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1 gh the phosphorylated enzyme IIA(glu) of the phosphotransferase system.
2 sequence of the phosphoenolpyruvate:glucose phosphotransferase system.
3 in the N,N'-diacetylchitobiose branch of the phosphotransferase system.
4 s of the phosphoenolpyruvate-dependent:sugar phosphotransferase system.
5 via the phosphoenolpyruvate-dependent:sugar phosphotransferase system.
6 t of the phosphoenolpyruvate-dependent sugar:phosphotransferase system.
7 egulation of fruA expression by the fructose phosphotransferase system.
8 r protein of the phosphoenolpyruvate:glycose phosphotransferase system.
9 permease of the phosphoenolpyruvate:glycose phosphotransferase system.
10 ier protein of the phosphoenolpyruvate-sugar phosphotransferase system.
11 hydrate uptake via the bacterial PEP:glycose phosphotransferase system.
12 ssion of the glcP gene required a functional phosphotransferase system.
13 zyme IIAglc of the phosphoenolpyruvate:sugar phosphotransferase system.
14 t by the bacterial phosphoenolpyruvate:sugar phosphotransferase system.
15 in the bacterial phosphoenolpyruvate: sugar phosphotransferase system.
16 and by HPr, a phosphocarrier protein of the phosphotransferase system.
17 er, ptsM, of the phosphoenolpyruvate:glycose phosphotransferase system.
18 e glucose-specific phosphoenolpyruvate/sugar phosphotransferase system.
19 encoding Enzyme I of the phosphoenolpyruvate phosphotransferase system.
20 ongs to the phosphoenolpyruvate carbohydrate phosphotransferase system.
21 coding the glucose-specific enzyme II of the phosphotransferase system.
22 phosphoenolpyruvate (PEP)-dependent:glucose phosphotransferase system.
23 e mtl operon, encoding the mannitol-specific phosphotransferase system.
24 ibits the synthesis of the mannitol-specific phosphotransferase system.
25 rotein-protein interactions of the bacterial phosphotransferase system.
26 archaeon found to have a transporter of the phosphotransferase system.
27 phocarrier protein that is part of the sugar phosphotransferase system.
28 t of the phosphoenolpyruvate-dependent sugar phosphotransferase system.
29 of the bacterial phosphoenolpyruvate:glycose phosphotransferase system.
30 (EI) is the first component in the bacterial phosphotransferase system, a signal transduction pathway
33 r, a phosphocarrier protein of the bacterial phosphotransferase system and a transcriptional cofactor
34 sence of fructose induces the synthesis of a phosphotransferase system and glycolytic enzymes that al
35 d out by the phosphoenolpyruvate (PEP):sugar phosphotransferase system and involves five phosphoryl g
37 onfirmed the absence of a galactose-specific phosphotransferase system and suggested the presence of
38 The agaZVWEFASYBCDI gene cluster encodes the phosphotransferase systems and enzymes responsible for t
39 in with the sugar permeases of the bacterial phosphotransferase system, and (iii) catalysis of phosph
40 residues), the first enzyme in the bacterial phosphotransferase system, and its complex with HPr ( ap
41 nce of bacterial phosphoenolpyruvate:glycose phosphotransferase systems are the autophosphorylation o
42 EI monomer/dimer transition may regulate the phosphotransferase system because only the EI dimer is a
43 glucose-specific arm of the Escherichia coli phosphotransferase system, between enzyme IIAGlucose (II
44 I of the bacterial phosphoenolpyruvate:sugar phosphotransferase system can be phosphorylated by PEP o
45 he transhydrogenase genes sthA and pntAB The phosphotransferase system component crr was also found t
46 mology to a gene encoding a glucose-specific phosphotransferase system component, and the resT gene,
47 l enzymes of sugar metabolism at low pH: the phosphotransferase system components ManX and PtsH and t
48 permeases of the phosphoenolpyruvate:glycose phosphotransferase system comprise one to five separatel
49 ansporter (IIB(Mtl)) of the Escherichia coli phosphotransferase system, containing a mutation of the
51 cytosolic component, Enzyme 1 of the glucose phosphotransferase system, demonstrated that the spherop
52 activates the dhaKLM operon that encodes the phosphotransferase system, DhfA is involved in formate,
53 oxyacetone kinase-linked phosphoenolpyruvate phosphotransferase system (EI, DhaK), and oxidoreductase
54 nd the two upstream complexes of the glucose phosphotransferase system (EI.HPr and IIAGlc.HPr) reveal
55 inal region of Mga, possessing similarity to phosphotransferase system EIIB proteins, plays a critica
57 Thus, both phosphoenolpyruvate-dependent phosphotransferase system enzymes exist in soluble and m
58 n sugar transport (phosphoenolpyruvate (PEP) phosphotransferase system), EPS assembly (epsG1D) and am
59 kingdoms, the phosphoenolpyruvate-dependent phosphotransferase system exists almost exclusively in b
61 ng enzyme I of the phosphoenolpyruvate:sugar phosphotransferase system from an Escherichia coli enzym
64 e Escherichia coli phosphoenolpyruvate:sugar phosphotransferase system has been investigated by heter
65 the mannitol branch of the Escherichia coli phosphotransferase system has been solved by multidimens
66 f the mannose branch of the Escherichia coli phosphotransferase system has been solved by NMR using c
67 arrier protein (HPr) of the Escherichia coli phosphotransferase system has been solved by NMR, includ
70 components of all branches of the bacterial phosphotransferase system, have been examined using NMR
71 hocarrier of the phosphoenolpyruvate:glycose phosphotransferase system, IIA(Glc) (formerly known as I
72 r protein of the phosphoenolpyruvate:glycose phosphotransferase system, IIAGlc (also known as IIIGlc)
75 The various substrate specificities among phosphotransferase systems in different genomes apparent
76 ng trypotophan production and the galactitol phosphotransferase system (including dihydroxyacetone ph
77 e Escherichia coli phosphoenolpyruvate:sugar phosphotransferase system inhibits transport catalyzed b
78 in IIA(Glc) of the phosphoenolpyruvate:sugar phosphotransferase system is an activator of adenylyl cy
81 hat NagE, a putative component of the GlcNAc phosphotransferase system, is required for growth on and
82 ptsI of the phosphoenolpyruvate:carbohydrate phosphotransferase system lowered transformation frequen
83 by means of the phosphoenolpyruvate/glycose phosphotransferase system mutate further to permit growt
84 e phosphoenolpyruvate-dependent carbohydrate phosphotransferase system of Escherichia coli carries ou
85 yme I (EIN) of the phosphoenolpyruvate:sugar phosphotransferase system of Escherichia coli has been d
87 glc) (EIIA) of the phosphoenolpyruvate:sugar phosphotransferase system of Mycoplasma capricolum was c
88 ties between the phosphoenolpyruvate:glycose phosphotransferase system of V. furnissii and enteric ba
89 There are two paralogous Escherichia coli phosphotransferase systems, one for sugar import (PTS(su
90 lin2907 within a beta-glucoside (cellobiose):phosphotransferase system operon, may presage both enzym
92 o phosphorylation by the phosphoenolpyruvate phosphotransferase system (PEP-PTS) and for their impact
95 ediate, fructose 1,6-biphosphate, and by the phosphotransferase system phosphocarrier protein, IIIGlc
96 Escherichia coli phosphoenolpyruvate:glucose phosphotransferase system plays a direct role in regulat
97 e bacterial phosphoenolpyruvate:carbohydrate phosphotransferase system plays a key role in the regula
98 rotein IIAGlc, the phosphoenolpyruvate:sugar phosphotransferase system plays a role in the regulation
99 he crr gene of the phosphoenolpyruvate:sugar phosphotransferase system, plays an important role in re
100 nd ptsH2(encoding a homolog of the bacterial phosphotransferase system protein Hpr) genes were transc
102 s: a domain that binds the partner PEP:sugar phosphotransferase system protein, HPr; a domain that ca
103 HPr with three other structurally unrelated phosphotransferase system proteins, enzymes I, IIA(gluco
107 specific phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS II transport enzyme).
108 plus validation work with bacterial mannose phosphotransferase system (PTS(man))-defective strains,
112 s is accomplished by the phosphoenolpyruvate-phosphotransferase system (PTS) and ATP-binding cassette
113 t requires the phosphoenolpyruvate-dependent phosphotransferase system (PTS) and is independent of an
114 des the Aga phosphoenolpyruvate:carbohydrate phosphotransferase system (PTS) and other catabolic enzy
115 components of the phosphoenolpyruvate-sugar phosphotransferase system (PTS) and their subsequent reg
116 lation, likely due to its ability to use the phosphotransferase system (PTS) as regulatory machinery
117 depends on the phosphoenolpyruvate: sucrose phosphotransferase system (PTS) but is unaffected by a m
118 ry proteins of the phosphoenolpyruvate:sugar phosphotransferase system (PTS) but no recognizable homo
119 The bacterial phosphoenolpyruvate/glycose phosphotransferase system (PTS) comprises a group of pro
120 The bacterial phosphoenolpyruvate-dependent phosphotransferase system (PTS) consists of a set of cyt
121 e bacterial phosphoenolpyruvate-carbohydrate phosphotransferase system (PTS) consists of cascading ph
124 we report that cells defective for the sugar phosphotransferase system (PTS) exhibited a magnesium-in
125 mutants in the phosphoenolpyruvate-dependent phosphotransferase system (PTS) exhibited Streptolysin S
128 phoenolpyruvate-dependent sugar-transporting phosphotransferase system (PTS) have previously been ide
129 not fully known, one implicated pathway is a phosphotransferase system (PTS) in E. faecalis strain OG
131 e Escherichia coli phosphoenolpyruvate:sugar phosphotransferase system (PTS) in prokaryotes mediates
138 of the bacterial phosphoenolpyruvate:glycose phosphotransferase system (PTS) is autocatalytically pho
139 Escherichia coli phosphoenolpyruvate: sugar phosphotransferase system (PTS) is the 64-kDa protein en
142 bacterial phosphoenolpyruvate (PEP):glycose phosphotransferase system (PTS) mediates uptake/phosphor
143 e phosphoenolpyruvate-dependent carbohydrate phosphotransferase system (PTS) of Escherichia coli, bot
144 of the glucose-specific phosphoenolpyruvate:phosphotransferase system (PTS) of Escherichia coli, is
145 ase/phosphatase is a common component of the phosphotransferase system (PTS) of gram-positive bacteri
148 d "bepA," putatively encoding a carbohydrate phosphotransferase system (PTS) permease (biofilm and en
149 idase (CelA) and a cellobiose-specific sugar phosphotransferase system (PTS) permease (EII(Cel)).
150 a previously uncharacterized mannose family phosphotransferase system (PTS) permease, and we designa
152 The phosphoenolpyruvate (PEP)-dependent phosphotransferase system (PTS) phosphorylates sugars an
153 The bacterial phosphoenolpyruvate:glycose phosphotransferase system (PTS) plays a central role in
155 virulence regulator Mga contains homology to phosphotransferase system (PTS) regulatory domains (PRDs
156 genome-wide approach, we identified the GAS phosphotransferase system (PTS) responsible for non-MalE
158 influenced by environmental signals, such as phosphotransferase system (PTS) sugars, biotin, and amin
159 One such pathway is the phosphoenolpyruvate phosphotransferase system (PTS), a multicomponent sugar
160 erichia coli phosphoenolpyruvate (PEP):sugar phosphotransferase system (PTS), and a cloned amino-term
161 zyme II of the phosphoenolpyruvate-dependent phosphotransferase system (PTS), contains a duplicated I
163 fructose via the phosphoenolpyruvate/glycose phosphotransferase system (PTS), further mutants were se
164 ucose-specific phosphocarrier protein of the phosphotransferase system (PTS), IIAGlc (IIIGlc in older
165 was abolished when a plasmid containing the phosphotransferase system (PTS), phospho-beta-galactosid
167 e Escherichia coli phosphoenolpyruvate:sugar phosphotransferase system (PTS), the sugar-specific enzy
168 strates of the phosphoenolpyruvate-dependent phosphotransferase system (PTS), we show that PTS sugar
169 scription factor and a sugar permease of the phosphotransferase system (PTS), which are predicted to
170 switching can occur in the Escherichia coli phosphotransferase system (PTS), which regulates the upt
171 nse to glucose-specific phosphoenolypyruvate phosphotransferase system (PTS)-dependent phosphosugar s
181 ncluding three phosphoenolpyruvate-dependent phosphotransferase systems (PTS) and a binding protein-d
182 copiotrophs, like Vibrios, possess numerous phosphotransferase systems (PTS), prototypical oligotrop
184 ride synthase), and the scrAB pathway (sugar-phosphotransferase system [PTS] permease and sucrose-6-P
185 ntal caries, possesses at least two fructose phosphotransferase systems (PTSs), encoded by fruI and f
188 HTH2) and phosphoenolpyruvate: carbohydrate phosphotransferase system-regulated domains (PRD1 and PR
189 of an RNA-binding domain and two reiterated phosphotransferase system regulation domains (PRDs).
190 AtxA of two PTS (phosphenolpyruvate : sugar phosphotransferase system) regulation domains (PRD) gene
192 that connect elevated PEP/pyruvate ratios to phosphotransferase system signaling and adenylate cyclas
193 predicting the rates of phosphoenolpyruvate phosphotransferase system sugar uptake in whole cells.
194 of the phosphoenol pyruvate dependent:sugar phosphotransferase system suggests participation of MalB
195 hia coli encodes a phosphoenolpyruvate:sugar phosphotransferase system that metabolizes the hexitol D
196 is of RMC26 produced defects in the sorbitol phosphotransferase system that prevented the transport o
197 Escherichia coli phosphoenolpyruvate: sugar phosphotransferase system, that between histidine-contai
198 omplexes of HPr with partner proteins of the phosphotransferase system, the N-terminal domain of enzy
199 P phosphomimetic mutant HPr S46D had reduced phosphotransferase system transport rates and limited in
200 ly regulated by coaggregation, including two phosphotransferase system transporters and several other
201 sphocarrier protein (HPr) from the bacterial phosphotransferase system, we have identified a minor sp
202 olic pathways, i.e. benzoate degradation and phosphotransferase system, were identified to be closely