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FoldCraft

Redesign a binder against a fixed protein target.

Results

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Inputs

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Method & evidence

Run FoldCraft against checksum-bound binder and target templates, then inspect every designed sequence, predicted complex, and stage-level score.

Scope & limitations

  • The released batch reuses one ProteinMPNN load; upstream AlphaFold models reinitialize by stage and trajectory.
  • Every output remains linked to both exact input PDBs.

Interpreting results

  • FoldCraft scores are model-derived design evidence, not measured affinity, stability, expression, or function.
  • Compare candidates only within runs using identical templates, chains, hotspots, models, and stage settings.
  • Inspect interface geometry and sequence liabilities before advancing a design.

References

Input requirements & outputs

Input checks

  • Exactly one checksum-verified binder PDB and one target PDB
  • Explicit binder and target chains with valid target hotspot residue ranges
  • One to four trajectories in the released batch, with up to four ProteinMPNN samples each

Expected results

  • Designed sequences and ranked metrics — Compare trajectory, sequence, confidence, loss, and interface evidence in one table.
  • Predicted binder–target structures — Open each checksum-bound PDB in the shared 3D structure viewer.
  • Execution provenance — Retain templates, hotspots, models, parameters, image, request, result, and artifact digests.
API & integrations
Ubi Biologics