Evidence map›Paper›PMID 42278661›Full record

ArticleInternational journal of molecular sciences2026

Identifying Conserved Regions in HIV-1 Proteins by Entropy Analysis of Sequence Variability.

Alexandr N Shchemelev, Elena N Serikova, Yulia V Ostankova, Vladimir S Davydenko, Edward S Ramsay, Areg A Totolian

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Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

6 authors.

Alexandr N ShchemelevSaint Petersburg Pasteur Institute, 197101 St. Petersburg, Russia.ORCID 0000-0002-3139-3674
Elena N SerikovaSaint Petersburg Pasteur Institute, 197101 St. Petersburg, Russia.
Yulia V OstankovaSaint Petersburg Pasteur Institute, 197101 St. Petersburg, Russia.ORCID 0000-0003-2270-8897
Vladimir S DavydenkoSaint Petersburg Pasteur Institute, 197101 St. Petersburg, Russia.ORCID 0000-0003-0078-9681
Edward S RamsaySaint Petersburg Pasteur Institute, 197101 St. Petersburg, Russia.ORCID 0000-0001-7086-5825
Areg A TotolianSaint Petersburg Pasteur Institute, 197101 St. Petersburg, Russia.ORCID 0000-0003-4571-8799

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The extraordinary genetic diversity of human immunodeficiency virus type 1 (HIV-1), driven by high mutation and recombination rates, poses significant challenges for diagnostics, therapy, and vaccine development. While variable regions enable immune escape, hyperconserved regions are critical for viral function and represent promising targets for novel therapeutic interventions. This study aimed to develop and validate a bioinformatic algorithm for quantitative assessment of sequence conservation and automated identification of functionally significant conserved regions across all major HIV-1 proteins. A total of 1119 full-length HIV-1 genome sequences representing major subtypes (A1, A2, A6, B, C, D, F1, F2, G, H, J, K) were analyzed. Normalized Shannon entropy (S-index) was calculated for each alignment column. Statistical thresholds for conserved regions were established using 95% confidence intervals derived from bootstrap resampling. Two complementary algorithms, clustering and local maxima detection, were applied to identify conserved regions, which were subsequently mapped to known functional domains based on literature data. Protein conservation varied markedly, with S

Indexed as

Conserved SequenceHIV-1Human Immunodeficiency Virus ProteinsAlgorithmsAmino Acid SequenceComputational BiologyEntropyGenetic VariationHumansHuman Immunodeficiency Virus Proteinsaccessory proteinsbioinformaticsconserved regionsenvgaggenetic diversityHIV-1polsequence conservationShannon entropy

Identifiers

PMID42278661
PMCPMC13257677

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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.