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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.
6 channels in planar bilayers were occluded by colicins E3 and E1, respectively, from the trans-side of
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
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 x of BtuB and the receptor binding domain of colicin E3 forms a basis for further analysis of the mec
15 t-defective protein, or by the addition of a Colicin E3 fragment, which stabilizes the Ton box in a f
17 is system for cloning a highly potent toxin, Colicin E3, in the absence of its cognate immunity prote
22 th the crystallographic observation that the colicin E3 receptor-binding domain can contact almost al
25 within the hydrophobic core of the isolated colicin E3 rRNase domain causes the enzyme to become an
26 by inducing one partner of the high-affinity colicin E3 rRNase domain-Im3 complex (K(d) approximately
27 3 residue glycine-rich N-terminal segment of colicin E3 (T83) that occludes OmpF ion channels yielded
28 domain of colicin Ia is replaced by that of colicin E3, this chimera effectively kills cells, provid
29 fer the C-terminal cytotoxic domain (C96) of colicin E3 through the Escherichia coli outer membrane.
30 e translocation and cytotoxic domains of the colicin E3 was observed upon colicin binding in vitro to
31 -domain of colicin E2, compared with that of colicin E3, was extended by two and five residues at the
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