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  • Title: Conformational changes of the Tet repressor induced by tetracycline trapping.
    Author: Orth P, Cordes F, Schnappinger D, Hillen W, Saenger W, Hinrichs W.
    Journal: J Mol Biol; 1998 Jun 05; 279(2):439-47. PubMed ID: 9642048.
    Abstract:
    The X-ray crystal structure analysis of inducer-free Tet repressor, TetR, at 2.4 A resolution identifies one of two openings of the tunnel-like binding site as the entrance for the inducer tetracycline-Mg2+, [Mg Tc]+. Recognition and binding of the inducer unleashes conformational changes leading to the induced state of TetR. In the first step, the C-terminal turn of alpha-helix 6 unwinds, thereby altering the orientation of alpha-helix 4. This different orientation of alpha-helix 4 is stabilized by a series of hydrogen bonds mediated through a chain of eight water molecules. The alpha-helix 4 connects the DNA-binding domain (alpha-helices 1 to 3) to the rigid TetR core, and thus regulates gene expression through its respective orientations.
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