The Eyes Absent Proteins: Unusual HAD Family Tyrosine Phosphatases

Here, we review the haloacid dehalogenase (HAD) class of protein phosphatases, with a particular emphasis on an unusual group of enzymes, the eyes absent (EYA) family. EYA proteins have the unique distinction of being structurally and mechanistically classified as HAD enzymes, yet, unlike other HAD phosphatases, they are protein tyrosine phosphatases (PTPs). Further, the EYA proteins are unique among the 107 classical PTPs in the human genome because they do not use a Cysteine residue as a nucleophile in the dephosphorylation reaction. We will provide an overview of HAD phosphatase structure-function, describe unique features of the EYA family and their tyrosine phosphatase activity, provide a brief summary of the known substrates and cellular functions of the EYA proteins, and speculate about the evolutionary origins of the EYA family of proteins.

Automated summary

This review focuses on the haloacid dehalogenase (HAD) class of protein phosphatases, particularly the unique group of enzymes known as the eyes absent (EYA) family. EYA proteins are structurally and mechanistically classified as HAD enzymes, but they function as protein tyrosine phosphatases (PTPs) and do not use a Cysteine residue as a nucleophile in their dephosphorylation reaction. The article provides an overview of HAD phosphatase structure-function, describes the unique features of the EYA family and their tyrosine phosphatase activity, summarizes the known substrates and cellular functions of EYA proteins, and speculates about the evolutionary origins of the EYA family of proteins.