Literature DB >> 20663481

The tuberculosis structural genomics consortium: a structural genomics approach to drug discovery.

Tracey L Musa1, Thomas R Ioerger, James C Sacchettini.   

Abstract

Structural genomics is changing the way we study and understand biological systems, providing insight into the biology and life cycle of an organism at the molecular level through determination of protein structures. Structural genomics can be a particularly useful tool in the study of infectious diseases, especially to facilitate the development of new chemotherapeutics by providing a structural foundation for drug discovery. The Tuberculosis Structural Genomics Consortium (TBSGC) is applying a structural genomics approach to solving the structures of biologically and medically important proteins in the pathogenic bacterium Mycobacterium tuberculosis, adding to the scientific knowledge base essential for developing novel and effective antitubercular drugs. Tuberculosis (TB) has been declared a global health emergency by the World Health Organization (WHO). With the rise in the number of multidrug resistant (MDR) and extensively drug resistant (XDR) TB strains, the need for more effective TB treatments has become urgent. In contrast to other structural genomics projects, the TBSGC specifically prioritizes proteins based on their potential as drug targets. We describe the consortium's high-throughput (HT) structure determination pipeline that enables an efficient distribution of resources while also incorporating knowledge from several scientific fields. The success of this pipeline is illustrated in the number of successful structure solutions as demonstrated in the case studies presented in this chapter. Copyright 2009 Elsevier Inc. All rights reserved.

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Year:  2009        PMID: 20663481     DOI: 10.1016/S1876-1623(09)77003-8

Source DB:  PubMed          Journal:  Adv Protein Chem Struct Biol        ISSN: 1876-1623            Impact factor:   3.507


  4 in total

1.  Modeling Protein-Ligand Binding by Mining Minima.

Authors:  Wei Chen; Michael K Gilson; Simon P Webb; Michael J Potter
Journal:  J Chem Theory Comput       Date:  2010-10-08       Impact factor: 6.006

2.  Mycobacterium thermoresistibile as a source of thermostable orthologs of Mycobacterium tuberculosis proteins.

Authors:  Thomas E Edwards; Reiling Liao; Isabelle Phan; Peter J Myler; Christoph Grundner
Journal:  Protein Sci       Date:  2012-05-24       Impact factor: 6.725

Review 3.  The impact of structural genomics: the first quindecennial.

Authors:  Marek Grabowski; Ewa Niedzialkowska; Matthew D Zimmerman; Wladek Minor
Journal:  J Struct Funct Genomics       Date:  2016-03-02

4.  Crystal structure of decaprenylphosphoryl-β- D-ribose 2'-epimerase from Mycobacterium smegmatis.

Authors:  Hua Li; Gerwald Jogl
Journal:  Proteins       Date:  2012-12-24
  4 in total

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