4FE1 : Improving the Accuracy of Macromolecular Structure Refinement at 7 A Resolution

  • Gunnar F. Schröder (Contributor)
  • Paul D. Adams (Contributor)
  • Michael Levitt (Contributor)
  • Petra Fromme (Contributor)
  • Raimund Fromme (Contributor)
  • Paul D. Adams (Contributor)
  • Axel T. Brunger (Contributor)
  • Petra Fromme (Contributor)

Dataset

Description

Experimental Technique/Method:X-RAY DIFFRACTION
Resolution:4.92
Classification:PHOTOSYNTHESIS
Release Date:2012-08-15
Deposition Date:2012-05-29
Revision Date:2012-08-29
Molecular Weight:359700.12
Macromolecule Type:Protein
Residue Count:2334
Atom Site Count:23997
DOI:10.2210/pdb4fe1/pdb

Abstract:
In X-ray crystallography, molecular replacement and subsequent refinement is challenging at low resolution. We compared refinement methods using synchrotron diffraction data of photosystem I at 7.4 Å resolution, starting from different initial models with increasing deviations from the known high-resolution structure. Standard refinement spoiled the initial models, moving them further away from the true structure and leading to high R(free)-values. In contrast, DEN refinement improved even the most distant starting model as judged by R(free), atomic root-mean-square differences to the true structure, significance of features not included in the initial model, and connectivity of electron density. The best protocol was DEN refinement with initial segmented rigid-body refinement. For the most distant initial model, the fraction of atoms within 2 Å of the true structure improved from 24% to 60%. We also found a significant correlation between R(free) values and the accuracy of the model, suggesting that R(free) is useful even at low resolution.
Date made availableAug 15 2012
PublisherRCSB-PDB

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