BioinformaticsBioinformaticsPeer-reviewed journal article
Protlego: A Python package for the analysis and design of chimeric proteins
Abstract
MotivationGene duplication and recombination of protein fragments have led to the highly diverse protein space that we observe today. By mimicking this natural process, the design of protein chimeras via fragment recombination has proven experimentally successful and has opened a new era for the design of customizable proteins. The in-silico building of structural models for these chimeric proteins, however, remains a manual task that requires a considerable degree of expertise and is not amenable for high-throughput studies. Energetic and structural analysis of the designed proteins often require the use of several tools, each with their unique technical difficulties and available in different programming languages or web servers. ResultsWe have implemented a Python package that enables automated, high-throughput design of chimeras and their structural analysis. First, it is possible to fetch evolutionarily conserved fragments from a built-in database (also available at fuzzle.uni-bayreuth.de). These relationships can then be represented via networks or further selected for chimera construction via recombination. Designed chimeras or natural proteins are then scored and minimised with the Charmm and Amber forcefields and their diverse structural features can be analysed at ease. Here, we showcase Protlegos pipeline by exploring the relationships between the P-loop and Rossmann superfolds and building and characterising their offspring chimeras. We believe that Protlego provides a powerful new tool for the protein design community. Availability and implementationProtlego is freely available at (https://hoecker-lab.github.io/protlego/) with tutorials and documentation.
- Citations
- 17
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
- A general-purpose protein design framework based on mining sequence-structure relationships in known protein structures
J. Zhou, A. E. Panaitiu, G. Grigoryan·bioRxiv·Oct 1, 2018
- Prosculpt: Lowering the Barrier to Computational Protein Design
Federico Olivieri, Alina V. Konstantinova, … Ajasja Ljubetič·bioRxiv·Jun 26, 2026
- De Novo Protein Fold Design Through Sequence-Independent Fragment Assembly Simulations
Robin Pearce, Xiaoqiang Huang, … Yang Zhang·Proceedings of the National Academy of SciencesPeer-reviewed·Jan 19, 2023
- pyFoldX: enabling biomolecular analysis and engineering along structural ensembles
Leandro Radusky, Luis G. Serrano·BioinformaticsPeer-reviewed·Feb 9, 2022
- rstoolbox: management and analysis of computationally designed structural ensembles.
Jaume Bonet, Zander Harteveld, … Bruno E. Correia·bioRxiv·Sep 27, 2018
- BioPipelines: Accessible Computational Protein and Ligand Design for Chemical Biologists
Gianluca Quargnali, Pablo Rivera‐Fuentes·Computational and Structural Biotechnology JournalPeer-reviewed·Mar 1, 2026