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1 the polyP-binding domain of Escherichia coli exopolyphosphatase.
2 ood fold similarity between NTPDase3 and the exopolyphosphatase.
3 ficiency or neutralization using recombinant exopolyphosphatase.
4 ge disk on which it is hydrolyzed by a yeast exopolyphosphatase.
5 ate hydrolysis with Saccharomyces cerevisiae exopolyphosphatase 1 and S. cerevisiae inorganic pyropho
6  biallelic variants in PRUNE1 encoding prune exopolyphosphatase 1.
7 re shown to contain polyphosphate kinase and exopolyphosphatase activities.
8 anules, and genetic engineering to eliminate exopolyphosphatase activity increases metal accumulation
9 lization of protein structure and/or loss of exopolyphosphatase activity.
10                   Starved cells treated with exopolyphosphatase failed to aggregate effectively, sugg
11                                      Whereas exopolyphosphatases have been purified from yeast and a
12 tion and found genes associated with growth (exopolyphosphatase, HesB_IscA_SufA family protein), deto
13                      TcPPX differs from most exopolyphosphatases in its preference for short-chain po
14 t, in contrast to the yeast enzyme and other exopolyphosphatases investigated before, acts on polyP o
15 ion of NTPDase3, based on homology with this exopolyphosphatase, is consistent with the assignment of
16                                  Because the exopolyphosphatase leaves one pyrophosphate per polyphos
17 and characterization of the Leishmania major exopolyphosphatase (LmPPX).
18 of PPN1 and PPX1 (the gene encoding a potent exopolyphosphatase) loses viability rapidly in stationar
19                                              Exopolyphosphatase of Escherichia coli (PPX) is a highly
20                                          The exopolyphosphatase of Saccharomyces cerevisiae degraded
21  structural fold similarity with a bacterial exopolyphosphatase (PDB ).
22 entration is assayed by coupling the enzymes exopolyphosphatase (polyP into pyrophosphate), ATP sulfu
23  were reversed concomitantly when expressing exopolyphosphatase PPX from a recombinant plasmid, or by
24                 Recombinant Escherichia coli exopolyphosphatase (PPX) specifically degrades polyphosp
25 synthesizes poly-P reversibly from ATP, (ii) exopolyphosphatase (PPX), which hydrolyzes poly-P to P(i
26 of an operon with ppx, the gene that encodes exopolyphosphatase (PPX).
27 in devoid of vacuolar polyP by targeting the exopolyphosphatase Ppx1 to the vacuole and concomitantly
28 tis and Aquifex, PRUNE of Drosophila, and an exopolyphosphatase (PPX1) of Saccharomyces cereviseae.
29 1 (PPK1), polyphosphate kinase-2 (PPK2), and exopolyphosphatases (PPXs).
30                     LmPPX differs from other exopolyphosphatases previously investigated.
31 ideum and macrophages with recombinant yeast exopolyphosphatase reduced the survival of phagocytosed
32 nd characterization of the Trypanosoma cruzi exopolyphosphatase (TcPPX).
33 convert poly P and ADP to ATP and of a yeast exopolyphosphatase that can hydrolyze poly P to Pi, prov
34 des for a 45 kDa, metal-dependent, cytosolic exopolyphosphatase that processively cleaves the termina
35 pGpp of the hydrolytic breakdown of polyP by exopolyphosphatase, thereby blocking the dynamic turnove
36 J motifs are shared between exonucleases and exopolyphosphatases, they may constitute an ancient phos
37                                    Adding an exopolyphosphatase to cell cultures or stationary phase
38 ctional enzyme that was similar to the yeast exopolyphosphatase with respect to its Mg(2+) requiremen
39 d after addition of Saccharomyces cerevisiae exopolyphosphatase X to the bilayer, providing functiona