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