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dc.contributor.authorLiu, Yang
dc.contributor.authorYe, Qing
dc.contributor.authorPeng, Jian
dc.contributor.authorPalmedo, Peter Franklin
dc.contributor.authorBerger Leighton, Bonnie
dc.date.accessioned2018-05-16T13:26:52Z
dc.date.available2018-05-16T13:26:52Z
dc.date.issued2017-12
dc.date.submitted2017-10
dc.identifier.issn2405-4712
dc.identifier.urihttp://hdl.handle.net/1721.1/115385
dc.description.abstractWhile genes are defined by sequence, in biological systems a protein's function is largely determined by its three-dimensional structure. Evolutionary information embedded within multiple sequence alignments provides a rich source of data for inferring structural constraints on macromolecules. Still, many proteins of interest lack sufficient numbers of related sequences, leading to noisy, error-prone residue-residue contact predictions. Here we introduce DeepContact, a convolutional neural network (CNN)-based approach that discovers co-evolutionary motifs and leverages these patterns to enable accurate inference of contact probabilities, particularly when few related sequences are available. DeepContact significantly improves performance over previous methods, including in the CASP12 blind contact prediction task where we achieved top performance with another CNN-based approach. Moreover, our tool converts hard-to-interpret coupling scores into probabilities, moving the field toward a consistent metric to assess contact prediction across diverse proteins. Through substantially improving the precision-recall behavior of contact prediction, DeepContact suggests we are near a paradigm shift in template-free modeling for protein structure prediction. Many protein structures of interest remain out of reach for both computational prediction and experimental determination. DeepContact learns patterns of co-evolution across thousands of experimentally determined structures, identifying conserved local motifs and leveraging this information to improve protein residue-residue contact predictions. DeepContact extracts additional information from the evolutionary couplings using its knowledge of co-evolution and structural space, while also converting coupling scores into probabilities that are comparable across protein sequences and alignments. Keywords: contact prediction; convolutional neural networks; deep learning; protein structure prediction; structure prediction; co-evolution; evolutionary couplingsen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01GM081871)en_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/J.CELS.2017.11.014en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourceElsevieren_US
dc.titleEnhancing Evolutionary Couplings with Deep Convolutional Neural Networksen_US
dc.typeArticleen_US
dc.identifier.citationLiu, Yang et al. “Enhancing Evolutionary Couplings with Deep Convolutional Neural Networks.” Cell Systems 6, 1 (January 2018): 65–74 © 2017 The Authorsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratoryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mathematicsen_US
dc.contributor.mitauthorPalmedo, Peter Franklin
dc.contributor.mitauthorBerger Leighton, Bonnie
dc.relation.journalCell Systemsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-05-15T18:41:59Z
dspace.orderedauthorsLiu, Yang; Palmedo, Perry; Ye, Qing; Berger, Bonnie; Peng, Jianen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-2724-7228
mit.licensePUBLISHER_CCen_US


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