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models / protein / la-proteina
Protein
NVIDIAReleased January 2026

La-Proteina

Partially latent flow-matching model for de novo protein design, jointly generating sequence and all-atom structure for proteins up to 800 residues.

The short version

  • —Side chains come out with the backbone, so no separate sequence-design step follows
  • —Backbone frames stay in Cartesian space while atomic coordinates live in a learned latent
  • —Explores designable protein space as a starting point for scaffolding or target conditioning
  • —The same architecture with target conditioning underpins the Proteina-Complexa binder system
69Openness
155HF downloads
304GitHub stars

Or self-host

Weights are downloadable

  • Hugging Face
Where to run

La-Proteina is a partially latent flow-matching generative model from NVIDIA's GenAIR group for joint generation of protein amino-acid sequence and full atomistic structure (backbone plus side chains). Originally announced as an ICLR 2026 paper and released publicly on GitHub in early 2026, La-Proteina is the architectural backbone underlying NVIDIA's later Proteina-Complexa target-conditioned binder design system.

The model generates proteins up to 800 residues in length with both sequence identity and complete atomic coordinates produced jointly. La-Proteina advances unconditional all-atom protein generation past the regime where most prior baselines fail to produce designable, foldable proteins at this length.

#Key Features

  • Joint sequence-structure generation: Produces amino-acid sequence and full atomistic structure (backbone plus side chains) jointly within a single generative pass.
  • Up to 800 residues: Handles substantially longer proteins than prior all-atom generative baselines that typically saturate around 200 to 300 residues.
  • Partially latent flow matching: Combines explicit and latent representations to balance geometric fidelity against computational tractability.
  • All-atom output: Side chains generated alongside backbone, removing the need for a separate sequence-design pipeline.
  • Architectural backbone for Proteina-Complexa: Same architecture, with target conditioning, underlies NVIDIA's binder design system.

#Technical Details

La-Proteina represents proteins in a partially latent space where backbone frames are modeled in an explicit Cartesian representation and atomic-level coordinates are encoded in a learned latent space. Flow matching transports samples from a Gaussian prior to the joint sequence-structure data distribution. The ICLR 2026 paper provides architectural details, training corpus (PDB-derived), and ablations on representation choices.

The released code and weights are available through NVIDIA's research GitHub. Inference can be performed at moderate compute cost on single high-end GPUs.

#Applications

La-Proteina is suited for unconditional generative protein design at lengths where prior atomic-level baselines fail. Researchers can use La-Proteina to explore the space of designable proteins for downstream conditioning, scaffolding, or as a starting point for target-conditioned design through extensions like Proteina-Complexa.

#Impact

La-Proteina advances the state of the art in unconditional all-atom protein generation by handling longer proteins than prior baselines and producing designable sequence-structure pairs jointly. As the architectural foundation for Proteina-Complexa, La-Proteina is a key piece of NVIDIA's growing protein-design ecosystem and a useful open-source reference implementation for future flow-matching-based generative protein models.

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At a glance

Released
January 2026
Category
Protein
Organization
NVIDIA

Related models

  • Proteina

    NVIDIA

  • Proteina-Complexa

    NVIDIA

  • ProteinZen

    UCSF

  • ProtFlow

    Zhejiang University

  • GPFlow

    University of Illinois Urbana-Champaign

Links

GitHub RepositoryResearch PaperOfficial WebsiteHuggingFace ModelDataset

Tags

de_novo_designsequence_structure_co_designstructure_generationflow_matchingtransformergenerativefoundation_modelall_atomprotein

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