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• W2130506955 endingPage "634" @default.
• W2130506955 startingPage "628" @default.
• W2130506955 abstract "Abstract Psalmopeotoxin I (PcFK1) is a 33‐amino‐acid residue peptide isolated from the venom of the tarantula Psalmopoeus cambridgei . It has been recently shown to possess strong antiplasmodial activity against the intra‐erythrocyte stage of Plasmodium falciparum in vitro. Although the molecular target for PcFK1 is not yet determined, this peptide does not lyse erythrocytes, is not cytotoxic to nucleated mammalian cells, and does not inhibit neuromuscular function. We investigated the structural properties of PcFK1 to help understand the unique mechanism of action of this peptide and to enhance its utility as a lead compound for rational development of new antimalarial drugs. In this paper, we have determined the three‐dimensional solution structure by 1 H two‐dimensional NMR means of recombinant PcFK1, which is shown to belong to the ICK structural superfamily with structural determinants common to several neurotoxins acting as ion channels effectors." @default.
• W2130506955 created "2016-06-24" @default.
• W2130506955 creator A5001708789 @default.
• W2130506955 date "2006-03-01" @default.
• W2130506955 modified "2023-10-17" @default.
• W2130506955 title "Solution structure of PcFK1, a spider peptide active against Plasmodium falciparum" @default.
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• W2130506955 doi "https://doi.org/10.1110/ps.051860606" @default.
• W2130506955 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2249782" @default.
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• W2130506955 hasPublicationYear "2006" @default.
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