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Detalle de: Using Situs for the registration of protein structures with low-resolution bead models from x-ray solution scattering

Title Using Situs for the registration of protein structures with low-resolution bead models from x-ray solution scattering
Abstract

Three-dimensional bead models of proteins in solution are routinely determined from one-dimensional small-angle X-ray scattering (SAXS) data. The Situs software provides a novel set of visualization and registration procedures to facilitate the localization of protein structures in low-resolution SAXS bead models. The docking algorithm takes advantage of a reduced representation of the input data sets by means of topology-representing neural networks to expedite the rigid-body search. The precision of the docking was tested on ten different simulated bead models: for >100 beads typically arising in SAXS models, a docking precision of the order of an ångström can be achieved. The shape-matching score captured the correct solutions in all ten trial cases and was sufficiently stringent to yield unique matches in seven systems. A size-invariant shape descriptor of `sphericity' is proposed to assess the onset of ambiguity in the matching of globular molecules. The software, a tutorial and supplementary data are available at http://situs.scripps.edu/saxs.

Apa Reference Wriggers, W., & Chacón, P. (2001). UsingSitusfor the registration of protein structures with low-resolution bead models from X-ray solution scattering. Journal of Applied Crystallography, 34(6), 773–776. 10.1107/s0021889801012869
Doi 10.1107/S0021889801012869
Publication Date 17 Nov 2001
Publication Type Article
Researcher Pablo Chacón
Ontology Artificial Intelligence, Bioinformatics Software and Tools, Structural bioinformatics, Experimental structure determination, Molecular Interactions/Docking, Deep Learning in Biology
Research Groups Structural Bioinformatics, Genomics of ancient crops and domestication
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