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. 2013 Mar 21;288(18):12777–12790. doi: 10.1074/jbc.M112.431320

TABLE 1.

Assignments for peptide sequences identified from trypsin digestion of captured FLIP protein bands

The whole lane of c-FLIP protein bands were excised from the SDS-PAGE gel, reduced, alkylated, digested by trypsin, and subjected to LC/MS-MS analysis using the Michrom Paradigm MS4 HPLC.HTC-PAL autosampler/LTQ Orbitrap XL mass spectrometery for the analyses. The first column indicates the number of the first and last amino acid of the identified FLIP peptides, whereas the second column shows the corresponding amino acid sequences. TP or T(181 amu) indicates Thr mass + phospho group; KUb or K(242 amu) indicates Lys mass + ubiquitin GG tag; and MO or M(147 amu) indicates Met mass + oxidation.

Residues Sequence
27–38 DVAIDVVPPNVR
39–45 DLLDILR
50–61 LSVGDLAELLYR
77–85 KAVETHLLR
95–106 VLMOAEIGEDLDK
141–154 LNLVAPDQLDLLEK
162–170 IDLKTpKUbIQK
213–226 LKEQLGAQQEPVKK
227–243 SIQESEAFLPQSIPEER
269–280 DTFTSLGYEVQK