CIDER

CIDER classifies intrinsically disordered ensemble regions from protein amino acid sequences and quantifies sequence-encoded physicochemical properties of intrinsically disordered proteins (IDPs).


Key Features:

  • Sequence-based classification: Classifies intrinsically disordered ensemble regions using protein amino acid sequences.
  • Physicochemical property computation: Computes sequence-encoded physicochemical properties that characterize IDP conformational ensembles.
  • localCIDER support: Includes a complementary high-performance localCIDER package for a broader range of IDP sequence analyses.
  • IDP-centered analysis: Focuses analyses specifically on intrinsically disordered proteins and regions (IDPs) to derive biophysical insights from sequences.

Scientific Applications:

  • Conformational ensemble characterization: Characterizes sequence determinants of conformational heterogeneity in IDPs.
  • Disease-related IDP analysis: Supports investigation of IDP dysregulation implicated in neurodegeneration and cancer.
  • Biophysical parameter extraction: Enables extraction of biophysical parameters from sequence data to inform studies of protein disorder.
  • Comparative sequence analyses: Facilitates broader comparative analyses of IDP sequences using localCIDER.

Methodology:

Analyses compute sequence-derived physicochemical properties from amino acid sequences and use those properties to classify intrinsically disordered ensemble regions; a related localCIDER package supports broader sequence analyses.

Topics

Details

Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
8/7/2018
Last Updated:
12/10/2018

Operations

Publications

Holehouse AS, Das RK, Ahad JN, Richardson MO, Pappu RV. CIDER: Resources to Analyze Sequence-Ensemble Relationships of Intrinsically Disordered Proteins. Biophysical Journal. 2017;112(1):16-21. doi:10.1016/j.bpj.2016.11.3200. PMID:28076807. PMCID:PMC5232785.

PMID: 28076807
PMCID: PMC5232785
Funding: - National Science Foundation: MCB 1121867, MCB 1614766

Documentation