Evidence map›Paper›PMID 39968854›Full record

ArticleProtein science : a publication of the Protein Society2025

Refinement and curation of homologous groups facilitated by structure prediction.

Richard Dustin Schaeffer, Jimin Pei, Jing Zhang, Qian Cong, Nick V Grishin

Abstract read
In one paragraph

Article in Protein science : a publication of the Protein Society, 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. Refinement and curation of homologous groups facilitated by structure prediction.Protein science : a publication of the Protein Society · 2025
    Article
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

5 authors.

Richard Dustin SchaefferDepartment of Biophysics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID 0000-0001-6502-1425
Jimin PeiDepartment of Biophysics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID 0000-0002-3505-9665
Jing ZhangEugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID 0000-0003-4190-3065
Qian CongDepartment of Biophysics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID 0000-0002-8909-0414
Nick V GrishinDepartment of Biophysics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Funding

Computational analysis of proteinsR35GM127390 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI GRISHIN, NICK V. · 2018 to 2022
$1.5M
ECOD: Large scale classification of predicted and experimental protein structuresR01GM147367 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI Richard Dustin Schaeffer · 2023 to 2026
$1.4M
Functions of Rapidly-Evolving Proteins and Their Roles in PathogenicityK99AI180984 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI ZHANG, JING · 2024 to 2025
$210k
National Institute of Allergy and Infectious Diseases 1K99AI180984-01National Science Foundation DBI 2224128National Science Foundation MED230034National Science Foundation MED240004NIAID NIH HHS K99 AI180984NIGMS NIH HHS GM127390NIGMS NIH HHS GM147367NIGMS NIH HHS R01 GM147367NIGMS NIH HHS R35 GM127390Welch Foundation I-1505Welch Foundation I-2095-20220331
6 · The paper itself

Abstract

Domain classification of protein predictions released in the AlphaFold Database (AFDB) has been a recent focus of the Evolutionary Classification of protein Domains (ECOD). Although a primary focus of our recent work has been the partition and assignment of domains from these predictions, we here show how these diverse predictions can be used to examine the reference domain set more closely. Using results from DPAM, our AlphaFold-specific domain parsing algorithm, we examine hierarchical groupings that share significant levels of homologous links, both between groups that were not previously assessed to be definitively homologous and between groups that were not previously observed to share significant homologous links. Combined with manual analysis, these large datasets of structural and sequence similarities allow us to merge homologous groups in multiple cases which we detail within. These domains tend to be families of domains from families that are either small, previously had few experimental representatives, or had unknown function. The exception to this is the chromodomains, a large homologous group which were increased from "possibly homologous" to "definitely homologous" to increase the consistency of ECOD based their strong homologous links to the SH3 domains.

Indexed as

ProteinsAlgorithmsComputational BiologyDatabases, ProteinModels, MolecularProtein DomainsProteinsdomain classificationDPAMECODprotein homologystructure prediction

Identifiers

PMID39968854
PMCPMC11836899

What OpenQuestion holds

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Registered trials

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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.