Curated Information
Javascript is not enabled on this browser. This site will not work properly without Javascript.
PhosphoSitePlus Homepage PhosphoSitePlus® v6.7.1.1
Powered by Cell Signaling Technology
Home > Curated Information Page > PubMed Id: 22430208
Liu J, et al. (2013) Phosphorylation of Mps1 by BRAFV600E prevents Mps1 degradation and contributes to chromosome instability in melanoma. Oncogene 32, 713-23 22430208
This page summarizes selected information from the record referenced above and curated into PhosphoSitePlus®, a comprehensive online resource for the study of protein post-translational modifications (NAR, 2015, 43:D512-20). To learn more about the scope of PhosphoSitePlus®, click here.
Click on the protein name to open the protein page, and on the RSD number to open the site page.
Download

S281-p - TTK (human)
Modsite: VPVNLLNsPDCDVkt SwissProt Entrez-Gene
Orthologous residues
TTK (human): S281‑p, TTK iso2 (human): S281‑p, TTK (mouse): S277‑p, TTK iso2 (mouse): S277‑p, TTK (rat): S277‑p, TTK (frog): S283‑p
Characterization
Methods used to characterize site in vivo immunoprecipitation, mass spectrometry, phospho-antibody, western blotting
Disease tissue studied:  melanoma skin cancer
Relevant cell lines - cell types - tissues:  HEK293T (epithelial), Sbcl2 (melanocyte)
Cellular systems studied:  cell lines
Species studied:  human
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE BRAF (human) phosphopeptide analysis, pharmacological inhibitor of upstream enzyme, phospho-antibody, mutation in upstream enzyme recognition motif
Downstream Regulation
Effect of modification (function):  protein stabilization, ubiquitination
Effect of modification (process):  carcinogenesis, induced, cytoskeletal reorganization
Modification regulates interactions with: 
Interacting molecule Interacting domains Effect Consequences (function) Consequences (process) Detection assays
CDC27 (human) Disrupts co-immunoprecipitation
Comments:  accumulation at centrosomes, aneuploidy, correlated with p-ERK, in human metastatic melanoma, centrosome reduplication

S436-p - TTK (human)
Modsite: VFSVskQsPPIsTSk SwissProt Entrez-Gene
Orthologous residues
TTK (human): S436‑p, TTK iso2 (human): S435‑p, TTK (mouse): S435‑p, TTK iso2 (mouse): S409‑p, TTK (rat): S414‑p, TTK (frog): S459‑p
Characterization
Methods used to characterize site in vivo immunoprecipitation, mass spectrometry, phospho-antibody, western blotting
Disease tissue studied:  melanoma skin cancer
Relevant cell lines - cell types - tissues:  HEK293T (epithelial), Sbcl2 (melanocyte)
Cellular systems studied:  cell lines
Species studied:  human
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE BRAF (human) phosphopeptide analysis, pharmacological inhibitor of upstream enzyme, phospho-antibody, mutation in upstream enzyme recognition motif
Downstream Regulation
Effect of modification (process):  cytoskeletal reorganization
Comments:  centrosome reduplication

S821-p - TTK (human)
Modsite: GQLVGLNsPNsILkA SwissProt Entrez-Gene
Orthologous residues
TTK (human): S821‑p, TTK iso2 (human): S820‑p, TTK (mouse): S820‑p, TTK iso2 (mouse): S794‑p, TTK (rat): S799‑p, TTK (frog): S844‑p
Characterization
Methods used to characterize site in vivo immunoprecipitation, mass spectrometry, phospho-antibody, western blotting
Disease tissue studied:  melanoma skin cancer
Relevant cell lines - cell types - tissues:  HEK293T (epithelial), Sbcl2 (melanocyte)
Cellular systems studied:  cell lines
Species studied:  human