Journal article
Probing the equatorial groove of the hookworm protein and vaccine candidate antigen, Na-ASP-2
L Mason, L Tribolet, A Simon, N Von Gnielinski, L Nienaber, P Taylor, C Willis, MK Jones, PW Sternberg, RB Gasser, A Loukas, A Hofmann
International Journal of Biochemistry and Cell Biology | PERGAMON-ELSEVIER SCIENCE LTD | Published : 2014
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 fur..
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Awarded by Australian Research Council
Funding Acknowledgements
This study was supported by the Australian Research Council (ARC LP100100092 to RBG, AH, AL and PWS). We also gratefully acknowledge funding of our laboratories by the National Health and Medical Research Council (AH, MKJ, AL, RBG). LT is the recipient of an Australian Postgraduate Award. AL is the recipient of a principal research fellowship from NHMRC. Parts of this research were undertaken on the MX1 beamline at the Australian Synchrotron, Victoria, Australia.