Data from: Biochemical, structural and dynamical characterizations of the lactate dehydrogenase from Selenomonas ruminantium provide information about an intermediate evolutionary step prior to complete allosteric regulation acquisition in the super family of lactate and malate dehydrogenases.

This data accompanies the paper entitled <strong><em>Biochemical, structural and dynamical characterizations of the lactate dehydrogenase from Selenomonas ruminantium provide information about an intermediate evolutionary step prior to complete allosteric regulation acquisition in the super family of lactate and malate dehydrogenases.</em></strong> The zip archive contains the results of molecular dynamics simulations of the 2 systems investigated in the paper: <em>S. rum</em> and <em>T. mar</em> LDHs. The systems have been simulated at 315 K for <em>S. rum </em>and 340 K for <em>T. mar</em>. Final configurations of the proteins after productions are provided for all the systems in GRO Gromos87 format. Trajectories with the positions of the proteins every 100 ps are provided for all the systems in XTC gromacs format.