FLEXR GUI : a graphical user interface for multi-conformer modeling of proteins

© Stachowski and Fischer 2024.

Détails bibliographiques
Publié dans:Journal of applied crystallography. - 1998. - 57(2024), Pt 2 vom: 01. Apr., Seite 580-586
Auteur principal: Stachowski, Timothy R (Auteur)
Autres auteurs: Fischer, Marcus
Format: Article en ligne
Langue:English
Publié: 2024
Accès à la collection:Journal of applied crystallography
Sujets:Journal Article Coot FLEXR conformational heterogeneity electron-density maps flexibility graphical user interfaces model building multi-conformer models proteins
Description
Résumé:© Stachowski and Fischer 2024.
Proteins are well known 'shapeshifters' which change conformation to function. In crystallography, multiple conformational states are often present within the crystal and the resulting electron-density map. Yet, explicitly incorporating alternative states into models to disentangle multi-conformer ensembles is challenging. We previously reported the tool FLEXR, which, within a few minutes, automatically separates conformational signal from noise and builds the corresponding, often missing, structural features into a multi-conformer model. To make the method widely accessible for routine multi-conformer building as part of the computational toolkit for macromolecular crystallography, we present a graphical user interface (GUI) for FLEXR, designed as a plugin for Coot 1. The GUI implementation seamlessly connects FLEXR models with the existing suite of validation and modeling tools available in Coot. We envision that FLEXR will aid crystallographers by increasing access to a multi-conformer modeling method that will ultimately lead to a better representation of protein conformational heterogeneity in the Protein Data Bank. In turn, deeper insights into the protein conformational landscape may inform biology or provide new opportunities for ligand design. The code is open source and freely available on GitHub at https://github.com/TheFischerLab/FLEXR-GUI
Description:Date Revised 23.11.2024
published: Electronic-eCollection
Citation Status PubMed-not-MEDLINE
ISSN:0021-8898
DOI:10.1107/S1600576724001523