Evidence map›Paper›PMID 39868321›Full record

ArticlebioRxiv : the preprint server for biology2025

Assessing Generative Model Coverage of Protein Structures with SHAPES.

Tianyu Lu, Melissa Liu, Yilin Chen, Jinho Kim, Po-Ssu Huang

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Tianyu LuDepartment of Bioengineering, Stanford University, Stanford, CA, USA.ORCID 0000-0002-3365-1542
Melissa LiuDepartment of Bioengineering, Stanford University, Stanford, CA, USA.
Yilin ChenDepartment of Bioengineering, Stanford University, Stanford, CA, USA.
Jinho KimDepartment of Physics, Stanford University, Stanford, CA, USA.
Po-Ssu HuangDepartment of Bioengineering, Stanford University, Stanford, CA, USA.ORCID 0000-0002-7948-2895

Funding

Generative neural networks for structure-based antibody designR01GM147893 · NIGMS · STANFORD UNIVERSITY · PI Possu Huang · 2022 to 2026
$1.9M
NIGMS NIH HHS R01 GM147893
6 · The paper itself

Abstract

Recent advances in generative modeling enable efficient sampling of protein structures, but their tendency to optimize for designability imposes a bias toward idealized structures at the expense of loops and other complex structural motifs critical for function. We introduce SHAPES (Structural and Hierarchical Assessment of Proteins with Embedding Similarity) to evaluate five state-of-the-art generative models of protein structures. Using structural embeddings across multiple structural hierarchies, ranging from local geometries to global protein architectures, we reveal substantial undersampling of the observed protein structure space by these models. We use Fréchet Protein Distance (FPD) to quantify distributional coverage. Different models are distinct in their coverage behavior across different sampling noise scales and temperatures; the frequency of TERtiary Motifs (TERMs) further supports the observations. More robust sequence design and structure prediction methods are likely crucial in guiding the development of models with improved coverage of the designable protein space.

Identifiers

PMID39868321
PMCPMC11761634

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.