Abstract
O‐linked β‐N‐acetylglucosamine (O‐GlcNAc) transferase (OGT) transfers O‐GlcNAc from the nucleotide‐sugar UDP‐GlcNAc to thousands of nuclear and cytoplasmic proteins. OGT is an essential enzyme, and misregulation of O‐GlcNAcylation has been linked to cancers or neurodegeneration. Most eukaryotic organisms possess a single structural homolog of OGT. However, Arabidopsis thaliana has two: Spindly (SPY) and Secret Agent (SEC). Whilst being structurally similar, SPY and SEC select different nucleotide sugars, GDP‐fucose and UDP‐GlcNAc, respectively. To determine which of SPY's active site amino acids govern GDP‐fucose selection, residues equivalent to those necessary for OGT's function were mutated and expressed in E. coli. Using the in vitro malachite green glycosyltransferase assay, the mutants’ activity was analyzed and compared to wildtype. One mutant displayed wild‐type levels of glycosylation, while another exhibited partial activity. The remaining three mutants lost glycosylation activity, suggesting essentiality for GDP‐fucose selection.
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