Evidence map›Paper›PMID 41432288›Full record

ReviewProtein science : a publication of the Protein Society2026

Exploring the protein universe with distant similarity detection methods.

Harutyun Sahakyan, Pascal Mutz, Victor Tobiasson, Eugene V Koonin

Abstract readReview
In one paragraph

Review in Protein science : a publication of the Protein Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Systematic discovery of circular permutations across the protein universe using CIRPIN.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Exploring the protein universe with distant similarity detection methods.Protein science : a publication of the Protein Society · 2026
    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

4 authors.

Harutyun SahakyanComputational Biology Branch, Division of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-3750-8118
Pascal MutzComputational Biology Branch, Division of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0002-0430-2095
Victor TobiassonComputational Biology Branch, Division of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0001-8920-017X
Eugene V KooninComputational Biology Branch, Division of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-3943-8299

Funding

NIH HHS
6 · The paper itself

Abstract

During the last few years, the body of data on proteins is expanding almost exponentially with the development of advanced methods for gene sequencing, protein structure determination, particularly by cryoelectron microscopy, and structure prediction using artificial intelligence-based approaches. These developments create the potential for a comprehensive exploration of the protein universe, the entirety of the proteins existing in the biosphere. Elucidation of the relationships among proteins including the most distant ones, where only the core fold is shared, is crucial for understanding protein functions, folding mechanisms, and evolution, as well as the evolution of cellular life forms and viruses. In this brief review, we discuss methods that shaped the field of protein bioinformatics, first, through comparative sequence analysis, and the recent developments in protein structure prediction that transformed the state of the art in the comparative analysis of distantly related proteins. The combination of the rapidly growing databases of genome and metagenome sequences with sensitive methods for sequence comparison and the new generation of structure analysis tools can make charting the protein universe at the structural level a realistic goal.

Indexed as

Computational BiologyProteinsDatabases, ProteinModels, MolecularProtein ConformationSequence Analysis, ProteinProteinsdistant homology detectionprotein universesequence alignmentstructural searchstructure alignment

Identifiers

PMID41432288
PMCPMC12723729

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.