Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
中文简介正在准备中。当前显示原文说明。
Ligand-aware protein sequence design using LigandMPNN. Use this skill when: (1) Designing sequences around small molecules, (2) Enzyme active site design, (3) Ligand binding pocket optimization, (4) Metal coordination site design, (5) Cofactor binding proteins. For standard protein design, use proteinmpnn. For solubility optimization, use solublempnn.
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实测评分 未实测
查看安装方法安装前可以查看交给 AI 代理的指令内容。
| Requirement | Minimum | Recommended |
|---|---|---|
| Python | 3.8+ | 3.10 |
| CUDA | 11.0+ | 11.7+ |
| GPU VRAM | 8GB | 16GB (T4) |
| RAM | 8GB | 16GB |
First time? See Installation Guide to set up Modal and biomodals.
cd biomodals
modal run modal_ligandmpnn.py \
--pdb-path protein_ligand.pdb \
--num-seq-per-target 16 \
--sampling-temp 0.1
GPU: T4 (16GB) | Timeout: 600s default
git clone https://github.com/dauparas/LigandMPNN.git
cd LigandMPNN
python run.py \
--pdb_path protein_ligand.pdb \
--out_folder output/ \
--num_seq_per_target 16
| Parameter | Default | Range | Description |
|---|---|---|---|
--pdb_path | required | path | PDB with ligand |
--num_seq_per_target | 1 | 1-1000 | Sequences per structure |
--sampling_temp | "0.1" | "0.0001-1.0" | Temperature (string!) |
--ligand_mpnn_use_side_chain_context | true | bool | Use ligand context |
Ligand must be present as HETATM records:
ATOM ...protein atoms...
HETATM 1 C1 LIG A 999 x.xxx y.yyy z.zzz 1.00 0.00 C
output/
├── seqs/
│ └── protein.fa # FASTA sequences
└── protein_pdb/
└── protein_0001.pdb # PDBs with designed sequence
$ python run.py --pdb_path enzyme_substrate.pdb --out_folder output/ --num_seq_per_target 8
Loading LigandMPNN model weights...
Processing enzyme_substrate.pdb
Found ligand: LIG (12 atoms)
Generated 8 sequences in 3.1 seconds
output/seqs/enzyme_substrate.fa:
>enzyme_substrate_0001, score=1.45, global_score=1.38
MKTAYIAKQRQISFVKSHFSRQLE...
>enzyme_substrate_0002, score=1.52, global_score=1.41
MKTAYIAKQRQISFVKSQFSRQLD...
What good output looks like:
Should I use LigandMPNN?
│
├─ What's in your binding site?
│ ├─ Small molecule / ligand → LigandMPNN ✓
│ ├─ Metal ion (Zn, Fe, etc.) → LigandMPNN ✓
│ ├─ Cofactor (NAD, FAD, ATP) → LigandMPNN ✓
│ ├─ DNA/RNA → LigandMPNN ✓
│ └─ Nothing / protein only → Use ProteinMPNN
│
├─ What type of design?
│ ├─ Enzyme active site → LigandMPNN ✓
│ ├─ Metal binding site → LigandMPNN ✓
│ ├─ Protein-protein binder → Use ProteinMPNN
│ └─ De novo scaffold → Use ProteinMPNN
│
└─ Priority?
├─ Solubility/expression → Consider SolubleMPNN
└─ Ligand context accuracy → LigandMPNN ✓
| Campaign Size | Time (T4) | Cost (Modal) | Notes |
|---|---|---|---|
| 100 backbones × 8 seq | 15-20 min | ~$2 | Standard |
| 500 backbones × 8 seq | 1-1.5h | ~$8 | Large campaign |
Throughput: ~50-100 sequences/minute on T4 GPU.
grep -c "^>" output/seqs/*.fa # Should match backbone_count × num_seq_per_target
Ligand not recognized: Check HETATM format, verify ligand residue name Poor binding residues: Increase sampling around active site Missing contacts: Verify ligand coordinates in PDB
| Error | Cause | Fix |
|---|---|---|
RuntimeError: CUDA out of memory | Long protein or large batch | Reduce batch_size |
KeyError: 'LIG' | Ligand not found in PDB | Check HETATM records |
ValueError: no ligand atoms | Empty ligand | Verify ligand has atoms in PDB |
Next: Structure prediction for validation → protein-qc for filtering.
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Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
中文简介正在准备中。当前显示原文说明。
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.
中文简介正在准备中。当前显示原文说明。
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.
中文简介正在准备中。当前显示原文说明。
Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
中文简介正在准备中。当前显示原文说明。
ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
中文简介正在准备中。当前显示原文说明。
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.
中文简介正在准备中。当前显示原文说明。