5
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Evaluation of template‐based modeling in CASP13

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Performance in the template‐based modeling (TBM) category of CASP13 is assessed here, using a variety of metrics. Performance of the predictor groups that participated is ranked using the primary ranking score that was developed by the assessors for CASP12. This reveals that the best results are obtained by groups that include contact predictions or inter‐residue distance predictions derived from deep multiple sequence alignments. In cases where there is a good homolog in the wwPDB (TBM‐easy category), the best results are obtained by modifying a template. However, for cases with poorer homologs (TBM‐hard), very good results can be obtained without using an explicit template, by deep learning algorithms trained on the wwPDB. Alternative metrics are introduced, to allow testing of aspects of structural models that are not addressed by traditional CASP metrics. These include comparisons to the main‐chain and side‐chain torsion angles of the target, and the utility of models for solving crystal structures by the molecular replacement method. The alternative metrics are poorly correlated with the traditional metrics, and it is proposed that modeling has reached a sufficient level of maturity that the best models should be expected to satisfy this wider range of criteria.

          Related collections

          Most cited references35

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          The worldwide Protein Data Bank (wwPDB): ensuring a single, uniform archive of PDB data

          The worldwide Protein Data Bank (wwPDB) is the international collaboration that manages the deposition, processing and distribution of the PDB archive. The online PDB archive is a repository for the coordinates and related information for more than 38 000 structures, including proteins, nucleic acids and large macromolecular complexes that have been determined using X-ray crystallography, NMR and electron microscopy techniques. The founding members of the wwPDB are RCSB PDB (USA), MSD-EBI (Europe) and PDBj (Japan) [H.M. Berman, K. Henrick and H. Nakamura (2003) Nature Struct. Biol., 10, 980]. The BMRB group (USA) joined the wwPDB in 2006. The mission of the wwPDB is to maintain a single archive of macromolecular structural data that are freely and publicly available to the global community. Additionally, the wwPDB provides a variety of services to a broad community of users. The wwPDB website at provides information about services provided by the individual member organizations and about projects undertaken by the wwPDB.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: found
            Is Open Access

            The RCSB Protein Data Bank: new resources for research and education

            The Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB) develops tools and resources that provide a structural view of biology for research and education. The RCSB PDB web site (http://www.rcsb.org) uses the curated 3D macromolecular data contained in the PDB archive to offer unique methods to access, report and visualize data. Recent activities have focused on improving methods for simple and complex searches of PDB data, creating specialized access to chemical component data and providing domain-based structural alignments. New educational resources are offered at the PDB-101 educational view of the main web site such as Author Profiles that display a researcher’s PDB entries in a timeline. To promote different kinds of access to the RCSB PDB, Web Services have been expanded, and an RCSB PDB Mobile application for the iPhone/iPad has been released. These improvements enable new opportunities for analyzing and understanding structure data.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              A new clustering of antibody CDR loop conformations.

              Previous analyses of the complementarity-determining regions (CDRs) of antibodies have focused on a small number of "canonical" conformations for each loop. This is primarily the result of the work of Chothia and coworkers, most recently in 1997. Because of the widespread utility of antibodies, we have revisited the clustering of conformations of the six CDR loops with the much larger amount of structural information currently available. In this work, we were careful to use a high-quality data set by eliminating low-resolution structures and CDRs with high B-factors or high conformational energies. We used a distance function based on directional statistics and an effective clustering algorithm with affinity propagation. With this data set of over 300 nonredundant antibody structures, we were able to cover 28 CDR-length combinations (e.g., L1 length 11, or "L1-11" in our CDR-length nomenclature) for L1, L2, L3, H1, and H2. The Chothia analysis covered only 20 CDR-lengths. Only four of these had more than one conformational cluster, of which two could easily be distinguished by gene source (mouse/human; κ/λ) and one could easily be distinguished purely by the presence and the positions of Pro residues (L3-9). Thus, using the Chothia analysis does not require the complicated set of "structure-determining residues" that is often assumed. Of our 28 CDR-lengths, 15 have multiple conformational clusters, including 10 for which the Chothia analysis had only one canonical class. We have a total of 72 clusters for non-H3 CDRs; approximately 85% of the non-H3 sequences can be assigned to a conformational cluster based on gene source and/or sequence. We found that earlier predictions of "bulged" versus "nonbulged" conformations based on the presence or the absence of anchor residues Arg/Lys94 and Asp101 of H3 have not held up, since all four combinations lead to a majority of conformations that are bulged. Thus, the earlier analyses have been significantly enhanced by the increased data. We believe that the new classification will lead to improved methods for antibody structure prediction and design. Copyright © 2010 Elsevier Ltd. All rights reserved.
                Bookmark

                Author and article information

                Contributors
                rjr27@cam.ac.uk
                Journal
                Proteins
                Proteins
                10.1002/(ISSN)1097-0134
                PROT
                Proteins
                John Wiley & Sons, Inc. (Hoboken, USA )
                0887-3585
                1097-0134
                20 August 2019
                December 2019
                : 87
                : 12 , Critical Assessment of Methods of Protein Structure Prediction (CASP) Special Issue ( doiID: 10.1002/prot.v87.12 )
                : 1113-1127
                Affiliations
                [ 1 ] Department of Haematology University of Cambridge, Cambridge Institute for Medical Research Cambridge UK
                [ 2 ] Genome Center University of California Davis California
                Author notes
                [*] [* ] Correspondence

                Randy J. Read, Department of Haematology, University of Cambridge, Cambridge Institute for Medical Research, The Keith Peters Building, Hills Road, Cambridge CB2 0XY, UK.

                Email: rjr27@ 123456cam.ac.uk

                Author information
                https://orcid.org/0000-0002-3514-8377
                https://orcid.org/0000-0002-8346-9247
                https://orcid.org/0000-0001-5066-7178
                https://orcid.org/0000-0001-8273-0047
                Article
                PROT25800
                10.1002/prot.25800
                6851432
                31407380
                034dd1a9-bf73-4a5d-9671-d545117169e8
                © 2019 The Authors. Proteins: Structure, Function, and Bioinformatics published by Wiley Periodicals, Inc.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 10 May 2019
                : 29 July 2019
                : 08 August 2019
                Page count
                Figures: 10, Tables: 1, Pages: 15, Words: 10461
                Funding
                Funded by: H2020 Marie Skłodowska‐Curie Actions , open-funder-registry 10.13039/100010665;
                Award ID: 790122
                Funded by: Wellcome Trust , open-funder-registry 10.13039/100010269;
                Award ID: 209407/Z/17/Z
                Categories
                Research Article
                3d Structure Modeling
                Research Articles
                Custom metadata
                2.0
                December 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.2 mode:remove_FC converted:05.12.2019

                Biochemistry
                casp,molecular replacement,structure prediction,template‐based modeling
                Biochemistry
                casp, molecular replacement, structure prediction, template‐based modeling

                Comments

                Comment on this article