Re-refinement from deposited X-ray data can deliver improved models for most PDB entries
Open Access
- 20 January 2009
- journal article
- research article
- Published by International Union of Crystallography (IUCr) in Acta Crystallographica Section D-Biological Crystallography
- Vol. 65 (2) , 176-185
- https://doi.org/10.1107/s0907444908037591
Abstract
The deposition of X-ray data along with the customary structural models defining PDB entries makes it possible to apply large-scale re-refinement protocols to these entries, thus giving users the benefit of improvements in X-ray methods that have occurred since the structure was deposited. Automated gradient refinement is an effective method to achieve this goal, but real-space intervention is most often required in order to adequately address problems detected by structure-validation software. In order to improve the existing protocol, automated re-refinement was combined with structure validation and difference-density peak analysis to produce a catalogue of problems in PDB entries that are amenable to automatic correction. It is shown that re-refinement can be effective in producing improvements, which are often associated with the systematic use of the TLS parameterization of B factors, even for relatively new and high-resolution PDB entries, while the accompanying manual or semi-manual map analysis and fitting steps show good prospects for eventual automation. It is proposed that the potential for simultaneous improvements in methods and in re-refinement results be further encouraged by broadening the scope of depositions to include refinement metadata and ultimately primary rather than reduced X-ray data.Keywords
This publication has 30 references indexed in Scilit:
- Crystal Structures and Mutagenesis of Sucrose Hydrolase from Xanthomonas axonopodis pv. glycines: Insight into the Exclusively Hydrolytic Amylosucrase FoldJournal of Molecular Biology, 2008
- Crystal structure of the extracellular domain of nAChR α1 bound to α-bungarotoxin at 1.94 Å resolutionNature Neuroscience, 2007
- Correlating EPR and X-ray structural analysis of arsenite-inhibited forms of aldehyde oxidoreductaseJBIC Journal of Biological Inorganic Chemistry, 2006
- Structural and Spectroscopic Studies Shed Light on the Mechanism of Oxalate OxidaseJournal of Biological Chemistry, 2006
- The Uppsala Electron-Density ServerActa Crystallographica Section D-Biological Crystallography, 2004
- Making optimal use of empirical energy functions: Force‐field parameterization in crystal spaceProteins-Structure Function and Bioinformatics, 2004
- Structures of Ser205 mutant plasmepsin II fromPlasmodium falciparumat 1.8 Å in complex with the inhibitors rs367 and rs370Acta Crystallographica Section D-Biological Crystallography, 2002
- Homo Crystallographicus—Quo Vadis?Structure, 2002
- The Protein Data BankNucleic Acids Research, 2000
- wARP: Improvement and Extension of Crystallographic Phases by Weighted Averaging of Multiple-Refined Dummy Atomic ModelsActa Crystallographica Section D-Biological Crystallography, 1997