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Nucleic Acids Research | 2010

PDBe: Protein Data Bank in Europe

Sameer Velankar; Y. Alhroub; C. Best; S. Caboche; M. J. Conroy; Jose M. Dana; M. A. Fernandez Montecelo; G. van Ginkel; A. Golovin; Swanand Gore; Aleksandras Gutmanas; P. Haslam; P. M. S. Hendrickx; E. Heuson; M. Hirshberg; M. John; I. Lagerstedt; S. Mir; L. E. Newman; Thomas J. Oldfield; Ardan Patwardhan; L. Rinaldi; G. Sahni; E. Sanz-García; Sanchayita Sen; R. Slowley; A. Suarez-Uruena; G. J. Swaminathan; M. F. Symmons; Wim F. Vranken

The Protein Data Bank in Europe (PDBe; pdbe.org) is a partner in the Worldwide PDB organization (wwPDB; wwpdb.org) and as such actively involved in managing the single global archive of biomacromolecular structure data, the PDB. In addition, PDBe develops tools, services and resources to make structure-related data more accessible to the biomedical community. Here we describe recently developed, extended or improved services, including an animated structure-presentation widget (PDBportfolio), a widget to graphically display the coverage of any UniProt sequence in the PDB (UniPDB), chemistry- and taxonomy-based PDB-archive browsers (PDBeXplore), and a tool for interactive visualization of NMR structures, corresponding experimental data as well as validation and analysis results (Vivaldi).


Nucleic Acids Research | 2016

PDBe: improved accessibility of macromolecular structure data from PDB and EMDB

Sameer Velankar; Glen van Ginkel; Younes Alhroub; Gary M. Battle; John M. Berrisford; Matthew J. Conroy; Jose M. Dana; Swanand Gore; Aleksandras Gutmanas; Pauline Haslam; Pieter M. S. Hendrickx; Ingvar Lagerstedt; Saqib Mir; Manuel A. Fernandez Montecelo; Abhik Mukhopadhyay; Thomas J. Oldfield; Ardan Patwardhan; Eduardo Sanz-García; Sanchayita Sen; Robert A. Slowley; Michael E. Wainwright; Mandar Deshpande; Andrii Iudin; Gaurav Sahni; José Salavert Torres; Miriam Hirshberg; Lora Mak; Nurul Nadzirin; David R. Armstrong; Alice R. Clark

The Protein Data Bank in Europe (http://pdbe.org) accepts and annotates depositions of macromolecular structure data in the PDB and EMDB archives and enriches, integrates and disseminates structural information in a variety of ways. The PDBe website has been redesigned based on an analysis of user requirements, and now offers intuitive access to improved and value-added macromolecular structure information. Unique value-added information includes lists of reviews and research articles that cite or mention PDB entries as well as access to figures and legends from full-text open-access publications that describe PDB entries. A powerful new query system not only shows all the PDB entries that match a given query, but also shows the ‘best structures’ for a given macromolecule, ligand complex or sequence family using data-quality information from the wwPDB validation reports. A PDBe RESTful API has been developed to provide unified access to macromolecular structure data available in the PDB and EMDB archives as well as value-added annotations, e.g. regarding structure quality and up-to-date cross-reference information from the SIFTS resource. Taken together, these new developments facilitate unified access to macromolecular structure data in an intuitive way for non-expert users and support expert users in analysing macromolecular structure data.


Biopolymers | 2014

Improving the representation of peptide‐like inhibitor and antibiotic molecules in the Protein Data Bank

Shuchismita Dutta; Dimitris Dimitropoulos; Zukang Feng; Irina Persikova; Sanchayita Sen; Chenghua Shao; John D. Westbrook; Jasmine Young; Marina Zhuravleva; Gerard J. Kleywegt; Helen M. Berman

With the accumulation of a large number and variety of molecules in the Protein Data Bank (PDB) comes the need on occasion to review and improve their representation. The Worldwide PDB (wwPDB) partners have periodically updated various aspects of structural data representation to improve the integrity and consistency of the archive. The remediation effort described here was focused on improving the representation of peptide-like inhibitor and antibiotic molecules so that they can be easily identified and analyzed. Peptide-like inhibitors or antibiotics were identified in over 1000 PDB entries, systematically reviewed and represented either as peptides with polymer sequence or as single components. For the majority of the single-component molecules, their peptide-like composition was captured in a new representation, called the subcomponent sequence. A novel concept called “group” was developed for representing complex peptide-like antibiotics and inhibitors that are composed of multiple polymer and nonpolymer components. In addition, a reference dictionary was developed with detailed information about these peptide-like molecules to aid in their annotation, identification and analysis. Based on the experience gained in this remediation, guidelines, procedures, and tools were developed to annotate new depositions containing peptide-like inhibitors and antibiotics accurately and consistently.


Structure | 2017

OneDep: Unified wwPDB System for Deposition, Biocuration, and Validation of Macromolecular Structures in the PDB Archive

Jasmine Young; John D. Westbrook; Zukang Feng; Raul Sala; Ezra Peisach; Thomas J. Oldfield; Sanchayita Sen; Aleksandras Gutmanas; David R. Armstrong; John M. Berrisford; Li Chen; Minyu Chen; Luigi Di Costanzo; Dimitris Dimitropoulos; Guanghua Gao; Sutapa Ghosh; Swanand Gore; Vladimir Guranovic; Pieter M. S. Hendrickx; Brian P. Hudson; Reiko Igarashi; Yasuyo Ikegawa; Naohiro Kobayashi; Catherine L. Lawson; Yuhe Liang; Steve Mading; Lora Mak; M. Saqib Mir; Abhik Mukhopadhyay; Ardan Patwardhan

OneDep, a unified system for deposition, biocuration, and validation of experimentally determined structures of biological macromolecules to the PDB archive, has been developed as a global collaboration by the worldwide PDB (wwPDB) partners. This new system was designed to ensure that the wwPDB could meet the evolving archiving requirements of the scientific community over the coming decades. OneDep unifies deposition, biocuration, and validation pipelines across all wwPDB, EMDB, and BMRB deposition sites with improved focus on data quality and completeness in these archives, while supporting growth in the number of depositions and increases in their average size and complexity. In this paper, we describe the design, functional operation, and supporting infrastructure of the OneDep system, and provide initial performance assessments.


Structure | 2017

Validation of Structures in the Protein Data Bank

Swanand Gore; Eduardo Sanz García; Pieter M. S. Hendrickx; Aleksandras Gutmanas; John D. Westbrook; Huanwang Yang; Zukang Feng; Kumaran Baskaran; John M. Berrisford; Brian P. Hudson; Yasuyo Ikegawa; Naohiro Kobayashi; Catherine L. Lawson; Steve Mading; Lora Mak; Abhik Mukhopadhyay; Thomas J. Oldfield; Ardan Patwardhan; Ezra Peisach; Gaurav Sahni; Monica Sekharan; Sanchayita Sen; Chenghua Shao; Oliver S. Smart; Eldon L. Ulrich; Reiko Yamashita; Martha Quesada; Jasmine Young; Haruki Nakamura; John L. Markley

Summary The Worldwide PDB recently launched a deposition, biocuration, and validation tool: OneDep. At various stages of OneDep data processing, validation reports for three-dimensional structures of biological macromolecules are produced. These reports are based on recommendations of expert task forces representing crystallography, nuclear magnetic resonance, and cryoelectron microscopy communities. The reports provide useful metrics with which depositors can evaluate the quality of the experimental data, the structural model, and the fit between them. The validation module is also available as a stand-alone web server and as a programmatically accessible web service. A growing number of journals require the official wwPDB validation reports (produced at biocuration) to accompany manuscripts describing macromolecular structures. Upon public release of the structure, the validation report becomes part of the public PDB archive. Geometric quality scores for proteins in the PDB archive have improved over the past decade.


Database | 2014

Small molecule annotation for the Protein Data Bank

Sanchayita Sen; Jasmine Young; John M. Berrisford; Minyu Chen; Matthew J. Conroy; Shuchismita Dutta; Luigi Di Costanzo; Guanghua Gao; Sutapa Ghosh; Brian P. Hudson; Reiko Igarashi; Yumiko Kengaku; Yuhe Liang; Ezra Peisach; Irina Persikova; Abhik Mukhopadhyay; Buvaneswari Coimbatore Narayanan; Gaurav Sahni; Junko Sato; Monica Sekharan; Chenghua Shao; Lihua Tan; Marina Zhuravleva

The Protein Data Bank (PDB) is the single global repository for three-dimensional structures of biological macromolecules and their complexes, and its more than 100 000 structures contain more than 20 000 distinct ligands or small molecules bound to proteins and nucleic acids. Information about these small molecules and their interactions with proteins and nucleic acids is crucial for our understanding of biochemical processes and vital for structure-based drug design. Small molecules present in a deposited structure may be attached to a polymer or may occur as a separate, non-covalently linked ligand. During curation of a newly deposited structure by wwPDB annotation staff, each molecule is cross-referenced to the PDB Chemical Component Dictionary (CCD). If the molecule is new to the PDB, a dictionary description is created for it. The information about all small molecule components found in the PDB is distributed via the ftp archive as an external reference file. Small molecule annotation in the PDB also includes information about ligand-binding sites and about covalent and other linkages between ligands and macromolecules. During the remediation of the peptide-like antibiotics and inhibitors present in the PDB archive in 2011, it became clear that additional annotation was required for consistent representation of these molecules, which are quite often composed of several sequential subcomponents including modified amino acids and other chemical groups. The connectivity information of the modified amino acids is necessary for correct representation of these biologically interesting molecules. The combined information is made available via a new resource called the Biologically Interesting molecules Reference Dictionary, which is complementary to the CCD and is now routinely used for annotation of peptide-like antibiotics and inhibitors.


Acta Crystallographica Section D-biological Crystallography | 2013

The role of structural bioinformatics resources in the era of integrative structural biology

Aleksandras Gutmanas; Thomas J. Oldfield; Ardan Patwardhan; Sanchayita Sen; Sameer Velankar; Gerard J. Kleywegt

The integration of structural data on atomistic to cellular scales with genetic, taxonomic and functional information is discussed. The challenges to the PDB and EMDB archives and some pertinent developments at PDBe to address these are discussed.


Nucleic Acids Research | 2018

PDBe: towards reusable data delivery infrastructure at protein data bank in Europe.

Saqib Mir; Younes Alhroub; Stephen Anyango; David R. Armstrong; John M. Berrisford; Alice R. Clark; Matthew J. Conroy; Jose M. Dana; Mandar Deshpande; Deepti Gupta; Aleksandras Gutmanas; Pauline Haslam; Lora Mak; Abhik Mukhopadhyay; Nurul Nadzirin; Typhaine Paysan-Lafosse; David Sehnal; Sanchayita Sen; Oliver S. Smart; Mihaly Varadi; Gerard J. Kleywegt; Sameer Velankar

Abstract The Protein Data Bank in Europe (PDBe, pdbe.org) is actively engaged in the deposition, annotation, remediation, enrichment and dissemination of macromolecular structure data. This paper describes new developments and improvements at PDBe addressing three challenging areas: data enrichment, data dissemination and functional reusability. New features of the PDBe Web site are discussed, including a context dependent menu providing links to raw experimental data and improved presentation of structures solved by hybrid methods. The paper also summarizes the features of the LiteMol suite, which is a set of services enabling fast and interactive 3D visualization of structures, with associated experimental maps, annotations and quality assessment information. We introduce a library of Web components which can be easily reused to port data and functionality available at PDBe to other services. We also introduce updates to the SIFTS resource which maps PDB data to other bioinformatics resources, and the PDBe REST API.


Database | 2018

Worldwide Protein Data Bank biocuration supporting open access to high-quality 3D structural biology data

Jasmine Young; John D. Westbrook; Zukang Feng; Ezra Peisach; Irina Persikova; Raul Sala; Sanchayita Sen; John M. Berrisford; Jawahar Swaminathan; Thomas J. Oldfield; Aleksandras Gutmanas; Reiko Igarashi; David R. Armstrong; Kumaran Baskaran; Li Chen; Minyu Chen; Alice R. Clark; Luigi Di Costanzo; Dimitris Dimitropoulos; Guanghua Gao; Sutapa Ghosh; Swanand Gore; Vladimir Guranovic; Pieter M. S. Hendrickx; Brian P. Hudson; Yasuyo Ikegawa; Yumiko Kengaku; Catherine L. Lawson; Yuhe Liang; Lora Mak

Abstract The Protein Data Bank (PDB) is the single global repository for experimentally determined 3D structures of biological macromolecules and their complexes with ligands. The worldwide PDB (wwPDB) is the international collaboration that manages the PDB archive according to the FAIR principles: Findability, Accessibility, Interoperability and Reusability. The wwPDB recently developed OneDep, a unified tool for deposition, validation and biocuration of structures of biological macromolecules. All data deposited to the PDB undergo critical review by wwPDB Biocurators. This article outlines the importance of biocuration for structural biology data deposited to the PDB and describes wwPDB biocuration processes and the role of expert Biocurators in sustaining a high-quality archive. Structural data submitted to the PDB are examined for self-consistency, standardized using controlled vocabularies, cross-referenced with other biological data resources and validated for scientific/technical accuracy. We illustrate how biocuration is integral to PDB data archiving, as it facilitates accurate, consistent and comprehensive representation of biological structure data, allowing efficient and effective usage by research scientists, educators, students and the curious public worldwide. Database URL: https://www.wwpdb.org/


Acta Crystallographica Section A | 2006

AutoDep 4.0: a web-based deposition and archival system

Sanchayita Sen; G. Van Ginkel; A. Kapopoulou; Gaurav Sahni; G. J. Swaminathan; Richard Newman; Sameer Velankar; Kim Henrick

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Aleksandras Gutmanas

European Bioinformatics Institute

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John M. Berrisford

European Bioinformatics Institute

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Sameer Velankar

European Bioinformatics Institute

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Swanand Gore

European Bioinformatics Institute

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Thomas J. Oldfield

European Bioinformatics Institute

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Abhik Mukhopadhyay

European Bioinformatics Institute

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