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. Author manuscript; available in PMC: 2019 May 1.
Published in final edited form as: J Am Soc Mass Spectrom. 2018 Mar 19;29(5):935–947. doi: 10.1007/s13361-018-1915-0

Table 2. Direct Identification and Calculation of Phosphosite Occupancy for Prohormone-Derived Peptides.

Summary of phosphosite occupancies for known endogenous peptides, calculated by comparison of phosphopeptide intensity with intensity of its non-phosphorylated counterpart. Bold and underlined residues indicate a localized residue (AScore > 13). Multiple entries for the same sequences are due to multiple, distinct phosphopeptides. Lowercase “m” indicates oxidized methionine.

Name Sequence Gene Localized* Occupancy (%)
C-terminal peptide SVPHFSDEDKDPE SCG5 98.7
Enkelytin FAEPLPSEEEGESYSKEVPEmEKRYGGFm PENK 77.0
Enkelytin FAEPLPSEEEGESYSKEVPEmEKRYGGFm PENK 10.3
VIF HSSYEDELSEVLEKPNDQAEPKEVTEEVSSKDAAE CHGA 4.7
P01211(192–203) SPHLEDETKELQ PENK 0.3
Secretolytin QKIAEKFSGTRRG CHGB 0.1
P01211(192–203) SPHLEDETKELQ PENK 0.02
*

Refers to phosphosite localization on intact peptide sequence—localization may have been achieved on related extensions and fragments. Peptide phosphosite occupancy was determined by the direct method of LC-MS/MS.