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1 the cytoplasmic membrane through a type III protein secretion system.
2 imers, to engineer the first light-triggered protein secretion system.
3 is injected into plant cells by the type III protein secretion system.
4 (S. typhimurium-NY-ESO-1) through a type III protein secretion system.
5 determinant of this pathogen is its type III protein secretion system.
6 components, nitrogen fixation and a type-III protein secretion system.
7 dependent on a functional type III bacterial protein secretion system.
8 ella pathogenicity island 1-encoded type III protein secretion system.
9 henotypes associated with the SPI-1 type III protein secretion system.
10 ted into host mammalian cells via a type III protein secretion system.
11 that R. l. bv. viciae 3841 has ten putative protein secretion systems.
12 E (GspE) family of proteins found in type II protein secretion systems.
13 se of other loci that encode DNA transfer or protein secretion systems, all of which are members of t
14 ce modifications but more genes for Sec-like protein secretion systems, anaplerotic CO(2) incorporati
15 gen Pseudomonas syringae requires a type-III protein secretion system and the effector proteins it in
16 nsitive response and pathogenicity) type III protein secretion system and the effector proteins it tr
17 hese events chiefly depend upon the type III protein secretion system and the effector proteins that
18 n Pseudomonas syringae depends on a type III protein secretion system and the effector proteins that
19 y express both the HR and pathogenesis (Hrp) protein secretion system and the HrpZ harpin from P. syr
20 hanisms of substrate recognition by type III protein secretion systems and AAA + ATPase disassembly m
21 MFPs) are essential components of the type I protein secretion systems and drug efflux pumps in Gram-
22 ion system that is conserved in all type III protein secretion systems and is required for most patho
23 rmation for further understanding chlamydial protein secretion systems and modeling COMC and EB struc
24 process found to be dependent on a type III protein secretion system, and SipB, a protein with membr
26 hylum Bacteroidetes, suggesting that similar protein secretion systems are common among members of th
30 e that GBPs detect the presence of bacterial protein secretion systems as "patterns of pathogenesis"
31 O, which encode components of a bacteroidete protein secretion system, blocked the transport of RemA
35 tures with the previously described type III protein secretion system effector ILEs and are considere
36 Salmonella typhimurium uses of a type III protein secretion system encoded at centisome 63 of its
41 rapid, specific, and depends on the type III protein secretion system encoded within Salmonella patho
42 gely dependent on the function of a type III protein-secretion system encoded at centisome 63 of its
43 pression of the invasion-associated Type III protein-secretion system encoded at centisome 63 of the
44 ncodes a component of a virulence-associated protein secretion system, enhanced the apoptosis of infe
45 virulence mechanisms, including the type VII protein secretion system ESX-1, biosynthesis of polyketi
47 aureus pathogenesis depends on a specialized protein secretion system (ESX-1) that delivers a range o
48 ow 20 degrees C and that a bacterial type II protein secretion system facilitates growth at low tempe
49 s include the switching between two type III protein secretion systems, flagellum biosynthesis (</=30
50 ) whose products show similarity to type III protein secretion systems found in plant and animal path
56 considerably advance knowledge of the plant protein secretion system in general and emphasize the ve
57 also hinted at the existence of a dedicated protein secretion system in Gram-positive bacteria, targ
60 aments analogous to curli are formed by many protein secretion systems, including the type III secret
61 land 1 controls the expression of a type III protein secretion system involved in the invasion of hos
64 with the general rule that the expression of protein secretion systems is tightly regulated, expressi
66 t eukaryotic hosts is a class of specialized protein secretion systems (known as type III protein sec
69 e Hrp pilus is assembled by the Hrp type III protein secretion system of Pseudomonas syringae pv. tom
72 are also conserved in the type III virulence protein secretion systems of animal pathogenic Yersinia,
74 ponents of multidrug efflux pumps and type I protein secretion systems of gram-negative bacteria.
77 ly secretory antigen target 6 kDa secretion) protein secretion systems require FtsK/SpoIIIE family AT
79 rect or indirect restriction of the type III protein secretion system's (T3SS) ability to inject type
81 s a Gram-negative bacterium that possesses a protein secretion system similar to those found in Salmo
82 We have shown here that two targets of this protein-secretion system, SipB and SipC, are translocate
83 genome of Q8r1-96 and identified a type III protein secretion system (T3SS) gene cluster that has ov
84 herichia coli (EPEC and EHEC) use a type III protein secretion system (T3SS) to inject microbial prot
88 e pathogenic bacteria have evolved a complex protein secretion system termed type III to deliver bact
89 thogenic bacteria have evolved a specialized protein secretion system termed type III to secrete and
91 lants and animals have evolved a specialized protein-secretion system termed type III to deliver bact
92 host-cell cytosol by means of a specialized protein-secretion system (termed type III), which causes
93 consequence of this interaction, a dedicated protein secretion system, termed type III, is activated
94 enesis pathway is one of the best-understood protein secretion systems, thanks largely to innovative
95 Salmonella enterica has evolved a type III protein secretion system that allows these enteropathoge
96 P. syringae hrp/hrc genes encode a type III protein secretion system that appears to translocate Avr
97 is interaction is the function of a type III protein secretion system that delivers effector proteins
98 en Pseudomonas syringae possesses a type III protein secretion system that delivers many virulence pr
99 the Salmonella chromosome encodes a type III protein secretion system that is essential for its patho
100 ealed that this region encodes a specialized protein secretion system that mediates the export and/or
101 rous bacterial pathogens possess specialized protein secretion systems that are dedicated to the expo
102 lence factors and contains three of the four protein secretion systems that have been described in gr
103 eria, type II secretion (T2S) is one of five protein secretion systems that permit the export of prot
104 protein secretion systems (known as type III protein secretion systems) that deliver bacterial virule
112 Many bacterial pathogens use a type III protein secretion system to deliver virulence effector p
113 hogens use at least 6 distinct extracellular protein secretion systems to export proteins through the
115 ant pathogen that is dependent on a type III protein secretion system (TTSS) and the effector protein
116 ected with Salmonella: SipB and the type III protein secretion system (TTSS) encoded by Salmonella pa
118 hrp pathogenicity island encodes a type III protein secretion system (TTSS) that is required for pat
120 into host cells via the hrp-encoded type III protein secretion system (TTSS) to facilitate pathogenes
123 predicted amino acid homologies with type I protein secretion systems (typified by Escherichia coli
124 nd ChiX operate in tandem as components of a protein secretion system used by gram-negative bacteria.
125 lE, a pectate lyase secreted via the type II protein secretion system, was not associated with the Hr
127 ions in genes that encode components of this protein-secretion system were devoid of macrophage cytot
128 and HrpT are all components of the type III protein secretion system whereas HrpV is a negative regu
129 of Salmonella typhimurium encode a type III protein secretion system which is essential for the abil
131 DC3000 to infect host plants is the type III protein secretion system, which is thought to deliver mu
132 umophila is dependent on the Dot/Icm type IV protein secretion system, which translocates effectors i
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