ライフサイエンスコーパス: phosphotransferase

1 cetylglucosmine-1-phosphotrans ferase(GlcNAc-phosphotransferase).

2 etylglucosamine-1-phosphotransferase (GlcNAc-phosphotransferase).

3 me N-acetylglucosamine-1-phosphotransferase (phosphotransferase).

4 es characterized by a deficiency in GlcNAc-1-phosphotransferase.

5 st notably those encoding Lipin1 and choline phosphotransferase.

6 nd state, and in an interacting state with a phosphotransferase.

7 and genomic DNA of the precursor of Glc-NAc-phosphotransferase.

8 anism similar to most known aminoglycoside 3-phosphotransferases.

9 ses/heat shock cognate/actin) superfamily of phosphotransferases.

10 brane enzymes that is unrelated to all other phosphotransferases.

11 ation among all characterized aminoglycoside phosphotransferases.

12 is part of the phosphoenolpyruvate-dependent phosphotransferases.

13 erfamily, which comprises a vast majority of phosphotransferases.

14 inin signaling pathway mediated by histidine phosphotransferases.

15 o the membrane topology of other CDP-alcohol phosphotransferases.

16 etabolism, we perturbed choline/ethanolamine phosphotransferase 1 (CEPT1), the terminal enzyme in the

17 side acetyltransferase(6')-Ie/aminoglycoside phosphotransferase(2'')-Ia possesses an N-terminal acety

18 side acetyltransferase(6')-Ie/aminoglycoside phosphotransferase(2'')-Ia, or AAC(6')-Ie/APH(2'')-Ia, i

19 the dynamic properties of the aminoglycoside phosphotransferase 3'-IIIa (APH), a protein of intense i

20 A variety of heterodimers of aminoglycoside phosphotransferase (3')-IIa (Neo) were created in which

21 d to study its binding to the aminoglycoside phosphotransferase(3')-IIIa (APH) by 15N NMR spectroscop

22 f solvent in complexes of the aminoglycoside phosphotransferase(3')-IIIa (APH) with different aminogl

23 of RP, and although RP1 has both kinase and phosphotransferase activities, to date RP2 has only been

24 protein (RP) that possesses both kinase and phosphotransferase activities.

25 a common mechanism for stimulation of their phosphotransferase activities.

26 Thus, C1 domains positively regulated phosphotransferase activity by docking DKF-1 with pools

27 combination of mutation detection and GlcNAc-phosphotransferase activity determination.

28 A neighboring glutamate (E67), essential for phosphotransferase activity hydrogen bonds directly to H

29 ults in a 3.6- or 17-fold increase in GlcNAc-phosphotransferase activity in cell lysates, suggesting

30 nking intronic sequences and measured GlcNAc-phosphotransferase activity in patient fibroblasts.

31 A balance of phosphotransferase activity is necessary for optimal NFA

32 domain from the pore without disrupting the phosphotransferase activity of the released kinase but s

33 I) regulate tyrosine autophosphorylation and phosphotransferase activity of VEGFR-2.

34 kinase reaction was severely compromised but phosphotransferase activity remained unaffected.

35 F-ATPase activity, although bacterial sugar:phosphotransferase activity was elevated in the mutants.

36 he mutations were analyzed along with GlcNAc-phosphotransferase activity, it was possible to confiden

37 , mutation of 15 of these reduced kinase and phosphotransferase activity, while mutation of six resid

38 nt lysates, consistent with the reduction in phosphotransferase activity.

39 able to modulate cellular signaling by their phosphotransferase activity.

40 ocking interactions does not compromise ERK2 phosphotransferase activity.

41 the kinase domain of the reductase inhibits phosphotransferase activity.

42 pshots of conformational fluctuations in the phosphotransferase adenylate kinase (AK) throughout its

43 igated the roles of TCS genes, the histidine phosphotransferase AHP2 and the histidine kinases AHK2 a

44 described, their role and that of histidine phosphotransferases (AHPs) in guard cell signalling rema

45 tion of cloning all three subunits of GlcNAc-phosphotransferase allows expression of recombinant enzy

46 seases are caused by mutations in the GlcNAc-phosphotransferase alpha / beta -subunits precursor gene

47 ylglucosamine-1-phosphotransferase (GlcNAc-1-phosphotransferase), an alpha2beta2gamma2hexamer, mediat

48 main involved in Golgi retention of GlcNAc-1-phosphotransferase and its ability to specifically recog

49 The RPH enzyme is a RIF-inactivating phosphotransferase and represents a new protein family i

50 ses, the Spo0F response regulator, the Spo0B phosphotransferase and the Spo0A transcription factor th

51 ha-glucosidase (GAA) with recombinant GlcNAc-phosphotransferase and uncovering enzyme (N-acetylglucos

52 ences similar to the wild type bovine GlcNAc-phosphotransferase and was able to phosphorylate a lysos

53 al a novel role for tau in modulating axonal phosphotransferases and provide a molecular basis for a

54 ylglucosamine-1-phosphotransferase (GlcNAc-1-phosphotransferase) and GlcNAc-1-phosphodiester alpha-N-

55 wn that KSHV encodes two lytic genes, ORF36 (phosphotransferase) and KSHV ORF21 (thymidine kinase), w

56 FlaC, and FlaD), phosphoenolpyruvate-protein phosphotransferase, and diaminobutyrate-2-oxoglutarate a

57 odes the alpha and beta subunits of GlcNAc-1-phosphotransferase, and mutations in this gene cause the

58 ytic genes (ORF34-37) that includes ORF36, a phosphotransferase, and ORF37, a shutoff exonuclease.

59 ity among choline kinase A-2, aminoglycoside phosphotransferases, and protein kinases, together with

60 Aminoglycoside 3'-phosphotransferases (APH(3')s) are common bacterial resi

61 Aminoglycoside 2''-Ib phosphotransferase [APH(2'')-Ib] produces resistance to

62 a family of enzymes called aminoglycoside O-phosphotransferases (APHs) is a major mechanism by which

63 Aminoglycoside 2''-phosphotransferases are clinically important enzymes tha

64 ied a CDP-ethanolamine:ceramide ethanolamine phosphotransferase as the enzyme responsible for CPE pro

65 integration of a beta-galactosidase-neomycin phosphotransferase (betageo) cassette into the GR gene c

66 s a soluble form of human recombinant GlcNAc-phosphotransferase by removing the putative transmembran

67 The CDP-alcohol phosphotransferase (CDP-AP) family of integral membrane

68 serine decarboxylase (psd-1) and choline/ETA phosphotransferase (cept-1), which encodes the last enzy

69 al foundations of signaling from the central phosphotransferase, ChpT, to its response regulator subs

70 Cho phosphotransferase CHPT1, identified as a direct ERalpha

71 ter-specific membranes with purified general phosphotransferase components showed that although PtsG

72 ome enriched genes, such as aminoglycoside O-phosphotransferases, confer resistance to antibiotics th

73 Second, recombinant GlcNAc-1-phosphotransferase containing a missense mutation in the

74 The structural bases of HK phosphatase/phosphotransferase control are uncovered, and the unexpe

75 (TTMs) are a newly recognized superfamily of phosphotransferases defined by a unique active site resi

76 ain (IPCT) fused with a membrane CDP-alcohol phosphotransferase domain (DIPPS) at 2.65 A resolution.

77 phosphorylating a conserved histidine on its phosphotransferase domain (P1).

78 we reevaluated the substrate profile of the phosphotransferase domain of this clinically important e

79 al acetyltransferase domain and a C-terminal phosphotransferase domain that can act synergistically a

80 ated by phosphorylation, which (via the ChpT phosphotransferase) enables the phosphorylation and acti

81 e in acceptor specificity of the galactose-1-phosphotransferases encoded by downstream wefC in S. gor

82 olecule in which a promoterless hygromycin B phosphotransferase-encoding gene (hpt) was flanked by ZF

83 led conformational transition pathway of the phosphotransferase enzyme adenylate kinase (AdK) in the

84 -phosphate tag by the action of the GlcNAc-1-phosphotransferase enzyme, allowing them to bind recepto

85 Adenylate kinase (AdK), a phosphotransferase enzyme, plays an important role in ce

86 II (EII(Lev)) for a fructose/mannose sugar : phosphotransferase enzyme, which was found to negatively

87 erred from phosphoenolpyruvate (PEP) via the phosphotransferases enzyme I (EI) and HPr to the EIIs, w

88 ough the characterization of an ethanolamine phosphotransferase (EPT) mutant.

89 Recombinant soluble GlcNAc-phosphotransferase exhibited specific activity and subst

90 The P-loop phosphotransferase fold of the kinase is embellished by

91 Whereas lipid allostery impacts the phosphotransferase function of the kinase, extracellular

92 kinase, separated into membrane association, phosphotransferase function, and stimulus recognition.

93 by expressing a phosphoribulokinase-neomycin phosphotransferase fusion protein to produce a high-fide

94 g sequence and expressed functional neomycin phosphotransferase fusion proteins.

95 ression levels of the neighboring hygromycin phosphotransferase gene.

96 ations in the two genes that encode GlcNAc-1-phosphotransferase give rise to lysosomal storage diseas

97 mine: lysosomal enzyme N-acetylglucosamine-1-phosphotransferase (GlcNAc-1-phosphotransferase) and Glc

98 lcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase (GlcNAc-1-phosphotransferase) is an a

99 lcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase (GlcNAc-1-phosphotransferase) mediate

100 GlcNAc:lysosomal enzymeN-acetylglucosamine-1-phosphotransferase (GlcNAc-1-phosphotransferase), an alp

101 amine:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase (GlcNAc-phosphotransferase) is absent

102 amine:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase (GlcNAc-phosphotransferase).

103 alpha and beta catalytic subunits of GlcNAc-phosphotransferase (GNPT [EC 2.7.8.15]), that was associ

104 ant cells, the HPT gene, encoding hygromycin phosphotransferase, has become one of the most widely us

105 f this enzyme is unique among aminoglycoside phosphotransferases, having the ability to inactivate an

106 d cpt) encoding a 1,2-diacylglycerol choline phosphotransferase homologous to choline phosphotransfer

107 nscriptional regulators, fimbrial, and sugar phosphotransferase homologues, as well as genetic loci o

108 ent phosphorylation at its PRD1, whereas the phosphotransferase HPr phosphorylates PRD2.

109 n a receiver domain, and H2 in the histidine phosphotransferase (HPt) domain.

110 regulator domains, but it lacks a histidine phosphotransferase (HPT) domain.

111 in, a receiver (Rec) domain, and a histidine phosphotransferase (Hpt) domain.

112 Helical histidine phosphotransferase (HPt) domains play a central role in

113 Insertion of a hygromycin B phosphotransferase (HPT) gene cassette in place of the m

114 y regulates the expression of a macrolide 2'-phosphotransferase I resistance gene (mphA) via binding

115 members of the bacterial aminoglycoside 2''-phosphotransferase IIIa (APH(2'')) aminoglycoside kinase

116 nal cytoplasmic tail of the alpha subunit of phosphotransferase impair retention of the catalytically

117 We have also identified the first histidine phosphotransferase in C. crescentus, ShpA, and show that

118 as further determined that K1648R-TRPM7, the phosphotransferase-inactive TRPM7 mutant, was unresponsi

119 GlcNAc-phosphotransferase is a multisubunit enzyme with an alph

120 lcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase is an alpha(2)beta(2)gamma(2) hexamer

121 Depending on the yeast strains, the GTP:AMP phosphotransferase is encoded by the nuclear gene ADK2 w

122 A key property of GlcNAc-1-phosphotransferase is its unique ability to distinguish

123 ich a purified histidine kinase or histidine phosphotransferase is simultaneously assayed for the abi

124 The finding that mislocalization of active phosphotransferase is the basis for mucolipidosis III al

125 etylglucosamine-1-phosphotransferase (GlcNAc-phosphotransferase) is absent or reduced, respectively.

126 ylglucosamine-1-phosphotransferase (GlcNAc-1-phosphotransferase) is an alpha2beta2gamma2 heterohexame

127 the phosphate donor, with aminoglycoside 2''-phosphotransferase IVa (APH(2'')-IVa) being a member tha

128 istic characterization of aminoglycoside 2''-phosphotransferase, known as type Ic enzyme.

129 uminescence in concert with the SK AinR, the phosphotransferase LuxU and the RR LuxO.

130 Aminoglycoside 2''-phosphotransferases mediate high level resistance to ami

131 ylglucosamine-1-phosphotransferase (GlcNAc-1-phosphotransferase) mediates the first step in the synth

132 ient in UDP-GlcNAc:lysosomal enzyme GlcNAc-1-phosphotransferase (mucolipidosis type II or Gnptab -/-

133 inhibitory activities against the bacterial phosphotransferases (MurX and WecA) (IC50 = 0.096-0.69 m

134 ons and containing mutations in the neomycin phosphotransferase (neo) gene were corrected by adeno-as

135 cells with a plasmid containing the neomycin phosphotransferase (neo) selectable marker resulted in s

136 when fused to the reporter protein neomycin phosphotransferase (Npt), are sufficient for the secreti

137 ted of a positive selection for the neomycin phosphotransferase (nptII) gene positioned within Ds fol

138 We identified the phosphotransferase nucleoside diphosphate kinase (NDPK),

139 The phosphotransferases of the haloalkanoate dehalogenase su

140 Different from CAP IIA UW-1, the phosphotransferase (pap) in polyphosphate metabolism and

141 rolyzes poly-P to P(i), and (iii) poly-P/AMP phosphotransferase (PAP), which uses poly-P as a donor t

142 ase in the level of the choline/ethanolamine-phosphotransferase (PfCEPT), a key enzyme involved in th

143 rophosphate-dependent fructose-6-phosphate 1-phosphotransferase (PFP) catalyzes the ATP-independent c

144 lcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase (phosphotransferase).

145 In a variety of bacteria, the phosphotransferase protein IIA(Glc) plays a key regulato

146 uorum sensing process is the function of the phosphotransferase protein, LuxU.

147 rization of an isolated, monomeric bacterial phosphotransferase protein.

148 by most CheA kinases, but absent in related phosphotransferase proteins.

149 The Golgi-resident N-acetylglucosamine-1-phosphotransferase (PT) complex is composed of two alpha

150 h encodes enzyme I of the nitrogen-regulated phosphotransferase (PTS(Ntr)) system, as being important

151 nucleolin through a novel kinase-independent phosphotransferase reaction.

152 higher observed specific activities for the phosphotransferase reaction.

153 These findings serve to explain how GlcNAc-1-phosphotransferase recognizes a large number of proteins

154 t conserved phosphoenolpyruvate:carbohydrate phosphotransferase regulation domain (PRD) histidines of

155 Here we show that Enzyme I, the terminal phosphotransferase responsible for the conversion of PEP

156 Loss of GlcNAc-1-phosphotransferase results in hydrolase hypersecretion a

157 heretofore unknown RIF resistance gene, RIF phosphotransferase (rph).

158 ,N'-diacetylchitobiose/lactose branch of the phosphotransferase signal transduction system, has been

159 In the Golgi, a phosphotransferase specifically labels lysosomal protein

160 rate enhancement by salt occurs for only the phosphotransferase step of the reaction.

161 c [dibutroylphosphatidylinositol (diC(4)PI)] phosphotransferase substrates and inositol 1,2-(cyclic)-

162 utation in the Gnptab (N-acetylglucosamine-1-phosphotransferase subunits alpha/beta) gene with wild-t

163 se belonging to the family of aminoglycoside phosphotransferases suggested that AGXT2L1 and AGXT2L2 a

164 stitutes a new branch within the CDP-alcohol phosphotransferase superfamily with homologues in Arthro

165 f ack as the potential urkinase in the ASKHA phosphotransferase superfamily, an origin hypothesis doe

166 terminal kinase domain belongs to the P-loop phosphotransferase superfamily.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

234 AtxA is a phosphotransferase system regulatory domain-containing p

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

252 rotein-protein interactions of the bacterial phosphotransferase system.

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

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

255 t of the phosphoenolpyruvate-dependent sugar phosphotransferase system.

256 of the bacterial phosphoenolpyruvate:glycose phosphotransferase system.

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

258 sequence of the phosphoenolpyruvate:glucose phosphotransferase system.

259 ongs to the phosphoenolpyruvate carbohydrate phosphotransferase system.

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

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

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

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

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

265 UDP-GlcNAc:lysosomal enzyme GlcNAc-1-phosphotransferase tags newly synthesized lysosomal enzy

266 ere we identify ChpT, an essential histidine phosphotransferase that controls the activity of CtrA, t

267 n alpha-Gal transferase, wefJ for a GalNAc-1-phosphotransferase that has a unique acceptor specificit

268 activities with a 1,2-diacylglycerol choline phosphotransferase that is common in eukaryotes.

269 r AvrRxo1 of plant pathogens is an authentic phosphotransferase that produces two novel metabolites b

270 established as an ATP-dependent capuramycin phosphotransferase that regio-specifically transfers the

271 a gene encoding a putative aminoglycoside 3-phosphotransferase that was previously demonstrated to b

272 Fcp1 belongs to the DXDX(T/V) family of phosphotransferases that act via an acyl-phosphoenzyme i

273 ine phosphotransferase homologous to choline phosphotransferases that catalyze the final step of the

274 ansferase system (PTS) consists of cascading phosphotransferases that couple the simultaneous import

275 Adenylate kinases (AKs) are phosphotransferases that regulate the cellular adenine n

276 e focus on protein kinases, a superfamily of phosphotransferases that share homologous sequences and

277 ting the expression of N-acetylglucosamine-1-phosphotransferase, the enzyme that initiates mannose 6-

278 lcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase, the initial enzyme in the biosynthes

279 he human and zebrafish N-acetylglucosamine-1-phosphotransferase to recognize and modify certain lysos

280 or kinase CckA and proceeds through the ChpT phosphotransferase to two regulatory substrates: CtrA an

281 This results in mistargeting of the mutant phosphotransferases to lysosomes, where they are degrade

282 system could deliver enzymes (Cre, neomycin phosphotransferase), transcription factors (NANOG, MYOD)

283 tol biosynthesis is catalysed by CDP-alcohol phosphotransferases, transmembrane enzymes that use CDP-

284 -phosphofructokinase enzyme and linked sugar phosphotransferase transport system were most strongly u

285 lized to genes c3405-10, encoding a putative phosphotransferase transport system, which is common to

286 ers of bacterial origin such as the neomycin phosphotransferase type II gene, which can confer kanamy

287 le, the enzyme is renamed aminoglycoside 2''-phosphotransferase type IIIa.

288 resistance associated with mutations in the phosphotransferase UL97 and the DNA polymerase UL54.

289 reactions, two of the four aminoglycoside 2'-phosphotransferases utilize GTP as the phosphate donor.

290 Bovine GlcNAc-phosphotransferase was isolated using monoclonal antibod

291 enzyme in de novo PC synthesis, and choline phosphotransferase were increased by 64 and 53%, respect

292 ylglycerol acyltransferase, and ethanolamine phosphotransferase were not affected by Scd1 mutation.

293 er with a selectable marker gene (hygromycin phosphotransferase), were cloned between two loxP recomb

294 rder caused by loss of N-acetylglucosamine-1-phosphotransferase, which tags lysosomal enzymes with a

295 s poly P reversibly from ATP, and poly P:AMP phosphotransferase, which uses poly P as a donor to also

296 -terminal kinase (JNK) is a serine/threonine phosphotransferase whose sustained activation in respons

297 e profiles of four common aminoglycoside 2''-phosphotransferases widely distributed in clinically imp

298 duced an active and processed soluble GlcNAc-phosphotransferase with an alpha'2beta'2gamma2-subunits

299 properties of a lipid phosphate phosphatase/phosphotransferase with distinct substrate preference fo

300 l metalloenzymes (TTMs) are a superfamily of phosphotransferases with a distinctive active site locat