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1 ve "3A-like" protein), and p39 (the putative nucleoside triphosphatase).
2 ng two-thirds of NS3 serve as a helicase and nucleoside triphosphatase.
3 a point mutation, leaving a fully functional nucleoside triphosphatase.
4 ked to several large structural proteins and nucleoside triphosphatases.
5  in the following order: N-terminal protein; nucleoside triphosphatase; 20-kDa protein (p20); virus p
6 hat NTPDase2 (CD39L1, 75 kd), a preferential nucleoside triphosphatase, activates platelet aggregatio
7 ain-containing protein 1 (ELMOD1), a guanine nucleoside triphosphatase activating protein (GAP) for A
8 purified protein has been characterized as a nucleoside triphosphatase active on all of the canonical
9  strain differences in the transcriptase and nucleoside triphosphatase activities of cores.
10 eoside triphosphatase of Cet1p resembles the nucleoside triphosphatase activities of the baculovirus
11 This hexamer has ATPase and, more generally, nucleoside triphosphatase activities that are indistingu
12 ses primase, DNA helicase, and DNA-dependent nucleoside triphosphatase activities.
13                      A previously identified nucleoside triphosphatase activity in mammalian reovirus
14                          To characterize the nucleoside triphosphatase activity of 2C, we purified po
15                                          The nucleoside triphosphatase activity of the UL5/UL52 subas
16                            2C binds RNA, has nucleoside triphosphatase activity, and shares three mot
17  the M1 gene in viral RNA synthesis and core nucleoside triphosphatase activity, but there have been
18 elix-destabilizing properties, NSP2 exhibits nucleoside triphosphatase activity.
19 d nsP2 consists of an N-terminal domain with nucleoside triphosphatase and helicase activities and a
20 controlling the BAG1 and bradyzoite-specific nucleoside triphosphatase (B-NTPase) promoters.
21 ional inactivation of RNA triphosphatase and nucleoside triphosphatase functions (to approximately 1%
22 tinctive catalytic domains resembling P-loop nucleoside triphosphatases, have uniquely adapted this a
23 nd replicase activities through protease and nucleoside triphosphatase/helicase domains.
24      We report that protein 2C, the putative nucleoside triphosphatase/helicase protein of poliovirus
25  related but helicase-inactive RNA-dependent nucleoside-triphosphatase, HrpB.
26  is a metal-dependent tripolyphosphatase and nucleoside triphosphatase; it is not an adenylate cyclas
27                            Whereas all other nucleoside triphosphatase members of the superfamily rel
28  revealed that rNSP2 possessed an associated nucleoside triphosphatase (NTPase) activity in vitro, wh
29  nonspecifically, possesses a Mg2+-dependent nucleoside triphosphatase (NTPase) activity, and is a co
30 to 40S subunits and possesses 40S-stimulated nucleoside triphosphatase (NTPase) activity.
31 the N-terminal one-third of the protein, and nucleoside triphosphatase (NTPase) and helicase activiti
32                                     Here, by nucleoside triphosphatase (NTPase) assay and comparisons
33 -FLAG fusion protein was used in an in vitro nucleoside triphosphatase (NTPase) assay to show that UL
34                                    The LEF-4 nucleoside triphosphatase (NTPase) is activated by manga
35                                     Helicase/nucleoside triphosphatase (NTPase) motifs have been iden
36                                            A nucleoside triphosphatase (NTPase) present in highly pur
37 nging to the phosphate-binding loop (P-loop) nucleoside triphosphatase (NTPase) superfamily.
38                     A CDNA encoding a 47 kDa nucleoside triphosphatase (NTPase) that is associated wi
39  and frequently involves viral proteins with nucleoside triphosphatase (NTPase)/helicase motifs or ac
40                NS3 is also an RNA-stimulated nucleoside triphosphatase (NTPase)/RNA helicase and a 5'
41 tifs present in several viral RNA-stimulated nucleoside triphosphatase (NTPase)/RNA helicases.
42 ins annotated as putative nucleotide binding nucleoside triphosphatases (NTPases) or nucleoside triph
43 he DExH box family of nucleic acid-dependent nucleoside triphosphatases (NTPases), which is defined b
44          The manganese- and cobalt-dependent nucleoside triphosphatase of Cet1p resembles the nucleos
45 nd AVAST (antiviral adenosine triphosphatase/nucleoside triphosphatase of the STAND superfamily, Avs)
46           Many bacteria harbor RNA-dependent nucleoside-triphosphatases of the DEAH/RHA family, whose
47                           Orf141 (yfaO) is a nucleoside triphosphatase preferring pyrimidine deoxynuc
48  possesses a number of activities, including nucleoside triphosphatase, RNA binding, and helicase act
49 rotavirus nonstructural proteins, NSP2 (with nucleoside triphosphatase, single-stranded RNA [ssRNA] b
50 al protein NSP2 of rotavirus, which exhibits nucleoside triphosphatase, single-stranded RNA binding,
51 ed mu2 is itself a divalent cation-dependent nucleoside triphosphatase that can remove the 5' gamma-p
52 dent RNA polymerase (RdRp) 3, and RdRp-bound nucleoside triphosphatase u2 with a unique RNA-binding d
53 e the energy requirements for Ran from other nucleoside triphosphatases, we constructed a mutant deri
54 (ecto-ATPase) is a divalent cation-dependent nucleoside triphosphatase with an unusually high specifi
55 ombinant protein is active as a non-specific nucleoside triphosphatase, with k(cat)=7.6x10(-3) s(-1).