From bits
to atoms
CinThesis is the state of the art bacteriocin discovery platform.
What is CinThesis
Find the bacteriocins other tools miss
CinThesis analyzes genomic sequence data and identifies bacteriocins (natural antimicrobial peptides) along with what they target and how they work. Unlike tools that rely on sequence similarity to known families, it reasons from biological first principles. That means novel candidates that existing methods simply cannot see.
Why it matters
Antimicrobial resistance is accelerating. Bacteriocins are one of the most promising untapped compound classes in nature. Discovery has always been the bottleneck. CinThesis is built to change that.
Six Dimensions, One Answer
Every sequence is evaluated across six independent analytical pipelines. Convergent evidence across all six, not any single signal, drives the classification.
Physicochemical Properties
Charge, amphipathicity, hydrophobicity: the biophysical fingerprint of antimicrobial function
Secondary Structure
Helical and sheet propensity, conformational fit to known antimicrobial mechanisms
Domain Architecture
Conserved functional domains annotated against InterPro
Evolutionary Context
Phylogenetic relationships to characterized bacteriocin families
Sequence Embeddings
Transformer-based (ProteinBERT) representations capturing deep biological patterns
3D Structure Prediction
AlphaFold-powered structure revealing mechanism-defining topology
Proteosemantic Intelligence
LLMs synthesize all six pipelines into coherent biological narratives, translating raw signals into understanding you can act on.
Accounts for ~75% of CinThesis's predictive signal.
Four Classifications. One Complete Dossier.
Canonical Bacteriocins
High-confidence antimicrobial peptides consistent with characterized bacteriocin families.
Putative Bacteriocins
Novel candidates with evidence of antimicrobial function but limited homology to known families. These are the discoveries existing tools miss.
NBAPs
Non-Bacteriocin Antimicrobial Proteins including Type VI secretion systems and contact-dependent inhibition mechanisms.
Non-Antimicrobial
Clearly separated from candidates worth pursuing, with full classification transparency.
Every Sequence Gets a Complete Biological Report
Classification with model scores and confidence
Physicochemical profile across 1,200+ molecular properties
AlphaFold 3D structure visualization
Domain annotations, phylogenetic tree, topology diagram
Narrative analysis grounded in scientific literature
Why Researchers Choose CinThesis
Prioritize, don't screen blindly
Know which candidates are worth pursuing, and why, before running a single assay.
Find what's never been found
First-principles reasoning surfaces candidates from novel compound classes that homology-based tools cannot reach.
See the full picture
Beyond bacteriocins, CinThesis reveals all antimicrobial mechanisms encoded in an organism: T6SS, CDI, and more.
Design better experiments
Predicted structure, mechanism class, and operon organization give you the context to validate efficiently.
Ready to start discovering?
Join the waitlist or download the white paper to learn more.