Evidence map›Paper›PMID 37868056›Full record

ArticlePeerJ2023

Predicting protein and pathway associations for understudied dark kinases using pattern-constrained knowledge graph embedding.

Mariah V Salcedo, Nathan Gravel, Abbas Keshavarzi, Liang-Chin Huang, Krzysztof J Kochut, Natarajan Kannan

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 32% of its field
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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Heterogeneous network approaches to protein pathway prediction.Computational and structural biotechnology journal · 2024
    Review
  2. 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

6 authors at 1 institution in 1 country.

Mariah V Salcedo *Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA, United States of America.
Nathan Gravel *Institute of Bioinformatics, University of Georgia, Athens, GA, United States of America.
Abbas KeshavarziSchool of Computing, University of Georgia, Athens, GA, United States of America.
Liang-Chin HuangInstitute of Bioinformatics, University of Georgia, Athens, GA, United States of America.
Krzysztof J KochutSchool of Computing, University of Georgia, Athens, GA, United States of America.
Natarajan KannanDepartment of Biochemistry and Molecular Biology, University of Georgia, Athens, GA, United States of America.
University of Georgia · US

Funding

A data analytics framework for mining the dark kinomeU01CA239106 · NCI · UNIVERSITY OF GEORGIA · PI KANNAN, NATARAJAN, KOCHUT, KRZYSZTOF J · 2019 to 2021
$1.3M
Annotating dark ion-channel functions using evolutionary features, machine learning and knowledge graph mining (Rayna Carter)U01CA271376 · NCI · UNIVERSITY OF GEORGIA · PI KANNAN, NATARAJAN, LU, WEI · 2022 to 2023
$973k
NCI NIH HHS U01 CA239106
6 · The paper itself

Abstract

The 534 protein kinases encoded in the human genome constitute a large druggable class of proteins that include both well-studied and understudied "dark" members. Accurate prediction of dark kinase functions is a major bioinformatics challenge. Here, we employ a graph mining approach that uses the evolutionary and functional context encoded in knowledge graphs (KGs) to predict protein and pathway associations for understudied kinases. We propose a new scalable graph embedding approach, RegPattern2Vec, which employs regular pattern constrained random walks to sample diverse aspects of node context within a KG flexibly. RegPattern2Vec learns functional representations of kinases, interacting partners, post-translational modifications, pathways, cellular localization, and chemical interactions from a kinase-centric KG that integrates and conceptualizes data from curated heterogeneous data resources. By contextualizing information relevant to prediction, RegPattern2Vec improves accuracy and efficiency in comparison to other random walk-based graph embedding approaches. We show that the predictions produced by our model overlap with pathway enrichment data produced using experimentally validated Protein-Protein Interaction (PPI) data from both publicly available databases and experimental datasets not used in training. Our model also has the advantage of using the collected random walks as biological context to interpret the predicted protein-pathway associations. We provide high-confidence pathway predictions for 34 dark kinases and present three case studies in which analysis of meta-paths associated with the prediction enables biological interpretation. Overall, RegPattern2Vec efficiently samples multiple node types for link prediction on biological knowledge graphs and the predicted associations between understudied kinases, pseudokinases, and known pathways serve as a conceptual starting point for hypothesis generation and testing.

Indexed as

Pattern Recognition, AutomatedProteinsComputational BiologyHumansKnowledgeLearningProteinsClassificationData integrationDrug discoveryEvolutionIlluminating Druggable Genome (IDG)Link predictionOntologiesPathway predictionRandom walkSignaling networks

Identifiers

PMID37868056
PMCPMC10590106
OpenAlexW4387741891

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.