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Record W2169151607 · doi:10.1186/1758-2946-2-s1-p35

Prediction of highly-connected 'hub'-proteins in protein interaction networks using QSAR

2010· article· en· W2169151607 on OpenAlexaff
Michael Hsing, Kendall Byler, Artem Cherkasov

Bibliographic record

VenueJournal of Cheminformatics · 2010
Typearticle
Languageen
FieldComputer Science
TopicComputational Drug Discovery Methods
Canadian institutionsUniversity of British Columbia
Fundersnot available
KeywordsQuantitative structure–activity relationshipComputer scienceInterpretabilityCheminformaticsComputational biologyMachine learningProteomeArtificial intelligenceDrug discoveryVirtual screeningData miningChemistryBiologyBiochemistryComputational chemistry

Abstract

fetched live from OpenAlex

Proteins that are most essential for functioning and viability of bacterial cell have been shown to exhibit larger number of interactions with other cell components. Thus, by identifying the most connected proteins (or hubs) in protein interaction networks (PINs), one may discover prospective drug targets that can be utilized to combat emergent and drug-resistant pathogens such as Methicillin-Resistant Staphylococcus aureus 252 (MRSA). The advantage of using such hub proteins as drug targets lies in their essentiality, non-replaceable position in the PIN and lower rate of mutation, which can help to counter bacterial resistance. However, finding or predicting such hub proteins remains a challenging task as the corresponding experiments are very costly, while traditional bioinformatics approaches generally fail in forecasting PIN data due to the general lack of agreement between the existing datasets [1]. Thus, we have decided to utilize various structural and physicochemical features of proteins, related to traditional QSAR properties for predicting highly connected proteins. Using our own in-house generated PIN for the MRSA cell we have trained a boosting tree-based classifier that uses 75 physical and chemical QSAR descriptors computed for all proteins in the interaction network [2]. The utilized parameters included molecular weight, net charge, isoelectric point, hydrophobicity, surface area, solvent accessibilities, electronegativity, secondary structure composition, surface coils and flexibility among other QSAR descriptors. The developed QSAR model has yielded a high prediction accuracy of 80% for the validation set and was used to predict additional hubs in the rest of the MRSA proteome. The predicted hubs have then been evaluated experimentally and 55% of them were confirmed as high interactors what corresponds to >5 fold dataset enrichment for potential hub-proteins provided by the developed QSAR model. Thus, the successful development of accurate hub classifiers demonstrated that highly-connected proteins tend to share certain structural and physicochemical features that can be characterized and quantified by conventional QSAR descriptors. It is anticipated that the developed hub classifiers will represent a useful tool for the prediction of highly-interacting proteins and can find broad application for planning and executing large-scale proteomic experiments and for identification of novel and prospective antibacterial drug targets – even in those organisms that currently lack protein interaction data.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Simulation or modeling · Consensus signal: Simulation or modeling
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.006
Threshold uncertainty score0.012

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0020.001
Science and technology studies0.0000.000
Scholarly communication0.0010.001
Open science0.0010.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.028
GPT teacher head0.282
Teacher spread0.254 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designSimulation or modeling
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2010
Admission routes1
Has abstractyes

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