Adaptive conformational restraints for interactive model rebuilding in Cartesian and torsion space
Abstract
When building atomic models into weak and/or low-resolution density, a common strategy is to restrain its conformation to that of a higher-resolution model of the same or similar sequence. When doing so, it is important to avoid over-restraining to the reference model in the face of disagreement with the experimental data. The most common strategy for this is the use of "top-out" potentials. These act like simple harmonic restraints within a defined range, but gradually weaken when the deviation between the model and reference grows larger than a defined transition point. In each current implementation, the rate at which the potential flattens beyond the transition region follows a fixed form - although the form chosen varies between implementations. A restraint potential with a tuneable rate of flattening would provide greater flexibility to encode the confidence in any given restraint. Here we describe two new such potentials: a Cartesian distance restraint derived from a recent generalisation of common loss functions, and a periodic torsion restraint based on a renormalisation of the von Mises distribution. Further, we describe their implementation as user-adjustable/switchable restraints in ISOLDE, and demonstrate their use in some real-world examples. SynopsisNew forms of adaptive or top-out distance and torsion restraints are described, suitable for restraining a model to match a reference structure during interactive rebuilding. In addition, their implementation in ISOLDE is described along with some illustrative example applications.
02 /Specification & Classification
Click any tag to browse matching papers- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Optimizing the connectivity of protein conformations to untangle ensemble refinement
Spencer K. Passmore, James M. Holton, … Andrew V. Martin·bioRxiv·Sep 26, 2026
- Pose: a pure-NumPy, chirality-aware, structural engine for building and manipulating the molecular structures of proteins, nucleic acids, and small organic molecules
Sari Sabban·bioRxiv·Oct 22, 2026
- Improved chemistry restraints for crystallographic refinement by integrating the Amber force field into Phenix
Nigel W. Moriarty, Pawel A. Janowski, … Paul D. Adams·Acta Crystallographica Section D Structural BiologyPeer-reviewed·Dec 20, 2019
- The Untangle Challenge for accurate ensemble models
Mehagan Susan Hopkins, Thomas C. Terwilliger, … James M. Holton·bioRxiv·Feb 22, 2026
- STRIDER: Steric hindrance estimator
L. Ponoop Prasad Patro, Thenmalarchelvi Rathinavelan·bioRxiv·Feb 7, 2020
- Restraint Validation of Biomolecular Structures Determined by NMR in the Protein Data Bank
Kumaran Baskaran, Eliza Płoskoń, … Jasmine Y. Young·StructurePeer-reviewed·Mar 14, 2024