Bio2Rxn
Bio2Rxn predicts putative enzymatic reactions for uncharacterized protein sequences by applying a consensus strategy that integrates six distinct enzyme prediction tools to support characterization of protein functions within metabolic pathways.
Key Features:
- Consensus integration: Integrates six distinct enzyme prediction tools to produce consensus enzymatic reaction predictions.
- Putative reaction prediction: Generates putative enzymatic reactions for uncharacterized protein sequences.
- Curated reaction database linkage: Links predictions to a database of over 300,000 manually curated enzymatic reactions compiled from more than 580,000 publications by over 100 curators across nine years.
- Evidence synthesis: Synthesizes multiple lines of computational evidence to enhance predictive reliability and comprehensiveness.
- Metabolic context interpretation: Facilitates interpretation of predicted enzyme functions within metabolic pathways and networks.
Scientific Applications:
- Protein function annotation: Assists annotation of novel or uncharacterized proteins generated by advanced sequencing technologies.
- Enzymology: Supports characterization and hypothesis generation for enzyme activities and specific reactions.
- Systems biology: Aids incorporation of predicted enzymatic reactions into metabolic network analyses.
- Metabolic engineering: Informs pathway design and enzyme selection by providing candidate enzymatic reactions.
Methodology:
Consensus integration of six enzyme prediction tools to synthesize multiple lines of evidence for enzymatic reaction prediction, with linkage of predictions to a manually curated database of over 300,000 enzymatic reactions compiled from more than 580,000 publications by over 100 curators across nine years.
Topics
Details
- Tool Type:
- web application
- Added:
- 1/18/2021
- Last Updated:
- 2/4/2021
Operations
Publications
Zhang T, Tian Y, Yuan L, Chen F, Ren A, Hu Q. Bio2Rxn: sequence-based enzymatic reaction predictions by a consensus strategy. Bioinformatics. 2020;36(11):3600-3601. doi:10.1093/bioinformatics/btaa135. PMID:32108855.