Towards automated crystallographic structure refinement with phenix.refine

被引:4188
作者
Afonine, Pavel V. [1 ]
Grosse-Kunstleve, Ralf W. [1 ]
Echols, Nathaniel [1 ]
Headd, Jeffrey J. [1 ]
Moriarty, Nigel W. [1 ]
Mustyakimov, Marat [2 ,3 ]
Terwilliger, Thomas C. [2 ,3 ]
Urzhumtsev, Alexandre [4 ]
Zwart, Peter H. [1 ]
Adams, Paul D. [1 ,5 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
[2] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
[3] CNRS INSERM UdS, IGBMC, F-67404 Illkirch Graffenstaden, France
[4] Univ Henri Poincare, Fac Sci & Technol, Dept Phys, F-54506 Vandoeuvre Les Nancy, France
[5] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2012年 / 68卷
关键词
REAL-SPACE REFINEMENT; ELECTRON-DENSITY MAPS; X-RAY-DIFFRACTION; FREE R-VALUE; CRYSTAL-STRUCTURE; PROTEIN-STRUCTURE; MACROMOLECULAR REFINEMENT; STRUCTURE VALIDATION; THERMAL-MOTION; DATA-BANK;
D O I
10.1107/S0907444912001308
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
phenix.refine is a program within the PHENIX package that supports crystallographic structure refinement against experimental data with a wide range of upper resolution limits using a large repertoire of model parameterizations. It has several automation features and is also highly flexible. Several hundred parameters enable extensive customizations for complex use cases. Multiple user-defined refinement strategies can be applied to specific parts of the model in a single refinement run. An intuitive graphical user interface is available to guide novice users and to assist advanced users in managing refinement projects. X-ray or neutron diffraction data can be used separately or jointly in refinement. phenix.refine is tightly integrated into the PHENIX suite, where it serves as a critical component in automated model building, final structure refinement, structure validation and deposition to the wwPDB. This paper presents an overview of the major phenix.refine features, with extensive literature references for readers interested in more detailed discussions of the methods.
引用
收藏
页码:352 / 367
页数:16
相关论文
共 140 条
  • [31] X-ray structure determination at low resolution
    Brunger, Axel T.
    DeLaBarre, Byron
    Davies, Jason M.
    Weis, William I.
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2009, 65 : 128 - 133
  • [32] RESTRAINED REAL-SPACE MACROMOLECULAR ATOMIC REFINEMENT USING A NEW RESOLUTION-DEPENDENT ELECTRON-DENSITY FUNCTION
    CHAPMAN, MS
    [J]. ACTA CRYSTALLOGRAPHICA SECTION A, 1995, 51 : 69 - 80
  • [33] Conformational strictness required for maximum activity and stability of bovine pancreatic ribonuclease A as revealed by crystallographic study of three Phe 120 mutants at 1.4 Å resolution
    Chatani, E
    Hayashi, R
    Moriyama, H
    Ueki, T
    [J]. PROTEIN SCIENCE, 2002, 11 (01) : 72 - 81
  • [34] REFINEMENT OF AN ENZYME COMPLEX WITH INHIBITOR BOUND AT PARTIAL OCCUPANCY - HEN EGG-WHITE LYSOZYME AND TRI-N-ACETYLCHITOTRIOSE AT 1-BULLET-75-ANGSTROM RESOLUTION
    CHEETHAM, JC
    ARTYMIUK, PJ
    PHILLIPS, DC
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1992, 224 (03) : 613 - 628
  • [35] MolProbity: all-atom structure validation for macromolecular crystallography
    Chen, Vincent B.
    Arendall, W. Bryan, III
    Headd, Jeffrey J.
    Keedy, Daniel A.
    Immormino, Robert M.
    Kapral, Gary J.
    Murray, Laura W.
    Richardson, Jane S.
    Richardson, David C.
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2010, 66 : 12 - 21
  • [36] Crystal Structure of the GluR2 Amino-Terminal Domain Provides Insights into the Architecture and Assembly of Ionotropic Glutamate Receptors
    Clayton, Amber
    Siebold, Christian
    Gilbert, Robert J. C.
    Sutton, Geoffrey C.
    Harlos, Karl
    McIlhinney, R. A. Jeffrey
    Jones, E. Yvonne
    Aricescu, A. Radu
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2009, 392 (05) : 1125 - 1132
  • [37] ELECTRON POPULATION ANALYSIS OF ACCURATE DIFFRACTION DATA .10. JOINT X-RAY AND NEUTRON DATA REFINEMENT OF STRUCTURAL AND CHARGE-DENSITY PARAMETERS
    COPPENS, P
    BOEHME, R
    PRICE, PF
    STEVENS, ED
    [J]. ACTA CRYSTALLOGRAPHICA SECTION A, 1981, 37 (NOV): : 857 - 863
  • [38] Proteins at atomic resolution
    Dauter, Z
    Lamzin, VS
    Wilson, KS
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 1995, 5 (06) : 784 - 790
  • [39] The benefits of atomic resolution
    Dauter, Z
    Lamzin, VS
    Wilson, KS
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 1997, 7 (05) : 681 - 688
  • [40] MolProbity: all-atom contacts and structure validation for proteins and nucleic acids
    Davis, Ian W.
    Leaver-Fay, Andrew
    Chen, Vincent B.
    Block, Jeremy N.
    Kapral, Gary J.
    Wang, Xueyi
    Murray, Laura W.
    Arendall, W. Bryan, III
    Snoeyink, Jack
    Richardson, Jane S.
    Richardson, David C.
    [J]. NUCLEIC ACIDS RESEARCH, 2007, 35 : W375 - W383