Evidence map›Paper›PMID 40569950›Full record

ArticlePloS one2025

Using computer-generated protein models to analyze mutations linked to Amelogenesis Imperfecta.

Nazlee Sharmin, Jerald Yuan, Ava K Chow

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Nazlee SharminMike Petryk School of Dentistry, Faculty of Medicine and Dentistry, College of Health Sciences, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0002-2408-2333
Jerald YuanMike Petryk School of Dentistry, Faculty of Medicine and Dentistry, College of Health Sciences, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0001-6799-7579
Ava K ChowMike Petryk School of Dentistry, Faculty of Medicine and Dentistry, College of Health Sciences, University of Alberta, Edmonton, Alberta, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amelogenesis Imperfecta (AI) is a disorder of tooth development caused by mutations in genes involved in several stages of tooth enamel formation. Few proteins involved in tooth development or developmental anomalies are explored in detail. Knowledge of 3D protein structure is essential to studying protein function. However, crystallized complete protein structures related to teeth and oral development are rare in the Protein Data Bank. Computational approaches for automated protein structure prediction have become a popular alternative for generating protein 3D structures. In this study, we aimed to explore the potential of using computer-generated protein models to analyze mutations linked to AI. We took a systematic approach to identify, screen, and analyze AI-linked protein variants. Proteins with AI-linked mutations were identified from the NCBI and OMIM databases, followed by screening of sequences for intrinsically disordered regions (IDRs). The iterative threading assembly refinement (I-TASSER) server was used to generate homology models for the wildtype and mutant proteins. PyMOL was used to analyze and compare the 3D structures of the proteins. Nineteen human genes with AI-associated mutations were identified from NCBI and OMIM. We identified multiple AI-associated protein variants with structural differences compared to their wildtype form. The current evidence aligns with several of the structural alterations identified in our study. Our findings suggest the potential of utilizing computer-generated protein models to investigate disease-associated mutations. However, careful consideration of models, templates, and alignments over the regions of interest is necessary to predict any potential structural impact of a disease-causing protein variant.

Indexed as

Amelogenesis ImperfectaModels, MolecularMutationProteinsDatabases, ProteinHumansProtein ConformationProteins

Identifiers

PMID40569950
PMCPMC12200857

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.