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Protein Secondary Structure Detection in Intermediate Resolution Cryo-EM Maps Using Deep Learning
An increasing number of protein structures have been solved by cryo-electron microscopy (cryo-EM). Although structures determined at near-atomic resolution are now routinely reported, many density maps are still determined at an intermediate resolution, where extracting structure information is stil...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717539/ https://www.ncbi.nlm.nih.gov/pubmed/31358979 http://dx.doi.org/10.1038/s41592-019-0500-1 |
Sumario: | An increasing number of protein structures have been solved by cryo-electron microscopy (cryo-EM). Although structures determined at near-atomic resolution are now routinely reported, many density maps are still determined at an intermediate resolution, where extracting structure information is still a challenge. We have developed a computational method, Emap2sec, which identifies the secondary structures of proteins (α helices, β sheets, and other structures) in an EM map of 5 to 10 Å resolution. Emap2sec uses a 3D deep convolutional neural network to assign secondary structure to each grid point in an EM map. We tested Emap2sec on 6.0 and 10.0 Å resolution EM maps simulated from 34 structures, as well as on 43 maps determined experimentally at 5.0 to 9.5 Å resolution. Emap2sec was able to clearly identify the secondary structures in many maps tested, and showed substantially better performance than existing methods. |
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