Acyl - in Biochemistry

In Biochemistry

In biochemistry there are many instances of acyl groups, in all major categories of biochemical molecules.

Acyl-CoAs are acyl derivatives formed via fatty acid metabolism. Acetyl-CoA, the most common derivative, serves as an acyl donor in many biosynthetic transformations. Such acyl compounds are thioesters.

Names of acyl groups of amino acids are formed by the replacement of the ending -ine by the ending -yl. For example the acyl group of glycine is glycyl-, and of lysine is lysyl-.

Names of acyl groups of ribonucleoside monophosphates such as AMP (5'-adenylic acid), GMP (5'-guanylic acid), CMP (5'-cytidylic acid), and UMP (5'-uridylic acid) are adenylyl-, guanylyl-, cytidylyl-, and uridylyl- respectively.

In phospholipids, the acyl group of phosphatidic acid is called phosphatidyl-.

Finally, many saccharides are acylated.

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