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. 2023 Jun 9;22(7):100590. doi: 10.1016/j.mcpro.2023.100590

Table 1.

Curated list of proteins annotated from LC–MS/MS data processed via MaxQuant

Protein Gene Molecular weight (kDa) Sequence coverage (%) Unique sequence coverage (%) Sequence length PEP score PEP
Caspase-14 CASP14 27.679 14.9 14.9 242 22.3 4.75e-11
Heat shock protein beta 1 HSPB1 22.782 19.0 19.0 205 11.1 7.93e-04
Histone H1.2/H1.3/H1.4 H1-2/H1-3/H1-4 21.316 16.0 16.0 212 18.2 6.50e-07
Calmodulin-like protein 5 CALML5 15.892 47.3 47.3 146 79.5 2.87e-60
Fatty acid–binding protein 5 FABP5 15.164 24.4 24.4 135 24.8 1.44e-13
Protein S100-A9 S100A9 13.242 24.6 24.6 114 32.8 1.49e-25
Histone H2B1 H2B1 13.990 16.0 16.0 125 42.8 1.77e-13
Protein S100-A7 S100A7 11.471 28.7 28.7 101 15.7 1.90e-08
Histone H4 H4c1 11.367 26.2 26.2 103 12.0 9.65e-05
Dermicidin DCD 11.284 16.4 16.4 110 13.7 2.05e-06
Cystatin-A CSTA 11.006 39.8 39.8 98 36.7 1.99e-21
Protein S100-A8 S100A8 10.834 45.2 45.2 93 42.7 2.10e-23
Ubiquitin-60S ribosomal protein L40 7.132 49.2 49.2 63 109.3 4.52e-102

Proteins with <2 unique peptides and >30 kDa were filtered out. Six proteins found in MALDI-TOF MS protein profiles are shaded in bold. Q values for all annotations (not shown) were found to be 0. MS/MS spectra for peptides used by MaxQuant for annotation are found in supplemental Figs. S9–S21. The PEP score is defined in MaxQuant as derived from peptide posterior error probabilities (PEPs), which have been described by Käll et al. (96). The PEP score calculated in MaxQuant is inversely related to the protein group PEPs and should be treated as a thresholded value. More detailed identification data can be found in supplementary File 2. Furthermore, a brief discussion of other microproteins of interest in the context of ovarian cancer can be found in the supplemental data.