ライフサイエンスコーパス: nucleoside diphosphate kinase

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 ucleotide reductase, thymidine kinase 1, and nucleoside-diphosphate kinase.

6 e describe a new phagocytic function for the nucleoside diphosphate kinase 1 (NDK-1), the nematode co

7 to interact with the H2O2 signaling protein nucleoside diphosphate kinase 2 (NDPK2) and to inhibit i

8 Arabidopsis nucleoside diphosphate kinase 2 (NDPK2) is a component i

9 ous H2O2, as well as analysis of a mutant in nucleoside diphosphate kinase 2 which also had increased

10 A high level of nucleoside diphosphate kinase A (NDPK A/nm23-H1) in neur

11 We report that nucleoside diphosphate kinase A (NDPK-A) interacts with

12 Nucleoside diphosphate kinase A (NDPK-A) regulates the a

13 e the turnover of the multifunctional enzyme nucleoside diphosphate kinase A (NDPK-A) that controls c

14 idated the molecular interaction between the nucleoside diphosphate kinase A (NDPK-A)/AMP-activated p

15 goes endocytosis due to the induction of the nucleoside diphosphate kinase Abnormal Wing Disc (AWD).

16 Distinctive features of the poly P-driven nucleoside diphosphate kinase activity and structural as

17 re that such protein-lipid complexes inhibit nucleoside diphosphate kinase activity but are necessary

18 Therefore, nucleoside diphosphate kinase activity cannot explain th

19 a complex with RCC1L, which together perform nucleoside diphosphate kinase activity to maintain local

20 Nucleoside diphosphate kinase activity was present in bo

21 l defects; histidine 118, involved in Nm23's nucleoside diphosphate kinase activity; and serine 120,

22 Most NM23 proteins have phosphotransferase (nucleoside diphosphate kinase) activity, and the second

23 ficiencies in the ndk or dcd genes, encoding nucleoside diphosphate kinase and dCTP deaminase, respec

24 ential reactions catalyzed by luciferase and nucleoside diphosphate kinase and further illustrate thi

25 he mouse homologue of the rat gene), Ndk3 (a nucleoside diphosphate kinase), and six additional putat

26 a ubiquitous c-Myc transcription-activating nucleoside diphosphate kinase, and the core histone H2B

27 ch as peroxiredoxins, thioredoxin reductase, nucleoside-diphosphate kinase, and ribonucleotide-diphos

28 e analogs, disputing the classic notion that nucleoside diphosphate kinases are responsible for the p

29 ymatic activities, the 3'-5' exonuclease and nucleoside diphosphate kinase, are novel participants in

30 Metabolic bottleneck analysis identified nucleoside diphosphate kinase as a central regulator of

31 ate was based on ATP as the phosphate donor, nucleoside diphosphate kinase as the catalyst, coupled w

32 d support to the recently discovered role of nucleoside-diphosphate kinases as regulatory components

33 tional characterization, we identified Nme1 (nucleoside diphosphate kinase) as an Mga target, which d

34 nase-like protein 1, guanylate kinase 1, and nucleoside diphosphate kinase at 2.09, 2.44, 1.76, and 1

35 We show that nucleoside diphosphate kinase B (NDPK-B), a mammalian hi

36 Here we show that the histidine kinase, nucleoside diphosphate kinase B (NDPK-B), activates TRPV

37 dephosphorylates the catalytic histidine on nucleoside diphosphate kinase B (NDPK-B).

38 e isomerase, aconitate hydratase, M-protein, nucleoside diphosphate kinase B, and myoglobin are S-thi

39 creasing pancreatic Zn(2+) (hZnT8WT) induced nucleoside diphosphate kinase B, and Zn(2+) reduction (h

40 sidue (His358) in the cytoplasmic region, by nucleoside diphosphate kinase-B (NDPK-B).

41 We previously showed that nucleoside diphosphate kinase beta (NDPK-B), a mammalian

42 that an Escherichia coli ndk mutant, lacking nucleoside diphosphate kinase, can use adenylate kinase

43 synthesis, whereas NME6, an uncharacterized nucleoside diphosphate kinase, controls OXPHOS biogenesi

44 ages, we identified the mitochondrial enzyme nucleoside diphosphate kinase D (NDPK-D) as a regulator

45 ITP, XTP, and ATP to E-site nucleotide- and nucleoside diphosphate kinase-depleted tubulin.

46 Nucleoside diphosphate kinase (EC 2.7.4.6) (Ndk) is a ub

47 2.7.1.40), creatine kinase (EC 2.7.3.2), and nucleoside diphosphate kinase (EC 2.7.4.6) were found to

48 Here, we characterized the M. oryzae nucleoside diphosphate kinase-encoding gene NDK1 and dis

49 Escherichia coli nucleoside diphosphate kinase (eNDK) is an XTP:XDP phosp

50 i subunit of DNA polymerase, or loss of ndk (nucleoside diphosphate kinase) function fall into the la

51 --> ATP + polyP(n - 1) (Equation 2); general nucleoside-diphosphate kinase, GDP + polyP(n) --> GTP +

52 When coupled with nucleoside diphosphate kinase, gp1.7 exponentially conve

53 Secreted nucleoside diphosphate kinases have previously been iden

54 Nm23 genes, which encode nucleoside diphosphate kinases, have been implicated in

55 ein S23, putative 60S ribosomal protein L15, nucleoside diphosphate kinase III protein, regulator of

56 We show that GAAD is NM23-H1, a nucleoside diphosphate kinase implicated in suppression

57 trometry as Nm23H2, one of eight isoforms of nucleoside diphosphate kinase in mammalian cells.

58 inase, pyruvate kinase, creatine kinase, and nucleoside diphosphate kinase increased 2-, 1.3-, 3-, an

59 n both prokaryotic and eukaryotic organisms, nucleoside diphosphate kinase is a multifunctional prote

60 ding cofactor C-like domain and a C-terminal nucleoside diphosphate kinase-like domain.

61 A nucleoside diphosphate kinase mechanism was proposed to

62 P1 functions as a molecular scaffold for the nucleoside diphosphate kinase-mediated phosphorylation o

63 th in host cells, an effect regulated by the nucleoside diphosphate kinase ndk-1.

64 The nucleoside diphosphate kinase NDK-1/NME1 promotes phagoc

65 This nucleoside diphosphate kinase (NDK) activity resides in

66 vis BCG secretes two ATP-scavenging enzymes, nucleoside diphosphate kinase (Ndk) and ATPase, during g

67 Pseudomonas aeruginosa positively regulates nucleoside diphosphate kinase (Ndk) and succinyl-CoA syn

68 formation with the truncated 12-kDa form of nucleoside diphosphate kinase (Ndk) but not with the 16-

69 Escherichia coli nucleoside diphosphate kinase (Ndk) catalyzes ATP-depend

70 ification and characterization of the enzyme nucleoside diphosphate kinase (Ndk) from Mycobacterium s

71 mutagenesis procedures in the gene encoding nucleoside diphosphate kinase (ndk) from Pseudomonas aer

72 the nucleotide sequence of the gene encoding nucleoside diphosphate kinase (Ndk) from Pseudomonas aer

73 Here, we describe a novel nucleoside diphosphate kinase (NDK) from the Chlamydomon

74 Loss of nucleoside diphosphate kinase (Ndk) function in Escheric

75 Nucleoside diphosphate kinase (Ndk) is a ubiquitous enzy

76 Nucleoside diphosphate kinase (Ndk) is an important enzy

77 ontribute to the pathogenesis of infections, nucleoside diphosphate kinase (Ndk) mediates bacterially

78 cellular protease cleaves the 16 kDa form of nucleoside diphosphate kinase (Ndk) to a truncated 12 kD

79 matis can form complexes with human or yeast nucleoside diphosphate kinase (Ndk) to modulate their nu

80 at 650 nm is about 0.4, and they demonstrate nucleoside diphosphate kinase (Ndk), 5' nucleotidase, an

81 le all the strains secrete enzymes that have nucleoside diphosphate kinase (Ndk), adenylate kinase (A

82 (CF) patient secretes multiple enzymes with nucleoside diphosphate kinase (Ndk), ATPase, adenylate k

83 ccinyl-coenzyme A (CoA) synthetase (Scs) and nucleoside diphosphate kinase (Ndk), implying coregulati

84 lfilled largely by the ubiquitous and potent nucleoside diphosphate kinase (NDK), most commonly using

85 otein (Ap2), Rhomboid protein 1 (Rom 1), and nucleoside diphosphate kinase (NDK).

86 vity led to the identification of the enzyme nucleoside diphosphate kinase (Ndk).

87 e pathway requires the gene for any of three nucleoside diphosphate kinases (ndk, pykA, or pykF) and

88 s and sea urchin sperm flagella also exhibit nucleoside-diphosphate kinase (NDK) activity, suggesting

89 omplex with both the 12- and 16-kDa forms of nucleoside-diphosphate kinase (Ndk) and predominantly sy

90 Escherichia coli nucleoside-diphosphate kinase (Ndk) catalyzes nucleoside

91 Nucleoside diphosphate kinases (NDKs) play a central rol

92 Nucleoside diphosphate kinases (NDKs), an evolutionarily

93 Nucleoside-diphosphate-kinases (NDKs) are leaderless, mu

94 ne encodes the subunit of a protein that has nucleoside diphosphate kinase (NDP kinase) activity.

95 Nucleoside-diphosphate kinase (NDP kinase) from the matr

96 DnaK purified from ndk::km cells shows that nucleoside-diphosphate kinase (NDP kinase) is responsibl

97 Nucleoside-diphosphate kinase (NDP kinase), a key enzyme

98 llection of biochemical properties including nucleoside-diphosphate kinase (NDP kinase), DNA binding

99 tidine protein kinase activity but retaining nucleoside diphosphate kinase (NDPK) activity showed tha

100 iphosphates were not phosphorylated by their nucleoside diphosphate kinase (NDPK) activity.

101 NME3 is a member of the nucleoside diphosphate kinase (NDPK) family localized on

102 is and enzymatic activities of mitochondrial nucleoside diphosphate kinase (NDPK) in prostate cancer

103 We have explored the ability of a nucleoside diphosphate kinase (NDPK) mutant in which the

104 mone complex with adenosine kinase (ADK) and nucleoside diphosphate kinase (NDPK) to regulate extrace

105 ggest that the deregulation of mitochondrial nucleoside diphosphate kinase (NDPK) together with defec

106 We identified the phosphotransferase nucleoside diphosphate kinase (NDPK), which maintains po

107 Nucleoside-diphosphate kinase (NDPK) 2 in Arabidopsis ha

108 og, exhibited normal autophosphorylation and nucleoside-diphosphate kinase (NDPK) characteristics but

109 ession and activity of the energy-generating nucleoside-diphosphate kinase (NDPK), and knockdown of h

110 Nucleoside diphosphate kinases (NDPKs) are encoded by th

111 Nucleoside diphosphate kinases (NDPKs) are enriched at t

112 We found that knockdown of nucleoside diphosphate kinases (NDPKs) NM23-H1/H2, which

113 Here, we describe how the nucleoside diphosphate kinase Nm23-H1, a protein with a

114 The nucleoside diphosphate kinase Nm23-H4/NDPK-D forms symme

115 Nucleoside diphosphate kinase, NME1/NM23-H1, has been id

116 Here, we report that a mitochondrial nucleoside diphosphate kinase, NME6, supplies mitochondr

117 immobilization of the mycobacterial nucleoside diphosphate kinase on a Sepharose 4 B matrix

118 ll three of these activities, as well as the nucleoside-diphosphate kinase, reside in the same protei

119 metabolite, PSI-7409, by UMP-CMP kinase and nucleoside diphosphate kinase, respectively.

120 the fold of the monomer is similar to other nucleoside diphosphate kinase structures.

121 chemical mechanism(s) by which Nm23 proteins/nucleoside diphosphate kinases suppress tumor metastasis

122 The reverse reaction, a poly P-driven nucleoside diphosphate kinase synthesis of GTP from GDP,

123 Like other nucleoside diphosphate kinases, the retinal enzyme showe

124 and structural properties of bovine retinal nucleoside diphosphate kinase were investigated.

125 demonstrate that infective larvae secrete a nucleoside diphosphate kinase when maintained in vitro.

126 is regulated by Abnormal wing disc (Awd), a nucleoside diphosphate kinase which converts nucleoside

127 With deficient adenylate kinase, nucleoside diphosphate kinase, which secures phosphoryl