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1 p in InsP6 biosynthesis) or Escherichia coli polyphosphate kinase.
2 ARG82/IPK2, which encodes a nuclear inositol polyphosphate kinase.
3 e phospholipase C and two potential inositol polyphosphate kinases.
4 , we pay particular attention to the enzyme, polyphosphate kinase 1 (Poly P kinase 1 or PPK1), respon
5 quantitative real-time PCR (qPCR) assays for polyphosphate kinase 1 (ppk1) and 16S rRNA genes to asse
7 ed consequences of inactivating the gene for polyphosphate kinase 1 (ppk1) in strains of Helicobacter
9 nsport (pstSCAB-phoU) operon: no increase in polyphosphate kinase 1 (ppk1) transcript abundance was o
12 hosphate (polyP) is primarily synthesized by Polyphosphate Kinase-1 (PPK-1) and regulates numerous ce
13 of PolyP are modulated by the activities of polyphosphate kinase-1 (PPK1), polyphosphate kinase-2 (P
14 activities of polyphosphate kinase-1 (PPK1), polyphosphate kinase-2 (PPK2), and exopolyphosphatases (
15 catalyzed by starch and glycogen synthases, polyphosphate kinase (a polymerase), cyanophycin synthet
16 hydroxybutyrate synthesis, and ppk, encoding polyphosphate kinase, all indicated no defect in Ca(2+)
17 h, we employ an engineered acid phosphatase, polyphosphate kinase and acetate kinase to produce 2'-O-
18 sults, acidocalcisomes were shown to contain polyphosphate kinase and exopolyphosphatase activities.
20 Here, we report a requirement for inositol polyphosphate kinases, AtIPK1 and AtIPK2beta, for the la
23 ication and characterization of two inositol polyphosphate kinases from Arabidopsis thaliana, designa
25 d provide insights into the role of inositol polyphosphate kinases in phosphate signaling biology.
27 are a group of calmodulin-regulated inositol polyphosphate kinases (IPKs) that convert the second mes
28 per tetramer by an enzymatic assay in which polyphosphate kinase is used to transfer phosphates from
29 ositol kinases, including the yeast inositol polyphosphate kinase Kcs1, which principally generates p
30 ity and resistance to heat and H2O2; neither polyphosphate kinase nor long-chain poly P was restored.
36 n and ready availability of Escherichia coli polyphosphate kinase (PPK) that can convert poly P and A
37 xiliary NDK-like activity in the capacity of polyphosphate kinase (PPK) to use inorganic polyphosphat
40 sformation protocol to create mutants in the polyphosphate kinase (ppk), the major enzyme responsible
43 an additional component of the degradosome, polyphosphate kinase (PPK), which catalyses the reversib
44 inorganic polyphosphate (polyP) from ATP by polyphosphate kinase (PPK; EC 2.7.4.1) of Escherichia co
45 s trigger polyphosphate (polyP) synthesis by polyphosphate kinase (PPK1), including heat, nutrient re
46 that heterologous expression of rat inositol polyphosphate kinases rIPK2, a dual specificity inositol
47 t the yeast protein, ArgRIII, is an inositol-polyphosphate kinase that can convert InsP(3) to InsP(4)
48 polyphosphate, and reduced expression of the polyphosphate kinase that synthesizes polyphosphate decr
49 ed a new family of highly conserved inositol-polyphosphate kinases that contain a newly identified, u
50 te that mutations in genes encoding inositol polyphosphate kinases that produce IP4, IP5, and IP6 imp
51 erichia coli mutant (ppk) lacking the enzyme polyphosphate kinase, which makes long chains of inorgan