Evidence map›Paper›PMID 38808365›Full record

ArticleProteins2024

Application of artificial intelligence and machine learning techniques to the analysis of dynamic protein sequences.

David C Kombo, Matthew J LaMarche, Chilaluck C Konkankit, S Rackovsky

Abstract read
In one paragraph

Article in Proteins, 2024. 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. Review
  2. The Spatial Distribution of Local Mobility in Folded Proteins.The journal of physical chemistry. B · 2026
    Article
  3. Techniques for Bioinformatic Applications in Protein Dynamics.Methods in molecular biology (Clifton, N.J.) · 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

4 authors.

David C KomboDepartment of Medicinal Chemistry, Integrated Drug Discovery, Sanofi, Cambridge, Massachusetts, USA.
Matthew J LaMarcheDepartment of Medicinal Chemistry, Integrated Drug Discovery, Sanofi, Cambridge, Massachusetts, USA.
Chilaluck C KonkankitDepartment of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, New York, USA.
S RackovskyDepartment of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, New York, USA.ORCID 0000-0002-6186-7893

Funding

INTERNAL BONDIN IN PROTEINSR01GM014312 · NIGMS · CORNELL UNIVERSITY ITHACA · PI MAISURADZE, GIA, RACKOVSKY, SHALOM R · 1985 to 2021
$9.4M
NIGMS NIH HHS R01 GM014312NIH HHS GM14312
6 · The paper itself

Abstract

We apply methods of Artificial Intelligence and Machine Learning to protein dynamic bioinformatics. We rewrite the sequences of a large protein data set, containing both folded and intrinsically disordered molecules, using a representation developed previously, which encodes the intrinsic dynamic properties of the naturally occurring amino acids. We Fourier analyze the resulting sequences. It is demonstrated that classification models built using several different supervised learning methods are able to successfully distinguish folded from intrinsically disordered proteins from sequence alone. It is further shown that the most important sequence property for this discrimination is the sequence mobility, which is the sequence averaged value of the residue-specific average alpha carbon B factor. This is in agreement with previous work, in which we have demonstrated the central role played by the sequence mobility in protein dynamic bioinformatics and biophysics. This finding opens a path to the application of dynamic bioinformatics, in combination with machine learning algorithms, to a range of significant biomedical problems.

Indexed as

Artificial IntelligenceComputational BiologyMachine LearningAlgorithmsAmino Acid SequenceDatabases, ProteinFourier AnalysisIntrinsically Disordered ProteinsProtein FoldingProteinsSequence Analysis, ProteinIntrinsically Disordered ProteinsProteinsartificial intelligencedynamicsfolded proteinsintrinsically disordered proteins

Identifiers

PMID38808365
PMCPMC11511649

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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.