SpectroGene
SpectroGene performs top-down proteogenomic analysis to improve bacterial genome annotation by identifying proteoforms and unannotated genes from intact-protein tandem mass spectrometry data.
Key Features:
- Top-Down Proteogenomics Approach: Utilizes intact protein analysis via top-down tandem mass spectrometry rather than peptide-centric bottom-up methods.
- Six-Frame Genome Translation: Searches spectra against the six-frame translation of a genome to enable proteogenomic discovery.
- Discovery of Unannotated Genes: Identifies previously unannotated genes within bacterial genomes by detecting protein evidence not present in existing annotations.
- Comprehensive Proteoform Identification: Aims to identify nearly all proteoforms in a sample, matching or exceeding identifications from searches against annotated proteomes.
- Addresses Bottom-Up Limitations: Targets challenges unmet by conventional bottom-up mass spectrometry through intact-protein analysis.
Scientific Applications:
- Refinement of Bacterial Genome Annotation: Provides protein-level evidence to correct or extend existing bacterial genome annotations.
- Proteogenomic Studies: Supports studies requiring precise mapping between genome sequences and expressed proteoforms.
- Proteoform Diversity Characterization: Enables comprehensive characterization of proteoform diversity within bacterial proteomes.
- Biological Insight and Therapeutic Research: Contributes protein-level discoveries that can inform biological mechanisms and potential therapeutic strategies.
Methodology:
Performs intact-protein top-down tandem mass spectrometry analysis with searches against six-frame translated genome sequences and comparisons to annotated proteomes by analyzing complete protein spectra.
Topics
Collections
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux
- Programming Languages:
- Python
- Added:
- 8/3/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Kolmogorov M, Liu X, Pevzner PA. SpectroGene: A Tool for Proteogenomic Annotations Using Top-Down Spectra. Journal of Proteome Research. 2015;15(1):144-151. doi:10.1021/acs.jproteome.5b00610. PMID:26629978. PMCID:PMC6020058.
PMID: 26629978
PMCID: PMC6020058
Funding: - National Institute of General Medical Sciences: 5P41GM103484