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Using this optimized DIA method with 15 min LC gradients, we identified almost three times as many elution group precursors and twice as many phosphopeptides compared to the number of DDA peptide-spectrum matches and phosphopeptides, respectively (Fig

MYC degradation is controlled by phosphorylation at Thr58, which helps recruit ubiquitin ligases, hence targeting MYC for proteasomal degradation [63]

Their findings indicated that the polysaccharides from HEFB were predominantly composed of fucose, galactose, and glucose [36]

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however, the commercial production from these approaches is not sufficiently cost-effective