Hydration in drug design. 2. Influence of local site surface shape on water binding
- 1 December 1995
- journal article
- research article
- Published by Springer Nature in Journal of Computer-Aided Molecular Design
- Vol. 9 (6) , 513-520
- https://doi.org/10.1007/bf00124322
Abstract
Summary If water molecules are strongly bound at a protein-ligand interface, they are unlikely to be displaced during ligand binding. Such water molecules can change the shape of the ligand binding site and thus affect strategies for drug design. To understand the nature of water binding, and factors influencing it, water molecules at the ligand binding sites of 26 high-resolution protein-ligand complexes have been examined here. Water molecules bound in deep grooves and cavities between the protein and the ligand are located in the indentations on the protein-site surface, but not in the indentations on the ligand surface. The majority of the water molecules bound in deep indentations on the protein-site surface make multiple polar contacts with the protein surface. This may indicate a strong binding of water molecules in deep indentations on protein-site surfaces. The local shape of the site surface may influence the binding of water molecules that mediate protein-ligand interactions.Keywords
This publication has 53 references indexed in Scilit:
- The interpretation of protein structures: Estimation of static accessibilityPublished by Elsevier ,2004
- Detection of Long-lived Bound Water Molecules in Complexes of Human Dihydrofolate Reductase with Methotrexate and NADPHJournal of Molecular Biology, 1995
- Hydration of ProteinsJournal of Molecular Biology, 1993
- The interdependence of protein surface topography and bound water molecules revealed by surface accessibility and fractal density measuresJournal of Molecular Biology, 1992
- Refined structure of the complex between guanylate kinase and its substrate GMP at 2·0 Å resolutionJournal of Molecular Biology, 1992
- Determination of the positions of bound water molecules in the solution structure of reduced human thioredoxin by heteronuclear three-dimensional nuclear magnetic resonance spectroscopyJournal of Molecular Biology, 1991
- Refined crystal structure of type III chloramphenicol acetyltransferase at 1·75 Å resolutionJournal of Molecular Biology, 1990
- Structure of holo-glyceraldehyde-3-phosphate dehydrogenase from Bacillus stearothermophilus at 1.8 Å resolutionJournal of Molecular Biology, 1987
- Crystallographic refinement and atomic models of two different forms of citrate synthase at 2·7 and 1·7 Å resolutionJournal of Molecular Biology, 1982
- Structures of product and inhibitor complexes of Streptomyces griseus protease A at 1.8 Å resolutionJournal of Molecular Biology, 1980