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1 s diadenosine tetraphosphate and diadenosine pentaphosphate.
2 kinase activity with P1,P5-di(adenosine-5') pentaphosphate.
5 on, bacterial organisms synthesize guanosine pentaphosphate and tetraphosphate, collectively denoted
6 s work showed that P(1),P(5)-di(adenosine-5')pentaphosphate (Ap(5)A), a specific adenylate kinases in
7 in that Ap(n)A's, in particular diadenosine pentaphosphate (Ap(5)A), were the preferred substrates.
9 , we identified P (1),P (5)-di(adenosine-5')-pentaphosphate (Ap5A) ammonium salt as an LdHSP78 inhibi
10 ine tetraphosphate (AP4A), P1,P5-diadenosine pentaphosphate (AP5A) and P1,P6-diadenosine hexaphosphat
11 bstrate inhibitor P(1),P(5)-di(adenosine-5') pentaphosphate (Ap5A) suggests that AMP binds to the con
14 ammaSL) or (2) ADP (i.e., P1, P5-diadenosine pentaphosphate, AP5A), reduced the affinity by only appr
15 ds for synthesizing nucleoside 5'-tetra- and pentaphosphates as well as dinucleoside 5',5'-oligophosp
16 the preparation and properties of dimerized pentaphosphate-bridged deoxynucleotides (dicaptides) tha
18 one nucleotides guanosine tetraphosphate and pentaphosphate, commonly referred to as (p)ppGpp, regula
21 tive center probe P(1),P(5)-di(adenosine-5') pentaphosphate interacted simultaneously with an AMP-bin
23 hA, catalyzing the hydrolysis of diadenosine pentaphosphates, may also play a role in facilitating P.
24 ATP conversion was inhibited by diadenosine pentaphosphate, oligomycin, and UDP, suggesting the invo
25 The purinergic P2/P4 antagonist di-inosine pentaphosphate or P1-receptor antagonist sulfonylphenyl
26 for a guanosine tetraphosphate and guanosine pentaphosphate [(p)ppGpp] synthetase/hydrolase, in biofi
27 the nucleotides guanosine tetraphosphate and pentaphosphate [(p)ppGpp], which interact with target pr
30 ndent on the UvrD helicase and the guanosine pentaphosphate (ppGpp) alarmone/stringent response regul
31 anosine tetraphosphate (ppGpp) and guanosine pentaphosphate (pppGpp) [collectively named "(p)ppGpp"]
33 ponse alarmones guanosine tetra- (ppGpp) and pentaphosphate (pppGpp) control a global response allowi
34 anosine tetraphosphate (ppGpp) and guanosine pentaphosphate (pppGpp) in response to nutrient deprivat
35 anosine tetraphosphate (ppGpp) and guanosine pentaphosphate (pppGpp), generated in response to amino
36 two synthetic derivatives: namely quercetin pentaphosphate (QPP) and quercetin sulfonic acid (QSA).
37 and the impermeant AK inhibitor, diadenosine pentaphosphate, reduced ADPase activity by more than 70%
38 h polynucleotide phosphorylase and guanosine pentaphosphate synthetase activities in the cloning host
40 Further investigation showed that guanosine pentaphosphate/tetraphosphate (henceforth ppGpp) and SOS
41 nable to catalyze the synthesis of guanosine pentaphosphate under conditions in which GPSI was highly
43 o biosynthesize guanosine tetraphosphate and pentaphosphate was severely affected; the mutant showed
45 reus is mediated by the nucleotide guanosine pentaphosphate, whose synthesis is catalyzed by the prod