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1  support the assigned in vivo function as an inorganic pyrophosphatase.
2 t these enzymes reversibly phosphorylated an inorganic pyrophosphatase.
3 a protein that was 80% similar to the enzyme inorganic pyrophosphatase.
4 TP sulfurylase, a recombinant APS kinase and inorganic pyrophosphatase.
5    NURF-38 is strikingly homologous to known inorganic pyrophosphatases.
6 c enzymes including glutamine synthetase and inorganic pyrophosphatase 1 in vitro, in cells and in vi
7 isiae exopolyphosphatase 1 and S. cerevisiae inorganic pyrophosphatase 1, followed by colorimetric or
8    ZmCIPK12 interacts with the maize-soluble inorganic pyrophosphatase 4 (ZmPPase4) and inhibits its
9                                  Further, an inorganic pyrophosphatase activity was identified which
10  the purified NURF complex are shown to have inorganic pyrophosphatase activity.
11             Acetone carboxylase did not have inorganic pyrophosphatase activity.
12 was evaluated in the absence and presence of inorganic pyrophosphatase and elongation factor Tu.
13              Structural comparisons with the inorganic pyrophosphatases and analysis of the ligand-bo
14  been described as the DHH family, including inorganic pyrophosphatases and RecJ ssDNA exonucleases.
15  the action of acetyl coenzyme A synthetase, inorganic pyrophosphatase, and the bifunctional Escheric
16                                              Inorganic pyrophosphatases are required for anabolism to
17               To estimate the proficiency of inorganic pyrophosphatase as a catalyst, (31)P NMR was u
18 f phosphoesterases, which includes: family-2 inorganic pyrophosphatases, found in Gram-positive bacte
19 tb DnaG to that of another essential enzyme, inorganic pyrophosphatase from M. tuberculosis (Mtb PPia
20  is a coupled assay in which the addition of inorganic pyrophosphatase initially cleaves the pyrophos
21                                              Inorganic pyrophosphatase (IPPase) from Thermococcus thi
22 e (P(i)) concentrations after degradation by inorganic pyrophosphatase of the PP(i) released during a
23 s reveal a strong similarity to the family-2 inorganic pyrophosphatases, particularly in the active-s
24 tations in the nuclear-encoded mitochondrial inorganic pyrophosphatase (PPA2) that are associated wit
25  both Stk1 and Stp1 as a manganese-dependent inorganic pyrophosphatase (PpaC) by liquid chromatograph
26                                      Soluble inorganic pyrophosphatase (PPase), which converts inorga
27 te, Trypanosoma, encodes soluble versions of inorganic pyrophosphatases (PPase), also called vacuolar
28                               Type I soluble inorganic pyrophosphatases (PPases) are well characteriz
29 n [pH]cyt inhibits the activity of a soluble inorganic pyrophosphatase required for pollen tube growt
30                 Addition of commercial yeast inorganic pyrophosphatase shifts the equilibrium of the
31 translational regulation of Family I soluble inorganic pyrophosphatases (sPPases) may affect their ac
32 , Pr-p26.1a and Pr-p26.1b, which are soluble inorganic pyrophosphatases (sPPases).
33 xI which is also found at the active site of inorganic pyrophosphatases, suggesting a potential pyrop
34 alcification induced in aortas cultured with inorganic pyrophosphatase, the inhibition of calcificati
35 yltransferase reaction is rapidly cleaved by inorganic pyrophosphatase to form phosphate (Pi), which
36             Recently, a new class of soluble inorganic pyrophosphatase (type-C PPase) has been descri
37 r the reaction catalyzed by Escherichia coli inorganic pyrophosphatase using isothermal titration cal
38            Plant vacuolar H(+)-translocating inorganic pyrophosphatases (V-PPases; EC 3.6.1.1) have b
39 from fibroblasts showed that the activity of inorganic pyrophosphatase was significantly reduced in a
40 1, peroxiredoxin 2, nucleophosmin 1/B23, and inorganic pyrophosphatase were decreased in MCF7/AdVp300