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1 s bound tightly in a complex with the folded colicin E3.
2 366-Arg399 of the helix-loop-helix region of colicin E3.
3 llular import of colicins such as the rRNase colicin E3.
4  in colicin E9 is identical to that found in colicin E3, an RNase type E colicin.
5             Comparative sequence analysis of colicin E3 and cloacin DF13, which is also an RNase-type
6 channels in planar bilayers were occluded by colicins E3 and E1, respectively, from the trans-side of
7                The OmpF recognition sites of colicins E3 and N, and the TolC recognition site of coli
8 mplex, the colicin translocon, consisting of colicin E3, BtuB and OmpF.
9 coefficient appropriate for a BtuB-detergent-colicin E3 complex, demonstrating that monomeric BtuB re
10  with the coiled-coil BtuB-binding domain of colicin E3 did not reveal displacement of the BtuB plug
11       Surprisingly, the crystal structure of colicin E3 does not possess a recognizable globular fold
12 e effect of the receptor binding fragment of colicin E3 (E3R) on the conformation of the Ton box was
13 due coiled-coil receptor-binding R-domain of colicin E3 (E3R135) suggested a novel mechanism for impo
14 avage of 16S rRNA at position 1493 using the colicin E3 endonuclease and replacing the resulting 3'-t
15 x of BtuB and the receptor binding domain of colicin E3 forms a basis for further analysis of the mec
16 t-defective protein, or by the addition of a Colicin E3 fragment, which stabilizes the Ton box in a f
17       The 315-residue N-terminal T domain of colicin E3 functions in translocation of the colicin acr
18 is system for cloning a highly potent toxin, Colicin E3, in the absence of its cognate immunity prote
19                         The lethal action of colicin E3 is a specific cleavage in the ribosomal decod
20                           Cellular import of colicin E3 is initiated by high affinity binding of the
21 lease-fold, and RNases of the EndoU-like and colicin E3-like cytotoxic RNases-folds.
22                                              Colicin E3 molecules of sufficient length display normal
23 th the crystallographic observation that the colicin E3 receptor-binding domain can contact almost al
24                     The crystal structure of colicin E3, reported here in a binary complex with its i
25 constitution of Imm in a complex with C96 or colicin E3 restored the native structure.
26  within the hydrophobic core of the isolated colicin E3 rRNase domain causes the enzyme to become an
27 by inducing one partner of the high-affinity colicin E3 rRNase domain-Im3 complex (K(d) approximately
28 3 residue glycine-rich N-terminal segment of colicin E3 (T83) that occludes OmpF ion channels yielded
29  domain of colicin Ia is replaced by that of colicin E3, this chimera effectively kills cells, provid
30 fer the C-terminal cytotoxic domain (C96) of colicin E3 through the Escherichia coli outer membrane.
31 e translocation and cytotoxic domains of the colicin E3 was observed upon colicin binding in vitro to
32 -domain of colicin E2, compared with that of colicin E3, was extended by two and five residues at the
33               The receptor-binding domain of colicin E3, which binds to BtuB competitively with CNCbl
34                         The preincubation of colicin E3 with stoichiometric levels of BtuB protects s