Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2080961 | Drug Discovery Today | 2008 | 8 Pages |
Abstract
The continued success of genome sequencing projects has resulted in a wealth of information, but 40-50% of identified genes correspond to hypothetical proteins or proteins of unknown function. The functional annotation screening technology by NMR (FAST-NMR) screen was developed to assign a biological function for these unannotated proteins with a structure solved by the protein structure initiative. FAST-NMR is based on the premise that a biological function can be described by a similarity in binding sites and ligand interactions with proteins of known function. The resulting co-structure and functional assignment may provide a starting point for a drug discovery effort.
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Authors
Robert Powers, Kelly A. Mercier, Jennifer C. Copeland,