Understanding Enzyme Superfamilies

Abstract

We have described four superfamilies of enzymes where the members within each catalyze different overall reactions using broadly varied substrates. Within each superfamily, the different overall reactions are facilitated by a common mechanistic strategy that can be rationalized in the context of the structural scaffold. Although space limitations prevent their discussion, a number of additional superfamilies have been described in which these principles appear to obtain. Analyses of the relationships between structure and function in all of these superfamilies suggest two general conclusions regarding the evolution of new catalytic activities. 1) Nature discovered that chemistry, and not binding specificity, is the dominant factor in the evolution of new enzymatic activities. New enzymatic activities evolve by duplication of the gene for a preexisting enzyme that provides a structural strategy for a mechanistically difficult chemical step. As a result, related enzymes can differ broadly in the identity of the overall reactions they mediate as well as in substrate specificity. 2) The catalytic activity of a newly sequenced but uncharacterized open reading frame cannot necessarily be inferred from the overall reactions catalyzed by homologous enzymes. Rather, the chemical step common to the superfamily scaffold must be identified and correlated with conserved structural features. These conclusions should be useful in developing new strategies for solving problems of current interest in mechanistic enzymology and structural biology as well as in the emerging disciplines of bioinformatics. For example, determination of the principles that govern the structure-function correlations for any particular superfamily will likely play an important role in assigning catalytic function to unknown sequences. Finally, by providing a more contextual basis for understanding both the rapid rates and mechanisms of enzyme-catalyzed reactions, superfamily analysis has the potential to offer insights that cannot be obtained even from the most elegant studies of a single enzyme.