Conjunts de dades de producció científicaBioquímica i Biotecnologia

Site contribution to the energy-optimized pharmacophores obtained from PDB complexes in bold from Table 1.

  • Identification data

    Identifier:  PC:4052
    Authors:  Guasch, Laura
    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.
  • Others:

    Document type: info:eu-repo/semantics/other
    DOI: 10.1371/journal.pone.0044971.t002
    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
    Research group: Nutrigenòmica
    Departament: Bioquímica i Biotecnologia
    Author: Guasch, Laura
    Repository ingest date: 2012-09-12
    Dataset publication year: 2012
    Subject matter: Bioquímica
    Researcher identifier: 0000-0003-4990-7765
    Related publication's DOI: 10.1371/journal.pone.0044971
    Language: en
    Published by (editorial): Universitat Rovira i Virgili (URV)
    Access rights: info:eu-repo/semantics/openAccess
    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.
  • Keywords:

    energy-optimized
    pharmacophores
    pdb
    complexes
    Bioquímica
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