Extending the resolution and phase-quality limits in automated model building with iterative refinement

被引:7
作者
Skubák, P [1 ]
Ness, S [1 ]
Pannu, NS [1 ]
机构
[1] Leiden Univ, Inst Chem, Gorlaeus Labs, NL-2300 RA Leiden, Netherlands
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2005年 / 61卷
关键词
D O I
10.1107/S0907444905032233
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Previously, the direct use of prior phase information from a single-wavelength anomalous diffraction (SAD) experiment with a multivariate likelihood function applied to automated model building with iterative refinement has been proposed [Skubak et al. (2004), Acta Cryst. D60, 2196-2201]. In this approach, the anomalous information from the experimental data is used in refinement to derive phase information in a maximum-likelihood formalism and provided a more theoretically valid way of incorporating prior phase information compared with current approaches. In the present work, the SAD multivariate likelihood function that directly uses prior phase information is tested against currently used functions on many different SAD data sets which exhibit a wide range of resolution limits and anomalous signal. The results clearly show the importance of the more theoretically valid utilization of prior phase information: the SAD function extends the resolution and phase-quality limits needed for successful automated model building with iterative refinement. Indeed, the multivariate likelihood function reduces the overfitting in the refinement procedure and performs consistently better than the current refinement targets in terms of the quality of the models obtained and the number of residues built.
引用
收藏
页码:1626 / 1635
页数:10
相关论文
共 40 条
[1]   An evaluation of automated model-building procedures for protein crystallography [J].
Badger, J .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2003, 59 :823-827
[2]   THE CCP4 SUITE - PROGRAMS FOR PROTEIN CRYSTALLOGRAPHY [J].
BAILEY, S .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1994, 50 :760-763
[3]   Difference structure-factor normalization for heavy-atom or anomalous-scattering substructure determinations [J].
Blessing, RH ;
Smith, GD .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1999, 32 :664-670
[4]   Structural and thermodynamic dissection of specific mannan recognition by a carbohydrate binding module, TmCBM27 [J].
Boraston, AB ;
Revett, TJ ;
Boraston, CM ;
Nurizzo, D ;
Davies, GJ .
STRUCTURE, 2003, 11 (06) :665-675
[5]  
Bricogne G., 1996, P CCP4 STUD WEEK MAC, P85
[6]   FREE R-VALUE - A NOVEL STATISTICAL QUANTITY FOR ASSESSING THE ACCURACY OF CRYSTAL-STRUCTURES [J].
BRUNGER, AT .
NATURE, 1992, 355 (6359) :472-475
[7]   Low-resolution crystallography is coming of age [J].
Brunger, AT .
STRUCTURE, 2005, 13 (02) :171-172
[8]   The crystal structure of yeast copper thionein: The solution of a long-lasting enigma [J].
Calderone, V ;
Dolderer, B ;
Hartmann, HJ ;
Echner, H ;
Luchinat, C ;
Del Bianco, C ;
Mangani, S ;
Weser, U .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (01) :51-56
[9]   Practical aspects of the integration of different software in protein structure solution [J].
Calderone, V .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2004, 60 :2150-2155
[10]   Degradation pathway of the phosphonate ciliatine: Crystal structure of 2-aminoethylphosphonate transaminase [J].
Chen, CCH ;
Zhang, H ;
Kim, AD ;
Howard, A ;
Sheldrick, GM ;
Mariano-Dunaway, D ;
Herzberg, O .
BIOCHEMISTRY, 2002, 41 (44) :13162-13169