| Literature DB >> 24631931 |
Lyndel Mason1, Leon Tribolet2, Anne Simon3, Natascha von Gnielinski1, Lisa Nienaber1, Paul Taylor4, Charlene Willis5, Malcolm K Jones6, Paul W Sternberg7, Robin B Gasser8, Alex Loukas9, Andreas Hofmann10.
Abstract
Hookworm activation-associated secreted proteins can be structurally classified into at least three different groups. The hallmark feature of Group 1 activation-associated secreted proteins is a prominent equatorial groove, which is inferred to form a ligand binding site. Furthermore, a conserved tandem histidine motif is located in the centre of the groove and believed to provide or support a yet to be determined catalytic activity. Here, we report three-dimensional crystal structures of Na-ASP-2, an L3-secreted activation-associated secreted protein from the human hookworm Necator americanus, which demonstrate transition metal binding ability of the conserved tandem histidine motif. We further identified moderate phosphohydrolase activity of recombinant Na-ASP-2, which relates to the tandem histidine motif. By panning a random 12-mer peptide phage library, we identified a peptide with high similarity to the human calcium-activated potassium channel SK3, and confirm binding of the synthetic peptide to recombinant Na-ASP-2 by differential scanning fluorimetry. Potential binding modes of the peptide to Na-ASP-2 were studied by molecular dynamics simulations which clearly identify a preferred topology of the Na-ASP-2:SK3 peptide complex.Entities:
Keywords: Activation-associated secreted proteins; Host–parasite interactions; Pathogenesis-related proteins; Protein structure; SCP/TAPS proteins
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Year: 2014 PMID: 24631931 DOI: 10.1016/j.biocel.2014.03.003
Source DB: PubMed Journal: Int J Biochem Cell Biol ISSN: 1357-2725 Impact factor: 5.085