Theoretical Model: The protein structure described on this page was determined theoretically, and hence should be interpreted with caution.


Model: Botulinum Neurotoxin Serotype A Endopeptidase Liganded with a Small-Molecule Inhibitor HAB

Botulinum neurotoxin serotype A (BoNTA) causes botulism[1][2][3]. Small-molecule inhibitors of BoNTA endopeptidase (BoNTAe) are sought in our laboratories as potential antidotes to antagonize the extracellular or intracellular BoNTA[4][5][6]. HAB is one such inhibitor that exhibits nanomolar potency in inhibiting BoNTAe (to be published). Multiple molecular dynamics simulations of HAB•BoNTAe (20 10-ns-long simulations) suggest that one functional group of HAB is highly flexible or intrinsically disordered; the percentages of the top three most-populated conformations of the complex (Models 1-3) are 21%, 13% and 12%, respectively. To evaluate the computational methods, the coordinates of the three models were released before the forthcoming crystal structure of HAB•BoNTAe. Only 33% of the heavy atoms of HAB are provided in the released models[7]. The full structure of HAB will be released upon manuscript acceptance[8].

Download the coordinates of Models 1 (Hab1.pdb), 2 (Hab2.pdb), and 3 (Hab3.pdb) (PDB format)

References & Notes