Evidence map›Paper›PMID 39543043›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Secondary Structure Detection and Structure Modeling for Cryo-EM.

Pranav Punuru, Anika Jain, Daisuke Kihara

Abstract read
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In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Pranav PunuruDepartment of Biological Sciences, Purdue University, West Lafayette, IN, USA.
Anika JainDepartment of Biological Sciences, Purdue University, West Lafayette, IN, USA.
Daisuke KiharaDepartment of Biological Sciences, Purdue University, West Lafayette, IN, USA. dkihara@purdue.edu.

Funding

Building protein structure models for intermediate resolution cryo-electron microscopy mapsR01GM133840 · NIGMS · PURDUE UNIVERSITY · PI KIHARA, DAISUKE · 2020 to 2023
$1.6M
National Science Foundation CMMI1825941National Science Foundation DBI2003635National Science Foundation DBI2146026National Science Foundation DMS2151678National Science Foundation IIS2211598National Science Foundation MCB1925643NIGMS NIH HHS R01 GM133840
6 · The paper itself

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/ .

Indexed as

Cryoelectron MicroscopyModels, MolecularSoftwareDeep LearningProteinsProtein Structure, SecondaryProteinscryo-EMCryoREADDAQDeep learningDeepMainmastEmap2secStructural biologyStructure detectionStructure modeling

Identifiers

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Registered trials

None linked

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.