Evidence map›Paper›PMID 40631196›Full record

ArticlebioRxiv : the preprint server for biology2025

Multimodal deep learning integration of cryo-EM and AlphaFold3 for high-accuracy protein structure determination.

Rajan Gyawali, Ashwin Dhakal, Jianlin Cheng

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.

0numbers the graph read from it
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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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

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

3 authors.

Rajan GyawaliDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia, MO, 65211, United States.ORCID 0000-0002-7052-4964
Ashwin DhakalDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia, MO, 65211, United States.ORCID 0000-0002-4047-9947
Jianlin ChengDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia, MO, 65211, United States.ORCID 0000-0003-0305-2853

Funding

Deep learning methods for automated and accurate reconstruction of protein structures from cryo-EM image dataR01GM146340 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI CHENG, JIANLIN · 2022 to 2025
$1.4M
NIGMS NIH HHS R01 GM146340
6 · The paper itself

Abstract

Cryo-electron microscopy (cryo-EM) is a key technology for determining the structures of proteins, particularly large protein complexes. However, automatically building high-accuracy protein structures from cryo-EM density maps remains a crucial challenge. In this work, we introduce MICA, a fully automatic and multimodal deep learning approach combining cryo-EM density maps with AlphaFold3-predicted structures at both input and output levels to improve cryo-EM protein structure modeling. It first uses a multi-task encoder-decoder architecture with a feature pyramid network to predict backbone atoms, Cα atoms and amino acid types from both cryo-EM maps and AlphaFold3-predicted structures, which are used to build an initial backbone model. This model is further refined using AlphaFold3-predicted structures and density maps to build final atomic structures. MICA significantly outperforms other state-of-the-art deep learning methods in terms of both modeling accuracy and completeness and is robust to protein size and map resolution. Additionally, it builds high-accuracy structural models with an average template-based modeling score (TM-score) of 0.93 from recently released high-resolution cryo-EM density maps, showing it can be used for real-world, automated, accurate protein structure determination.

Identifiers

PMID40631196
PMCPMC12236472

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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.