| Literature DB >> 24240508 |
Karine Bastard1, Adam Alexander Thil Smith2, Carine Vergne-Vaxelaire3, Alain Perret3, Anne Zaparucha3, Raquel De Melo-Minardi4, Aline Mariage3, Magali Boutard3, Adrien Debard3, Christophe Lechaplais3, Christine Pelle3, Virginie Pellouin3, Nadia Perchat3, Jean-Louis Petit3, Annett Kreimeyer3, Claudine Medigue3, Jean Weissenbach3, François Artiguenave3, Véronique De Berardinis3, David Vallenet3, Marcel Salanoubat3.
Abstract
Millions of protein database entries are not assigned reliable functions, preventing the full understanding of chemical diversity in living organisms. Here, we describe an integrated strategy for the discovery of various enzymatic activities catalyzed within protein families of unknown or little known function. This approach relies on the definition of a generic reaction conserved within the family, high-throughput enzymatic screening on representatives, structural and modeling investigations and analysis of genomic and metabolic context. As a proof of principle, we investigated the DUF849 Pfam family and unearthed 14 potential new enzymatic activities, leading to the designation of these proteins as β-keto acid cleavage enzymes. We propose an in vivo role for four enzymatic activities and suggest key residues for guiding further functional annotation. Our results show that the functional diversity within a family may be largely underestimated. The extension of this strategy to other families will improve our knowledge of the enzymatic landscape.Mesh:
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Year: 2013 PMID: 24240508 DOI: 10.1038/nchembio.1387
Source DB: PubMed Journal: Nat Chem Biol ISSN: 1552-4450 Impact factor: 15.040