STRuster
Version 3.1, March 2007
Thank you very much for your interest in using the Struster service. Unfortunately we had to discontinue the service due to the closing of the Department for Computaional Biology and Applied Algrithms at the Max Planck Institute for Informatics, in the wake of the retirement of its Director Thomas Lengauer. We ask for your understanding.
For many proteins, alternative structural models determined by X-ray
crystallography or NMR spectroscopy, are frequently available in
PDB.
These models can present significant structural
dissimilarity. STRuster is a method for comparison and analysis of these alternative
structural models. |
Two main type of analyses are performed:
clustering and identification of variable and invariant regions.
Hierarchical clustering
reflects the hierarchy of similarities between all pairs of models.
A dissimilarity value based on the differences between carbon alpha distances
is used for clustering. The identification of variable and invariant regions is
based on the analysis of the distribution of the standard deviations of the carbon alpha distances,
where variable regions have higher (absolute or relative) distance standard
deviations. The different invariant regions are visualised by optimal
structural superposition.
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The method is described in:
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The method has been applied to analyse the domains at the
species level of SCOP (1.71
release). You can query the results by PDB ID, SCOP species sunid code, or
access the list of all available results. For more information see
Help/Info.
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- Source code of the STRuster library is available.
- The estimates of coordinate uncertainty based on DPI are available.
For questions comments contact:
Francisco S. Domingues doming@mpi-sb.mpg.de
Computational Biology and Applied Algorithmics
STRuster is part of the
BioSapiens Network of Excellence.