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Home > Curated Information Page > PubMed Id: 22210881
Ma P, et al. (2012) A newly identified complex of spinophilin and the tyrosine phosphatase, SHP-1, modulates platelet activation by regulating G protein-dependent signaling. Blood 119, 1935-45 22210881
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.
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Y536-p - SHP-1 (mouse)
Modsite: QKGQEsEyGNItyPP SwissProt Entrez-Gene
Orthologous residues
SHP‑1 (human): Y536‑p, SHP‑1 iso2 (human): Y497‑p, SHP‑1 iso3 (human): Y538‑p, SHP‑1 iso4 (human): Y536‑p, SHP‑1 (mouse): Y536‑p, SHP‑1 (rat): Y538‑p
Characterization
Methods used to characterize site in vivo mutation of modification site, phospho-antibody, western blotting
Relevant cell lines - cell types - tissues:  CHO (fibroblast), platelet-blood
Cellular systems studied:  cell lines, primary cultured cells
Species studied:  hamster, human
Upstream Regulation
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
thrombin increase
PP2 thrombin inhibit treatment-induced increase
Downstream Regulation
Effect of modification (function):  enzymatic activity, induced

S591-p - SHP-1 (mouse)
Modsite: DKEKNKGsLKRK___ SwissProt Entrez-Gene
Orthologous residues
SHP‑1 (human): S591‑p, SHP‑1 iso2 (human): S552‑p, SHP‑1 iso3 (human): S593‑p, SHP‑1 iso4 (human): , SHP‑1 (mouse): S591‑p, SHP‑1 (rat): S593‑p

Y398-p - Spinophilin (mouse)
Modsite: DLVDVSAySGLGEDS SwissProt Entrez-Gene
Orthologous residues
Spinophilin (human): Y398‑p, Spinophilin (mouse): Y398‑p, Spinophilin (rat): Y398‑p
Characterization
Methods used to characterize site in vivo mutation of modification site
Relevant cell lines - cell types - tissues:  CHO (fibroblast), platelet-blood
Cellular systems studied:  cell lines, primary cultured cells
Species studied:  hamster, human
Upstream Regulation
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
PAR1-activating_peptide decrease
U46619 decrease
NSC-87877 PAR1-activating_peptide inhibit treatment-induced decrease
SHP-1 (human) decrease
thrombin SHP-1 (human) augment treatment-induced decrease
Downstream Regulation
Effect of modification (function):  molecular association, regulation
Modification regulates interactions with: 
Interacting molecule Interacting domains Effect Consequences (function) Consequences (process) Detection assays
SHP-1 (human) Induces co-immunoprecipitation

Y483-p - Spinophilin (mouse)
Modsite: PMAASAEyELEKRVE SwissProt Entrez-Gene
Orthologous residues
Spinophilin (human): Y483‑p, Spinophilin (mouse): Y483‑p, Spinophilin (rat): Y483‑p
Characterization
Methods used to characterize site in vivo mutation of modification site
Relevant cell lines - cell types - tissues:  CHO (fibroblast), platelet-blood
Cellular systems studied:  cell lines, primary cultured cells
Species studied:  hamster, human
Upstream Regulation
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
PAR1-activating_peptide decrease
U46619 decrease
NSC-87877 PAR1-activating_peptide inhibit treatment-induced decrease
SHP-1 (human) decrease
thrombin SHP-1 (human) augment treatment-induced decrease