Ximdisp--A visualization tool to aid structure determination from electron microscope images.

The display of digitized electron microscope images on a computer screen is a crucial first step in the computation of macromolecular structures. It is also essential to be able to visualize the final computed density map in a way that reveals its shape in three dimensions. Ximdisp is an X-windows based, menu-driven computer program that forms the core of the MRC image processing package. Raw electron microscope images, Fourier transforms, and computed density maps may all be displayed in a variety of ways with a choice of colour representations suitable for manuscript illustration purposes. It gives the user full interactive control over its many functions with clear, simple menus, labels, and editable dialogue boxes. Ximdisp plays a part in single-particle analysis with a straightforward particle selection procedure, in processing 2D crystal and electron diffraction data with extended lattice refinement, and in the analysis of helical structures with filament straightening and interactive Fourier transform display of automatically rotated, padded, and floated particles. The role of Ximdisp in all of these analyses and the most effective ways in which it can be used to display images are described.

[1]  R A Crowther,et al.  Three‐dimensional structure of clathrin cages in ice. , 1986, The EMBO journal.

[2]  N Grigorieff,et al.  Clathrin coats at 21 Å resolution: a cellular assembly designed to recycle multiple membrane receptors , 1998, The EMBO journal.

[3]  G. Schertler,et al.  Characterisation of an improved two-dimensional p22121 crystal from bovine rhodopsin. , 1998, Journal of molecular biology.

[4]  E. Egelman,et al.  An algorithm for straightening images of curved filamentous structures. , 1986, Ultramicroscopy.

[5]  G. Mosser,et al.  Bio-Beads: an efficient strategy for two-dimensional crystallization of membrane proteins. , 1997, Journal of structural biology.

[6]  J Smith,et al.  System for accurate one-dimensional gel analysis including high-resolution quantitative footprinting. , 1996, BioTechniques.

[7]  P E Fraser,et al.  Examination of the structure of the transthyretin amyloid fibril by image reconstruction from electron micrographs. , 1995, Journal of molecular biology.

[8]  A Leith,et al.  SPIDER and WEB: processing and visualization of images in 3D electron microscopy and related fields. , 1996, Journal of structural biology.

[9]  James R. Harris,et al.  Electron Microscopy of Proteins , 1982 .

[10]  B. Böttcher,et al.  Determination of the fold of the core protein of hepatitis B virus by electron cryomicroscopy , 1997, Nature.

[11]  M van Heel,et al.  A new generation of the IMAGIC image processing system. , 1996, Journal of structural biology.

[12]  D. J. Thomas,et al.  A false‐colour look‐up table for images of large dynamic range , 1989 .

[13]  T Yasunaga,et al.  Extensible and object-oriented system Eos supplies a new environment for image analysis of electron micrographs of macromolecules. , 1996, Journal of structural biology.

[14]  K. Hirose,et al.  Nucleotide-dependent structural changes in dimeric NCD molecules complexed to microtubules. , 1998, Journal of molecular biology.

[15]  R A Crowther,et al.  MRC image processing programs. , 1996, Journal of structural biology.

[16]  D G Morgan,et al.  Image analysis of helical objects: the Brandeis Helical Package. , 1996, Journal of structural biology.