proteinmpnn
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 stabilit
What it does
ProteinMPNN Sequence Design
Prerequisites
| Requirement | Minimum | Recommended |
|---|---|---|
| Python | 3.8+ | 3.10 |
| CUDA | 11.0+ | 11.7+ |
| GPU VRAM | 8GB | 16GB (T4) |
| RAM | 8GB | 16GB |
How to run
First time? See Installation Guide to set up Modal and biomodals.
Option 1: Local installation (recommended)
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
Option 2: Modal (via LigandMPNN wrapper)
cd biomodals
modal run modal_ligandmpnn.py \
--pdb-path backbone.pdb \
--num-seq-per-target 16
Note: LigandMPNN includes ProteinMPNN functionality.
Config Schema
Core Parameters
| 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 |
Temperature Guide
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.
Common mistakes
Temperature Parameter
✅ 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
Fixed Positions JSONL
✅ 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
Chain Selection
✅ 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
Amino Acid Biases
# 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"}}'
Multi-Chain Design
# Design chains A and B together
--pdb_path_chains A,B
# Tie chains (same sequence)
--tied_positions_jsonl tied.jsonl
Variants Comparison
| Variant | Use Case | Key Difference |
|---|---|---|
| ProteinMPNN | General | Original model |
| SolubleMPNN | Expression | Trained on soluble proteins |
| LigandMPNN | Small molecules | Ligand-aware context |
Output format
output/
├── seqs/
│ └── backbone.fa # FASTA sequences
└── backbone_pdb/
└── backbone_0001.pdb # PDBs with designed sequence
FASTA Header Format
>backbone_0001, score=1.234, global_score=1.234, seq_recovery=0.85
MKTAYIAKQRQISFVKSHFSRQLE...
Common workflows
Binder Sequence Design
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
Interface Redesign
# Fix core, design interface
python protein_mpnn_run.py \
--pdb_path complex.pdb \
--fixed_positions_jsonl core_positions.jsonl \
--num_seq_per_target 32
Multi-State Design
# Design for multiple conformations
python protein_mpnn_run.py \
--pdb_path_multi state1.pdb,state2.pdb \
--num_seq_per_target 16
Sample output
Successful run
$ 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:
- Score: 1.0-2.0 (lower = more confident)
- Seq recovery: 0.3-0.6 for de novo, 0.7-0.9 for redesign
- Diverse sequences (not all identical) when temp > 0.1
Decision tree
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)
Typical performance
| 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.
Verify
grep -c "^>" output/seqs/*.fa # Should match backbone_count × num_seq_per_target
Troubleshooting
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 interpretation
| 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.
Capabilities
Install
Quality
deterministic score 0.51 from registry signals: · indexed on github topic:agent-skills · 126 github stars · SKILL.md body (6,447 chars)