PAD, a growing family of citrullinating enzymes: genes, features and involvement in disease

ER Vossenaar, AJW Zendman, WJ van Venrooij… - …, 2003 - Wiley Online Library
ER Vossenaar, AJW Zendman, WJ van Venrooij, GJM Pruijn
Bioessays, 2003Wiley Online Library
Abstract Peptidylarginine deiminase (PAD, EC 3.5. 3.15) enzymes catalyze the conversion
of protein‐bound arginine to citrulline. This post‐translational modification may have a big
impact on the structure and function of the target protein. In this review, we will discuss the
effects of citrullination and its involvement in several human diseases, including rheumatoid
arthritis and multiple sclerosis. So far, four isotypes of PAD have been described in
mammals. We describe the existence of PAD in non‐mammalian vertebrates and the …
Abstract
Peptidylarginine deiminase (PAD, EC 3.5.3.15) enzymes catalyze the conversion of protein‐bound arginine to citrulline. This post‐translational modification may have a big impact on the structure and function of the target protein. In this review, we will discuss the effects of citrullination and its involvement in several human diseases, including rheumatoid arthritis and multiple sclerosis. So far, four isotypes of PAD have been described in mammals. We describe the existence of PAD in non‐mammalian vertebrates and the existence of a fifth mammalian PAD. In addition, tissue‐specific expression, genomic organization and evolutionary conservation of the different PAD isotypes will be discussed in detail. This article contains supplementary material which may be viewed at the BioEssays website at http://www.interscience.wiley.com/jpages/0265‐9247/suppmat/2003/25/v25.1106.html. BioEssays 25:1106–1118, 2003. © 2003 Wiley Periodicals, Inc.
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