Molecular Recognition at the Active Site of Catechol‐O‐Methyltransferase: Energetically Favorable Replacement of a Water Molecule Imported by a Bisubstrate Inhibitor
- 11 November 2009
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 48 (48) , 9092-9096
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- Crystal structures of rat catechol-O-methyltransferase complexed with coumarine-based inhibitorBiochemical and Biophysical Research Communications, 2009
- Exploiting Ordered Waters in Molecular DockingJournal of Medicinal Chemistry, 2008
- Analysis of Ligand-Bound Water Molecules in High-Resolution Crystal Structures of Protein−Ligand ComplexesJournal of Chemical Information and Modeling, 2007
- Synthesis and Biological Evaluation of Potent Bisubstrate Inhibitors of the Enzyme CatecholO-Methyltransferase (COMT) Lacking a Nitro GroupHelvetica Chimica Acta, 2006
- WaterScore: a novel method for distinguishing between bound and displaceable water molecules in the crystal structure of the binding site of protein-ligand complexesJournal of Molecular Modeling, 2003
- COMT and schizophrenia: biology meets geneticsTrends in Biotechnology, 2001
- EntacaponeDrugs, 1999
- Just add water! The effect of water on the specificity of protein-ligand binding sites and its potential application to drug designChemistry & Biology, 1996
- Water: now you see it, now you don'tStructure, 1993
- Effects of methylation on the stability of nucleic acid conformations. Monomer levelBiochemistry, 1974