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1 protective antigen, lethal factor (LF), and edema factor.
2 -protective antigen (PA), lethal factor, and edema factor.
3 rate proteins, called lethal factor (LF) and edema factor.
4 ive antigen (PA) with lethal factor (LF) and edema factor.
5 protective antigen (PA), lethal factor, and edema factor.
6 nated protective Ag (PA), lethal factor, and edema factor.
7 protective antigen (PA), lethal factor, and edema factor.
8 nergic effects provided by lethal factor and edema factor.
9 tance of LeTx, very recent studies show that edema factor, a potent adenyl cyclase, has the ability t
11 o other enzyme components, lethal factor and edema factor, across the plasma membrane and into the cy
13 aired in pore formation and in translocating edema factor and lethal factor across the endosomal memb
16 igen (PA) moiety of anthrax toxin transports edema factor and lethal factor to the cytosol of mammali
17 slocation of the enzymatic toxin components, edema factor and lethal factor, across the target cell m
18 y binds the enzymatic moieties of the toxin, edema factor and lethal factor, and translocates them ac
20 lasmid-encoded A/B-type toxins, edema toxin (edema factor and protective antigen) and lethal toxin (l
21 ted channel, which unfolds lethal factor and edema factor and translocates them into the host cytosol
22 protective antigen (PA), lethal factor, and edema factor and virulence plasmid pXO2 that encodes cap
23 ur MAb react with three different domains of edema factor, and all were able to detect purified edema
24 ther toxin components, the lethal factor and edema factor, and domain 4, the receptor binding domain
26 iphtheria toxin that is conserved in anthrax edema factor, anthrax lethal factor, and botulinum neuro
27 g domain (RBD or domain 4) or the lethal and edema factor binding domain (LEF or domain 1') were engi
31 i.e., protective antigen, lethal factor, and edema factor, disseminated from the lung to the spleen a
35 surface involves competitive binding of the edema factor (EF) and lethal factor (LF) to heptameric o
36 membranes that leads to the translocation of edema factor (EF) and lethal factor (LF) to the cytosol.
38 he anthrax toxins that act by binding to the edema factor (EF) and/or lethal factor (LF) components.
40 rough which catalytic lethal factor (LF) and edema factor (EF) are believed to translocate to the cyt
41 PA(63)), translocates lethal factor (LF) and edema factor (EF) from endosomes into the cytosol of the
42 ective antigen (PA), lethal factor (LF), and edema factor (EF) in a growth phase-dependent manner whe
43 -terminal segments of lethal factor (LF) and edema factor (EF) in anthrax toxin, we asked whether LF
46 tective Ag (PA) together with a B. anthracis edema factor (EF) mutant having reduced adenylate cyclas
49 (63) oligomerizes into heptamers, which bind edema factor (EF) or lethal factor (LF) to form the toxi
51 mediates the entry of lethal factor (LF) or edema factor (EF) through a membranal pore into target c
52 ly) form by binding of lethal factor (LF) or edema factor (EF) to the pore-forming moiety protective
57 nd Bacillus pertussis produce the AC toxins, edema factor (EF), and adenylyl cyclase toxin (ACT), res
58 e proteins, namely, protective antigen (PA), edema factor (EF), and lethal factor (LF), encoded by th
61 rotective antigen (PA), the adenylyl cyclase edema factor (EF), and the metalloproteinase lethal fact
62 the proteins, called Lethal Factor (LF) and Edema Factor (EF), are enzymes that act on cytosolic sub
63 nts of anthrax toxin, lethal factor (LF) and edema factor (EF), are transported to the cytosol of mam
64 n, consisting of protective antigen (PA) and edema factor (EF), causes the edema associated with cuta
65 protective antigen and an adenylate cyclase edema factor (EF), elicits edema in host tissues, but th
66 er enzyme components, lethal factor (LF) and edema factor (EF), into the cytosol of the host cell und
67 hrax toxin is made up of three proteins: the edema factor (EF), lethal factor (LF) enzymes, and the m
68 three proteins that comprise anthrax toxin, edema factor (EF), lethal factor (LF), and protective an
70 ), necessary for host cell toxin uptake, and edema factor (EF), the toxic moiety which increases host
72 ective antigen (PA), lethal factor (LF), and edema factor (EF), which interact at the surface of mamm
73 oieties of the toxin--lethal factor (LF) and edema factor (EF)--across the endosomal membrane of mamm
74 ective antigen (PA), lethal factor (LF), and edema factor (EF)-that come together in binary combinati
85 the effects of the anthrax edema toxin (ET; edema factor [EF] plus protective antigen [PA]) and leth
88 ent corresponding to the catalytic domain of edema factor (EF3) was cloned, overexpressed in Escheric
89 ino-terminal 32-kDa fragment of B. anthracis edema factor, EGFP-EF32, was used to confirm specificity
90 pose that the N terminus of PA63-bound LF or edema factor enters the PA63-channel under the influence
92 ected mutations based on the homology of the edema factor family revealed a conserved pair of asparta
93 Da domain (EF3-N) of EF3, the sole domain of edema factor homologous to adenylyl cyclases from Bordet
98 entry of the toxin's lethal factor (LF) and edema factor into the cytosolic compartment of mammalian
101 its two enzyme components, lethal factor and edema factor, into the host cytosol under the proton mot
102 nts of anthrax toxin [lethal factor (LF) and edema factor] into the cytosol of mammalian cells depend
104 d to establish lethal infection, whereas its edema factor modulates progression and dissemination of
106 h the two catalytic parts (lethal factor and edema factor) or other proteins can be transported into
107 surface and docking of lethal factor and/or edema factor, PA is internalized and undergoes a conform
108 Hence, ExoY is a promiscuous cyclase and edema factor that uses cAMP and, to some extent, cGMP to
111 Protective antigen (PA), lethal factor, and edema factor, the protein toxins of Bacillus anthracis ,
114 lethal factor, and/or the adenylate cyclase edema factor, to generate lethal toxin (LTx) and edema t
115 y the adenylyl cyclase domain of the anthrax edema factor toxin was simulated using the empirical val
116 ective antigen (PA), lethal factor (LF), and edema factor-translocates large proteins across membrane
117 roteolytically, attaches to lethal factor or edema factor, undergoes oligomerization and internalizat
118 Abs) produced against PA, lethal factor, and edema factor, were examined in animals infected with Bac
119 xins (lethal factor, protective antigen, and edema factor) where expressed 4-6-log10-fold less than i
120 ludes protective antigen, lethal factor, and edema factor, which are the components of anthrax toxin,
121 s from the interaction of N-CaM with anthrax edema factor, which binds N-CaM via its helical domain.
122 ve antigen (PA) and traces of the lethal and edema factors, which may contribute to adverse side effe
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