| Literature DB >> 20737579 |
Cheng Lei1, S Dean Rider, Cai Wang, Haili Zhang, Xiangshi Tan, Guan Zhu.
Abstract
We have successfully expressed recombinant mitochondrial-type ferredoxin (mtFd) and ferredoxin:NADP(+) reductase (mtFNR) from Cryptosporidium parvum and characterized their biochemical features for the first time for an apicomplexan. Both C. parvum mtFd (CpmtFd) and FNR (CpmtFNR) were obtained and purified as holo-proteins, in which the correct assembly of [2Fe-2S] cluster in Fd and that of FAD in FNR were confirmed and characterized by UV/vis and electron paramagnetic resonance. These proteins were fully functional and CpmtFNR was capable of transferring electrons from NADPH to CpmtFd in a cytochrome c-coupled assay that followed a typical Michaelis-Menten kinetics. Apicomplexan mtFd and mtFNR proteins were evolutionarily divergent from their counterparts in humans and animals and could be explored as potential drug targets in Cryptosporidium and other apicomplexans.Entities:
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Year: 2010 PMID: 20737579 PMCID: PMC3005779 DOI: 10.1002/pro.487
Source DB: PubMed Journal: Protein Sci ISSN: 0961-8368 Impact factor: 6.725