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Dive into the research topics where Helen M. Berman is active.

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Featured researches published by Helen M. Berman.


Acta Crystallographica Section D-biological Crystallography | 2002

The Protein Data Bank

Helen M. Berman; Tammy Battistuz; Talapady N. Bhat; Wolfgang F. Bluhm; Philip E. Bourne; Kyle Burkhardt; Zukang Feng; Gary L. Gilliland; Lisa Iype; Shri Jain; Phoebe Fagan; Jessica Marvin; David Padilla; Veerasamy Ravichandran; Bohdan Schneider; Narmada Thanki; Helge Weissig; John D. Westbrook; Christine Zardecki

The Protein Data Bank (PDB; http://www.rcsb.org/pdb/ ) is the single worldwide archive of structural data of biological macromolecules. This paper describes the goals of the PDB, the systems in place for data deposition and access, how to obtain further information, and near-term plans for the future development of the resource.


Nucleic Acids Research | 2007

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

Helen M. Berman; Kim Henrick; Haruki Nakamura; John L. Markley

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.


Structure | 1995

Hydration structure of a collagen peptide.

Jordi Bella; Barbara Brodsky; Helen M. Berman

BACKGROUND The collagen triple helix is a unique protein motif defined by the supercoiling of three polypeptide chains in a polyproline II conformation. It is a major domain of all collagen proteins and is also reported to exist in proteins with host defense function and in several membrane proteins. The triple-helical domain has distinctive properties. Collagen requires a high proportion of the post-translationally modified imino acid 4-hydroxyproline and water to stabilize its conformation and assembly. The crystal structure of a collagen-like peptide determined to 1.85 Angstrum showed that these two features may be related. RESULTS A detailed analysis of the hydration structure of the collagen-like peptide is presented. The water molecules around the carbonyl and hydroxyprolyl groups show distinctive geometries. There are repetitive patterns of water bridges that link oxygen atoms within a single peptide chain, between different chains and between different triple helices. Overall, the water molecules are organized in a semi-clathrate-like structure that surrounds and interconnects triple helices in the crystal lattice. Hydroxyprolyl groups play a crucial role in the assembly. CONCLUSIONS The roles of hydroxyproline and hydration are strongly interrelated in the structure of the collagen triple helix. The specific, repetitive water bridges observed in this structure buttress the triple-helical conformation. The extensively ordered hydration structure offers a good model for the interpretation of the experimental results on collagen stability and assembly.


Genome Biology | 2000

An overview of the structures of protein-DNA complexes

Nicholas M. Luscombe; Susan E Austin; Helen M. Berman; Janet M. Thornton

On the basis of a structural analysis of 240 protein-DNA complexes contained in the Protein Data Bank (PDB), we have classified the DNA-binding proteins involved into eight different structural/functional groups, which are further classified into 54 structural families. Here we present this classification and review the functions, structures and binding interactions of these protein-DNA complexes.


Nucleic Acids Research | 2011

The RCSB Protein Data Bank: redesigned web site and web services

Peter W. Rose; Bojan Beran; Chunxiao Bi; Wolfgang F. Bluhm; Dimitris Dimitropoulos; David S. Goodsell; Andreas Prlić; Martha Quesada; Gregory B. Quinn; John D. Westbrook; Jasmine Young; Benjamin T. Yukich; Christine Zardecki; Helen M. Berman; Philip E. Bourne

The RCSB Protein Data Bank (RCSB PDB) web site (http://www.pdb.org) has been redesigned to increase usability and to cater to a larger and more diverse user base. This article describes key enhancements and new features that fall into the following categories: (i) query and analysis tools for chemical structure searching, query refinement, tabulation and export of query results; (ii) web site customization and new structure alerts; (iii) pair-wise and representative protein structure alignments; (iv) visualization of large assemblies; (v) integration of structural data with the open access literature and binding affinity data; and (vi) web services and web widgets to facilitate integration of PDB data and tools with other resources. These improvements enable a range of new possibilities to analyze and understand structure data. The next generation of the RCSB PDB web site, as described here, provides a rich resource for research and education.


Nature Structural & Molecular Biology | 2000

The Protein Data Bank and the Challenge of Structural Genomics

Helen M. Berman; Talapady N. Bhat; Philip E. Bourne; Zukang Feng; Gary L. Gilliland; Helge Weissig; John D. Westbrook

The PDB has created systems for the processing, exchange, query, and distribution of data that will enable many aspects of high throughput structural genomics.


Nucleic Acids Research | 2012

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

Peter W. Rose; Chunxiao Bi; Wolfgang F. Bluhm; Cole Christie; Dimitris Dimitropoulos; Shuchismita Dutta; Rachel Kramer Green; David S. Goodsell; Andreas Prlić; Martha Quesada; Gregory B. Quinn; Alexander G. Ramos; John D. Westbrook; Jasmine Young; Christine Zardecki; Helen M. Berman; Philip E. Bourne

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.


Nature Structural & Molecular Biology | 1999

Sequence dependent conformational variations of collagen triple-helical structure

Rachel Z. Kramer; Jordi Bella; Patricia Mayville; Barbara Brodsky; Helen M. Berman

The 2 Å crystal structure reported here of the collagen-like model peptide, T3-785, provides the first visualization of how the sequence of collagen defines distinctive local conformational variations in triple-helical structure.


Nucleic Acids Research | 2003

The Protein Data Bank and structural genomics

John D. Westbrook; Zukang Feng; Li Chen; Huanwang Yang; Helen M. Berman

The Protein Data Bank (PDB; http://www.pdb.org/) continues to be actively involved in various aspects of the informatics of structural genomics projects--developing and maintaining the Target Registration Database (TargetDB), organizing data dictionaries that will define the specification for the exchange and deposition of data with the structural genomics centers and creating software tools to capture data from standard structure determination applications.


Nucleic Acids Research | 2004

The RCSB Protein Data Bank: a redesigned query system and relational database based on the mmCIF schema

Nita Deshpande; Kenneth J. Addess; Wolfgang F. Bluhm; Jeffrey C. Merino-Ott; Wayne Townsend-Merino; Qing-qing Zhang; Charlie Knezevich; Lie-jun Xie; Li Chen; Zukang Feng; Rachel Kramer Green; Judith L. Flippen-Anderson; John D. Westbrook; Helen M. Berman; Philip E. Bourne

The Protein Data Bank (PDB) is the central worldwide repository for three-dimensional (3D) structure data of biological macromolecules. The Research Collaboratory for Structural Bioinformatics (RCSB) has completely redesigned its resource for the distribution and query of 3D structure data. The re-engineered site is currently in public beta test at http://pdbbeta.rcsb.org. The new site expands the functionality of the existing site by providing structure data in greater detail and uniformity, improved query and enhanced analysis tools. A new key feature is the integration and searchability of data from over 20 other sources covering genomic, proteomic and disease relationships. The current capabilities of the re-engineered site, which will become the RCSB production site at http://www.pdb.org in late 2005, are described.

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Philip E. Bourne

National Institutes of Health

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John L. Markley

University of Wisconsin-Madison

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Gerard J. Kleywegt

European Bioinformatics Institute

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Bohdan Schneider

Academy of Sciences of the Czech Republic

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