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. 2019 Jun 20;116(28):13943–13951. doi: 10.1073/pnas.1903297116

Table 2.

Observed mass peaks of GST P1-1 and its mutant forms incubated with cis-DDP

Enzyme Peak Molecular mass, Da Assignment Relative abundance, %
GST P1-1 A 23,216 GST P1-1 monomer 50
B 23,347 GST P1-1* monomer 100
C 46,433 GST P1-1 dimer 4
D 23,216 GST P1-1 monomer 100
E 46,860 GST P1-1 dimer + 2×[Pt(NH3)] 74
F 47,093 GST P1-1 dimer + 2×[Pt(NH3)] + [Pt(NH3)2] 82
G 47,429 GST P1-1* dimer + 3×[Pt(NH3)Cl] 91
C47S A 23,199 C47S monomer 98
B 23,330 C47S* monomer 89
C 46,398 C47S dimer 5
D 23,753 C47S* monomer + 2×[Pt(NH3)] 100
E 46,824 C47S dimer + 2×[Pt(NH3)] 54
F 47,164 C47S dimer + 2×[PtCl2] + [Pt(NH3)2] 24
C101S A 23,199 C101S monomer 36
B 23,330 C101S* monomer 97
C 46,398 C101S dimer 5
D 23,199 C101S monomer 30
E 23,235.5 C101S monomer + MeOH 100
F 23,524 C101S* monomer + Pt 26
G 23,541 C101S* monomer + [Pt(NH3)] 16
H 23,734 C101S monomer + 2×[PtCl2] 28
I 23,752 C101S* monomer + 2×[Pt(NH3)] 74
L 46,464.5 C101S dimer + 2×MeOH 18

The relative abundance (%) of each peak is obtained after normalization to the tallest peak present in each spectra.

*

Enzymes characterized by the presence of the N-terminal methionine residue.