BASILIScan

BASILIScan facilitates high-throughput identification of homologous proteins and evaluation of intrinsic disorder to enable comparative analysis of intrinsically disordered regions (IDRs) across eukaryotic and viral proteomes.


Key Features:

  • BLAST-Based Homologue Search: Uses BLAST to identify close homologues of the query protein for comparative sequence analysis.
  • Intrinsic Disorder Prediction: Performs simultaneous prediction of intrinsic disorder to map disordered regions alongside sequence homology.
  • Homologue Scoring and Selection: Screens, scores, and selects homologues based on predicted structural order to identify more ordered counterparts of the target protein.
  • Comparative Analysis of Disorder Conservation: Conducts parallel comparative analysis to examine conservation of extended disordered regions across multiple sequences.

Scientific Applications:

  • Recombinant Protein Expression: Identifies intrinsically stable homologues with poorly conserved disordered regions to improve chances of successful recombinant expression.
  • Crystallization and Downstream Applications: Pinpoints structured homologues that are more compatible with crystallization and other structural or functional assays.
  • Biological Insights: Reveals that portions of the human proteome have homologous sequences in related species with superior intrinsic structural order, informing evolutionary and protein-engineering studies.

Methodology:

Performs a BLAST-based homologue search, simultaneous intrinsic disorder prediction, parallel comparative analysis of disorder conservation, and scoring/selection of homologues based on predicted structural order.

Topics

Details

License:
Unlicense
Maturity:
Mature
Cost:
Free of charge
Tool Type:
desktop application
Operating Systems:
Linux, Windows, Mac
Programming Languages:
Python
Added:
8/11/2019
Last Updated:
6/16/2020

Operations

Publications

Barski M. BASILIScan: a tool for high-throughput analysis of intrinsic disorder patterns in homologous proteins. BMC Genomics. 2018;19(1). doi:10.1186/s12864-018-5322-5. PMID:30537929. PMCID:PMC6290515.

Documentation

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