Proceedings of the National Academy of Sciences · 2011 · 196 citations · 35 references
Mycobacterium tuberculosis must import iron from its host for survival, and its siderophore-dependent iron acquisition pathways are well established. Here we demonstrate a newly characterized pathway, whereby M. tuberculosis can use free heme and heme from hemoglobin as an iron source. Significantly, we identified the genomic region, Rv0202c-Rv0207c, responsible for the passage of heme iron across the mycobacterial membrane. Key players of this heme uptake system were characterized including a secreted protein and two transmembrane proteins, all three specific to mycobacteria. Furthermore, the crystal structure of the key heme carrier protein Rv0203 was found to have a unique fold. The discovery of a unique mycobacterial heme acquisition pathway opens new avenues of exploration into mycobacterial therapeutics.
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Searching protein structure databases with DaliLite v.3
Liisa Holm, Sakari Kääriäinen, Päivi Rosenström et al. · Bioinformatics · 2008 · 1K citations · Full text
Passage of Heme-Iron Across the Envelope of <i>Staphylococcus aureus</i>
Sarkis K. Mazmanian, Eric P. Skaar, Andrew H. Gaspar et al. · Science · 2003 · 578 citations
Structural evidence for gene duplication in the evolution of the acid proteases
Jordan Tang, Michael N.G. James, I.-N. Hsu et al. · Nature · 1978 · 408 citations