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Oxford University Press, Nucleic Acids Research, suppl(39), p. W261-W269, 2011

DOI: 10.1093/nar/gkr287

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Swimming into peptidomimetic chemical space using pepMMsMIMIC

Journal article published in 2011 by Matteo Floris ORCID, Masciocchi Joel, J. Masciocchi, Marco Fanton, Stefano Moro
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

pepMMsMIMIC is a novel web-oriented peptidomimetic compound virtual screening tool based on a multi-conformers three-dimensional (3D)-similarity search strategy. Key to the development of pepMMsMIMIC has been the creation of a library of 17 million conformers calculated from 3.9 million commercially available chemicals collected in the MMsINC® database. Using as input the 3D structure of a peptide bound to a protein, pepMMsMIMIC suggests which chemical structures are able to mimic the protein-protein recognition of this natural peptide using both pharmacophore and shape similarity techniques. We hope that the accessibility of pepMMsMIMIC (freely available at http://mms.dsfarm.unipd.it/pepMMsMIMIC) will encourage medicinal chemists to de-peptidize protein-protein recognition processes of biological interest, thus increasing the potential of in silico peptidomimetic compound screening of known small molecules to expedite drug development.