Võrdle meetodeid

	Farmakofoorimudelite loomine	Homoloogia modelleerimine	Molekulaarne dokkimine
Valdkond	Bioinformaatika	Bioinformaatika	Bioinformaatika
Perekond	Process / pipeline	Process / pipeline	Process / pipeline
Tekkeaasta	1977	1993	1982
Looja	Peter Gund	Andrej Sali	Irwin Kuntz
Tüüp	Pattern-based virtual screening pipeline	Comparative structure prediction pipeline	Binding prediction pipeline
Algallikas	Wermuth, C. G., Ganellin, C. R., Lindberg, P., & Mitscher, L. A. (1998). Glossary of terms used in medicinal chemistry. Pure and Applied Chemistry, 70(5), 1129-1143.	Sali, A. & Blundell, T. L. (1993). Comparative protein modelling by satisfaction of spatial restraints. Journal of Molecular Biology, 234(3), 779-815.	Kuntz, I. D., Blaney, J. M., Oatley, S. J., Langridge, R., & Ferrin, T. E. (1982). A geometric approach to macromolecule-ligand interactions. Journal of Molecular Biology, 161(2), 269-288.
Rööpnimetused	pharmacophore pattern recognition, 3D pharmacophore	comparative modeling, template-based modeling	protein-ligand docking, binding prediction
Seotud	3	4	4
Kokkuvõte	Pharmacophore modeling identifies the spatial arrangement of molecular features (hydrogen bond donors, acceptors, aromatic rings) that are essential for biological activity. Introduced by Gund in 1977, this ligand-based method creates a three-dimensional pattern that can screen chemical libraries and design new active compounds without requiring receptor structure.	Homology modeling, also called comparative modeling, predicts the three-dimensional structure of a protein using an experimentally-solved structure of a homologous protein as a template. Introduced by Sali and Blundell in 1993, this method exploits the principle that homologous proteins share similar spatial structures despite differing in amino acid sequence.	Molecular docking predicts the preferred binding orientation and affinity of a ligand (small molecule) within a protein binding pocket. Pioneered by Kuntz and colleagues in 1982, this computational method searches conformational space to find energetically favorable ligand-protein complexes, enabling rapid screening of chemical libraries for drug discovery.