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1 to degrade (p)ppGpp by a Mn(2+)-dependent 3'-pyrophosphohydrolase.
2 , ribosome and tRNA-independent, (p)ppGpp 3'-pyrophosphohydrolase.
3 enzyme MTH1 and possibly other Nudix-related pyrophosphohydrolases.
4 sopentenyl pyrophosphate isomerases and MutT pyrophosphohydrolases.
5 biochemical characterization of adenosine 3'-pyrophosphohydrolase 1 (Aph1), the founding member of a
6 rotected against 8-oxo-dGTP by 8-oxo-dGTP 5'-pyrophosphohydrolases (8-oxo-dGTP-ases) that convert it
7 bodies contain alkaline phosphatase and NTP pyrophosphohydrolase activities and can precipitate calc
9 gh TGFbeta increased nucleoside triphosphate pyrophosphohydrolase activity and decreased alkaline pho
10 all possess deoxyribonucleoside triphosphate pyrophosphohydrolase activity and that all four RdgB hom
11 vels of extracellular ATP in the presence of pyrophosphohydrolase activity indicates that ATP was con
12 ) is produced by the nucleoside triphosphate pyrophosphohydrolase activity of a family of isozymes, w
13 ical studies demonstrate that Rai1 possesses pyrophosphohydrolase activity towards 5' triphosphorylat
14 tly reported that the yeast Rai1 protein has pyrophosphohydrolase activity towards mRNAs lacking a 5'
15 The recombinant protein showed high DHNTP pyrophosphohydrolase activity with a K(m) value of 2 mic
16 had no effect on ACV nucleoside triphosphate pyrophosphohydrolase activity, suggesting that none of t
17 gh the inhibition of nucleoside triphosphate pyrophosphohydrolase activity, which generates inorganic
19 Pi by the ectoenzyme nucleoside triphosphate pyrophosphohydrolase also results in excessive ossificat
20 provide evidence for several additional RNA pyrophosphohydrolases, among them MutT, NudF, YmaB, and
21 degraded by incubation with the nonspecific pyrophosphohydrolase apyrase or with hexokinase and was
22 lling firmicute species B. subtilis, the RNA pyrophosphohydrolase BsRppH, a member of the Nudix famil
23 describe the mammalian enzyme DXO, which has pyrophosphohydrolase, decapping, and 5'-3' exoribonuclea
24 molog, Dom3Z (referred to as DXO), possesses pyrophosphohydrolase, decapping, and 5'-to-3' exoribonuc
25 kinase, nucleoside monophosphate kinase, and pyrophosphohydrolase families in archaeal genomes were e
29 We considered that the UDP-diacylglucosamine pyrophosphohydrolase LpxH could be responsible for this
30 tes the interaction between the 5' end-bound pyrophosphohydrolase MERS1 and 3' end-associated KPAF4 t
31 M0913 gene, has both nucleoside triphosphate pyrophosphohydrolase (NTPase) and pyrophosphatase activi
33 n and PPi-generating nucleoside triphosphate pyrophosphohydrolase (NTPPPH) activity are strongly link
35 may be hydrolyzed by nucleoside triphosphate pyrophosphohydrolase (NTPPPH), yielding an elevated PPi
36 ght binding of 8-oxo-nucleotides to the MutT pyrophosphohydrolase of Escherichia coli (129 residues),
37 er whether this reaction requires a specific pyrophosphohydrolase or is a metal ion-dependent chemica
38 ncodes a guanosine 3',5'-bis(diphosphate) 3'-pyrophosphohydrolase (ppGppase) as well as an apparent g
42 coli cells experiencing such stress, the RNA pyrophosphohydrolase RppH assumes a leading role in deca
43 phosphates of primary transcripts by the RNA pyrophosphohydrolase RppH triggers rapid 5'-exonucleolyt
45 l triphosphate to a monophosphate by the RNA pyrophosphohydrolase RppH, an event that triggers rapid
46 ing degradation via this pathway are the RNA pyrophosphohydrolase RppH, its heteromeric partner DapF,
47 ed RNA is the preferred substrate of the RNA pyrophosphohydrolase RppH, whose biological function was
48 monophosphate by a Nudix protein called RNA pyrophosphohydrolase (RppH), allowing access to both end
49 minal domain is distantly related to MutT, a pyrophosphohydrolase specific for 2'-deoxy-8-oxoguanosin
50 its E. coli counterpart, the B. subtilis RNA pyrophosphohydrolase that catalyzes this event is a Nudi
51 or another conserved nucleotide triphosphate pyrophosphohydrolase that functions as a mutator gene, t
52 protein RppH (formerly NudH/YgdP) is the RNA pyrophosphohydrolase that initiates mRNA decay by this 5
53 of them, HP1228 (renamed HpRppH), is an RNA pyrophosphohydrolase that triggers RNA degradation in H.
54 s characterized as a nucleoside triphosphate pyrophosphohydrolase which can hydrolyze all eight of th
56 eaving group, unlike its homologues the MutT pyrophosphohydrolase, which requires two, or Ap4A pyroph
57 rf17 gene is a novel nucleoside triphosphate pyrophosphohydrolase with a preference for dATP over the
58 er, unlike the other nucleoside triphosphate pyrophosphohydrolases with this conserved sequence, the