Evidence map›Paper›PMID 42081565›Full record

ArticlePLoS computational biology2026

VUStruct: A compute pipeline for high throughput and personalized structural biology.

Christopher W Moth, Jonathan H Sheehan, Abdullah Al Mamun, R Michael Sivley, Alican Gulsevin, David C Rinker, Zenab F Mchaourab, Undiagnosed Diseases Network, John A Capra, Jens Meiler

Abstract read
In one paragraph

Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. MAVISp: A modular structure-based framework for protein variant effects.Protein science : a publication of the Protein Society · 2026
    Article
  3. CircadianiScience · 2026
    Article
  4. Article
  5. Review
  6. bioRxiv : the preprint server for biology · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Christopher W MothDepartments of Chemistry, Pharmacology, and Biomedical Informatics, Center for Structural Biology and Institute of Chemical Biology; Vanderbilt University, Nashville, Tennessee, United States of America.ORCID https://orcid.org/0000-0001-8867-9369
Jonathan H SheehanDivision of Infectious Diseases, Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Abdullah Al MamunDepartment of Biomedical Data Science, School of Applied Computational Sciences, Meharry Medical College, Nashville, Tennessee, United States of America.
R Michael SivleyBiomedical Informatics at 5Prime Sciences, Montreal, Quebec, Canada.
Alican GulsevinDepartment of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, Butler University, Indianapolis, Indiana, United States of America.
David C RinkerDepartment of Biological Sciences, Evolutionary Studies Initiative; Vanderbilt University, Nashville, Tennessee, United States of America.
Zenab F MchaourabMeharry Medical College, Nashville, Tennessee, United States of America.
Undiagnosed Diseases Network
John A CapraBakar Computational Health Science Institute and Department of Epidemiology and Biostatistics, University of California, San Francisco, California, United States of America.
Jens MeilerDepartments of Chemistry, Pharmacology, and Biomedical Informatics, Center for Structural Biology and Institute of Chemical Biology; Vanderbilt University, Nashville, Tennessee, United States of America.

Funding

Vanderbilt Center for Undiagnosed Diseases (VCUD) - BiorepositoryU01HG007674 · NHGRI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI COGAN, JOY D, HAMID, RIZWAN · 2014 to 2022
$13.7M
WASHINGTON UNIVERSITY SCHOOL OF MEDICINE UNDIAGNOSED DISEASES NETWORK CLINICAL SITEU01HG010215 · NHGRI · WASHINGTON UNIVERSITY · PI DICKSON, PATRICIA I · 2018 to 2022
$3.4M
Washington University School of Medicine Undiagnosed Diseases Network Clinical SiteU01NS134354 · NINDS · WASHINGTON UNIVERSITY · PI PATRICIA I DICKSON · 2023 to 2026
$3.3M
NHGRI NIH HHS U01 HG007674NHGRI NIH HHS U01 HG010215NINDS NIH HHS U01 NS134354
6 · The paper itself

Abstract

Effective diagnosis and treatment of rare genetic disorders requires the interpretation of a patient's genetic variants of unknown significance (VUSs). Today, clinical decision-making is primarily guided by gene-phenotype association databases and DNA-based scoring methods. Our web-accessible variant analysis pipeline, VUStruct, supplements these established approaches by deeply analyzing the downstream molecular impact of variation in context of 3D protein structure. VUStruct's growing impact is fueled by the co-proliferation of protein 3D structural models, gene sequencing, compute power, and artificial intelligence. Contextualizing VUSs in protein 3D structural models also illuminates longitudinal genomics studies and biochemical bench research focused on VUS, and we created VUStruct for clinicians and researchers alike. We now introduce VUStruct to the broad scientific community as a mature, web-facing, extensible, High-Performance Computing (HPC) software pipeline. VUStruct maps missense variants onto automatically selected protein structures and launches a broad range of analyses. These include energy-based assessments of protein folding and stability, pathogenicity prediction through spatial clustering analysis, and machine learning (ML) predictors of binding surface disruptions and nearby post-translational modification sites. The pipeline also considers the entire input set of VUS and identifies genes potentially involved in digenic disease. VUStruct's utility in clinical rare disease genome interpretation has been demonstrated through its analysis of over 175 Undiagnosed Disease Network (UDN) Patient cases. VUStruct-leveraged hypotheses have often informed clinicians in their consideration of additional patient testing, and we report here details from two cases where VUStruct was key to their solution. We also note successes with academic research collaborators, for whom VUStruct has informed research directions in both computational genomics and wet lab studies.

Indexed as

Computational BiologyGenetic VariationProteinsSoftwareHumansInternetModels, MolecularProtein ConformationProtein FoldingProteins

Identifiers

PMID42081565
PMCPMC13160433

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.