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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8069645/ https://www.ncbi.nlm.nih.gov/pubmed/33920226 http://dx.doi.org/10.3390/ijms22083925 |
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author | Roychoudhury, Kaushik Hegde, Rashmi S. |
author_facet | Roychoudhury, Kaushik Hegde, Rashmi S. |
author_sort | Roychoudhury, Kaushik |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8069645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80696452021-04-26 The Eyes Absent Proteins: Unusual HAD Family Tyrosine Phosphatases Roychoudhury, Kaushik Hegde, Rashmi S. Int J Mol Sci Review 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. MDPI 2021-04-10 /pmc/articles/PMC8069645/ /pubmed/33920226 http://dx.doi.org/10.3390/ijms22083925 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Roychoudhury, Kaushik Hegde, Rashmi S. The Eyes Absent Proteins: Unusual HAD Family Tyrosine Phosphatases |
title | The Eyes Absent Proteins: Unusual HAD Family Tyrosine Phosphatases |
title_full | The Eyes Absent Proteins: Unusual HAD Family Tyrosine Phosphatases |
title_fullStr | The Eyes Absent Proteins: Unusual HAD Family Tyrosine Phosphatases |
title_full_unstemmed | The Eyes Absent Proteins: Unusual HAD Family Tyrosine Phosphatases |
title_short | The Eyes Absent Proteins: Unusual HAD Family Tyrosine Phosphatases |
title_sort | eyes absent proteins: unusual had family tyrosine phosphatases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8069645/ https://www.ncbi.nlm.nih.gov/pubmed/33920226 http://dx.doi.org/10.3390/ijms22083925 |
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