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. 2020 Nov 18;21(22):8687. doi: 10.3390/ijms21228687

Table 2.

Good and weak substrates of CPZ identified using the HEK293T peptide library.

Ratio CPZ/No Enzyme
Type Protein Precursor Peptide Sequence Z T Obs M Theor M ppm 100 nM 10 nM 1 nM 0.1 nM
Good Histidine triad nucleotide-binding protein 1 Ac-ADEIAKAQVAR 2 1 1212.66 1212.65 14 0.02 0.94 1.08 1.00
Good Eukaryotic translation initiation factor 5A SAMoxTEEAAVAIKAMAK 3 3 1636.81 1636.82 −5 0.07 0.15 0.95 0.95
Good Vimentin AELEQLKGQGKSR 4 3 1442.78 1442.78 −3 0.18 1.00 1.03 0.95
Good Hematological and neurological expressed 1 protein Ac-TTTTTFKGVDPNSRNSSR 3 1 2010.00 2009.98 13 0.31 0.89 1.24 1.07
Weak Eukaryotic translation initiation factor 5A NMDVPNIKR 3 2 1085.56 1085.57 −6 0.45 n.d. n.d. 0.82
Weak Ubiquitin-60S ribosomal protein L40 IIEPSLR 2 1 826.49 826.49 0 0.60 1.00 1.13 1.04

Good substrates, peptides affected with a decrease ≥60% with the highest concentration of enzyme; weak substrates, peptides affected with a decrease ≥20% and <60% with the highest concentration of enzyme; Z, charge; T, number of isotopic tags incorporated into each peptide; Obs M, observed monoisotopic mass; Theor M, theoretical monoisotopic mass; ppm, difference between Obs M and Theor M (in parts per million); Ratio CPZ/no enzyme, the ratio in peak intensity between the sample incubated with enzyme and the sample incubated without enzyme.