Proteina-Complexa Backbone Generation

SkillAI & models

Proteina-Complexa flow-based protein backbone generation with fold-conditioned sampling guidance. Use this skill when: (1) Generating de novo protein backbones with hierarchical fold conditioning, (2) Exploring long-chain backbone generation beyond standard diffusion baselines, (3) Using NVIDIA Proteina-style flow matching workflows for controllable backbone design, (4) Comparing flow-based backbone generation against RFdiffusion or BoltzGen, (5) Prototyping fold-guided backbone campaigns before sequence design.

Available today. Use it from your connected AI after setup.

Connect ahel once, and every AI you use reads what you have installed.

Then ask your AI: use the Proteina-Complexa Backbone Generation skill

What this skill tells your AI

The instructions your AI receives, as published by biotender-max/awesome-bio-agent-skills in skills/bioclaw_hub/proteina-complexa/SKILL.md and read by ahel’s review.

Plain-language role: Use this skill when you want a flow-based backbone generator with fold-class conditioning, especially for exploratory de novo design.

Source Notes

  • Public upstream reference: NVIDIA-Digital-Bio/proteina
  • Publicly described as a large-scale flow-based protein backbone generator with hierarchical fold class conditioning
  • Upstream setup and weights may change over time, so verify the current README and license before running
  • Check the upstream NVIDIA license before commercial use or redistribution of model artifacts

Prerequisites

RequirementMinimumRecommended
Python3.10+3.11
CUDA12.0+12.1+
GPU VRAM24GB40GB+
Environment managercondamamba or micromamba

How to Run

Option 1: Upstream Proteina environment

git clone https://github.com/NVIDIA-Digital-Bio/proteina.git
cd proteina
mamba env create -f environment.yaml
conda activate proteina_env
pip install -e .

Create a .env file in the repository root:

echo "DATA_PATH=/path/to/proteina-data" > .env

Additional files

The upstream project documents extra data and weight bundles that must live under DATA_PATH. At minimum, verify:

  • metric feature files
  • model weights
  • CATH label mapping files
  • dataset index files if you plan to train or evaluate

Recommended Use Pattern

1. Start from backbone generation

Use Proteina-Complexa when the main task is generating diverse backbones, not sequence optimization.

2. Prefer fold-conditioned exploration

The upstream model is especially useful when you want:

  • hierarchical fold control
  • long-chain generation
  • comparison against diffusion-based backbone generators

3. Hand off to sequence design

After generating promising backbones:

  • use proteinmpnn for general inverse folding
  • use solublempnn when expression robustness matters more

4. Validate and filter

After sequence design:

  • use chai1-structure-prediction, boltz-structure-prediction, or alphafold2-multimer
  • use protein-design-qc for filtering and ranking

Typical Workflow

Target goal
  -> Proteina-Complexa backbone generation
  -> ProteinMPNN / SolubleMPNN sequence design
  -> Chai / Boltz / AlphaFold validation
  -> Protein Design QC

When to Prefer This Over Other Tools

NeedPrefer
Maximum backbone diversity with established community recipesrfdiffusion
All-atom generation with side-chain awarenessboltzgen
Flow-based backbone generation with fold conditioningproteina-complexa
End-to-end integrated binder pipelinebindcraft

Key Ideas to Preserve

  • Keep fold-conditioning choices explicit
  • Record which checkpoint and config produced each backbone batch
  • Separate backbone-generation artifacts from downstream sequence-design artifacts
  • Treat generated backbones as candidates that still require validation and QC

Common Mistakes

  • Treating Proteina-Complexa as a sequence-design tool
  • Skipping required upstream weight and data bundles
  • Comparing outputs against RFdiffusion or BoltzGen without matching length and conditioning settings
  • Moving generated backbones directly to experiments without refolding validation

Troubleshooting

ErrorLikely causeFix
Missing DATA_PATH filesRequired upstream bundles not downloadedRe-check upstream setup and place files under the documented directory tree
CUDA OOMBackbone length or batch too largeReduce batch size or use a larger GPU
Config mismatchWrong checkpoint/config pairKeep checkpoint, config, and conditioning mode aligned
Weak downstream foldabilityBackbone exploration too unconstrainedTighten fold conditioning and validate more aggressively

Inputs

  • A backbone-generation objective such as fold-conditioned sampling, long-chain exploration, or de novo backbone discovery.
  • A configured Proteina-style environment with checkpoints, configs, and required data bundles available under the configured data path.
  • Optional fold-class or topology guidance for controlled generation.

Outputs

  • Generated protein backbone candidates suitable for downstream inverse folding.
  • Run metadata describing checkpoint choice, conditioning mode, and generation settings.
  • Backbone batches ready for sequence design with proteinmpnn or solublempnn.

Next Step

Send promising backbones to proteinmpnn or solublempnn, then validate them structurally and filter with protein-design-qc.

Signals

GitHub stars
178
Forks
32
Last commit
Jul 2026
Advanced
Catalog kind
skill
Gateway key
proteina-complexa
Source
github.com/biotender-max/awesome-bio-agent-skills