| Literature DB >> 18275915 |
Robert Powers1, Kelly A Mercier, Jennifer C Copeland.
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.Entities:
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Year: 2008 PMID: 18275915 PMCID: PMC2754198 DOI: 10.1016/j.drudis.2007.11.001
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851