Proteina-Complexa Backbone Generation
SkillAI & modelsProteina-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.
No other account needed.
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
| Requirement | Minimum | Recommended |
|---|---|---|
| Python | 3.10+ | 3.11 |
| CUDA | 12.0+ | 12.1+ |
| GPU VRAM | 24GB | 40GB+ |
| Environment manager | conda | mamba 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
proteinmpnnfor general inverse folding - use
solublempnnwhen expression robustness matters more
4. Validate and filter
After sequence design:
- use
chai1-structure-prediction,boltz-structure-prediction, oralphafold2-multimer - use
protein-design-qcfor 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
| Need | Prefer |
|---|---|
| Maximum backbone diversity with established community recipes | rfdiffusion |
| All-atom generation with side-chain awareness | boltzgen |
| Flow-based backbone generation with fold conditioning | proteina-complexa |
| End-to-end integrated binder pipeline | bindcraft |
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
| Error | Likely cause | Fix |
|---|---|---|
Missing DATA_PATH files | Required upstream bundles not downloaded | Re-check upstream setup and place files under the documented directory tree |
| CUDA OOM | Backbone length or batch too large | Reduce batch size or use a larger GPU |
| Config mismatch | Wrong checkpoint/config pair | Keep checkpoint, config, and conditioning mode aligned |
| Weak downstream foldability | Backbone exploration too unconstrained | Tighten 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
proteinmpnnorsolublempnn.
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