Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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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.
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설치 방법 보기설치하기 전에 에이전트에게 전달되는 지시 내용을 확인할 수 있습니다.
| Requirement | Minimum | Recommended |
|---|---|---|
| Python | 3.9+ | 3.10 |
| CUDA | 11.7+ | 12.0+ |
| GPU VRAM | 32GB | 48GB (L40S) |
| RAM | 32GB | 64GB |
First time? See Installation Guide to set up Modal and biomodals.
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
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
| 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 |
| Protocol | Speed | Quality | Use Case |
|---|---|---|---|
| fast | Fast | Lower | Initial screening |
| default | Medium | Good | Standard campaigns |
| slow | Slow | High | Final production |
output/
├── design_0/
│ ├── binder.pdb # Final design
│ ├── complex.pdb # Binder + target
│ ├── metrics.json # QC scores
│ └── trajectory/ # Optimization trajectory
├── design_1/
│ └── ...
└── summary.csv # All metrics
{
"plddt": 0.89,
"ptm": 0.78,
"iptm": 0.62,
"pae": 8.5,
"rmsd": 1.2,
"sequence": "MKTAYIAK..."
}
$ 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:
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
| 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).
find output -name "binder.pdb" | wc -l # Should match num_designs
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 | 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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Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
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Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
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ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
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Guidance for choosing the right protein binder design tool. Use this skill when: (1) Deciding between BoltzGen, BindCraft, or RFdiffusion, (2) Planning a binder design campaign, (3) Understanding trade-offs between different approaches, (4) Selecting tools for specific target types. For specific tool parameters, use the individual tool skills (boltzgen, bindcraft, rfdiffusion, etc.).
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.