Related Experiment Video
Updated: Feb 19, 2026

Optimization of Synthetic Proteins: Identification of Interpositional Dependencies Indicating Structurally and/or Functionally Linked Residues
Published on: July 14, 2015
Self-Avoiding Conformational Sampling Based on Histories of Past Conformational Searches
Ryuhei Harada1, Yasuteru Shigeta1
1Center for Computational Sciences, University of Tsukuba , 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8577, Japan.
Abstract:
Self-avoiding conformational sampling (SACS) is proposed as an enhanced conformational sampling method for proteins. In SACS, the following conformational resampling is repeated for a given protein: (1) identification of newly visited states in a subspace and (2) conformational resampling by restarting short-time molecular dynamics (MD) simulations from the newly visited states. To identify the newly visited states, a set of history-dependent histograms projected onto the subspace is used. One is constructed from the trajectories sampled at the current (ith) cycle, and the other is constructed from all of the trajectories accumulated up through the previous ((i - 1)th) cycle. By reference to the history-dependent histograms, the newly visited states appearing at the current (ith) cycle are defined as a difference set between them. By repeating the cycle of conformational resampling, SACS prevents the system from revisiting states that have already been visited for previous cycles, promoting structural transitions via resampling from the newly visited states. To verify the conformational sampling efficiency of SACS, the present method was applied to reveal underlying mechanisms of biologically important domain motions of maltodextrin binding protein in explicit water and successfully reproduced the open-closed transition with a reasonable (nanosecond-order) computational cost.
Related Concept Videos
¹H NMR of Conformationally Flexible Molecules: Temporal Resolution
Conserved Binding Sites
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
Conserved Binding Sites
Chair Conformation of Cyclohexane
The hydrogen atoms linked to carbons are arranged in two different axial and equatorial orientations to achieve this...
Conformations of Cyclohexane
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal...
¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR

