ToxT

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<Structure load='3gbg' color='cpk' size='500' frame='true' align='right' caption='ToxT, 1.9 Angstrom resolution' />
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<Structure load='3gbg' color='cpk' size='500' frame='true' align='right' caption='ToxT, 1.9 Angstrom resolution crystal structure' />
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Revision as of 23:44, 26 November 2011

ToxT, 1.9 Angstrom resolution crystal structure

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Introduction

ToxT is a molecule at the end of a transcriptional cascade that autoregulates the transcription of the primary virulence factors of Vibrio cholerae[1] and itself. These two factors, cholera toxin (CT)[2] and the toxin co-regulated pilus (TCP), are instrumental in causing the disease cholera[3]. This is an intestinal infection resulting in massive water loss in the affected individual, causing extreme dehydration.[4]

Structural Features

ToxT belongs to a family of transcriptional regulators known as AraC.[1] The AraC family is defined by a 100 amino acid region of sequence similarity that forms a DNA-binding domain with two helix-turn-helix motifs. [2]
A nine-stranded beta sheet sandwich contains a binding pocket that contains cis-palmitoleate, [1] which appears to have a negative effect on virulence when present in vitro. This unsaturated fatty acid, like other UFAs,[5] tend to inhibit genes under the control of ToxT.

References

  1. 1.0 1.1 Lowden MJ, Skorupski K, Pellegrini M, Chiorazzo MG, Taylor RK, Kull FJ. Structure of Vibrio cholerae ToxT reveals a mechanism for fatty acid regulation of virulence genes. Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):2860-5. Epub 2010 Feb 1. PMID:20133655
  2. Martin RG, Rosner JL. The AraC transcriptional activators. Curr Opin Microbiol. 2001 Apr;4(2):132-7. PMID:11282467
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