Entropy and Free Energy of a Mobile Loop Based on the Crystal Structures of the Free and Bound Proteins
A mobile loop changes its conformation from “open” (free enzyme) to “closed” upon ligand binding. The difference in the Helmholtz free energy, ΔFloop between these states sheds light on the mechanism of binding. With our “hypothetical scanning molecular dynamics” (HSMD-TI) method ΔFloop = Ffree − Fb...
Main Authors: | Hagai Meirovitch, Mihail Mihailescu |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2010-08-01
|
Series: | Entropy |
Subjects: | |
Online Access: | http://www.mdpi.com/1099-4300/12/8/1946/ |
Similar Items
-
Improved Estimation of Protein-Ligand Binding Free Energy by Using the Ligand-Entropy and Mobility of Water Molecules
by: Haruki Nakamura, et al.
Published: (2013-04-01) -
Accurate Receptor-Ligand Binding Free Energies from Fast QM Conformational Chemical Space Sampling
by: Esra Boz, et al.
Published: (2021-03-01) -
Protein – Ligand Binding: Estimation of Binding Free Energies
by: Ranganathan, Anirudh
Published: (2012) -
Examination of the role of binding site water molecules in molecular recognition
by: Orro Graña, Adolfo
Published: (2012) -
Entropy, Free Energy, and Symbolization: Free Association at the Intersection of Psychoanalysis and Neuroscience
by: Thomas Rabeyron, et al.
Published: (2020-03-01)