| Literature DB >> 20345902 |
Kevin Bonham1, Saskia Hemmers, Yeon-Hee Lim, Dawn M Hill, M G Finn, Kerri A Mowen.
Abstract
The protein arginine methyltransferase (PRMT) family of enzymes catalyzes the transfer of methyl groups from S-adenosylmethionine to the guanidino nitrogen atom of peptidylarginine to form monomethylarginine or dimethylarginine. We created several less polar analogs of the specific PRMT inhibitor arginine methylation inhibitor-1, and one such compound was found to have improved PRMT inhibitory activity over the parent molecule. The newly identified PRMT inhibitor modulated T-helper-cell function and thus may serve as a lead for further inhibitors useful for the treatment of immune-mediated disease.Entities:
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Year: 2010 PMID: 20345902 PMCID: PMC2903848 DOI: 10.1111/j.1742-4658.2010.07623.x
Source DB: PubMed Journal: FEBS J ISSN: 1742-464X Impact factor: 5.542