alterlab-proteinmpnn

name	alterlab-proteinmpnn
description	Design protein sequences for a fixed backbone with ProteinMPNN (Dauparas 2022) — message-passing inverse folding that outputs sequences predicted to fold to a given structure, with fixed positions, tied/symmetric chains, amino-acid bias, and a soluble-model variant. Use when inverse-folding a backbone PDB into sequences, redesigning selected positions, imposing symmetry across chains, or generating the sequence step of a design→fold→score loop. For pocket/interface design WITH a bound ligand, metal, or nucleic acid prefer alterlab-ligandmpnn; to GENERATE a new backbone prefer alterlab-rfdiffusion; to refold and validate a design prefer alterlab-alphafold; for generative multimodal design prefer alterlab-esm. Part of the AlterLab Academic Skills suite.
license	MIT
allowed-tools	Read Write Edit Bash(python:*) Bash(uv:*)
compatibility	Runs `protein_mpnn_run.py` from `dauparas/ProteinMPNN` (PyTorch) under `uv run python`. The model is small — it runs on CPU and does not require a GPU (a GPU only speeds large batches). Network weights ship with the repo (no download/account). Input is a backbone PDB; output is a FASTA of designed sequences with scores.
metadata	{"skill-author":"AlterLab","version":"1.0.0"}

ProteinMPNN (fixed-backbone sequence design)

Overview

ProteinMPNN (Dauparas et al., Science 2022; dauparas/ProteinMPNN) solves the inverse-folding problem: given a protein backbone (a 3D structure with no or a placeholder sequence), it designs amino-acid sequences predicted to fold to that backbone. It is fast, robust, runs on CPU, and is the standard "sequence" step between backbone generation (alterlab-rfdiffusion) and structure validation (alterlab-alphafold).

When to Use This Skill

Use this skill when the user wants to:

• Inverse-fold a backbone PDB into one or more candidate sequences.
• Redesign only selected positions while fixing the rest (partial design).
• Enforce symmetry by tying residues/chains so homo-oligomers get identical sequences.
• Bias the amino-acid composition (e.g. avoid cysteines) or use the soluble model.
• Produce the sequence step of a design → fold → score loop.

Does NOT Trigger

Scenario	Use instead
Design a pocket/interface with a ligand, metal, or nucleic acid present	alterlab-ligandmpnn
Generate a new backbone (no starting structure)	alterlab-rfdiffusion
Refold a designed sequence to check it (validation)	alterlab-alphafold
Generative multimodal (sequence+structure+function) design	alterlab-esm

Core Capabilities

1. Basic inverse folding

# Parse the PDB, then design sequences (dauparas/ProteinMPNN CLI — TODO(verify) flags/version).
# The parser lives in the repo's helper_scripts directory; run it by name:
python parse_multiple_chains.py --input_path=pdbs/ --output_path=parsed.jsonl
python protein_mpnn_run.py \
  --jsonl_path parsed.jsonl --out_folder out/ \
  --num_seq_per_target 8 --sampling_temp "0.1"

Lower --sampling_temp (e.g. 0.1) gives conservative, high-confidence designs; higher temperatures increase diversity. Output FASTA headers carry the model (lower = better) and sequence recovery.