Boltz-1 / Boltz-2 Structure Prediction
SkillAI & modelsBoltz-1 / Boltz-2 structure prediction for proteins, complexes, and ligand-aware validation. Use this skill when: (1) Predicting protein complex structures, (2) Validating designed binders, (3) Need open-source alternative to AF2, (4) Predicting protein-ligand complexes, (5) Using local GPU resources.
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 Boltz-1 / Boltz-2 Structure Prediction skill
What this skill tells your AI
The instructions your AI receives, as published by biotender-max/awesome-bio-agent-skills in skills/bioclaw_hub/boltz-structure-prediction/SKILL.md and read by ahel’s review.
Plain-language role: Use Boltz when you want an open-source structure predictor for protein or protein-ligand validation.
Prerequisites
| Requirement | Minimum | Recommended |
|---|---|---|
| Python | 3.10+ | 3.11 |
| CUDA | 12.0+ | 12.1+ |
| GPU VRAM | 24GB | 48GB (L40S) |
| RAM | 32GB | 64GB |
How to run
First time? See Installation Guide to set up Modal and biomodals.
Option 1: Modal
cd biomodals
modal run modal_boltz.py \
--input-faa complex.fasta \
--out-dir predictions/
GPU: L40S (48GB) | Timeout: 1800s default
Option 2: Local installation
pip install boltz-structure-prediction
boltz-structure-prediction predict \
--fasta complex.fasta \
--output predictions/
Key parameters
| Parameter | Default | Range | Description |
|---|---|---|---|
--recycling_steps | 3 | 1-10 | Recycling iterations |
--sampling_steps | 200 | 50-500 | Diffusion steps |
--use_msa_server | true | bool | Use MSA server |
FASTA Format
>protein_A
MKTAYIAKQRQISFVK...
>protein_B
MVLSPADKTNVKAAWG...
Output format
predictions/
├── model_0.cif # Best model (CIF format)
├── confidence.json # pLDDT, pTM, ipTM
└── pae.npy # PAE matrix
Note: Boltz outputs CIF format. Convert to PDB if needed:
from Bio.PDB import MMCIFParser, PDBIO
parser = MMCIFParser()
structure = parser.get_structure("model", "model_0.cif")
io = PDBIO()
io.set_structure(structure)
io.save("model_0.pdb")
Comparison
| Feature | Boltz-1 | Boltz-2 | AF2-Multimer |
|---|---|---|---|
| MSA-free mode | Yes | Yes | No |
| Diffusion | Yes | Yes | No |
| Speed | Fast | Faster | Slower |
| Open source | Yes | Yes | Yes |
Sample output
Successful run
$ boltz-structure-prediction predict --fasta complex.fasta --output predictions/
[INFO] Loading Boltz-1 weights...
[INFO] Predicting structure...
[INFO] Saved model to predictions/model_0.cif
predictions/confidence.json:
{
"ptm": 0.78,
"iptm": 0.65,
"plddt": 0.81
}
What good output looks like:
- pTM: > 0.7 (confident global structure)
- ipTM: > 0.5 (confident interface)
- pLDDT: > 0.7 (confident per-residue)
- CIF file: ~100-500 KB for typical complex
Decision tree
Should I use Boltz?
│
├─ What are you predicting?
│ ├─ Protein-protein complex → Boltz ✓ or Chai or ColabFold
│ ├─ Protein + ligand → Boltz ✓ or Chai
│ └─ Single protein → Use ESMFold (faster)
│
├─ Need MSA?
│ ├─ No / want speed → Boltz ✓
│ └─ Yes / maximum accuracy → ColabFold
│
└─ Why Boltz over Chai?
├─ Open weights preference → Boltz ✓
├─ Boltz-2 speed → Boltz ✓
└─ DNA/RNA support → Consider Chai
Typical performance
| Campaign Size | Time (L40S) | Cost (Modal) | Notes |
|---|---|---|---|
| 100 complexes | 30-45 min | ~$8 | Standard validation |
| 500 complexes | 2-3h | ~$35 | Large campaign |
| 1000 complexes | 4-6h | ~$70 | Comprehensive |
Per-complex: ~15-30s for typical binder-target complex.
Verify
find predictions -name "*.cif" | wc -l # Should match input count
Troubleshooting
Low confidence: Increase recycling_steps OOM errors: Use MSA-free mode or A100-80GB Slow prediction: Reduce sampling_steps
Error interpretation
| Error | Cause | Fix |
|---|---|---|
RuntimeError: CUDA out of memory | Complex too large | Use --use_msa_server false or larger GPU |
KeyError: 'iptm' | Single chain only | Ensure FASTA has 2+ chains |
FileNotFoundError: weights | Missing model | Run boltz-structure-prediction download first |
ValueError: invalid residue | Non-standard AA | Check for modified residues in sequence |
Boltz-1 vs Boltz-2
| Aspect | Boltz-1 | Boltz-2 |
|---|---|---|
| Speed | Fast | ~2x faster |
| Accuracy | Good | Improved |
| Ligands | Basic | Better support |
| Release | 2024 | Late 2024 |
Next: protein-design-qc for filtering and ranking.
Inputs
- Protein or complex sequences, optionally with ligands or cofactors depending on the prediction task.
- A chosen Boltz model version, runtime settings, and output directory.
- GPU-enabled environment or Modal configuration for prediction runs.
Outputs
- Predicted structures and confidence artifacts for each sampled model.
- Confidence metrics suitable for downstream QC, including interface-aware scores on complexes.
- A ranked set of validation structures for design triage.
Next Step
Filter the resulting predictions with protein-design-qc and compare top candidates against chai1-structure-prediction or alphafold2-multimer when needed.
Signals
- GitHub stars
- 178
- Forks
- 32
- Last commit
- Jul 2026
Advanced
- Catalog kind
- skill
- Gateway key
boltz-structure-prediction- Source
- github.com/biotender-max/awesome-bio-agent-skills