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Abstract

Artificial intelligence has the potential to open insight into the structure of proteins at the scale of evolution. It has only recently been possible to extend protein structure prediction to two hundred million cataloged proteins. Characterizing the structures of the exponentially growing billions of protein sequences revealed by large scale gene sequencing experiments would necessitate a break-through in the speed of folding. Here we show that direct inference of structure from primary sequence using a large language model enables an order of magnitude speed-up in high resolution structure prediction. Leveraging the insight that language models learn evolutionary patterns across millions of sequences, we train models up to 15B parameters, the largest language model of proteins to date. As the language models are scaled they learn information that enables prediction of the three-dimensional structure of a protein at the resolution of individual atoms. This results in prediction that is up to 60x faster than state-of-the-art while maintaining resolution and accuracy. Building on this, we present the ESM Metage-nomic Atlas. This is the first large-scale structural characterization of metagenomic proteins, with more than 617 million structures. The atlas reveals more than 225 million high confidence predictions, including millions whose structures are novel in comparison with experimentally determined structures, giving an unprecedented view into the vast breadth and diversity of the structures of some of the least understood proteins on earth.

02 /Specification & Classification

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Abstract summary

Verified abstract synthesis

Claude Opus 5.5 · max effort · 17 Oct 2026 · from the abstract

Protein language models scaled to 15B parameters predict atomic-resolution structures from sequence up to 60x faster than the state of the art, producing over 617 million metagenomic structures.

Structure prediction has only recently reached two hundred million catalogued proteins, while sequencing keeps revealing billions more sequences, so folding has to become much faster. The work shows that a large protein language model can infer structure straight from primary sequence with an order-of-magnitude speed-up, making structural characterization of metagenomic proteins feasible at scale.

Key results

  1. ShownAs protein language models grow, up to 15B parameters (the largest protein language model to date, per the authors), they learn enough to predict three-dimensional protein structure at the resolution of individual atoms from primary sequence.

    Models of up to 15B parameters trained on evolutionary patterns across millions of sequences; the abstract reports no accuracy values across model sizes. · Abstract

  2. ShownInferring structure directly from sequence with the language model speeds up high-resolution structure prediction by an order of magnitude without losing resolution or accuracy.

    Up to 60x faster than the state of the art (the comparator is not named in the abstract) while resolution and accuracy are maintained; no accuracy metric or benchmark set is given. · Abstract

  3. ShownRunning the model on metagenomic proteins produced the ESM Metagenomic Atlas, a large-scale structural survey in which millions of confident predictions are novel compared with experimentally determined structures.

    More than 617 million predicted structures, more than 225 million of them high confidence, including millions novel relative to experimental structures; the abstract defines neither the confidence threshold nor the novelty criterion. · Abstract

Methods, data and reproducibility

Protein language models of up to 15B parameters were trained to capture evolutionary patterns across millions of sequences, and atomic-level structure was predicted directly from primary sequence using what the models learned; the approach was then applied to metagenomic proteins to build the ESM Metagenomic Atlas.

  • Protein sequences used to train the language models · n = millions of sequences
  • Metagenomic proteins characterized in the ESM Metagenomic Atlas · metagenomic (organisms not specified) · n = >617 million predicted structures; >225 million high confidence
Methods & tools
protein language models (up to 15B parameters), ESM Metagenomic Atlas
Reproducibility gaps
The abstract names no model release, code or atlas link, and gives no training or inference hardware.
Limitations (2)
  • The speed and accuracy comparison is against an unnamed 'state of the art', and the abstract gives no accuracy metric or benchmark set to judge the claim of maintained accuracy. · noted in this summary
  • Atlas structures are computational predictions; novelty is judged only against experimentally determined structures, with no experimental validation or definition of 'high confidence' in the abstract. · noted in this summary

Who should read:Read this if you need fast structure prediction for very large protein sequence sets, or want to explore predicted structures of metagenomic proteins, many unlike any experimentally determined structure.

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