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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 rotected against 8-oxo-dGTP by 8-oxo-dGTP 5'-pyrophosphohydrolases (8-oxo-dGTP-ases) that convert it
6 bodies contain alkaline phosphatase and NTP pyrophosphohydrolase activities and can precipitate calc
7 gh TGFbeta increased nucleoside triphosphate pyrophosphohydrolase activity and decreased alkaline pho
8 all possess deoxyribonucleoside triphosphate pyrophosphohydrolase activity and that all four RdgB hom
9 vels of extracellular ATP in the presence of pyrophosphohydrolase activity indicates that ATP was con
10 ) is produced by the nucleoside triphosphate pyrophosphohydrolase activity of a family of isozymes, w
11 ical studies demonstrate that Rai1 possesses pyrophosphohydrolase activity towards 5' triphosphorylat
12 tly reported that the yeast Rai1 protein has pyrophosphohydrolase activity towards mRNAs lacking a 5'
13 The recombinant protein showed high DHNTP pyrophosphohydrolase activity with a K(m) value of 2 mic
14 had no effect on ACV nucleoside triphosphate pyrophosphohydrolase activity, suggesting that none of t
15 gh the inhibition of nucleoside triphosphate pyrophosphohydrolase activity, which generates inorganic
17 Pi by the ectoenzyme nucleoside triphosphate pyrophosphohydrolase also results in excessive ossificat
18 degraded by incubation with the nonspecific pyrophosphohydrolase apyrase or with hexokinase and was
19 describe the mammalian enzyme DXO, which has pyrophosphohydrolase, decapping, and 5'-3' exoribonuclea
20 molog, Dom3Z (referred to as DXO), possesses pyrophosphohydrolase, decapping, and 5'-to-3' exoribonuc
21 kinase, nucleoside monophosphate kinase, and pyrophosphohydrolase families in archaeal genomes were e
24 M0913 gene, has both nucleoside triphosphate pyrophosphohydrolase (NTPase) and pyrophosphatase activi
26 n and PPi-generating nucleoside triphosphate pyrophosphohydrolase (NTPPPH) activity are strongly link
28 may be hydrolyzed by nucleoside triphosphate pyrophosphohydrolase (NTPPPH), yielding an elevated PPi
29 ght binding of 8-oxo-nucleotides to the MutT pyrophosphohydrolase of Escherichia coli (129 residues),
30 er whether this reaction requires a specific pyrophosphohydrolase or is a metal ion-dependent chemica
31 ncodes a guanosine 3',5'-bis(diphosphate) 3'-pyrophosphohydrolase (ppGppase) as well as an apparent g
35 phosphates of primary transcripts by the RNA pyrophosphohydrolase RppH triggers rapid 5'-exonucleolyt
37 l triphosphate to a monophosphate by the RNA pyrophosphohydrolase RppH, an event that triggers rapid
38 ed RNA is the preferred substrate of the RNA pyrophosphohydrolase RppH, whose biological function was
39 monophosphate by a Nudix protein called RNA pyrophosphohydrolase (RppH), allowing access to both end
40 minal domain is distantly related to MutT, a pyrophosphohydrolase specific for 2'-deoxy-8-oxoguanosin
41 its E. coli counterpart, the B. subtilis RNA pyrophosphohydrolase that catalyzes this event is a Nudi
42 or another conserved nucleotide triphosphate pyrophosphohydrolase that functions as a mutator gene, t
43 protein RppH (formerly NudH/YgdP) is the RNA pyrophosphohydrolase that initiates mRNA decay by this 5
44 of them, HP1228 (renamed HpRppH), is an RNA pyrophosphohydrolase that triggers RNA degradation in H.
45 s characterized as a nucleoside triphosphate pyrophosphohydrolase which can hydrolyze all eight of th
47 eaving group, unlike its homologues the MutT pyrophosphohydrolase, which requires two, or Ap4A pyroph
48 rf17 gene is a novel nucleoside triphosphate pyrophosphohydrolase with a preference for dATP over the
49 er, unlike the other nucleoside triphosphate pyrophosphohydrolases with this conserved sequence, the
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