PTPN18 dephosphorylates ERBB2 at Y1196, Y1112 and Y1248

Stable Identifier
Reaction [transition]
Homo sapiens
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Protein tyrosine kinase PTPN18 dephosphorylates ERBB2, activated in response to EGF stimulation (Gensler et al. 2004), at tyrosine residues Y1196, Y1112 and Y1248 (Wang et al. 2014). PTPN18 does not dephosphorylate activated EGFR. Dephosphorylation of ERBB2 tyrosines Y1196 and Y1248 attenuates downstream activation of PI3K/AKT and RAS signaling. Dephosphorylation of Y1112 interferes with the recruitment of CBL E3 ubiquitin ligase to activated ERBB2 and CBL-mediated lysosomal route of ERBB2 down-regulation. When phosphorylated by an unknown serine/threonine kinase in an AKT-dependent manner on serine residues S419 and S423, PTPN18 recruits beta-TRCP ubiquitin ligase complex to ERBB2, thus promoting proteasome-dependent ERBB2 degradation (Wang et al. 2014).

Literature References
PubMed ID Title Journal Year
14660651 Negative regulation of HER2 signaling by the PEST-type protein-tyrosine phosphatase BDP1

Gensler, M, Ullrich, A, Buschbeck, M

J. Biol. Chem. 2004
25081058 The catalytic region and PEST domain of PTPN18 distinctly regulate the HER2 phosphorylation and ubiquitination barcodes

Yang, F, Zhang, Y, Yang, DX, Wang, HM, Ning, SL, Sun, JP, Liang, N, Li, Y, Gu, LC, Chen, YX, Gao, CJ, Pang, Q, Ma, R, Xiao, KH, Yao, W, Xu, YF, Du, YJ, Zhang, LL, Yu, X

Cell Res. 2014
Event Information
Catalyst Activity

protein tyrosine phosphatase activity of Phosphorylated ERBB2:EGFR heterodimers:PTPN18 [plasma membrane]

Orthologous Events
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