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Exact(21)
Variable modifications were set to include oxidation of methionine and Gly-Gly addition to lysines, fixed modifications were set to include carbamidomethylation of cysteine residues.
The fixed and variable modifications were set to Carbamidomethyl (C) and oxidation (M) respectively.
Variable modifications were set to methionine oxidation, pyro-glutamate formation of amino terminal glutamine, acetylation of the N-terminus, deamidation of glutamine or asparagines.
Fixed modifications were set to tri-deuteroacetylation on lysine.
Fixed modifications were set to fixed carbamidomethyl modification for cysteines.
Fixed modifications were set for carbamidomethylation of cysteine and variable modifications were set for oxidation of methionine.
Similar(39)
Epigenetic modifications are set by cell-type specific transcriptional regulators and chromatin remodelling enzymes [3].
In this study, we identified H2AR11 and H2AR29 as novel arginine methylation sites, and showed that these modifications are set in vitro by the enzymes PRMT1 and PRMT6.
The rates of PKC modification were set by fitting data of the timecourse of IRS tyrosine phosphorylation from human adipocytes [ 27].
The fixed modification was set to carboxyamidomethylation of cysteine.
The variable modification was set to oxidation of methionine.
More suggestions(15)
modifications were explored
modifications were discussed
modifications were included
modifications were examined
modifications were considered
modifications were made
modifications were calculated
modifications were observed
modifications were followed
modifications were preserved
modifications were illustrated
modifications were performed
modifications were found
modifications were done
modifications were confirmed
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