Subject matter: Bioquímica
Access rights: info:eu-repo/semantics/openAccess
Researcher identifier: 0000-0003-4990-7765
Published by (editorial): Universitat Rovira i Virgili (URV)
Related publications: Guasch, L., Ojeda, M. J., González-Abuín, N., Sala, E., Cereto-Massagué, A., Mulero, M., Valls, C., Pinent, M., Ardévol, A., Garcia-Vallvé, S., & Pujadas, G. (2012). Identification of novel human dipeptidyl peptidase-iv inhibitors of natural origin (Part i): Virtual screening and activity assays. PLoS ONE, 7(9), e44971. https://doi.org/10.1371/journal.pone.0044971
Abstract: Required and optional sites at the structure-based common pharmacophore are shown in bold and italics, respectively. The other sites are not part of the structure-based common pharmacophore. Data at the same raw for different PDB complexes indicate that the pharmacophore site is shared by these complexes.
Departament: Bioquímica i Biotecnologia
DOI: 10.1371/journal.pone.0044971.t002
Document type: info:eu-repo/semantics/other
Related publication's DOI: 10.1371/journal.pone.0044971
Repository ingest date: 2012-09-12
Author: Guasch, Laura
Keywords: energy-optimized, pharmacophores, pdb, complexes
Research group: Nutrigenòmica
Dataset publication year: 2012
Dataset title: Site contribution to the energy-optimized pharmacophores obtained from PDB complexes in bold from Table 1.
Repositori URV