Author/Authors :
Valérie Campanacci، نويسنده , , Daniel Y. Dubois، نويسنده , , Hubert D. Becker، نويسنده , , Daniel Kern، نويسنده , , Silvia Spinelli، نويسنده , , Christel Valencia، نويسنده , , Fabienne Pagot، نويسنده , , Aurelia Salomoni، نويسنده , , Sacha Grisel، نويسنده , , Renaud Vincentelli، نويسنده , , Christophe Bignon، نويسنده , , Jacques Lapointe، نويسنده , , Richard Giegé، نويسنده , , Dominique Bourgeois and Christian Cambillau، نويسنده ,
Abstract :
In the course of a structural genomics program aiming at solving the structures of Escherichia coli open reading frame products of unknown function, we have determined the structure of YadB at 1.5 Å using molecular replacement. The YadB protein is 298 amino acid residues long and displays 34% sequence identity with E. coli glutamyl-tRNA synthetase (GluRS). It is much shorter than GluRS, which contains 468 residues, and lacks the complete domain interacting with the tRNA anticodon loop. As E. coli GluRS, YadB possesses a Zn2+ located in the putative tRNA acceptor stem-binding domain. The YadB cluster uses cysteine residues as the first three zinc ligands, but has a weaker tyrosine ligand at the fourth position. It shares with canonical amino acid RNA synthetases a major functional feature, namely activation of the amino acid (here glutamate). It differs, however, from GluRSs by the fact that the activation step is tRNA-independent and that it does not catalyze attachment of the activated glutamate to E. coli tRNAGlu, but to another, as yet unknown tRNA. These results suggest thus a novel function, distinct from that of GluRSs, for the yadB gene family.
Keywords :
YadB , glutamyl-tRNA synthetase , zinc cluster , aaRSs , structural genomics