3tao
Structure of Mycobacterium tuberculosis triosephosphate isomerase bound to phosphoglycolohydroxamateStructure of Mycobacterium tuberculosis triosephosphate isomerase bound to phosphoglycolohydroxamate
Structural highlights
Publication Abstract from PubMedTuberculosis (TB) is a major infectious disease that accounts for over 1.7 million deaths every year. Mycobacterium tuberculosis, the causative agent of tuberculosis, enters the human host by the inhalation of infectious aerosols. Additionally, one third of the world's population is likely to be infected with latent TB. The incidence of TB is on the rise owing in part to the emergence of multidrug-resistant strains. As a result, there is a growing need to focus on novel M. tuberculosis enzyme targets. M. tuberculosis triosephosphate isomerase (MtTPI) is an essential enzyme for gluconeogenetic pathways, making it a potential target for future therapeutics. In order to determine its structure, the X-ray crystal structure of MtTPI has been determined, as well as that of MtTPI bound with a reaction-intermediate analog. As a result, two forms of the active site were revealed. In conjunction with the kinetic parameters obtained for the MtTPI-facilitated conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (D-GAP), this provides a greater structural and biochemical understanding of this enzyme. Additionally, isothermal titration calorimetry was used to determine the binding constant for a reaction-intermediate analog bound to the active site of MtTPI. Structural and functional characterization of Mycobacterium tuberculosis triosephosphate isomerase.,Connor SE, Capodagli GC, Deaton MK, Pegan SD Acta Crystallogr D Biol Crystallogr. 2011 Dec;67(Pt 12):1017-22. Epub 2011 Nov 5. PMID:22120738[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See AlsoReferences
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