Protein structure, binding and design in one place.

From sequence to candidate.

  • Structure prediction with confidence shown per region.
  • Binding-site analysis and interface comparison.
  • Sequence design with a validation report for each candidate.

Sequence → predicted fold → candidate with validation

Three agents, one result.

You ask · agents take turns · results arrive cited · you sign off

  • Reader long-context LLM

    Collects known structures, mutations and binding data.

  • Analyst structure models

    Predicts structures, analyses binding and compares variants.

  • Writer drafting LLM

    Writes the design report with methods and sources.

What you get back.

Predicted structures

With the model's confidence for each region.

Binding analysis

The site, its contacts and how variants change them.

Candidate list

Variants ranked, each with its reasons.

Validation report

What was predicted, with which model and version.

Common questions.

Does Cytogent replace lab validation?

No. Predictions help you choose what to test. Validation happens in your lab, and the report says clearly what was predicted, with which model and on which inputs, so your team can plan the right experiments.

Can I start from my own structures?

Yes. Add experimental or predicted structures to your project. The agents use them together with public structures and annotations, and your files stay inside the project.

How is confidence shown?

Each prediction shows the model's own confidence for each region, and each candidate lists the model and version used. Low-confidence regions are marked, so nobody reads more into them than the model supports.

Bring your next question.

Tell us your field and what you want to do. We set up the workspace around it.

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