International Tables for Crystallography (2006). Vol. F, ch. 21.2, pp. 507-519   | 1 | 2 |
doi: 10.1107/97809553602060000708

Chapter 21.2. Assessing the quality of macromolecular structures

Contents

  • 21.2. Assessing the quality of macromolecular structures  (pp. 507-519) | html | pdf | chapter contents |
    • 21.2.1. Introduction  (p. 507) | html | pdf |
    • 21.2.2. Validating the geometric and stereochemical parameters of the model  (pp. 507-509) | html | pdf |
      • 21.2.2.1. Comparisons against standard values derived from crystals of small molecules  (pp. 507-508) | html | pdf |
      • 21.2.2.2. Comparisons against standard values derived from surveys of other macromolecules  (pp. 508-509) | html | pdf |
        • 21.2.2.2.1. Validation of stereochemical and non-bonded parameters   (p. 508) | html | pdf |
        • 21.2.2.2.2. Validation using knowledge-based interaction potentials and profiles   (pp. 508-509) | html | pdf |
        • 21.2.2.2.3. Deviations from standard atomic volumes as a quality measure for protein crystal structures  (p. 509) | html | pdf |
    • 21.2.3. Validation of a model versus experimental data  (pp. 509-517) | html | pdf |
      • 21.2.3.1. A systematic approach using the SFCHECK software  (pp. 510-517) | html | pdf |
        • 21.2.3.1.1. Tasks performed by SFCHECK   (pp. 510-511) | html | pdf |
          • 21.2.3.1.1.1. Treatment of structure-factor data and scaling  (pp. 510-511) | html | pdf |
          • 21.2.3.1.1.2. Global agreement between the model and experimental data  (p. 511) | html | pdf |
          • 21.2.3.1.1.3. Estimations of errors in atomic positions  (p. 511) | html | pdf |
          • 21.2.3.1.1.4. Local agreement between the model and the experimental data  (p. 511) | html | pdf |
        • 21.2.3.1.2. Evaluation of individual structures  (pp. 511-513) | html | pdf |
        • 21.2.3.1.3. Quality assessment based on surveys across structures  (pp. 513-517) | html | pdf |
          • 21.2.3.1.3.1. Assessing the quality of a structure as a whole  (pp. 513-514) | html | pdf |
          • 21.2.3.1.3.2. Assessing the quality in specific regions of a model  (pp. 514-517) | html | pdf |
    • 21.2.4. Atomic resolution structures  (pp. 517-518) | html | pdf |
    • 21.2.5. Concluding remarks  (p. 518) | html | pdf |
    • References | html | pdf |
    • Figures
      • Fig. 21.2.2.1. The Voronoi polyhedron  (p. 509) | html | pdf |
      • Fig. 21.2.2.2. Atomic volume Z score r.m.s. variation with nominal resolution ( d spacing) in 900 protein structures from the PDB  (p. 510) | html | pdf |
      • Fig. 21.2.3.1. Typical SFCHECK output in PostScript format, illustrated for the protein rusticyanin from Thiobacillus ferrooxidans (1RCY) (Walter et al   (p. 513) | html | pdf |
      • Fig. 21.2.3.2. Graphical output from the SFCHECK analysis of global characteristics of the structure-factor data and the model agreement with those data for the same structure as in Fig. 21.2.3.1  (p. 514) | html | pdf |
      • Fig. 21.2.3.3. SFCHECK evaluation summary of the local agreement between the model and the electron density for the same structure as in Fig. 21.2.3.1  (pp. 515-516) | html | pdf |
      • Fig. 21.2.3.4. Variation of global quality indicators with the nominal resolution ( d spacing) of the crystallographic data  (p. 517) | html | pdf |
      • Fig. 21.2.3.5. Pairwise correlations between the various local quality indicators computed by SFCHECK   (p. 518) | html | pdf |
      • Fig. 21.2.3.6. B factors and density indices for residues across different structures  (p. 519) | html | pdf |
    • Tables
      • Table 21.2.3.1. Parameters computed for the analysis of the structure-factor data  (p. 511) | html | pdf |
      • Table 21.2.3.2. Estimation of errors in atomic coordinates  (p. 512) | html | pdf |
      • Table 21.2.3.3. Parameters computed by SFCHECK to assess the quality of the model in specific regions  (p. 512) | html | pdf |