|Title||Combining data from genomes, Y2H and 3D structure indicates that BolA is a reductase interacting with a glutaredoxin|
|Publication Type||Journal Article|
|Year of Publication||2005|
|Authors||Huynen, MA, Spronk, CA, Gabaldón, T, Snel, B|
|Keywords||*Genome Glutaredoxins Models; Molecular Oxidoreductases/chemistry/*metabolism Phylogeny Protein Conformation|
Genomes, functional genomics data and 3D structure reflect different aspects of protein function. Here, we combine these data to predict that BolA, a widely distributed protein family with unknown function, is a reductase that interacts with a glutaredoxin. Comparisons at the 3D structure level as well as at the sequence profile level indicate homology between BolA and OsmC, an enzyme that reduces organic peroxides. Complementary to this, comparative analyses of genomes and genomics data provide strong evidence of an interaction between BolA and the mono-thiol glutaredoxin family. The interaction between BolA and a mono-thiol glutaredoxin is of particular interest because BolA does not, in contrast to its homolog OsmC, have evolutionarily conserved cysteines to provide it with reducing equivalents. We propose that BolA uses the mono-thiol glutaredoxin as the source for these.
Huynen, Martijn A Spronk, Chris A E M Gabaldon, Toni Snel, Berend Research Support, Non-U.S. Gov’t Netherlands FEBS letters FEBS Lett. 2005 Jan 31;579(3):591-6.