Literature DB >> 8347566

SETOR: hardware-lighted three-dimensional solid model representations of macromolecules.

S V Evans1.   

Abstract

SETOR is designed to exploit the hardware lighting capabilities of the IRIS-4D series graphics workstations to render high-quality raster images of macromolecules that can undergo rotation and translation interactively. SETOR can render standard all-atom and backbone models of proteins or nucleic acids, but focuses on displaying protein molecules by highlighting elements of secondary structure. The program has a very friendly user interface that minimizes the number of input files by allowing the user to interactively edit parameters, such as colors, lighting coefficients, and descriptions of secondary structure via mouse activated dialogue boxes. The choice of polymer chain representation can be varied from standard vector models and van der Waal models, to a B-spline fit of polymer backbones that yields a smooth ribbon that approximates the polymer chain, to strict Cardinal splines that interpolate the smoothest curve possible that will precisely follow the polymer chain. The program provides a photograph mode, save/restore facilities, and efficient generation of symmetry-related molecules and packing diagrams. Additionally, SETOR is designed to accept commands and model coordinates from the standard input stream, and to control standard output. Ancillary programs provide a method to interactively edit hardcopy plots of all vector and many solid models generated by SETOR, and to produce standard HPGL or PostScript files. Examples of figures rendered by SETOR of a number of macromolecules of various classes are presented.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8347566     DOI: 10.1016/0263-7855(93)87009-t

Source DB:  PubMed          Journal:  J Mol Graph        ISSN: 0263-7855


  231 in total

1.  The IMB Jena Image Library of biological macromolecules.

Authors:  J Reichert; A Jabs; P Slickers; J Sühnel
Journal:  Nucleic Acids Res       Date:  2000-01-01       Impact factor: 16.971

2.  Ice-binding surface of fish type III antifreeze.

Authors:  G Chen; Z Jia
Journal:  Biophys J       Date:  1999-09       Impact factor: 4.033

3.  Evolution of a light-harvesting protein by addition of new subunits and rearrangement of conserved elements: crystal structure of a cryptophyte phycoerythrin at 1.63-A resolution.

Authors:  K E Wilk; S J Harrop; L Jankova; D Edler; G Keenan; F Sharples; R G Hiller; P M Curmi
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

4.  X-ray structure of MalY from Escherichia coli: a pyridoxal 5'-phosphate-dependent enzyme acting as a modulator in mal gene expression.

Authors:  T Clausen; A Schlegel; R Peist; E Schneider; C Steegborn; Y S Chang; A Haase; G P Bourenkov; H D Bartunik; W Boos
Journal:  EMBO J       Date:  2000-03-01       Impact factor: 11.598

5.  Enantiomer discrimination illustrated by high-resolution crystal structures of the human nuclear receptor hRARgamma.

Authors:  B P Klaholz; A Mitschler; M Belema; C Zusi; D Moras
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-06       Impact factor: 11.205

6.  X-ray crystal structures of a severely desiccated protein.

Authors:  J A Bell
Journal:  Protein Sci       Date:  1999-10       Impact factor: 6.725

7.  Crystal structure of an OCA-B peptide bound to an Oct-1 POU domain/octamer DNA complex: specific recognition of a protein-DNA interface.

Authors:  D Chasman; K Cepek; P A Sharp; C O Pabo
Journal:  Genes Dev       Date:  1999-10-15       Impact factor: 11.361

8.  The design of a hyperstable mutant of the Abp1p SH3 domain by sequence alignment analysis.

Authors:  A Rath; A R Davidson
Journal:  Protein Sci       Date:  2000-12       Impact factor: 6.725

9.  Sm protein-Sm site RNA interactions within the inner ring of the spliceosomal snRNP core structure.

Authors:  H Urlaub; V A Raker; S Kostka; R Lührmann
Journal:  EMBO J       Date:  2001-01-15       Impact factor: 11.598

10.  A new crystal structure, Ca2+ dependence and mutational analysis reveal molecular details of E-cadherin homoassociation.

Authors:  O Pertz; D Bozic; A W Koch; C Fauser; A Brancaccio; J Engel
Journal:  EMBO J       Date:  1999-04-01       Impact factor: 11.598

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.