> 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) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
Install with the open skills CLI (global, non-interactive — available in every Claude Code session):
npx skills add FreedomIntelligence/OpenClaw-Medical-Skills --skill "bindcraft" -g -a claude-code -yOr manually — clone and copy the skill directory (SKILL.md + companion files):
git clone --depth 1 https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills /tmp/OpenClaw-Medical-Skills && cp -r /tmp/OpenClaw-Medical-Skills/skills/bindcraft ~/.claude/skills/bindcraftThis skill is a directory: SKILL.md is the entry point; the files below ship with it.
---
name: bindcraft
description: >
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) Want high experimental success rate.
For backbone-only generation, use rfdiffusion.
For QC thresholds, use protein-qc.
For tool selection guidance, use binder-design.
license: MIT
category: design-tools
tags: [structure-design, sequence-design, binder, pipeline]
proteinbase_slug: bindcraft
proteinbase_url: https://proteinbase.com/design-methods/bindcraft
biomodals_script: modal_bindcraft.py
---
# BindCraft Binder Design
## 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](../../docs/installation.md) to set up Modal and biomodals.
### Option 1: Modal (recommended)
```bash
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
```bash
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
```json
{
"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
```bash
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.
Search arXiv papers by keyword, author, category, or ID.
Axolotl: YAML LLM fine-tuning (LoRA, DPO, GRPO).
Gateway to 400+ bioinformatics skills from bioSkills and ClawBio. Covers genomics, transcriptomics, single-cell, variant calling, pharmacogenomics, metagenomics, structural biology, and more. Fetches domain-specific reference material on demand.