## Abstract Solvent effects play a crucial role in mediating the interactions between proteins and their ligands. Implicit solvent models offer some advantages for modeling these interactions, but they have not been parameterized on such complex problems, and therefore, it is not clear how reliable
Comparison of generalized born and poisson models: Energetics and dynamics of HIV protease
✍ Scribed by David, Laurent; Luo, Ray; Gilson, Michael K.
- Book ID
- 102646190
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 564 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0192-8651
No coin nor oath required. For personal study only.
✦ Synopsis
This study characterizes the accuracy of energies and forces computed with a generalized Born (GB) model and the distance-dependent dielectric (DDD) model with respect to detailed finite solutions of the Poisson equation (FDPE). Tests are done for a small molecule in solution and for HIV-1 protease with inhibitor, KNI-272. GB agrees well with FDPE for the small molecule, but less well for the protein system. The correlation between GB and FDPE energies is poorest in calculations of changes upon binding. Also, forces computed with the GB model are less accurate than energies. The DDD model is far less accurate than GB. Nanosecond stochastic dynamics simulations of HIV-1 protease with an empty active site are used to examine the consequence of the models for the conformational preferences of the active site. Interestingly, the active site flaps remain near their starting conformations in the FDPE and GB simulations but collapse into the active site in the DDD simulation.
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## Abstract This study compares generalized Born (GB) and Poisson (PB) methods for calculating electrostatic solvation energies of proteins. A large set of GB and PB implementations from our own laboratories as well as others is applied to a series of protein structure test sets for evaluating the