TransDFL

TransDFL identifies disordered flexible linkers (DFLs) within proteins to enable precise characterization of intrinsically disordered regions (IDRs) and their roles in inter-domain interactions.


Key Features:

  • Transfer learning: Leverages transfer learning techniques to enhance precision and reduce false-positive rates in DFL identification.
  • RFPR-IDP pre-training: Employs the RFPR-IDP predictor pre-trained on sequences known to contain IDRs to learn features distinguishing IDRs from ordered regions.
  • DFL-specific fine-tuning: Fine-tunes the pre-trained RFPR-IDP model with annotated DFL sequences to capture DFL-specific characteristics.
  • Prediction modes: Produces DFL predictions in two scenarios: restricted to IDRs and across entire protein sequences.
  • Performance: Experimental evaluations report reduced false-positive rates and higher accuracy compared to traditional machine-learning DFL predictors.

Scientific Applications:

  • IDR functional characterization: Supports study of functional dynamics of IDRs by precisely locating DFLs within disordered regions.
  • Inter-domain interaction analysis: Facilitates identification of linkers that connect protein domains and mediate inter-domain interactions.
  • Protein annotation: Enables annotation of DFLs both within IDRs and across whole proteins for structural and functional analyses.

Methodology:

Two-step transfer-learning approach using RFPR-IDP: RFPR-IDP is pre-trained on IDR-containing sequences to learn IDR versus ordered features, then fine-tuned on annotated DFL sequences to enable DFL prediction within IDRs or across whole proteins.

Topics

Details

Cost:
Free of charge
Tool Type:
web application
Operating Systems:
Mac, Linux, Windows
Added:
2/26/2023
Last Updated:
11/24/2024

Operations

Data Inputs & Outputs

Protein disorder prediction

Outputs

    Publications

    Pang Y, Liu B. TransDFL: Identification of Disordered Flexible Linkers in Proteins by Transfer Learning. Genomics, Proteomics & Bioinformatics. 2022;21(2):359-369. doi:10.1016/j.gpb.2022.10.004. PMID:36272675. PMCID:PMC10626177.

    PMID: 36272675
    Funding: - National Key R&D Program of China: 2018AAA0100100 - Beijing Natural Science Foundation, China: JQ19019 - Natural Science Foundation of Beijing Municipality: JQ19019 - National Key Research and Development Program of China: 2018AAA0100100