کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2047683 | 1074012 | 2013 | 5 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Structure of the (E)-4-hydroxy-3-methyl-but-2-enyl-diphosphate reductase from Plasmodium falciparum Structure of the (E)-4-hydroxy-3-methyl-but-2-enyl-diphosphate reductase from Plasmodium falciparum](/preview/png/2047683.png)
• LytB of the malaria pathogen Plasmodium falciparum was structurally characterized.
• The substrate and electron donor binding sites serve as targets for a search for antimalarian drugs.
• A LytB-[2Fe–2S] ferredoxin complex was modelled by docking calculations.
Terpenoid precursor biosynthesis occurs in human and many pathogenic organisms via the mevalonate and 2-C-methyl-d-erythritol-4-phosphate (MEP) pathways, respectively. We determined the X-ray structure of the Fe/S containing (E)-4-hydroxy-3-methyl-but-2-enyl-diphosphate reductase (LytB) of the pathogenic protozoa Plasmodium falciparum which catalyzes the terminal step of the MEP pathway. The cloverleaf fold and the active site of P. falciparum LytB corresponds to those of the Aquifex aeolicus and Escherichia coli enzymes. Its distinct electron donor [2Fe–2S] ferredoxin was modeled to its binding site by docking calculations. The presented structural data provide a platform for a rational search of anti-malarian drugs.
Journal: FEBS Letters - Volume 587, Issue 24, 11 December 2013, Pages 3968–3972