Evidence map›Paper›PMID 41638990›Full record

ArticleBioinformatics (Oxford, England)2026

PyTEA-O: a Python implementation of Two-Entropies Analysis for protein sequence variation analysis.

Rosan C M Kuin, Alexander T Julian, Jagriti Chander, Sunah Lee, Gerard J P van Westen

Abstract read
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Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Rosan C M KuinComputational Drug Discovery, Division of Medicinal Chemistry, Leiden Academic Centre of Drug Research, Leiden University, 2333 CC Leiden, The Netherlands.
Alexander T JulianDepartment of Biology, Illinois Institute of Technology, Chicago, IL 60616, United States.
Jagriti ChanderDepartment of Biology, Illinois Institute of Technology, Chicago, IL 60616, United States.
Sunah LeeDepartment of Biology, Illinois Institute of Technology, Chicago, IL 60616, United States.
Gerard J P van WestenComputational Drug Discovery, Division of Medicinal Chemistry, Leiden Academic Centre of Drug Research, Leiden University, 2333 CC Leiden, The Netherlands.ORCID 0000-0003-0717-1817

Funding

Pritzker Institute of Biomedical Science and Engineering
6 · The paper itself

Abstract

motivationProtein sequence variation analysis is a topic of broad interest in drug discovery and protein engineering to support modulation of protein function for diverse biotechnological and therapeutic applications. To assist in the analysis of multiple sequence alignments (MSAs) and identify residues that account for protein function specificity, computational tools have been developed. Yet, existing programs often omit consideration of amino acid properties, flexibility beyond fixed webserver interfaces, accessible source code, or compatibility with small MSAs.

resultsTo address these limitations, we present PyTEA-O, a Python implementation of Two-Entropies Analysis that has been developed to be easy to use for the analysis of protein sequence variation. To help users analyze the MSA and screen for residues of interest, we generate modifiable and intuitive visualizations. These visualizations, together with a scoring approach for identifying alignment positions with (dis-)similar physicochemical properties, presents a powerful tool for sequence variability analysis. To demonstrate its capabilities, we present a case study based on the deubiquitinase OTUD7B (Cezanne) where we identify a crucial position that modulates its affinity for its substrate. AVAILABILITY AND IMPLEMENTATION: PyTEA-O is available at https://github.com/CDDLeiden/PyTEA-O/ and archived via Zenodo (https://doi.org/10.5281/zenodo.15914598).

Indexed as

Computational BiologyProteinsSequence Analysis, ProteinSoftwareAmino Acid SequenceSequence AlignmentProteins

Identifiers

PMID41638990
PMCPMC12910380

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.