Skip to main content
bioRxiv
  • Home
  • About
  • Submit
  • ALERTS / RSS
Advanced Search
New Results

Explainable Deep Generative Models, Ancestral Fragments, and Murky Regions of the Protein Structure Universe

View ORCID ProfileEli J. Draizen, View ORCID ProfileCameron Mura, View ORCID ProfilePhilip E. Bourne
doi: https://doi.org/10.1101/2022.11.16.516787
Eli J. Draizen
1Department of Biomedical Engineering, University of Virginia, Charlottesville, VA 22903
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Eli J. Draizen
Cameron Mura
2School of Data Science, University of Virginia, Charlottesville, VA 22903
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Cameron Mura
Philip E. Bourne
2School of Data Science, University of Virginia, Charlottesville, VA 22903
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Philip E. Bourne
  • Abstract
  • Full Text
  • Info/History
  • Metrics
  • Data/Code
  • Preview PDF
Loading

Abstract

Modern proteins did not arise abruptly, as singular events, but rather over the course of at least 3.5 billion years of evolution. Can machine learning teach us how this occurred? The molecular evolutionary processes that yielded the intricate three-dimensional (3D) structures of proteins involve duplication, recombination and mutation of genetic elements, corresponding to short peptide fragments. Identifying and elucidating these ancestral fragments is crucial to deciphering the interrelationships amongst proteins, as well as how evolution acts upon protein sequences, structures & functions. Traditionally, structural fragments have been found using sequence-based and 3D structural alignment approaches, but that becomes challenging when proteins have undergone extensive permutations—allowing two proteins to share a common architecture, though their topologies may drastically differ (a phenomenon termed the Urfold). We have designed a new framework to identify compact, potentially-discontinuous peptide fragments by combining (i) deep generative models of protein superfamilies with (ii) layerwise relevance propagation (LRP) to identify atoms of great relevance in creating an embedding during an allsuperfamilies × alldomains analysis. Our approach recapitulates known relationships amongst the evolutionarily ancient small β-barrels (e.g. SH3 and OB folds) and amongst P-loop–containing proteins (e.g. Rossmann and P-loop NTPases), previously established via manual analysis. Because of the generality of our deep model’s approach, we anticipate that it can enable the discovery of new ancestral peptides. In a sense, our framework uses LRP as an ‘explainable AI’ approach, in conjunction with a recent deep generative model of protein structure (termed DeepUrfold), in order to leverage decades worth of structural biology knowledge to decipher the underlying molecular bases for protein structural relationships—including those which are exceedingly remote, yet discoverable via deep learning.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • edraizen{at}gmail.com, cmura{at}virginia.edu, peb6a{at}virginia.edu

  • ↵* https://edraizen.github.io

  • ↵† http://bournelab.org

  • https://doi.org/10.5281/zenodo.6873024

  • https://doi.org/10.5281/zenodo.6916524

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
Back to top
PreviousNext
Posted November 17, 2022.
Download PDF
Data/Code
Email

Thank you for your interest in spreading the word about bioRxiv.

NOTE: Your email address is requested solely to identify you as the sender of this article.

Enter multiple addresses on separate lines or separate them with commas.
Explainable Deep Generative Models, Ancestral Fragments, and Murky Regions of the Protein Structure Universe
(Your Name) has forwarded a page to you from bioRxiv
(Your Name) thought you would like to see this page from the bioRxiv website.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
Explainable Deep Generative Models, Ancestral Fragments, and Murky Regions of the Protein Structure Universe
Eli J. Draizen, Cameron Mura, Philip E. Bourne
bioRxiv 2022.11.16.516787; doi: https://doi.org/10.1101/2022.11.16.516787
Digg logo Reddit logo Twitter logo Facebook logo Google logo LinkedIn logo Mendeley logo
Citation Tools
Explainable Deep Generative Models, Ancestral Fragments, and Murky Regions of the Protein Structure Universe
Eli J. Draizen, Cameron Mura, Philip E. Bourne
bioRxiv 2022.11.16.516787; doi: https://doi.org/10.1101/2022.11.16.516787

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Subject Area

  • Bioinformatics
Subject Areas
All Articles
  • Animal Behavior and Cognition (4085)
  • Biochemistry (8755)
  • Bioengineering (6477)
  • Bioinformatics (23331)
  • Biophysics (11740)
  • Cancer Biology (9144)
  • Cell Biology (13237)
  • Clinical Trials (138)
  • Developmental Biology (7410)
  • Ecology (11364)
  • Epidemiology (2066)
  • Evolutionary Biology (15084)
  • Genetics (10397)
  • Genomics (14006)
  • Immunology (9115)
  • Microbiology (22036)
  • Molecular Biology (8777)
  • Neuroscience (47345)
  • Paleontology (350)
  • Pathology (1420)
  • Pharmacology and Toxicology (2480)
  • Physiology (3703)
  • Plant Biology (8045)
  • Scientific Communication and Education (1431)
  • Synthetic Biology (2207)
  • Systems Biology (6014)
  • Zoology (1249)