CSpritz

CSpritz predicts intrinsic protein disorder from amino acid sequences by integrating multiple prediction methods to produce consensus per-residue disorder probabilities for identifying short and long disordered regions.


Key Features:

  • Punch: Utilizes sequence and structural templates trained using support vector machines to enhance disorder prediction accuracy.
  • ESpritz: A single-sequence method based on bidirectional recursive neural networks for rapid disorder prediction.
  • Extended Spritz: Filters predictions by considering structural homologues to improve reliability.
  • Consensus integration: Averages probabilities from Punch, ESpritz, and extended Spritz to produce a robust consensus prediction.
  • Prediction outputs: Provides per-residue disorder predictions for short and long disordered regions, secondary structure details, and identification of short functional linear motifs within disordered segments.

Scientific Applications:

  • Disorder identification: Detection and characterization of short and long intrinsic disorder regions in proteins.
  • Structural annotation: Integration of structural homologue information and secondary structure details to inform structural biology analyses.
  • Benchmarking and evaluation: Performance assessed on the CASP9 dataset, reporting Sw = 49.27 and AUC = 0.828.

Methodology:

Predictions from Punch (SVMs on sequence and structural templates), ESpritz (bidirectional recursive neural networks on single sequences), and extended Spritz (filtering by structural homologues) are combined by averaging their per-residue disorder probabilities.

Topics

Details

Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
3/3/2016
Last Updated:
12/10/2018

Operations

Data Inputs & Outputs

Publications

Walsh I, Martin AJM, Di Domenico T, Vullo A, Pollastri G, Tosatto SCE. CSpritz: accurate prediction of protein disorder segments with annotation for homology, secondary structure and linear motifs. Nucleic Acids Research. 2011;39(suppl_2):W190-W196. doi:10.1093/nar/gkr411. PMID:21646342. PMCID:PMC3125791.

Documentation