ArticleMethods in molecular biology (Clifton, N.J.)2025
Secondary Structure Detection and Structure Modeling for Cryo-EM.
Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
- Computational Approaches for Protein-DNA/RNA Complex Modeling for Cryo-EM Maps.Current protocols · 2026Article
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Abstract
Rapid advancements in cryogenic electron microscopy (cryo-EM) have revolutionized the field of structural biology by enabling the determination of complex macromolecular structures at unprecedented resolutions. When cryo-EM density maps have a resolution around 3 Å, the atomic structure can be modeled manually. However, as the resolution decreases, analyzing these density maps becomes increasingly challenging. For modeling structures in lower resolution maps, deep learning can be used to identify structural features in the maps to assist in structure modeling.Here, we present a suite of deep learning-based tools developed by our lab that enable structural biologists to work with cryo-EM maps of a wide range of resolutions. For cryo-EM maps at near-atomic resolution (5 Å or better), DeepMainmast automatically models all-atom structures by tracing the main chain from local map features of amino acids and atoms detected by deep learning; DAQ score quantifies map-model fit and indicates potential misassignments in protein models. In intermediate resolution maps (5-10 Å), Emap2sec and Emap2sec+ can accurately detect protein secondary structures and nucleic acids. These tools and more are available at our web server: https://em.kiharalab.org/ .
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