ライフサイエンスコーパス: phosphotransferase

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

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

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

4 st notably those encoding Lipin1 and choline phosphotransferase.

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

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

7 anism similar to most known aminoglycoside 3-phosphotransferases.

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

9 brane enzymes that is unrelated to all other phosphotransferases.

10 ation among all characterized aminoglycoside phosphotransferases.

11 erfamily, which comprises a vast majority of phosphotransferases.

12 is part of the phosphoenolpyruvate-dependent phosphotransferases.

13 inin signaling pathway mediated by histidine phosphotransferases.

14 ipogenesis, mediated by choline-ethanolamine phosphotransferase 1 (CEPT1), is essential for phospholi

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

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

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

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

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

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

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

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

23 a common mechanism for stimulation of their phosphotransferase activities.

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

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

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

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

28 A balance of phosphotransferase activity is necessary for optimal NFA

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

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

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

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

33 Abrogation of this interaction increased phosphotransferase activity, promoted membrane associati

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

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

36 ocking interactions does not compromise ERK2 phosphotransferase activity.

37 the kinase domain of the reductase inhibits phosphotransferase activity.

38 able to modulate cellular signaling by their phosphotransferase activity.

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

40 The gene AK2 encodes the phosphotransferase adenylate kinase 2 (AK2).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

59 In applications to an aminoglycoside phosphotransferase [APH(3')-IIIa] and pantothenate kinas

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

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

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

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

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

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

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

67 ne histidine kinase CckA and the cytoplasmic phosphotransferase ChpT, provide the only phosphate sour

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

69 Cho phosphotransferase CHPT1, identified as a direct ERalpha

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 Recombinant soluble GlcNAc-phosphotransferase exhibited specific activity and subst

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

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

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

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

93 ression levels of the neighboring hygromycin phosphotransferase gene.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

115 promoted membrane association, and provoked phosphotransferase-independent alterations in cell morph

116 on, and localization, as well as mediating a phosphotransferase-independent function.

117 GlcNAc-phosphotransferase is a multisubunit enzyme with an alph

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 The phosphotransferases of the haloalkanoate dehalogenase su

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

138 ected weak encounters between two paralogous phosphotransferase pathways of Escherichia coli, which r

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

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

141 atalyzed by the cytidine diphosphate-alcohol phosphotransferase phosphatidylinositol-phosphate syntha

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

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

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

145 rization of an isolated, monomeric bacterial phosphotransferase protein.

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

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

148 nucleolin through a novel kinase-independent phosphotransferase reaction.

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

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

151 Deleting the phosphotransferase responsible for phosphoethanolamine m

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

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

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

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

156 cues from metformin and the diet through the phosphotransferase signaling pathway that converges on t

157 In the Golgi, a phosphotransferase specifically labels lysosomal protein

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

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

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

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

162 CPD belongs to the 2H phosphotransferase superfamily by dint of its conserved

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

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

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

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

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

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

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

170 o phosphorylation by the phosphoenolpyruvate phosphotransferase system (PEP-PTS) and for their impact

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

172 ing glutamine concentration using a nitrogen phosphotransferase system (PTS (Ntr)).

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

174 The nitrogen-related phosphotransferase system (PTS(Ntr)) of Rhizobium legumi

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

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

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

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

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

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

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

182 The phosphotransferase system (PTS) couples the import of ca

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

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

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

186 e encodes a phosphoenolpyruvate carbohydrate phosphotransferase system (PTS) for cellobiose.

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

188 not fully known, one implicated pathway is a phosphotransferase system (PTS) in E. faecalis strain OG

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

229 es a 6-phospho-beta-glucosidase (GenA) and a phosphotransferase system permease EIIC (GenB).

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

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

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

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

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

235 AtxA is a phosphotransferase system regulatory domain-containing p

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

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

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

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

240 ly regulated by coaggregation, including two phosphotransferase system transporters and several other

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

242 n sugar transport (phosphoenolpyruvate (PEP) phosphotransferase system), EPS assembly (epsG1D) and am

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

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

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

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

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

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

249 olic pathways, i.e. benzoate degradation and phosphotransferase system, were identified to be closely

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

251 ongs to the phosphoenolpyruvate carbohydrate phosphotransferase system.

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

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

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

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

256 rotein-protein interactions of the bacterial phosphotransferase system.

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

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

259 t of the phosphoenolpyruvate-dependent sugar phosphotransferase system.

260 of the bacterial phosphoenolpyruvate:glycose phosphotransferase system.

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

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

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

264 There are two paralogous Escherichia coli phosphotransferase systems, one for sugar import (PTS(su

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

289 Bovine GlcNAc-phosphotransferase was isolated using monoclonal antibod

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

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

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

293 ith mutations of the Golgi-resident GlcNAc-1-phosphotransferase, which generates mannose 6-phosphate

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