BioGraphX: Bridging the Sequence-Structure Gap via Physicochemical Graph Encoding for Interpretable Subcellular Localization Prediction
Clicks: 1
ID: 318495
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This
article has not been analysed, so there is no overall score —
reader engagement is measured and shown alongside.
Reader Engagement
0.0
/100
1 views
0 readers
AI Quality Assessment
Not analyzed
Readership in this journal
Ranked #87 of 104 articles by views in Bioinformatics advances
Most read
Least read
Bar heights use a square-root scale.
Mint this article as an NFT
Not yet mintedCreate a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.
5
SUSD
one-off · no wallet required
Abstract
Abstract Motivation Computational protein subcellular localization prediction is vital for understanding cellular mechanisms and disease treatments. However, current methods lack interpretability: they predict where a protein localizes but fail to explain why. Moreover, traditional approaches require costly, time-consuming three-dimensional structures. Results Here, we propose BioGraphX, a novel encoding framework that constructs protein interaction graphs directly from sequences using biochemical rules, providing a constraint-based structural proxy. Building upon this, BioGraphX-Net demonstrates superior performance on the DeepLoc 2.0 benchmark by integrating ESM-2 (Evolutionary Scale Modeling) embeddings with the proposed features via a gating mechanism. Gating analysis shows that while ESM-2 embeddings contribute strongly, BioGraphX features function as high-precision filters. SHAP (SHapley Additive exPlanations) analysis reveals feature importance patterns consistent with a sophisticated biophysical logic: sequence signals act as universal exclusion filters, while organelle-specific biophysical combinations enable precise compartment discrimination. Notably, Frustration features resolve targeting ambiguities in complex compartments, reflecting evolutionary constraints while preventing mislocalization from sequence mimicry. Cross-dataset validation on a protein solubility prediction task confirms the structural proxy captures genuine biophysical signal. Additionally, BioGraphX promotes Green AI in bioinformatics, matching state-of-the-art performance with a minimal parameter count of 13.46 million. In summary, BioGraphX provides accurate predictions and new insights into the language of life. Availability and implementation Source code is available at https://github.com/Abubakar-Saeed/BioGraphX.
| Reference Key |
openalex_W7165645840
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Abubakar Saeed, Waseem Abbas |
| Journal | Bioinformatics advances |
| Year | 2026 |
| DOI |
10.1093/bioadv/vbag181
|
| URL | |
| Keywords | Keywords not found |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.