We review various mathematical and computational techniques for drug discovery exemplifying
some recent works pertinent to group theory of nested structures of relevance to phylogeny, topological,
computational and combinatorial methods for drug discovery for multiple viral infections. We
have reviewed techniques from topology, combinatorics, graph theory and knot theory that facilitate
topological and mathematical characterizations of protein-protein interactions, molecular-target interactions,
proteomics, genomics and statistical data reduction procedures for a large set of starting chemicals
in drug discovery. We have provided an overview of group theoretical techniques pertinent to phylogeny,
protein dynamics especially in intrinsically disordered proteins, DNA base permutations and
related algorithms. We consider computational techniques derived from high level quantum chemical
computations such as QM/MM ONIOM methods, quantum chemical optimization of geometries complexes,
and molecular dynamics methods for providing insights into protein-drug interactions. We have
considered complexes pertinent to Hepatitis Virus C non-structural protein 5B polymerase receptor
binding of C5-Arylidebne rhodanines, complexes of synthetic potential vaccine molecules with dengue
virus (DENV) and HIV-1 virus as examples of various simulation studies that exemplify the utility of
computational tools. It is demonstrated that these combinatorial and computational techniques in conjunction
with experiments can provide promising new insights into drug discovery. These techniques
also demonstrate the need to consider a new multiple site or allosteric binding approach to drug discovery,
as these studies reveal the existence of multiple binding sites.
Quantitative Determination of the Conformational Properties of Partially Folded and Intrinsically Disordered Proteins Using NMR Dipolar Couplings