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PMID: 14579251 Published · ppublish English Journal Article Review

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

Vossenaar ER, Zendman AJ, van Venrooij WJ, Pruijn GJ

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.

MeSH Terms
Amino Acid Sequence Animals Arthritis, Rheumatoid/enzymology Humans Hydrolases/classification,genetics,metabolism Isoenzymes/classification,genetics,metabolism Molecular Sequence Data Multigene Family Multiple Sclerosis/enzymology Phylogeny Protein Conformation Protein-Arginine Deiminases Psoriasis/enzymology Sequence Alignment
Chemicals
Isoenzymes Hydrolases Protein-Arginine Deiminases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Vossenaar Erik R
Department of Biochemistry, University of Nijmegen, Nijmegen, The Netherlands. [email protected]
Zendman Albert J W
van Venrooij Walther J
Pruijn Ger J M
Article Info
Journal
BioEssays : news and reviews in molecular, cellular and developmental biology
Abbr.
Bioessays
ISSN
0265-9247
Published
2003-11-00
Pages
1106-18
Language
English
Region
United States
NLM ID
8510851
Subset
IM
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