Materia: Bioquímica
Derechos de acceso: info:eu-repo/semantics/openAccess
Identificador del investigador: 0000-0003-4990-7765
Publicado por (editorial): Universitat Rovira i Virgili (URV)
Publicaciones relacionadas: 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
Resumen: 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.
Departamento: Bioquímica i Biotecnologia
DOI: 10.1371/journal.pone.0044971.t002
Tipo de documento: info:eu-repo/semantics/other
DOI de la publicación relacionada: 10.1371/journal.pone.0044971
Fecha alta repositorio: 2012-09-12
Autor: Guasch, Laura
Palabras clave: energy-optimized, pharmacophores, pdb, complexes
Grupo de investigación: Nutrigenòmica
Año de publicación de la dataset: 2012
Título del conjunto de datos: Site contribution to the energy-optimized pharmacophores obtained from PDB complexes in bold from Table 1.
Repositori URV