Table 4.
Cysteines modified upon methyl viologen-mediated oxidation.
| No. | Protein name | Peptide sequence | Predicted mass | Observed mass in MV treatment | |
|---|---|---|---|---|---|
| NEM | Biotin maleimide | ||||
| 1 | RubisCO large subunit | AVYEC*LR | 978.0 | 1304.5 | 1304.61* | 
| 2 | Myrosinase | C*SPKIDVR | 1113.5 | 1440.0 | 1439.69* | 
| 19 | NAD(P)-binding Rossmann-fold-containing protein | SLVSDSTSICGPSKFTGK | 1938.9 | 2265.4 | 1938.1 | 
| 21 | Ferredoxin-NADP(+) oxidoreductase 1 (FNR1) | C*LLNTK | 815.9 | 1142.4 | 1142.57* | 
The table shows the peptide sequence and the predicted mass in the presence of the alkylating agents either NEM or biotin maleimide. The mass observed in MALDI-TOF MS of the MV-treated sample is shown. NEM-labeled cysteine (C) mass matches to experimental mass value suggesting that these Cys are not modified during oxidation. C* denotes Cys in the peptide sequence which is labeled with biotin maleimide, since the predicted mass matched to the experimentally observed value.The underlined peptides were addressed to be modified also in in vitro oxidation treatment (refer Table 2).