Literature DB >> 17970225

Drug targets in mycobacterial sulfur metabolism.

Devayani P Bhave1, Wilson B Muse, Kate S Carroll.   

Abstract

The identification of new antibacterial targets is urgently needed to address multidrug resistant and latent tuberculosis infection. Sulfur metabolic pathways are essential for survival and the expression of virulence in many pathogenic bacteria, including Mycobacterium tuberculosis. In addition, microbial sulfur metabolic pathways are largely absent in humans and therefore, represent unique targets for therapeutic intervention. In this review, we summarize our current understanding of the enzymes associated with the production of sulfated and reduced sulfur-containing metabolites in Mycobacteria. Small molecule inhibitors of these catalysts represent valuable chemical tools that can be used to investigate the role of sulfur metabolism throughout the Mycobacterial lifecycle and may also represent new leads for drug development. In this light, we also summarize recent progress in the development of inhibitors of sulfur metabolism enzymes.

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Year:  2007        PMID: 17970225      PMCID: PMC3106421          DOI: 10.2174/187152607781001772

Source DB:  PubMed          Journal:  Infect Disord Drug Targets        ISSN: 1871-5265


  193 in total

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5.  MmpL8 is required for sulfolipid-1 biosynthesis and Mycobacterium tuberculosis virulence.

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Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-30       Impact factor: 11.205

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5.  High-throughput screening for inhibitors of Mycobacterium tuberculosis H37Rv.

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6.  CysK2 from Mycobacterium tuberculosis is an O-phospho-L-serine-dependent S-sulfocysteine synthase.

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7.  Geometric and electrostatic study of the [4Fe-4S] cluster of adenosine-5'-phosphosulfate reductase from broken symmetry density functional calculations and extended X-ray absorption fine structure spectroscopy.

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