 an factor displayed a strong double-stranded DNA-dependent ATPase activity that was inhibited by sing
51                          DnaBbetagamma had a DNA-dependent ATPase activity that was kinetically compa
52 ve for DNA replication, was found to possess DNA-dependent ATPase activity that was not responsive to
53               The hHcsA protein had a strong DNA-dependent ATPase activity that was stimulated >/=5-f
54 omplex, like the five-subunit RFC, contained DNA-dependent ATPase activity that was stimulated by PCN
55  in its strong inhibition of single-stranded DNA-dependent ATPase activity when uncoupled from the DN
56                   The recombinant enzyme had DNA-dependent ATPase activity with an estimated kcat of
57 eSRS2-encodedproteinhasasingle-stranded (ss) DNA-dependent ATPase activity, a DNA helicase activity,
58                          Rad51 protein has a DNA-dependent ATPase activity, and it catalyzes ATP-depe
59 at Rad54 protein possesses a double-stranded DNA-dependent ATPase activity, and that it interacts wit
60 of the N and C termini affect differentially DNA-dependent ATPase activity, and whereas a C-terminal
61 RP/SMARCAL1 protein exhibits single-stranded DNA-dependent ATPase activity, consistent with it being
62 olase active site of the AdnB subunit ablate DNA-dependent ATPase activity, DSB end resection, and AT
63              The protein has single-stranded DNA-dependent ATPase activity, includes seven helicase m
64 opose that factor X, which has an associated DNA-dependent ATPase activity, mediates the requirement
65                The mutants also show altered DNA-dependent ATPase activity, suggesting that the latch
66 tor (GTF) TFIIH, drives scanning through its DNA-dependent ATPase activity, therefore potentially con
67 i2 protein family, and it possesses a robust DNA-dependent ATPase activity, uses free energy from ATP
68 lthough the afRFC complex showed significant DNA-dependent ATPase activity, which could be further st
69 ut 9% of wild type levels of single-stranded DNA-dependent ATPase activity.
70 dation, DNA and RNA helicase activities, and DNA-dependent ATPase activity.
71 ase II transcript release factor, exhibits a DNA-dependent ATPase activity.
72 dicating that SUMOylation might regulate its DNA-dependent ATPase activity.
73 three subunits (p40, p37, and p36) contained DNA-dependent ATPase activity.
74 otifs I and II exhibit profound decreases in DNA-dependent ATPase activity.
75 -stranded DNA, and possesses single-stranded DNA-dependent ATPase activity.
76  higher KM for single-stranded DNA and lower DNA-dependent ATPase activity.
77 d DNA and decreased Kcat for single-stranded DNA-dependent ATPase activity.
78 ->5' DNA helicase activity, and WRNIP1 has a DNA-dependent ATPase activity.
79 n addition, we show the YoaA-chi complex has DNA-dependent ATPase activity.
80 substrates by perturbing its DNA binding and DNA-dependent ATPase activity.
81  direction and unwind duplex DNA utilizing a DNA-dependent ATPase activity.
82 ant protein when expressed in E. coli showed DNA-dependent ATPase activity.
83     POLQ further exhibited a single-stranded DNA-dependent ATPase activity.
84                        All fragments exhibit DNA-dependent ATPase activity.
85 ee to which the G-quadruplex DNA can support DNA-dependent ATPase activity.
86                     hRad51 protein possesses DNA-dependent ATPase activity; however, the role of this
87           Here, we show that BACH1 is both a DNA-dependent ATPase and a 5'-to-3' DNA helicase.
88                     Mycobacterial UvrD1 is a DNA-dependent ATPase and a Ku-dependent 3' to 5' DNA hel
89                Therefore, (i) a prototypical DNA-dependent ATPase and ATP-stimulated DNA-binding prot
90             This enzyme is a double-stranded DNA-dependent ATPase and chromatin remodeller and was fo
91 nificantly attenuated DNA binding as well as DNA-dependent ATPase and DNA helicase activities, indica
92        Recombinant hDna2 has single-stranded DNA-dependent ATPase and DNA helicase activity.
93                  HEL308 is a single-stranded DNA-dependent ATPase and DNA helicase.
94 t yeast DNA topoisomerase II exhibits robust DNA-dependent ATPase and DNA transport activities.
95 ected trinucleotide-repeating sequences, the DNA-dependent ATPase and DNA-binding activities of RecA
96                            Purified WRNp has DNA-dependent ATPase and helicase activities consistent
97 l residues from RecQ severely diminishes its DNA-dependent ATPase and helicase activities, but does n
98 cells and demonstrated that hChlR1 possesses DNA-dependent ATPase and helicase activities.
99 ed levels of DNA binding and single-stranded DNA-dependent ATPase and helicase activities.
100  with and regulates the activity of DDX11, a DNA-dependent ATPase and helicase involved in DNA replic
101                                    RecA is a DNA-dependent ATPase and mediates homologous recombinati
102 he interaction between a particular class of DNA-dependent ATPase and their DNA effectors.
103   As a RecQ helicase family member, WRN is a DNA-dependent ATPase and unwinding enzyme, but also poss
104 s: (i) an ATP-dependent DNA helicase, (ii) a DNA-dependent ATPase, and (iii) a kinase with specificit
105 type of DNA synthesis which requires Rad5, a DNA-dependent ATPase, and also PCNA and Poldelta.
106 examined their role(s) in hexamer formation, DNA-dependent ATPase, and DNA helicase activities.
107 RNp, defective in WS, has helicase function, DNA-dependent ATPase, and exonuclease activity.
108       We find that the RFC(3/4) complex is a DNA-dependent ATPase, and we use this activity to determ
109 mon feature of fork remodeling, SNF2-family, DNA-dependent ATPases, and our study provides further me
110          Nuclear histone acetyltransferases, DNA-dependent ATPases, and transcriptional intermediary
111 ant hydrolyzes ATP rapidly, establishing the DNA-dependent ATPase as an intrinsic property of pol V M
112 in filaments, (ii) RadA is a single-stranded DNA-dependent ATPase at elevated temperatures, and (iii)
113 4/6/7 heterotrimer possessed single stranded DNA-dependent ATPase, ATP-dependent single stranded DNA
114 emodeling complexes based on the alternative DNA-dependent ATPases, Brg1 and Brm, plays essential rol
115                   UvrD1 per se is a vigorous DNA-dependent ATPase but a feeble DNA helicase.
116                                    RecA is a DNA-dependent ATPase, but ATP hydrolysis is not required
117             We show that SftH is a monomeric DNA-dependent ATPase/dATPase that translocates 3' to 5'
118                       We show that RqlH is a DNA-dependent ATPase/dATPase that translocates 3'-5' on
119 ciated with multiple biochemical activities: DNA-dependent ATPase, DNA helicase, and DNA nuclease.
120 erase II transcription factor that possesses DNA-dependent ATPase, DNA helicase, and protein kinase a
121        Mutation of lysine residue 798 in the DNA-dependent ATPase domain of BRG1 significantly reduce
122  by the catalytic subunit Snf2, containing a DNA-dependent ATPase domain.
123 ession, and provisional evidence for altered DNA-dependent ATPase expression in suicide only.
124 rand exchange protein: The RadA protein is a DNA-dependent ATPase, forms a nucleoprotein filament on
125 ight ( approximately 1.17 MDa) species, is a DNA-dependent ATPase, has 3'-->5' DNA helicase activity,
126                The heterotrimeric enzyme has DNA-dependent ATPase, helicase, and primase activities.
127 repair functions and harbors the XPB and XPD DNA-dependent ATPase/helicase subunits, which are affect
128        Rad5, a PCNA polyubiquitin ligase and DNA-dependent ATPase in yeast, is orthologous to putativ
129 ) and is a member of the SWI2/SNF2 family of DNA-dependent ATPases involved in chromatin remodeling.
130          Pontin/RUVBL1 and Reptin/RUVBL2 are DNA-dependent ATPases involved in numerous cellular proc
131 ease sensitivity of Ori(s) and single-strand DNA-dependent ATPase measurements of the UL9 protein ind
132 karos and Aiolos proteins associate with the DNA-dependent ATPase Mi-2 and histone deacetylases, in a
133 ap 2'-O-methyltransferase; A18 DNA helicase; DNA-dependent ATPase NPH-I; and DNA topoisomerase.
134 osphate phosphohydrolase-I), a virus-encoded DNA-dependent ATPase of the DExH-box family.
135        This screen identified BRM/SMARCA2, a DNA-dependent ATPase of the mammalian SWI/SNF (mSWI/SNF)
136                                  The lack of DNA-dependent ATPase of the mutant may indicate that bin
137 We demonstrate that it is feasible to target DNA-dependent ATPases of a particular type without affec
138                  hTid-1 had no effect on the DNA-dependent ATPase or helicase activities associated w
139 ex lacked any detectable catalytic activity (DNA-dependent ATPase, primase, or RNA polymerase using a
140 he direct association of RAP94 with NPH I, a DNA-dependent ATPase required for transcription terminat
141  is a single-stranded DNA endonuclease and a DNA-dependent ATPase, suggesting that both of these acti
142                                     Rad26, a DNA dependent ATPase that is homologous to human CSB, ha
143                We show that topo IIbeta is a DNA-dependent ATPase that appears to fit Michaelis-Mente
144  Rad54 (SsoRad54) protein is a double-strand DNA-dependent ATPase that can alter the topology of dupl
145      We find that Cdc6 is an ORC- and origin DNA-dependent ATPase that functions at a step preceding
146 tic activity of TraB, revealing that it is a DNA-dependent ATPase that is highly stimulated by dsDNA
147 triphosphate phosphohydrolase I (NPH-I) is a DNA-dependent ATPase that serves as a transcription term
148 III tau and gamma subunits are single-strand DNA-dependent ATPases (the latter requires the delta and
149 ation factor (VTF), NPH I, a single stranded DNA-dependent ATPase, the virion form of RNA polymerase
150 erved motifs that are present in a family of DNA-dependent ATPases, the SWI2/SNF2-like proteins.
151                    Within the superfamily of DNA-dependent ATPases, these compounds are most potent t
152      The SNF2/Brahma proteins are a class of DNA-dependent ATPases which activate gene expression by
153  and Rad26 belong to the Swi2/Snf2 family of DNA-dependent ATPases, which change DNA accessibility to
154 udied CS gene, CSB, codes for a Swi/Snf-like DNA-dependent ATPase, whose yeast homologue is called Ra
155                     Mycobacterial UvrD2 is a DNA-dependent ATPase with 3' to 5' helicase activity.

 
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