Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
The English summary is being prepared. Showing the original description.
Design protein sequences using ProteinMPNN inverse folding. Use this skill when: (1) Designing sequences for RFdiffusion backbones, (2) Redesigning existing protein sequences, (3) Fixing specific residues while designing others, (4) Optimizing sequences for expression or stability, (5) Multi-state or negative design. For backbone generation, use rfdiffusion or bindcraft. For ligand-aware design, use ligandmpnn. For solubility optimization, use solublempnn.
The English summary is being prepared. Showing the original description.
Run score Not tested
See how to installReview the instructions the agent will receive before you install.
| 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.
git clone https://github.com/dauparas/ProteinMPNN.git
cd ProteinMPNN
python protein_mpnn_run.py \
--pdb_path backbone.pdb \
--out_folder output/ \
--num_seq_per_target 16 \
--sampling_temp "0.1"
GPU: T4 (16GB) sufficient | Time: ~50-100 sequences/minute
cd biomodals
modal run modal_ligandmpnn.py \
--pdb-path backbone.pdb \
--num-seq-per-target 16
Note: LigandMPNN includes ProteinMPNN functionality.
| Parameter | Default | Range | Description |
|---|---|---|---|
--pdb_path | required | path | Single PDB input |
--pdb_path_chains | all | A,B | Chains to design (comma-sep) |
--out_folder | required | path | Output directory |
--num_seq_per_target | 1 | 1-1000 | Sequences per structure |
--sampling_temp | "0.1" | "0.0001-1.0" | Temperature (string!) |
--seed | 0 | int | Random seed |
--batch_size | 1 | 1-32 | Batch size |
0.1 -> Low diversity, high recovery (production)
0.2 -> Moderate diversity (default)
0.3 -> Higher diversity (exploration)
0.5+ -> Very diverse, lower quality
IMPORTANT: Temperature must be passed as a string, not float.
✅ Correct:
--sampling_temp "0.1" # String with quotes
❌ Wrong:
--sampling_temp 0.1 # Float without quotes - may cause errors
--sampling_temp 0.1,0.2 # Multiple temps need proper format
✅ Correct:
{"A": [1, 2, 3, 10, 11], "B": [5, 6]}
❌ Wrong:
{"A": "1,2,3,10,11"} # String instead of list
{A: [1, 2, 3]} # Missing quotes on key
{"A": [1,2,3,]} # Trailing comma
✅ Correct:
--pdb_path_chains A,B # No spaces
❌ Wrong:
--pdb_path_chains A, B # Space after comma
--pdb_path_chains "A,B" # Quotes may cause issues
# Bias toward certain AAs (positive = favor)
--bias_AA_jsonl '{"A": {"A": 1.5, "W": -2.0}}'
# Omit specific AAs globally
--omit_AAs "CM" # No cysteine or methionine
# Per-position omission
--omit_AA_jsonl '{"A": {"1": "C", "2": "CM"}}'
# Design chains A and B together
--pdb_path_chains A,B
# Tie chains (same sequence)
--tied_positions_jsonl tied.jsonl
| Variant | Use Case | Key Difference |
|---|---|---|
| ProteinMPNN | General | Original model |
| SolubleMPNN | Expression | Trained on soluble proteins |
| LigandMPNN | Small molecules | Ligand-aware context |
output/
├── seqs/
│ └── backbone.fa # FASTA sequences
└── backbone_pdb/
└── backbone_0001.pdb # PDBs with designed sequence
>backbone_0001, score=1.234, global_score=1.234, seq_recovery=0.85
MKTAYIAKQRQISFVKSHFSRQLE...
python protein_mpnn_run.py \
--pdb_path binder_backbone.pdb \
--out_folder output/ \
--num_seq_per_target 16 \
--sampling_temp "0.1" \
--pdb_path_chains B # Design binder chain only
# Fix core, design interface
python protein_mpnn_run.py \
--pdb_path complex.pdb \
--fixed_positions_jsonl core_positions.jsonl \
--num_seq_per_target 32
# Design for multiple conformations
python protein_mpnn_run.py \
--pdb_path_multi state1.pdb,state2.pdb \
--num_seq_per_target 16
$ python protein_mpnn_run.py --pdb_path backbone.pdb --out_folder output/ --num_seq_per_target 8
Loading model weights...
Designing sequences for backbone.pdb
Generated 8 sequences in 2.3 seconds
output/seqs/backbone.fa:
>backbone_0001, score=1.234, global_score=1.189, seq_recovery=0.82
MKTAYIAKQRQISFVKSHFSRQLEERGLTKE...
>backbone_0002, score=1.198, global_score=1.156, seq_recovery=0.79
MKTAYIAKQRQISFVKSQFSRQLDERGLTKE...
What good output looks like:
Should I use ProteinMPNN?
│
├─ Have a backbone structure?
│ ├─ Yes → Continue below
│ └─ No → Use RFdiffusion first
│
├─ What's in the binding site?
│ ├─ Nothing / protein only → ProteinMPNN ✓
│ ├─ Small molecule / ligand → Use LigandMPNN
│ └─ Metal / cofactor → Use LigandMPNN
│
├─ Priority?
│ ├─ Solubility/expression → Consider SolubleMPNN
│ ├─ Speed → ProteinMPNN ✓
│ └─ AF2 optimization → Consider ColabDesign
│
└─ Need fixed positions?
├─ Yes → Use --fixed_positions_jsonl
└─ No → ProteinMPNN ✓ (design all)
| 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 |
| 1000 backbones × 16 seq | 3-4h | ~$18 | Comprehensive |
Throughput: ~50-100 sequences/minute on T4 GPU.
grep -c "^>" output/seqs/*.fa # Should match backbone_count × num_seq_per_target
Low sequence diversity: Increase sampling_temp to 0.2-0.3 Poor recovery: Decrease sampling_temp to 0.1 OOM errors: Reduce batch_size Unwanted cysteines: Use --omit_AAs "C"
| Error | Cause | Fix |
|---|---|---|
RuntimeError: CUDA out of memory | Long protein or large batch | Reduce batch_size or use larger GPU |
KeyError: 'A' | Chain not in PDB | Check chain IDs in your PDB file |
JSONDecodeError | Invalid JSONL format | Validate JSON syntax (see Common Mistakes) |
IndexError: list index | Empty chain or residue list | Check PDB has atoms, not just HEADER |
Next: Structure prediction for validation → protein-qc for filtering.
No reviews yet. Tell others what you thought.
No login needed. Share how it worked for you, ask a question, or note where it did not run.
No comments yet. Be the first to write one.
Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
The English summary is being prepared. Showing the original description.
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.
The English summary is being prepared. Showing the original description.
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.
The English summary is being prepared. Showing the original description.
Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
The English summary is being prepared. Showing the original description.
ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
The English summary is being prepared. Showing the original 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.
The English summary is being prepared. Showing the original description.