Identification of Functional Subclasses in the DJ-1 Superfamily Proteins

• Main Authors: Ying Wei, Dagmar Ringe, Mark A Wilson, Mary Jo Ondrechen
• Format: Article
• Language: English
• Published: Public Library of Science (PLoS) 2007-01-01
• Series: PLoS Computational Biology
• Online Access: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1782040/?tool=EBI
• ISSN: 1553-734X; 1553-7358

Genomics has posed the challenge of determination of protein function from sequence and/or 3-D structure. Functional assignment from sequence relationships can be misleading, and structural similarity does not necessarily imply functional similarity. Proteins in the DJ-1 family, many of which are of unknown function, are examples of proteins with both sequence and fold similarity that span multiple functional classes. THEMATICS (theoretical microscopic titration curves), an electrostatics-based computational approach to functional site prediction, is used to sort proteins in the DJ-1 family into different functional classes. Active site residues are predicted for the eight distinct DJ-1 proteins with available 3-D structures. Placement of the predicted residues onto a structural alignment for six of these proteins reveals three distinct types of active sites. Each type overlaps only partially with the others, with only one residue in common across all six sets of predicted residues. Human DJ-1 and YajL from Escherichia coli have very similar predicted active sites and belong to the same probable functional group. Protease I, a known cysteine protease from Pyrococcus horikoshii, and PfpI/YhbO from E. coli, a hypothetical protein of unknown function, belong to a separate class. THEMATICS predicts a set of residues that is typical of a cysteine protease for Protease I; the prediction for PfpI/YhbO bears some similarity. YDR533Cp from Saccharomyces cerevisiae, of unknown function, and the known chaperone Hsp31 from E. coli constitute a third group with nearly identical predicted active sites. While the first four proteins have predicted active sites at dimer interfaces, YDR533Cp and Hsp31 both have predicted sites contained within each subunit. Although YDR533Cp and Hsp31 form different dimers with different orientations between the subunits, the predicted active sites are superimposable within the monomer structures. Thus, the three predicted functional classes form four different types of quaternary structures. The computational prediction of the functional sites for protein structures of unknown function provides valuable clues for functional classification. Author Summary Genome sequencing has led to the discovery of many new gene products, proteins. These discoveries hold tremendous potential for totally new approaches to the diagnosis and treatment of disease. To realize this potential, one important step is to understand the function of the thousands of proteins whose function is currently unknown. One of these proteins of unknown function is human DJ-1, a protein that appears to play a protective role against Parkinson and other neurodegenerative diseases. Here we present a computational approach to the classification by function of DJ-1 and its family members. Eight DJ-1 family members, all with similar 3-D structure, are analyzed. Three different probable functional classes emerge from this analysis on six of the family members, all with a simple calculation.