- A new forcefield for protein-ligand interactions has been added. It is a combination of MMFF94S (or MMFF94) with Amber. In this combined force field, MMFF94S is used to describe the intramolecular interactions of the ligand and the Amber force field is used for the VdW and Coulomb interactions between ligand and protein. Currently, this force field can be used only for ligands inside rigid proteins.
- Two new methods were added to the API:
`OESzybki.SetTorsionConstraint`and`OESzybki.ClearTorsionConstraint`. The first one adds a single-minimum harmonic torsional constraint for a torsion which is defined by a SMARTS pattern. It uses the functional form: \(V=k_c(cos(phi) - cos(phi0))^2\), where \(k_c\) is the user specified force constant and \(phi0\) is the reference torsion dihedral angle. The second method removes the torsional constraint if it exists. - Estimation of ligand entropy using analytical MMFF Hessian is extended for ligands bound in a rigid protein. Previously the entropy of only free ligands in vacuum or in solution could be estimated with analytical second derivatives.

- A few numerical errors in the calculation of analytical second derivatives (Hessian matrix) in MMFF torsion and out-of plane terms have been fixed.

- Constraint energy was reported twice by the method
`OESzybkiResults.Print`. The problem is fixed. - The method
`OESz::OESzybki::GetExactVdWProteinLigand`was misspelled (`GetExactVdEProteinLigand`instead of`GetExactVdWProteinLigand`). - When preoptimized ligands are used for entropy estimation it is necessary to gently move the ligand out of the minimum. The gradient normal below which such a perturbation was done was raised from 1 kcal/(mol Å\(\AA\)) to 10 kcal/(mol Å\(\AA\)). Research showed that for some conformations the above limit was too low which resulted in overestimation of its vibrational entropy.

© Copyright 2017, OpenEye Scientific Software, Inc. Last updated on Jun 17, 2017.