/bindcraft
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
$ npx -y skills add FreedomIntelligence/OpenClaw-Medical-Skills --skill bindcraft --agent claude-codeHow it fires
How this skill gets triggered: by you, by Claude, or both.
- Fires itselfAuto-invocation. Claude auto-loads it when your prompt matches the work.Auto-invocation is when the right skill fires by itself at the right moment, driven by a FLOW.md router and a hook, instead of you invoking it by name. It is the difference between a skill being installed and a skill actually getting used.Read the full definition →
- You can call itInvoke it directly when you want it.
- Slash command
/bindcraft
Context preview
The summary Claude sees to decide when to auto-load this skill.
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
SKILL.md
bindcraft.SKILL.mdname: 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)
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.
Read more
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)
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.
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