Abstract
Phosphorylase kinase is a four-subunit enzyme involved in the regulation of glycogen breakdown. The traditional textbook view is that only the gamma subunit has enzymatic activity, whereas the other three subunits have a regulatory role. Evidence from homology searches and sequence alignments, however, shows that the alpha- and beta-subunits possess amino-terminal glucoamylase-like domains and suggests that they might possess a previously overlooked amylase activity. If true, this would have important implications for the understanding, diagnosis, and management of glycogen storage diseases. There is thus a clear need to test this hypothesis through enzymatic assays and structural studies.
| Original language | English |
|---|---|
| Pages (from-to) | 1804-7 |
| Number of pages | 4 |
| Journal | Protein Science |
| Volume | 12 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 1 Aug 2003 |
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