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. 2013 Jun 29;4(9):1338–1348. doi: 10.18632/oncotarget.1060

Table 1. Post-translational modifications of the proteasomal subunits upon DNA damage induced by doxorubicin.

Subunit Control doxorubicin
PSMA6 (α1) Ub: Lys171
Ac: Ser2, Lys45, Lys104 Ac: Ser2, Lys30, Lys45, Lys54
PSMA2 (α2) Ub: Lys53, Lys64 Ub: Lys53
Ac: Ala2, Lys165 Ac: Ala2, Lys165
PSMA4 (α3) Ub: Lys195, Lys199
Ac: Lys127, Lys195 Ac: Lys187, Lys195, Lys199
PSMA5 (α5) Ub: Lys192, Lys196 Ub: Lys196, Lys203
P: Ser16 P: Ser16, Thr55, Ser56, Thr213 or Thr219
PSMA1 (α6) Ub: Lys115 Ub: Lys30, Lys115, Lys189, Lys208
Ac: Met1, Lys30, Lys39, Lys61 Ac: Met1, Lys50, Lys115
P: Tyr6, Thr11
PSMA3 (α7) Ub: Lys52
P: Ser250 P: Ser250; one of the four Serines (2-8)
PSMB6 (β1) Ac: Lys67
Ub: Lys67
P: Thr56, Ser58, Thr59 P: Thr56, Ser58, Thr59
PSMB7(β2) Ac: Lys72, Lys249
Ub: Lys249 Ub: Lys249
PSMB3 (β3) Ac: Ser2, Lys77 Ac: Ser2, Lys17
Ub: Lys15, Lys17, Lys77
PSMB5 (β5) Ub: Lys91
PSMB1 (β6) Ub: Lys94
PSMB4 (β7) Ac: Lys201
Ub: Lys201

Proteasomal subunits from normal (control) and DNA damaged cells (doxorubicin) were separated by 2D electrophoresis and analysed by mass-spectrometry. The following modifications are shown: P – phosphorylation, Ub – ubiquitylation (shown in italic), Ac – acetylation. Novel unpublished modification sites are shown in bold.