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. 2016 May 9;7(24):36971–36987. doi: 10.18632/oncotarget.9235

Table 1. Prediction of ubiquitination sites for cleaved-PAR-4.

Position* Sequence Database ressource
136 EPDGVPE-K-GKSSGPS BDM-PUB; Ubpred; Ubiprober
138 DGVPEKG-K-SSGPSAR BDM-PUB; Ubpred; Ubiprober
185 EDDEAGQ-K-ERKREDA BDM-PUB; Ubpred
188 EAGQKER-K-REDAITQ BDM-PUB; Ubpred
227 RTVSGRY-K-STTSVSE BDM-PUB; Ubpred
270 VSSSTLE-K-KIEDLEK BDM-PUB; Ubpred
271 SSSTLEK-K-IEDLEKE BDM-PUB; Ubpred
277 KKIEDLE-K-EVVRERQ Ubpred; Ubiprober
296 LVRLMQD-K-EEMIGKL Ubpred; Ubiprober
304 EEMIGKL-K-EEIDLLN Ubpred; Ubiprober
325 EDENEQL-K-QENKTLL Ubpred; Ubiprober
329 EQLKQEN-K-TLLKVVG Ubpred; Ubiprober
333 QENKTLL-K-VVGQLTR BDM-PUB; Ubiprober; Phosphosite plus

Ubiquitination sites were predicted using four bioinformatics database (BDM-Pub; Ubpred; Ubiprober and Phosphosite plus). 13 potential sites of ubiquitination were predicted considering they were provided by at least two bioinformatics tools. The position indicated in the table is based on the full length of Par-4 sequence (NP_002574.2). All sites are located on a Lysine (K).

*

Position is based on full length Par-4 sequence