ライフサイエンスコーパス: phosphotransferase system

1 in the N,N'-diacetylchitobiose branch of the phosphotransferase system.

2 s of the phosphoenolpyruvate-dependent:sugar phosphotransferase system.

3 via the phosphoenolpyruvate-dependent:sugar phosphotransferase system.

4 t of the phosphoenolpyruvate-dependent sugar:phosphotransferase system.

5 egulation of fruA expression by the fructose phosphotransferase system.

6 r protein of the phosphoenolpyruvate:glycose phosphotransferase system.

7 permease of the phosphoenolpyruvate:glycose phosphotransferase system.

8 ier protein of the phosphoenolpyruvate-sugar phosphotransferase system.

9 hydrate uptake via the bacterial PEP:glycose phosphotransferase system.

10 ssion of the glcP gene required a functional phosphotransferase system.

11 zyme IIAglc of the phosphoenolpyruvate:sugar phosphotransferase system.

12 t by the bacterial phosphoenolpyruvate:sugar phosphotransferase system.

13 in the bacterial phosphoenolpyruvate: sugar phosphotransferase system.

14 and by HPr, a phosphocarrier protein of the phosphotransferase system.

15 er, ptsM, of the phosphoenolpyruvate:glycose phosphotransferase system.

16 ongs to the phosphoenolpyruvate carbohydrate phosphotransferase system.

17 coding the glucose-specific enzyme II of the phosphotransferase system.

18 phosphoenolpyruvate (PEP)-dependent:glucose phosphotransferase system.

19 e mtl operon, encoding the mannitol-specific phosphotransferase system.

20 ibits the synthesis of the mannitol-specific phosphotransferase system.

21 rotein-protein interactions of the bacterial phosphotransferase system.

22 archaeon found to have a transporter of the phosphotransferase system.

23 phocarrier protein that is part of the sugar phosphotransferase system.

24 t of the phosphoenolpyruvate-dependent sugar phosphotransferase system.

25 of the bacterial phosphoenolpyruvate:glycose phosphotransferase system.

26 gh the phosphorylated enzyme IIA(glu) of the phosphotransferase system.

27 sequence of the phosphoenolpyruvate:glucose phosphotransferase system.

28 (EI) is the first component in the bacterial phosphotransferase system, a signal transduction pathway

29 The bacterial phosphoenolpyruvate:sugar phosphotransferase system accomplishes both the transpor

30 sphotransferase; EC 2.7.1.1) activity but no phosphotransferase system activities.

31 r, a phosphocarrier protein of the bacterial phosphotransferase system and a transcriptional cofactor

32 sence of fructose induces the synthesis of a phosphotransferase system and glycolytic enzymes that al

33 d out by the phosphoenolpyruvate (PEP):sugar phosphotransferase system and involves five phosphoryl g

34 The presence of genes for a unique phosphotransferase system and N-acetylglucosamine metabo

35 onfirmed the absence of a galactose-specific phosphotransferase system and suggested the presence of

36 The agaZVWEFASYBCDI gene cluster encodes the phosphotransferase systems and enzymes responsible for t

37 in with the sugar permeases of the bacterial phosphotransferase system, and (iii) catalysis of phosph

38 residues), the first enzyme in the bacterial phosphotransferase system, and its complex with HPr ( ap

39 nce of bacterial phosphoenolpyruvate:glycose phosphotransferase systems are the autophosphorylation o

40 EI monomer/dimer transition may regulate the phosphotransferase system because only the EI dimer is a

41 glucose-specific arm of the Escherichia coli phosphotransferase system, between enzyme IIAGlucose (II

42 I of the bacterial phosphoenolpyruvate:sugar phosphotransferase system can be phosphorylated by PEP o

43 he transhydrogenase genes sthA and pntAB The phosphotransferase system component crr was also found t

44 mology to a gene encoding a glucose-specific phosphotransferase system component, and the resT gene,

45 l enzymes of sugar metabolism at low pH: the phosphotransferase system components ManX and PtsH and t

46 permeases of the phosphoenolpyruvate:glycose phosphotransferase system comprise one to five separatel

47 ansporter (IIB(Mtl)) of the Escherichia coli phosphotransferase system, containing a mutation of the

48 The bacterial PEP:sugar phosphotransferase system couples the phosphorylation an

49 cytosolic component, Enzyme 1 of the glucose phosphotransferase system, demonstrated that the spherop

50 oxyacetone kinase-linked phosphoenolpyruvate phosphotransferase system (EI, DhaK), and oxidoreductase

51 nd the two upstream complexes of the glucose phosphotransferase system (EI.HPr and IIAGlc.HPr) reveal

52 inal region of Mga, possessing similarity to phosphotransferase system EIIB proteins, plays a critica

53 ssion is a component of the glucose-specific phosphotransferase system, enzyme IIA (EIIA(Glc)).

54 Thus, both phosphoenolpyruvate-dependent phosphotransferase system enzymes exist in soluble and m

55 kingdoms, the phosphoenolpyruvate-dependent phosphotransferase system exists almost exclusively in b

56 In addition, the native PEP-dependent phosphotransferase system for glucose uptake was inactiv

57 ng enzyme I of the phosphoenolpyruvate:sugar phosphotransferase system from an Escherichia coli enzym

58 The phosphoenolpyruvate:carbohydrate phosphotransferase system functions to maintain levels o

59 Phosphotransferase system genes are generally PHX with s

60 e Escherichia coli phosphoenolpyruvate:sugar phosphotransferase system has been investigated by heter

61 the mannitol branch of the Escherichia coli phosphotransferase system has been solved by multidimens

62 f the mannose branch of the Escherichia coli phosphotransferase system has been solved by NMR using c

63 arrier protein (HPr) of the Escherichia coli phosphotransferase system has been solved by NMR, includ

64 se (Chb) transporter of the Escherichia coli phosphotransferase system has been solved by NMR.

65 mannitol transporter of the Escherichia coli phosphotransferase system has been solved by NMR.

66 components of all branches of the bacterial phosphotransferase system, have been examined using NMR

67 hocarrier of the phosphoenolpyruvate:glycose phosphotransferase system, IIA(Glc) (formerly known as I

68 r protein of the phosphoenolpyruvate:glycose phosphotransferase system, IIAGlc (also known as IIIGlc)

69 ia the phosphoenolpyruvate-dependent glucose:phosphotransferase system (IICB(Glc)/IIA(Glc)).

70 ase and the phosphoenolpyruvate:carbohydrate phosphotransferase system in Escherichia coli.

71 The various substrate specificities among phosphotransferase systems in different genomes apparent

72 ng trypotophan production and the galactitol phosphotransferase system (including dihydroxyacetone ph

73 e Escherichia coli phosphoenolpyruvate:sugar phosphotransferase system inhibits transport catalyzed b

74 in IIA(Glc) of the phosphoenolpyruvate:sugar phosphotransferase system is an activator of adenylyl cy

75 The phosphotransferase system is less prevalent in the analy

76 (12) The phosphoenolpyruvate:sugar phosphotransferase system is prevalent in the large geno

77 hat NagE, a putative component of the GlcNAc phosphotransferase system, is required for growth on and

78 ptsI of the phosphoenolpyruvate:carbohydrate phosphotransferase system lowered transformation frequen

79 by means of the phosphoenolpyruvate/glycose phosphotransferase system mutate further to permit growt

80 e phosphoenolpyruvate-dependent carbohydrate phosphotransferase system of Escherichia coli carries ou

81 yme I (EIN) of the phosphoenolpyruvate:sugar phosphotransferase system of Escherichia coli has been d

82 Glc)) is a signal-transducing protein in the phosphotransferase system of Escherichia coli.

83 glc) (EIIA) of the phosphoenolpyruvate:sugar phosphotransferase system of Mycoplasma capricolum was c

84 ties between the phosphoenolpyruvate:glycose phosphotransferase system of V. furnissii and enteric ba

85 lin2907 within a beta-glucoside (cellobiose):phosphotransferase system operon, may presage both enzym

86 The phosphoenolpyruvate phosphotransferase system (PEP-PTS) and adenylate cyclas

87 ylation by the phosphoenolpyruvate-dependent phosphotransferase system (PEP-PTS).

88 ediate, fructose 1,6-biphosphate, and by the phosphotransferase system phosphocarrier protein, IIIGlc

89 Escherichia coli phosphoenolpyruvate:glucose phosphotransferase system plays a direct role in regulat

90 e bacterial phosphoenolpyruvate:carbohydrate phosphotransferase system plays a key role in the regula

91 rotein IIAGlc, the phosphoenolpyruvate:sugar phosphotransferase system plays a role in the regulation

92 he crr gene of the phosphoenolpyruvate:sugar phosphotransferase system, plays an important role in re

93 nd ptsH2(encoding a homolog of the bacterial phosphotransferase system protein Hpr) genes were transc

94 s influenzae, is inhibited allosterically by phosphotransferase system protein IIA(Glc).

95 s: a domain that binds the partner PEP:sugar phosphotransferase system protein, HPr; a domain that ca

96 HPr with three other structurally unrelated phosphotransferase system proteins, enzymes I, IIA(gluco

97 nd the accessory phosphoenolpyruvate:glycose phosphotransferase system proteins.

98 al, similar to that of the phosphohistidinyl phosphotransferase system proteins.

99 specific phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS II transport enzyme).

100 s influenced by a noncanonical nitrogen-type phosphotransferase system (PTS(Ntr)).

101 A phosphoenolpyruvate-dependent phosphotransferase system (PTS) and an unsaturated glucu

102 s is accomplished by the phosphoenolpyruvate-phosphotransferase system (PTS) and ATP-binding cassette

103 t requires the phosphoenolpyruvate-dependent phosphotransferase system (PTS) and is independent of an

104 des the Aga phosphoenolpyruvate:carbohydrate phosphotransferase system (PTS) and other catabolic enzy

105 lation, likely due to its ability to use the phosphotransferase system (PTS) as regulatory machinery

106 depends on the phosphoenolpyruvate: sucrose phosphotransferase system (PTS) but is unaffected by a m

107 ry proteins of the phosphoenolpyruvate:sugar phosphotransferase system (PTS) but no recognizable homo

108 The bacterial phosphoenolpyruvate/glycose phosphotransferase system (PTS) comprises a group of pro

109 The bacterial phosphoenolpyruvate-dependent phosphotransferase system (PTS) consists of a set of cyt

110 e bacterial phosphoenolpyruvate-carbohydrate phosphotransferase system (PTS) consists of cascading ph

111 lation utilizes specific phosphoenolpyruvate phosphotransferase system (PTS) enzymes.

112 we report that cells defective for the sugar phosphotransferase system (PTS) exhibited a magnesium-in

113 mutants in the phosphoenolpyruvate-dependent phosphotransferase system (PTS) exhibited Streptolysin S

114 Genes for an incomplete phosphotransferase system (PTS) have been found in the g

115 phoenolpyruvate-dependent sugar-transporting phosphotransferase system (PTS) have previously been ide

116 ssential component of the sugar-transporting phosphotransferase system (PTS) in many bacteria.

117 e Escherichia coli phosphoenolpyruvate:sugar phosphotransferase system (PTS) in prokaryotes mediates

118 e polypeptides that are part of the fructose phosphotransferase system (PTS) in S. gordonii.

119 The phosphoenolpyruvate-phosphotransferase system (PTS) is a global regulatory n

120 The bacterial phosphoenolpyruvate phosphotransferase system (PTS) is a highly conserved ph

121 The bacterial phosphoenolpyruvate phosphotransferase system (PTS) is a highly conserved ph

122 The phosphoenol phosphotransferase system (PTS) is a multicomponent sign

123 The bacterial phosphotransferase system (PTS) is a signal transduction

124 of the bacterial phosphoenolpyruvate:glycose phosphotransferase system (PTS) is autocatalytically pho

125 Escherichia coli phosphoenolpyruvate: sugar phosphotransferase system (PTS) is the 64-kDa protein en

126 The phosphoenolpyruvate:sugar phosphotransferase system (PTS) is the major carbohydrat

127 The phosphoenolpyruvate phosphotransferase system (PTS) is the primary mechanism

128 bacterial phosphoenolpyruvate (PEP):glycose phosphotransferase system (PTS) mediates uptake/phosphor

129 e phosphoenolpyruvate-dependent carbohydrate phosphotransferase system (PTS) of Escherichia coli, bot

130 of the glucose-specific phosphoenolpyruvate:phosphotransferase system (PTS) of Escherichia coli, is

131 ase/phosphatase is a common component of the phosphotransferase system (PTS) of gram-positive bacteri

132 promoter of a phosphoenolpyruvate-dependent phosphotransferase system (PTS) operon.

133 The phosphoenolpyruvate:glycose phosphotransferase system (PTS) participates in importan

134 d "bepA," putatively encoding a carbohydrate phosphotransferase system (PTS) permease (biofilm and en

135 idase (CelA) and a cellobiose-specific sugar phosphotransferase system (PTS) permease (EII(Cel)).

136 a previously uncharacterized mannose family phosphotransferase system (PTS) permease, and we designa

137 nents of phosphoenolpyruvate-dependent sugar:phosphotransferase system (PTS) permeases.

138 The phosphoenolpyruvate (PEP)-dependent phosphotransferase system (PTS) phosphorylates sugars an

139 The bacterial phosphoenolpyruvate:glycose phosphotransferase system (PTS) plays a central role in

140 The phosphoenolpyruvate-dependent phosphotransferase system (PTS) plays a major role in th

141 virulence regulator Mga contains homology to phosphotransferase system (PTS) regulatory domains (PRDs

142 genome-wide approach, we identified the GAS phosphotransferase system (PTS) responsible for non-MalE

143 Its genome also encodes an apparent fructose phosphotransferase system (PTS) sugar transporter.

144 influenced by environmental signals, such as phosphotransferase system (PTS) sugars, biotin, and amin

145 One such pathway is the phosphoenolpyruvate phosphotransferase system (PTS), a multicomponent sugar

146 erichia coli phosphoenolpyruvate (PEP):sugar phosphotransferase system (PTS), and a cloned amino-term

147 zyme II of the phosphoenolpyruvate-dependent phosphotransferase system (PTS), contains a duplicated I

148 The phosphotransferase system (PTS), encompassing EI, HPr, a

149 fructose via the phosphoenolpyruvate/glycose phosphotransferase system (PTS), further mutants were se

150 ucose-specific phosphocarrier protein of the phosphotransferase system (PTS), IIAGlc (IIIGlc in older

151 was abolished when a plasmid containing the phosphotransferase system (PTS), phospho-beta-galactosid

152 rotein and an enzyme IIA-like protein of the phosphotransferase system (PTS), respectively.

153 e Escherichia coli phosphoenolpyruvate:sugar phosphotransferase system (PTS), the sugar-specific enzy

154 strates of the phosphoenolpyruvate-dependent phosphotransferase system (PTS), we show that PTS sugar

155 scription factor and a sugar permease of the phosphotransferase system (PTS), which are predicted to

156 switching can occur in the Escherichia coli phosphotransferase system (PTS), which regulates the upt

157 nse to glucose-specific phosphoenolypyruvate phosphotransferase system (PTS)-dependent phosphosugar s

158 yzed by the phosphoenolpyruvate:carbohydrate phosphotransferase system (PTS).

159 mediated by the phosphoenolpyruvate:glycose phosphotransferase system (PTS).

160 tes internalized via the phosphoenolpyruvate phosphotransferase system (PTS).

161 nents of the V. cholerae phosphoenolpyruvate phosphotransferase system (PTS).

162 IA (IIAGlc) of the phosphoenolpyruvate:sugar phosphotransferase system (PTS).

163 e identified a locus that encodes a putative phosphotransferase system (PTS).

164 ) carbohydrate transporters of the bacterial phosphotransferase system (PTS).

165 species is the phosphoenolpyruvate-dependent phosphotransferase system (PTS).

166 d with the phosphoenolpyruvate: carbohydrate phosphotransferase system (PTS).

167 ncluding three phosphoenolpyruvate-dependent phosphotransferase systems (PTS) and a binding protein-d

168 cteria express phosphoenolpyruvate-dependent phosphotransferase systems (PTS).

169 ride synthase), and the scrAB pathway (sugar-phosphotransferase system [PTS] permease and sucrose-6-P

170 ntal caries, possesses at least two fructose phosphotransferase systems (PTSs), encoded by fruI and f

171 Chemotaxis of Escherichia coli toward phosphotransferase systems (PTSs)-carbohydrates requires

172 o the sugar uptake through a large family of phosphotransferase systems (PTSs).

173 HTH2) and phosphoenolpyruvate: carbohydrate phosphotransferase system-regulated domains (PRD1 and PR

174 of an RNA-binding domain and two reiterated phosphotransferase system regulation domains (PRDs).

175 AtxA of two PTS (phosphenolpyruvate : sugar phosphotransferase system) regulation domains (PRD) gene

176 AtxA is a phosphotransferase system regulatory domain-containing p

177 that connect elevated PEP/pyruvate ratios to phosphotransferase system signaling and adenylate cyclas

178 predicting the rates of phosphoenolpyruvate phosphotransferase system sugar uptake in whole cells.

179 of the phosphoenol pyruvate dependent:sugar phosphotransferase system suggests participation of MalB

180 hia coli encodes a phosphoenolpyruvate:sugar phosphotransferase system that metabolizes the hexitol D

181 is of RMC26 produced defects in the sorbitol phosphotransferase system that prevented the transport o

182 Escherichia coli phosphoenolpyruvate: sugar phosphotransferase system, that between histidine-contai

183 omplexes of HPr with partner proteins of the phosphotransferase system, the N-terminal domain of enzy

184 P phosphomimetic mutant HPr S46D had reduced phosphotransferase system transport rates and limited in

185 sphocarrier protein (HPr) from the bacterial phosphotransferase system, we have identified a minor sp