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1 te channels of sufficient length to span the periplasmic space.
2 long that spans both the outer membrane and periplasmic space.
3 nonfluorescent version was localized to the periplasmic space.
4 The latter is a lipoprotein located in the periplasmic space.
5 tes across the cytoplasmic membrane into the periplasmic space.
6 tions with other Mxi-Spa subunits within the periplasmic space.
7 ide bond in the oxidizing environment of the periplasmic space.
8 pI = 4.8) that probably is secreted into the periplasmic space.
9 ase that has its active site residing in the periplasmic space.
10 plex rather than being freely soluble in the periplasmic space.
11 li cells was found in the culture medium and periplasmic space.
12 e folding of proteins within the T. pallidum periplasmic space.
13 ts explain the stability of (GlcNAc)2 in the periplasmic space.
14 nant plasmid pHdSOD and was localized to the periplasmic space.
15 s surface and then translocating it into the periplasmic space.
16 s hydrophilic carboxyl domain located in the periplasmic space.
17 tive in the reduction environment within the periplasmic space.
18 sis upon their expression exclusively in the periplasmic space.
19 s that may connect cells at the level of the periplasmic space.
20 e channel, followed by diffusion towards the periplasmic space.
21 n outer and an inner membrane separated by a periplasmic space.
22 dominantly as internally oriented toward the periplasmic space.
23 r, whereas the other is pumped to the low-pH periplasmic space.
24 teins that are translocated to the bacterial periplasmic space.
25 membrane fusion protein (MFP) that spans the periplasmic space.
26 of biosynthesis of molecules located in the periplasmic space.
27 e passive diffusion of Hg(II) species to the periplasmic space.
28 proteins across the inner membrane into the periplasmic space.
29 mislocalized alginate that is trapped in the periplasmic space.
30 ts the transporter to the channel within the periplasmic space.
31 to the CM, and possibly having access to the periplasmic space.
32 tein PspA engineered to be secreted into the periplasmic space.
33 cilitate their rotation within the confining periplasmic space.
34 of flagellar filaments, displayed a uniform periplasmic space.
35 ester, is monomeric, and is localized to the periplasmic space.
36 oth inner and outer membranes separated by a periplasmic space.
37 lavins in RnfG and RnfD are localized in the periplasmic space.
38 domain (residues 46-618) protruding into the periplasmic space.
39 that formation of this complex occurs in the periplasmic space.
40 ytoplasm and only a fraction exported to the periplasmic space.
41 ps around the outside of the cell within the periplasmic space.
42 anslocation across the two membranes and the periplasmic space.
43 increasing the rate of Cbl release into the periplasmic space.
44 n digests the peptidoglycan cell wall in the periplasmic space.
45 ursor polypeptides from the cytoplasm to the periplasmic space.
46 hus demonstrating that the complex spans the periplasmic space.
47 ce is determined by the amount of GFP in the periplasmic space.
48 of the rod structure to proceed through the periplasmic space.
49 nt of iron associated with the cell wall and periplasmic space.
50 ization and protein folding in the bacterial periplasmic space.
51 in with calcofluor and aniline blue in their periplasmic space.
52 ortion of the exposure of the Ton box in the periplasmic space.
54 ranslocation across the OM and access to the periplasmic space (5-25 min later) correlates in time wi
55 pid moiety and oriented facing in toward the periplasmic space; a few lipoproteins have been shown to
56 -electron tomograms show that tubes span the periplasmic space and are present while the genome is be
57 s enable the colicin Ia molecule to span the periplasmic space and contact both the outer and plasma
59 mutants that would secrete FlgM-Bla into the periplasmic space and show ampicillin resistance (Ap(r))
60 The rod subunits self-assemble, spanning the periplasmic space and stopping at the outer membrane whe
61 lymerizes from the inner membrane across the periplasmic space and stops at a length of 25 nm at the
63 h itself was not resolved, is exposed to the periplasmic space and undergoes an extensive shift in po
64 of outer membrane protein precursors in the periplasmic space, and leads to the increased production
65 al being sent across the outer membrane, the periplasmic space, and the inner membrane, to a sigma fa
66 esis and translocation of DAT and PAT to the periplasmic space are coupled and topologically split ac
67 sing a library of proteins secreted into the periplasmic space are incubated with a fluorescent conju
68 e only portion of the protein exposed to the periplasmic space, are characterized by solution nuclear
69 1 remains unprocessed and is degraded in the periplasmic space, at least in part by the DegP protease
70 n the outer membrane and projects across the periplasmic space between inner and outer membranes.
71 at rod length is limited by the width of the periplasmic space between the inner and outer membranes.
72 t the SUN domain of Sun2 is localized to the periplasmic space between the inner and the outer nuclea
73 on is performed outside the cytoplasm in the periplasmic space between the plasma membrane and the ce
74 redoxin 1 can be efficiently exported to the periplasmic space by the signal sequence of the DsbA pro
75 ochromatium vinosum is translocated into the periplasmic space by the Tat system of Escherichia coli.
76 and C-terminal domains are positioned in the periplasmic space, connected by eight transmembrane segm
78 h the hypothesis that this protein spans the periplasmic space coordinating the concerted operation o
79 ccess of the Cbl-binding site of BtuB to the periplasmic space does not require removal of the hatch
80 Regions of subunit a that are exposed to the periplasmic space have been identified by a new procedur
81 gella are internalized, being incased in the periplasmic space; i.e., between the outer membrane and
84 TonB1, but not TonB2, can span the increased periplasmic space in high osmolarity and thus mediate ha
86 ne of these (the cytolysin/hemolysin) to the periplasmic space indicates that these proteins are norm
87 ively translocate virulence factors from the periplasmic space into the extracellular environment.
88 visualized as a thin layer that divided the periplasmic space into zones of higher and lower electro
90 ty of FbpA in the diverse composition of the periplasmic space is illustrated by the ex vivo exchange
94 as soluble antibody fragments (Fabs) in the periplasmic space of bacteria and isolated from small-sc
97 ng protein (FbpA) transports iron across the periplasmic space of certain Gram-negative bacteria and
98 is to transport unchelated Fe(3+) across the periplasmic space of certain Gram-negative bacteria, a p
99 combinant chimeras that were produced in the periplasmic space of E. coli as soluble pentamers, as co
100 ssembles with high fidelity and yield in the periplasmic space of E. coli cells, where it can success
101 in the production of holocytochrome f in the periplasmic space of E. coli, but the yield was low.
103 We show that rat PDI (rPDI) secreted in the periplasmic space of Escherichia coli can catalyze the f
105 ese mutants could be recovered form from the periplasmic space of Escherichia coli in a soluble form,
110 r layer and a low-density zone typifying the periplasmic space of gram-positive bacteria are apparent
111 T2SS) translocate virulence factors from the periplasmic space of many pathogenic bacteria into the e
112 9 kDa protein was expressed, exported to the periplasmic space of NovaBlue (DE) Escherichia coli, and
113 nFbp, a ferric-binding protein found in the periplasmic space of pathogenic Neisseria, has been char
115 itate the transport of naked Fe3+ across the periplasmic space of several Gram-negative bacteria.
117 , we propose that nitrate is detected in the periplasmic space of the cell, and that a signal-transdu
119 FbpA functions as an iron shuttle within the periplasmic space of these Gram-negative human pathogens
123 h the membrane and/or the environment of the periplasmic space results in improved folding of recombi
124 Experiments on the uptake of Cbl into the periplasmic space showed that this process is reversible
125 otein sites that are normally exposed in the periplasmic space tethers the scFv onto the inner membra
126 cetes, including a defined outer membrane, a periplasmic space that can be greatly enlarged and convo
127 riven by rotation of the flagella within the periplasmic space, the narrow ( approximately 20-40 nm i
137 li in a precursor form and exported into the periplasmic space upon cleavage of a 23-amino-acid leade
139 rA and PEB3, depends on translocation to the periplasmic space via the general secretory pathway.
140 in the cytoplasmic membrane and, ultimately, periplasmic space was confirmed using AnkB-BlaM and AnkB
142 hen upon activation is translocated into the periplasmic space, where it functions in pilus assembly.
143 cating its channel forming domain across the periplasmic space, where it inserts into the inner membr
144 ize that S. oneidensis secretes FAD into the periplasmic space, where it is hydrolysed by UshA to FMN
145 domain alpha-helical protein is found in the periplasmic space, where it supports an acid resistance
146 higher curvature of the outer membrane and a periplasmic space with 2-fold larger volume/area ratio t
147 permits reaction of sulfhydryl groups in the periplasmic space with MPB, but residues in the cytoplas
148 e as about 10 kDa can equilibrate within the periplasmic space without compromising the cell's integr
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