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1 e strain, suggesting that Ppk might act as a nucleoside diphosphate kinase.
2 eral phage-coded enzymes, as well as E. coli nucleoside diphosphate kinase.
3 The abnormal wing discs gene encodes a nucleoside diphosphate kinase.
4 s not support phosphotransferase activity by nucleoside diphosphate kinase.
5 to interact with the H2O2 signaling protein nucleoside diphosphate kinase 2 (NDPK2) and to inhibit i
7 ous H2O2, as well as analysis of a mutant in nucleoside diphosphate kinase 2 which also had increased
11 e the turnover of the multifunctional enzyme nucleoside diphosphate kinase A (NDPK-A) that controls c
12 idated the molecular interaction between the nucleoside diphosphate kinase A (NDPK-A)/AMP-activated p
13 Distinctive features of the poly P-driven nucleoside diphosphate kinase activity and structural as
14 re that such protein-lipid complexes inhibit nucleoside diphosphate kinase activity but are necessary
17 l defects; histidine 118, involved in Nm23's nucleoside diphosphate kinase activity; and serine 120,
18 Most NM23 proteins have phosphotransferase (nucleoside diphosphate kinase) activity, and the second
19 ficiencies in the ndk or dcd genes, encoding nucleoside diphosphate kinase and dCTP deaminase, respec
20 ential reactions catalyzed by luciferase and nucleoside diphosphate kinase and further illustrate thi
21 he mouse homologue of the rat gene), Ndk3 (a nucleoside diphosphate kinase), and six additional putat
22 a ubiquitous c-Myc transcription-activating nucleoside diphosphate kinase, and the core histone H2B
23 ch as peroxiredoxins, thioredoxin reductase, nucleoside-diphosphate kinase, and ribonucleotide-diphos
24 e analogs, disputing the classic notion that nucleoside diphosphate kinases are responsible for the p
25 ymatic activities, the 3'-5' exonuclease and nucleoside diphosphate kinase, are novel participants in
26 ate was based on ATP as the phosphate donor, nucleoside diphosphate kinase as the catalyst, coupled w
27 d support to the recently discovered role of nucleoside-diphosphate kinases as regulatory components
31 e isomerase, aconitate hydratase, M-protein, nucleoside diphosphate kinase B, and myoglobin are S-thi
32 creasing pancreatic Zn(2+) (hZnT8WT) induced nucleoside diphosphate kinase B, and Zn(2+) reduction (h
35 that an Escherichia coli ndk mutant, lacking nucleoside diphosphate kinase, can use adenylate kinase
38 2.7.1.40), creatine kinase (EC 2.7.3.2), and nucleoside diphosphate kinase (EC 2.7.4.6) were found to
40 i subunit of DNA polymerase, or loss of ndk (nucleoside diphosphate kinase) function fall into the la
41 --> ATP + polyP(n - 1) (Equation 2); general nucleoside-diphosphate kinase, GDP + polyP(n) --> GTP +
45 ein S23, putative 60S ribosomal protein L15, nucleoside diphosphate kinase III protein, regulator of
48 inase, pyruvate kinase, creatine kinase, and nucleoside diphosphate kinase increased 2-, 1.3-, 3-, an
49 n both prokaryotic and eukaryotic organisms, nucleoside diphosphate kinase is a multifunctional prote
54 vis BCG secretes two ATP-scavenging enzymes, nucleoside diphosphate kinase (Ndk) and ATPase, during g
55 Pseudomonas aeruginosa positively regulates nucleoside diphosphate kinase (Ndk) and succinyl-CoA syn
56 formation with the truncated 12-kDa form of nucleoside diphosphate kinase (Ndk) but not with the 16-
58 ification and characterization of the enzyme nucleoside diphosphate kinase (Ndk) from Mycobacterium s
59 mutagenesis procedures in the gene encoding nucleoside diphosphate kinase (ndk) from Pseudomonas aer
60 the nucleotide sequence of the gene encoding nucleoside diphosphate kinase (Ndk) from Pseudomonas aer
65 ontribute to the pathogenesis of infections, nucleoside diphosphate kinase (Ndk) mediates bacterially
66 cellular protease cleaves the 16 kDa form of nucleoside diphosphate kinase (Ndk) to a truncated 12 kD
67 matis can form complexes with human or yeast nucleoside diphosphate kinase (Ndk) to modulate their nu
68 at 650 nm is about 0.4, and they demonstrate nucleoside diphosphate kinase (Ndk), 5' nucleotidase, an
69 le all the strains secrete enzymes that have nucleoside diphosphate kinase (Ndk), adenylate kinase (A
70 (CF) patient secretes multiple enzymes with nucleoside diphosphate kinase (Ndk), ATPase, adenylate k
71 ccinyl-coenzyme A (CoA) synthetase (Scs) and nucleoside diphosphate kinase (Ndk), implying coregulati
72 lfilled largely by the ubiquitous and potent nucleoside diphosphate kinase (NDK), most commonly using
74 e pathway requires the gene for any of three nucleoside diphosphate kinases (ndk, pykA, or pykF) and
75 s and sea urchin sperm flagella also exhibit nucleoside-diphosphate kinase (NDK) activity, suggesting
76 omplex with both the 12- and 16-kDa forms of nucleoside-diphosphate kinase (Ndk) and predominantly sy
81 ne encodes the subunit of a protein that has nucleoside diphosphate kinase (NDP kinase) activity.
83 DnaK purified from ndk::km cells shows that nucleoside-diphosphate kinase (NDP kinase) is responsibl
85 llection of biochemical properties including nucleoside-diphosphate kinase (NDP kinase), DNA binding
88 ggest that the deregulation of mitochondrial nucleoside diphosphate kinase (NDPK) together with defec
91 og, exhibited normal autophosphorylation and nucleoside-diphosphate kinase (NDPK) characteristics but
92 ession and activity of the energy-generating nucleoside-diphosphate kinase (NDPK), and knockdown of h
99 ll three of these activities, as well as the nucleoside-diphosphate kinase, reside in the same protei
102 chemical mechanism(s) by which Nm23 proteins/nucleoside diphosphate kinases suppress tumor metastasis
106 demonstrate that infective larvae secrete a nucleoside diphosphate kinase when maintained in vitro.
107 is regulated by Abnormal wing disc (Awd), a nucleoside diphosphate kinase which converts nucleoside
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