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PRMT7
Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia
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Protein arginine methyltransferase 7 (PRMT7) is a protein that in humans is encoded by the PRMT7 gene.[1] Arginine methylation is an apparently irreversible protein modification catalyzed by arginine methyltransferases, such as PRMT7, using S-adenosylmethionine (AdoMet) as the methyl donor. Arginine methylation is implicated in signal transduction, RNA transport, and RNA splicing.[1][2]
PRMT7 was initially identified as a Type II protein lysine methyltransferase, indicating its role in the symmetric dimethylation of arginine residues. However, it was later reclassified as a Type III protein lysine methyltransferase, meaning it facilitates the mono-methylation of arginine residues. As of 2023, PRMT7 remains the sole member of the Type III PRMT category.[3]
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