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ABSTRACT: Summary
Automatic methods for macromolecular structure prediction (fold recognition, de novo folding and docking programs) produce large sets of alternative models. These large model sets often include many native-like structures, which are often scored as false positives. Such native-like models can be more easily identified based on data from experimental analyses used as structural restraints (e.g. identification of nearby residues by cross-linking, chemical modification, site-directed mutagenesis, deuterium exchange coupled with mass spectrometry, etc.). We present a simple server for scoring and ranking of models according to their agreement with user-defined restraints.Availability
FILTREST3D is freely available for users as a web server and standalone software at: ht
SUBMITTER: Gajda MJ
PROVIDER: S-EPMC2982159 | biostudies-literature | 2010 Dec
REPOSITORIES: biostudies-literature