Literature DB >> 27841751

A public database of macromolecular diffraction experiments.

Marek Grabowski1, Karol M Langner1, Marcin Cymborowski1, Przemyslaw J Porebski1, Piotr Sroka1, Heping Zheng1, David R Cooper1, Matthew D Zimmerman1, Marc André Elsliger2, Stephen K Burley3, Wladek Minor1.   

Abstract

The low reproducibility of published experimental results in many scientific disciplines has recently garnered negative attention in scientific journals and the general media. Public transparency, including the availability of `raw' experimental data, will help to address growing concerns regarding scientific integrity. Macromolecular X-ray crystallography has led the way in requiring the public dissemination of atomic coordinates and a wealth of experimental data, making the field one of the most reproducible in the biological sciences. However, there remains no mandate for public disclosure of the original diffraction data. The Integrated Resource for Reproducibility in Macromolecular Crystallography (IRRMC) has been developed to archive raw data from diffraction experiments and, equally importantly, to provide related metadata. Currently, the database of our resource contains data from 2920 macromolecular diffraction experiments (5767 data sets), accounting for around 3% of all depositions in the Protein Data Bank (PDB), with their corresponding partially curated metadata. IRRMC utilizes distributed storage implemented using a federated architecture of many independent storage servers, which provides both scalability and sustainability. The resource, which is accessible via the web portal at http://www.proteindiffraction.org, can be searched using various criteria. All data are available for unrestricted access and download. The resource serves as a proof of concept and demonstrates the feasibility of archiving raw diffraction data and associated metadata from X-ray crystallographic studies of biological macromolecules. The goal is to expand this resource and include data sets that failed to yield X-ray structures in order to facilitate collaborative efforts that will improve protein structure-determination methods and to ensure the availability of `orphan' data left behind for various reasons by individual investigators and/or extinct structural genomics projects.

Keywords:  IRRMC; data; diffraction experiment; metadata; protein crystallography; repository

Mesh:

Substances:

Year:  2016        PMID: 27841751      PMCID: PMC5108346          DOI: 10.1107/S2059798316014716

Source DB:  PubMed          Journal:  Acta Crystallogr D Struct Biol        ISSN: 2059-7983            Impact factor:   7.652


  52 in total

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Authors:  Gerard J Kleywegt; Mark R Harris; Jin Yu Zou; Thomas C Taylor; Anders Wählby; T Alwyn Jones
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2004-11-26

3.  The quality and validation of structures from structural genomics.

Authors:  Marcin J Domagalski; Heping Zheng; Matthew D Zimmerman; Zbigniew Dauter; Alexander Wlodawer; Wladek Minor
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4.  Storing diffraction data.

Authors:  T A Jones; G J Kleywegt; A T Brunger
Journal:  Nature       Date:  1996-09-05       Impact factor: 49.962

5.  Weak data do not make a free lunch, only a cheap meal.

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Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2014-01-17

6.  Better models by discarding data?

Authors:  K Diederichs; P A Karplus
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2013-06-15

7.  The Structural Biology Knowledgebase: a portal to protein structures, sequences, functions, and methods.

Authors:  Margaret J Gabanyi; Paul D Adams; Konstantin Arnold; Lorenza Bordoli; Lester G Carter; Judith Flippen-Andersen; Lida Gifford; Juergen Haas; Andrei Kouranov; William A McLaughlin; David I Micallef; Wladek Minor; Raship Shah; Torsten Schwede; Yi-Ping Tao; John D Westbrook; Matthew Zimmerman; Helen M Berman
Journal:  J Struct Funct Genomics       Date:  2011-04-07

8.  Reproducible Research Practices and Transparency across the Biomedical Literature.

Authors:  Shareen A Iqbal; Joshua D Wallach; Muin J Khoury; Sheri D Schully; John P A Ioannidis
Journal:  PLoS Biol       Date:  2016-01-04       Impact factor: 8.029

9.  Experience with exchange and archiving of raw data: comparison of data from two diffractometers and four software packages on a series of lysozyme crystals.

Authors:  Simon W M Tanley; Antoine M M Schreurs; John R Helliwell; Loes M J Kroon-Batenburg
Journal:  J Appl Crystallogr       Date:  2012-12-08       Impact factor: 3.304

10.  Case-controlled structure validation.

Authors:  Randy J Read; Gerard J Kleywegt
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2009-01-20
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Journal:  Drug Resist Updat       Date:  2018-08-25       Impact factor: 18.500

2.  A Gcn5-Related N-Acetyltransferase (GNAT) Capable of Acetylating Polymyxin B and Colistin Antibiotics in Vitro.

Authors:  Mateusz P Czub; Brian Zhang; M Paul Chiarelli; Karolina A Majorek; Layton Joe; Przemyslaw J Porebski; Alina Revilla; Weiming Wu; Daniel P Becker; Wladek Minor; Misty L Kuhn
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3.  Ab initio structure solution of a proteolytic fragment using ARCIMBOLDO.

Authors:  Jan Abendroth; Banumathi Sankaran; Peter J Myler; Donald D Lorimer; Thomas E Edwards
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2018-08-29       Impact factor: 1.056

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Journal:  Int J Biol Macromol       Date:  2019-06-15       Impact factor: 6.953

5.  Molstack-Interactive visualization tool for presentation, interpretation, and validation of macromolecules and electron density maps.

Authors:  Przemyslaw J Porebski; Piotr Sroka; Heping Zheng; David R Cooper; Wladek Minor
Journal:  Protein Sci       Date:  2017-09-13       Impact factor: 6.725

6.  Online tools for enhancing presentation, understanding, and retention of 3D structural data.

Authors:  Alexander Wlodawer
Journal:  FEBS J       Date:  2017-12       Impact factor: 5.542

7.  Refining the macromolecular model - achieving the best agreement with the data from X-ray diffraction experiment.

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Journal:  Crystallogr Rev       Date:  2018-09-21       Impact factor: 2.467

8.  Differences in substrate specificity of V. cholerae FabH enzymes suggest new approaches for the development of novel antibiotics and biofuels.

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9.  Albumin-Based Transport of Nonsteroidal Anti-Inflammatory Drugs in Mammalian Blood Plasma.

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10.  Comparison of metal-bound and unbound structures of aminopeptidase B proteins from Escherichia coli and Yersinia pestis.

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Journal:  Protein Sci       Date:  2020-05-08       Impact factor: 6.725

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