SCLpred-MEM

SCLpred-MEM predicts the subcellular localization of membrane proteins as an ab initio predictor that classifies sequences as membrane or non-membrane using an ensemble of Deep N-to-1 Convolutional Neural Networks (N1-NN) for biological annotation and analysis.


Key Features:

  • Deep Learning Architecture: Uses an ensemble of Deep N-to-1 Convolutional Neural Networks (N1-NN) to perform sequence-based classification.
  • Ab initio prediction: Operates without requiring homology-based transfer, relying on sequence-derived features learned by the networks.
  • Dataset quality: Trained and tested on strictly homology-reduced datasets to minimize redundancy and bias.
  • Performance metrics: Reports a Matthews correlation coefficient (MCC) of 0.52 on a strictly homology-reduced independent test set and MCC of 0.62 on a less strict homology-reduced dataset.
  • Benchmarking: Matches or surpasses other state-of-the-art subcellular localization predictors in comparative evaluations.

Scientific Applications:

  • Genomics: Assists annotation of genomic data by assigning subcellular localization to membrane protein sequences.
  • Drug design: Informs target selection and localization-aware drug targeting strategies for membrane proteins.
  • Theoretical and analytical bioinformatics: Provides localization predictions useful for modeling cellular processes and protein interaction contexts.

Methodology:

Ab initio prediction using an ensemble of Deep N-to-1 Convolutional Neural Networks (N1-NN) trained and evaluated on strictly homology-reduced datasets with independent test-set performance assessment.

Topics

Details

Tool Type:
web application
Added:
11/29/2021
Last Updated:
11/29/2021

Operations

Publications

Kaleel M, Ellinger L, Lalor C, Pollastri G, Mooney C. <scp>SCLpred‐MEM</scp>: Subcellular localization prediction of membrane proteins by deep N‐to‐1 convolutional neural networks. Proteins: Structure, Function, and Bioinformatics. 2021;89(10):1233-1239. doi:10.1002/prot.26144. PMID:33983651.

PMID: 33983651
Funding: - Irish Research Council: GOIPG/2014/603

Links