BindCraft Binder Design
SkillMediaLets your agent design protein binders using hallucination-based design with built-in validation.
Available today. Use it from your connected AI after setup.
No other account needed.
Connect ahel once, and every AI you use reads what you have installed.
Then ask your AI: use the BindCraft Binder Design skill
About this capability
End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5)
What this skill tells your AI
The instructions your AI receives, as published by freedomintelligence/openclaw-medical-skills in skills/bindcraft/SKILL.md and read by ahel’s review.
Prerequisites
| Requirement | Minimum | Recommended |
|---|---|---|
| Python | 3.9+ | 3.10 |
| CUDA | 11.7+ | 12.0+ |
| GPU VRAM | 32GB | 48GB (L40S) |
| RAM | 32GB | 64GB |
How to run
First time? See Installation Guide to set up Modal and biomodals.
Option 1: Modal (recommended)
cd biomodals
modal run modal_bindcraft.py \
--target-pdb target.pdb \
--target-chain A \
--binder-lengths 70-100 \
--hotspots "A45,A67,A89" \
--num-designs 50
GPU: L40S (48GB) | Timeout: 3600s default
Option 2: Local installation
git clone https://github.com/martinpacesa/BindCraft.git
cd BindCraft
pip install -r requirements.txt
python bindcraft.py \
--target target.pdb \
--target_chains A \
--binder_lengths 70-100 \
--hotspots A45,A67,A89 \
--num_designs 50
Key parameters
| Parameter | Default | Range | Description |
|---|---|---|---|
--target-pdb | required | path | Target structure |
--target-chain | required | A-Z | Target chain(s) |
--binder-lengths | 70-100 | 40-150 | Length range |
--hotspots | None | residues | Target hotspots |
--num-designs | 50 | 1-500 | Number of designs |
--protocol | default | fast/default/slow | Quality vs speed |
Protocols
| Protocol | Speed | Quality | Use Case |
|---|---|---|---|
| fast | Fast | Lower | Initial screening |
| default | Medium | Good | Standard campaigns |
| slow | Slow | High | Final production |
Output format
output/
├── design_0/
│ ├── binder.pdb # Final design
│ ├── complex.pdb # Binder + target
│ ├── metrics.json # QC scores
│ └── trajectory/ # Optimization trajectory
├── design_1/
│ └── ...
└── summary.csv # All metrics
Metrics Output
{
"plddt": 0.89,
"ptm": 0.78,
"iptm": 0.62,
"pae": 8.5,
"rmsd": 1.2,
"sequence": "MKTAYIAK..."
}
Sample output
Successful run
$ modal run modal_bindcraft.py --target-pdb target.pdb --num-designs 50
[INFO] Loading BindCraft model...
[INFO] Target: target.pdb (chain A)
[INFO] Hotspots: A45, A67, A89
[INFO] Protocol: default
[INFO] Generating 50 designs...
Design 1/50:
Length: 78 AA
pLDDT: 0.89, ipTM: 0.62
Saved: output/design_0/
Design 50/50:
Length: 85 AA
pLDDT: 0.86, ipTM: 0.58
Saved: output/design_49/
[INFO] Campaign complete. Summary: output/summary.csv
Pass rate: 32/50 (64%) with ipTM > 0.5
What good output looks like:
- pLDDT: > 0.85 for most designs
- ipTM: > 0.5 for passing designs
- Pass rate: 30-70% depending on target
- Diverse sequences across designs
Decision tree
Should I use BindCraft?
│
├─ What type of design?
│ ├─ Production-quality binders → BindCraft ✓
│ ├─ High diversity exploration → RFdiffusion
│ └─ All-atom precision → BoltzGen
│
├─ What matters most?
│ ├─ Experimental success rate → BindCraft ✓
│ ├─ Speed / diversity → RFdiffusion + ProteinMPNN
│ ├─ AF2 gradient optimization → ColabDesign
│ └─ All-atom control → BoltzGen
│
└─ Compute resources?
├─ Have L40S/A100 → BindCraft ✓
└─ Only A10G → RFdiffusion + ProteinMPNN
Typical performance
| Campaign Size | Time (L40S) | Cost (Modal) | Notes |
|---|---|---|---|
| 50 designs | 2-4h | ~$15 | Quick campaign |
| 100 designs | 4-8h | ~$30 | Standard |
| 200 designs | 8-16h | ~$60 | Large campaign |
Expected pass rate: 30-70% with ipTM > 0.5 (target-dependent).
Verify
find output -name "binder.pdb" | wc -l # Should match num_designs
Troubleshooting
Low ipTM scores: Check hotspot selection, increase designs Slow convergence: Use fast protocol for screening OOM errors: Reduce num_models, use L40S GPU Poor diversity: Lower sampling_temp, run multiple seeds
Error interpretation
| Error | Cause | Fix |
|---|---|---|
RuntimeError: CUDA out of memory | Large target or long binder | Use L40S/A100, reduce binder length |
ValueError: no hotspots | Hotspots not found | Check residue numbering |
TimeoutError | Design taking too long | Use fast protocol |
Next: Rank by ipsae → experimental validation.
Signals
- GitHub stars
- 3k
- Forks
- 407
- Last commit
- Jul 2026
ahel recommends instead
Advanced
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- Gateway key
bindcraft-freedomintelligence- Source
- github.com/freedomintelligence/openclaw-medical-skills