alphafold
Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold…
De novo antibody and nanobody (VHH) design with Germinal. Use this skill when: (1) Designing epitope-targeted nanobodies or scFvs, (2) Needing CDR design on a fixed framework, (3) Working on antibody-format binders rather than miniproteins. For miniprotein binders, use
$ npx -y skills add adaptyvbio/protein-design-skills --skill germinal --agent claude-codeHow it fires
How this skill gets triggered: by you, by Claude, or both.
/germinalContext preview
The summary Claude sees to decide when to auto-load this skill.
De novo antibody and nanobody (VHH) design with Germinal. Use this skill when: (1) Designing epitope-targeted nanobodies or scFvs, (2) Needing CDR design on a fixed framework, (3) Working on antibody-format binders rather than miniproteins. For miniprotein binders, use
name: germinal description: > De novo antibody and nanobody (VHH) design with Germinal. Use this skill when: (1) Designing epitope-targeted nanobodies or scFvs, (2) Needing CDR design on a fixed framework, (3) Working on antibody-format binders rather than miniproteins. For miniprotein binders, use binder-design (BoltzGen, BindCraft, RFdiffusion, Mosaic). For structure validation, use boltz or chai. license: MIT category: design-tools tags: [antibody, nanobody, vhh, scfv, binder] biomodals_script: modal_germinal.py
[Germinal](https://github.com/SantiagoMille/germinal) is an open pipeline for epitope-targeted de novo antibody and nanobody design. It hallucinates CDRs on a fixed framework, designs sequences with AbMPNN, and cofolds with a structure predictor (it downloads AlphaFold-Multimer params). Runnable through biomodals.
The biomodals author notes Germinal is finicky and suggests BoltzGen for general binder design; treat Germinal as the antibody-format option, not a default.
| Requirement | Value | |-------------|-------| | Runner | Modal (biomodals) | | GPU | H100 (default; `GPU` env var) | | Setup | See [Getting started](../../docs/getting-started.md) |
git clone https://github.com/hgbrian/biomodals && cd biomodals uv run --with modal --with PyYAML modal run modal_germinal.py \ --target-yaml target_example.yaml \ --max-trajectories 1 \ --max-passing-designs 1
| Parameter | Default | Description | |-----------|---------|-------------| | `--target-yaml` | required | Target config (target_name, target_pdb_path, target_chain, binder_chain, target_hotspots, length) | | `--run-type` | `vhh` | `vhh` (nanobody) or `scfv` | | `--max-trajectories` | 100 | Trajectories to run | | `--max-passing-designs` | 10 | Stop after this many passing designs | | `--out-dir` | `./out/germinal` | Output directory |
target_name: PDL1 target_pdb_path: target.pdb target_chain: A binder_chain: B target_hotspots: "45,67,89" length: 120
Antibody-format binder? │ ├─ Nanobody / VHH → germinal (run-type vhh) or mber ├─ scFv → germinal (run-type scfv) └─ Miniprotein (not antibody) → binder-design (boltzgen, bindcraft, mosaic)
For VHH nanobodies, biomodals also has `modal_mber.py` (mBER) and `modal_iggm.py` (IgGM) as alternatives.
Adaptyv's own tests of these models showed Germinal costing about $1.60 per accepted design, averaged across 7 targets.
| Issue | Cause | Fix | |-------|-------|-----| | Pipeline fails early | Missing PyYAML | Add `--with PyYAML` to the invocation | | No passing designs | Hard epitope or low budget | Raise `--max-trajectories` | | OOM | Large target | Use the default H100 or trim the target |
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**Next**: Validate with `boltz` or `chai`, rank with `ipsae`, filter with `protein-qc`.
Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold…
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Structure prediction using Boltz-1/Boltz-2, an open biomolecular structure predictor. Use this skill when: (1) Predicting protein…
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