Table 4.
Peptide Sequencea | Peptide Nameb | Gene | FC(log2)c |
---|---|---|---|
Q(−17.03)EDAELQPR | CARTPT | 1.57 | |
FLGEAYHHVPESQRD | CHGB | 1.25 | |
LGVLFNPYYDPLQWKSSRFE | CHGB | 0.94 | |
Q(−17.03)YDRVAELDQLLHY | BAM-1745 | CHGB | 1.03 |
YGGFLRKYP | β-neoendorphin | PDYN | 1.24 |
MDELYPVEPEEEANGGEVL | PENK | 1.72 | |
MDELYPVEPEEEANGGEVLA | PENK | 2.19 | |
SPQLEDEAKEL | PENK | 1.34 | |
VGRPEWWMDYQ | PENK | 1.60 | |
YGGFMRF | Met-enkephalin-Arg-Phe | PENK | 1.23 |
YGGFMRGL | Met-enkephalin-Arg-Gly-Leu | PENK | 1.05 |
ALNSVAYERNAMQNY | C-terminal flanking peptide(1-15) | TAC1 | 1.21 |
ALNSVAYERNAMQNYE | C-terminal flanking peptide | TAC1 | 1.53 |
ASWTREPLE | TRH | 1.18 |
Post-translational modifications are indicated by mass change observed by mass spectrometry. Pyroglutamylation = (−17.03).
Peptide common names inferred from analogy to well-annotated rat sequence.
Fold-change values are given for IBA/Torpor comparison. A positive value indicates the peptide is higher abundance in IBA.