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1  kinase activity with P1,P5-di(adenosine-5') pentaphosphate.
2 s diadenosine tetraphosphate and diadenosine pentaphosphate.
3 P and was prevented by P1,P5-di-adenosine-5'-pentaphosphate, an inhibitor of adenylate kinase.
4 s work showed that P(1),P(5)-di(adenosine-5')pentaphosphate (Ap(5)A), a specific adenylate kinases in
5  in that Ap(n)A's, in particular diadenosine pentaphosphate (Ap(5)A), were the preferred substrates.
6 h high specificity for diadenosine hexa- and pentaphosphates (Ap(6)A and Ap(5)A).
7 ine tetraphosphate (AP4A), P1,P5-diadenosine pentaphosphate (AP5A) and P1,P6-diadenosine hexaphosphat
8 bstrate inhibitor P(1),P(5)-di(adenosine-5') pentaphosphate (Ap5A) suggests that AMP binds to the con
9                ADP, UTP, P1, P5-di-adenosine pentaphosphate (AP5A), adenosine and alpha, beta-methyle
10 isubstrate inhibitor P1, P5-bis(5'-adenosyl) pentaphosphate (AP5A).
11 ammaSL) or (2) ADP (i.e., P1, P5-diadenosine pentaphosphate, AP5A), reduced the affinity by only appr
12 phosphates with a preference for diadenosine pentaphosphate, from which it forms ATP and ADP.
13              With P(1),P(5)-di(adenosine 5')-pentaphosphate (inhibitor of AK activity), no extracellu
14 tive center probe P(1),P(5)-di(adenosine-5') pentaphosphate interacted simultaneously with an AMP-bin
15 cap with guanosine 5'-tetraphosphate to form pentaphosphate-linked G(5')pppppRNA.
16 hA, catalyzing the hydrolysis of diadenosine pentaphosphates, may also play a role in facilitating P.
17  ATP conversion was inhibited by diadenosine pentaphosphate, oligomycin, and UDP, suggesting the invo
18   The purinergic P2/P4 antagonist di-inosine pentaphosphate or P1-receptor antagonist sulfonylphenyl
19 for a guanosine tetraphosphate and guanosine pentaphosphate [(p)ppGpp] synthetase/hydrolase, in biofi
20 the nucleotides guanosine tetraphosphate and pentaphosphate [(p)ppGpp], which interact with target pr
21  activity with GTP, followed by adenosine 5'-pentaphosphate (p5A) and dGTP.
22 ndent on the UvrD helicase and the guanosine pentaphosphate (ppGpp) alarmone/stringent response regul
23 anosine tetraphosphate (ppGpp) and guanosine pentaphosphate (pppGpp) [collectively named "(p)ppGpp"]
24           The alarmone nucleotides guanosine pentaphosphate (pppGpp) and tetraphosphate (ppGpp), coll
25 ponse alarmones guanosine tetra- (ppGpp) and pentaphosphate (pppGpp) control a global response allowi
26 anosine tetraphosphate (ppGpp) and guanosine pentaphosphate (pppGpp), generated in response to amino
27  two synthetic derivatives: namely quercetin pentaphosphate (QPP) and quercetin sulfonic acid (QSA).
28 and the impermeant AK inhibitor, diadenosine pentaphosphate, reduced ADPase activity by more than 70%
29 h polynucleotide phosphorylase and guanosine pentaphosphate synthetase activities in the cloning host
30            The gene for the enzyme guanosine pentaphosphate synthetase I (GPSI) from Streptomyces ant
31 nable to catalyze the synthesis of guanosine pentaphosphate under conditions in which GPSI was highly
32                      P1, P5-di(adenosine-5') pentaphosphate was found to be a competitive inhibitor o
33 o biosynthesize guanosine tetraphosphate and pentaphosphate was severely affected; the mutant showed
34 reus is mediated by the nucleotide guanosine pentaphosphate, whose synthesis is catalyzed by the prod

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