This allows us to determine how well the validation stages predict consistent contacts that may play an important role in the inhibitory properties of the peptides. Such knowledge is important for future design studies. Taking the four lowest energy structures from the docking runs for the top peptide SQ037, the contacts observed consistently across the four structures were identified. The PDB files used in the analysis are provided in File S1. The analysis of the structures reveal three distinct contacts, found in all or most of the four structures. These include a contact between K24 of the peptide and D41 of the protein, W26 of the peptide and M57 of the protein, and N32 of the peptide and D108/Y109. While all of these contacts are interesting in interpreting the results of the study, the contact between K24 and D41 is intriguing in two regards. The first is that this constitutes a potential salt bridge, previously unexploited in the native structure. Further, the D41 amino acid is a position of conservation between the human and viral SET domains. Such novel contacts to the conserved binding site 1000669-72-6 residues may help determine which amino acid positions in the MS023 customer reviews designed sequence are important for antagonistic binding. Further analysis of the mutation constraints can be performed using structural analysis. The allowed mutations in each position are chosen based on the Solvent Accessible Surface Area of the template structure. This is such that buried polar groups would have the opportunity to mutate to hydrophobic residues that may fit the structural environment better. In the successful design from Run 4, there was one interesting position that mutated from a buried charged amino acid to a hydrophobic amino acid consistently, R26W. As mentioned previously, W26 is an interesting position due to its novel interactions with the hydrophobic M57 position in the structure of the top inhibitor, SQ037. However, upon visual inspection of the SQ037 structure, the interaction occurs primarily between the side-chain atoms of W26 and the main-chain atoms of M57. More interestingly, adjacent to the M57 position there is a negatively charged lysine re
