Curated Information
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PubMed Id: 18451171 
This page summarizes selected information from the article referenced above and curated into PhosphoSitePlus®, a comprehensive online resource for the study of protein post-translational modifications (NAR, 2012,40:D261-70). To learn more about the scope of PhosphoSitePlus®, click here.
Information from this record has been curated, but not yet edited in PhosphoSitePlus® and may be incomplete.
Cheung M, Sharma A, Madhunapantula SV, Robertson GP (2008) Akt3 and mutant V600E B-Raf cooperate to promote early melanoma development. Cancer Res 68, 3429-39 18451171
Only sites from this record are displayed on this page. Click on the protein name to open the protein page, and on the RSD number to open the site page. For the complete dataset, click the download button, on the right.
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S365-p - B-Raf (human) ▲
Orthologous residues
B‑Raf (human): S365‑p, B‑Raf (mouse): S348‑p, B‑Raf iso3 (mouse): S298‑p, B‑Raf (rat): S347‑p, B‑Raf (chicken): S365‑p, B‑Raf (quail): S365‑p
Characterization
 Methods used to characterize site in vivo:  mutation of modification site
 Disease tissue studied:  melanoma skin cancer
 Cellular systems studied:  cell lines
 Species studied:  mouse
 Comments:  Melan-a cells
 Enzymes shown to modify site in vitro: 
Type Enzyme
KINASE Akt3 (human)
Upstream Regulation
 Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE Akt3 (human) modification site within consensus motif, transfection of inactive enzyme, transfection of constitutively active enzyme
Downstream Regulation
 Effect of modification (function):  enzymatic activity, inhibited
 Effect of modification (process):  cell growth, altered, transcription, altered

S429-p - B-Raf (human) ▲
Orthologous residues
B‑Raf (human): S429‑p, B‑Raf (mouse): S464‑p, B‑Raf iso3 (mouse): S362‑p, B‑Raf (rat): S463‑p, B‑Raf (chicken): S469‑p, B‑Raf (quail): S469‑p
Characterization
 Methods used to characterize site in vivo:  mutation of modification site
 Disease tissue studied:  melanoma skin cancer
 Cellular systems studied:  cell lines
 Species studied:  mouse
 Comments:  Melan-a cells
 Enzymes shown to modify site in vitro: 
Type Enzyme
KINASE Akt3 (human)
Upstream Regulation
 Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE Akt3 (human) modification site within consensus motif, transfection of inactive enzyme, transfection of constitutively active enzyme
Downstream Regulation
 Effect of modification (function):  enzymatic activity, inhibited
 Effect of modification (process):  cell growth, altered, transcription, altered

T599-p - B-Raf (human) ▲
Orthologous residues
B‑Raf (human): T599‑p, B‑Raf (mouse): T636‑p, B‑Raf iso3 (mouse): ‑, B‑Raf (rat): T636‑p, B‑Raf (chicken): T639‑p, B‑Raf (quail): T639‑p
Downstream Regulation
 Effect of modification (function):  enzymatic activity, induced

S602-p - B-Raf (human) ▲
Orthologous residues
B‑Raf (human): S602‑p, B‑Raf (mouse): S639‑p, B‑Raf iso3 (mouse): ‑, B‑Raf (rat): S639‑p, B‑Raf (chicken): S642‑p, B‑Raf (quail): S642‑p
Downstream Regulation
 Effect of modification (function):  enzymatic activity, induced

T202-p - ERK1 (human) ▲
Orthologous residues
ERK1 (human): T202‑p, ERK1 (mouse): T203‑p, ERK1 (rat): T203‑p, ERK1 (hamster): T192‑p
Characterization
 Methods used to characterize site in vivo:  phospho-antibody, western blotting
 Disease tissue studied:  melanoma skin cancer
 Relevant cell lines - cell types - tissues:  NHEM (melanocyte), SK-MEL24 (melanocyte), WM35 (melanocyte)
 Cellular systems studied:  cell lines
 Species studied:  human
 Comments:  UACC-903 cells
Upstream Regulation
 Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
siRNA Akt3 (human) no change compared to control normal melanocytes
siRNA Akt3 (human) increase melanoma cells
LY294002 increase melanoma cells
Akt3 (human) decrease activated, melanoma cells

Y204-p - ERK1 (human) ▲
Orthologous residues
ERK1 (human): Y204‑p, ERK1 (mouse): Y205‑p, ERK1 (rat): Y205‑p, ERK1 (hamster): Y194‑p
Characterization
 Methods used to characterize site in vivo:  phospho-antibody, western blotting
 Disease tissue studied:  melanoma skin cancer
 Relevant cell lines - cell types - tissues:  NHEM (melanocyte), SK-MEL24 (melanocyte), WM35 (melanocyte)
 Cellular systems studied:  cell lines
 Species studied:  human
 Comments:  UACC-903 cells
Upstream Regulation
 Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
siRNA Akt3 (human) no change compared to control normal melanocytes
siRNA Akt3 (human) increase melanoma cells
LY294002 increase melanoma cells
Akt3 (human) decrease activated, melanoma cells

T185-p - ERK2 (human) ▲
Orthologous residues
ERK2 (human): T185‑p, ERK2 (mouse): T183‑p, ERK2 (rat): T183‑p, ERK2 (chicken): T193‑p
Characterization
 Methods used to characterize site in vivo:  phospho-antibody, western blotting
 Disease tissue studied:  melanoma skin cancer
 Relevant cell lines - cell types - tissues:  NHEM (melanocyte), SK-MEL24 (melanocyte), WM35 (melanocyte)
 Cellular systems studied:  cell lines
 Species studied:  human
 Comments:  UACC-903 cells
Upstream Regulation
 Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
siRNA Akt3 (human) no change compared to control normal melanocytes
siRNA Akt3 (human) increase melanoma cells
LY294002 increase melanoma cells
Akt3 (human) decrease activated, melanoma cells

Y187-p - ERK2 (human) ▲
Orthologous residues
ERK2 (human): Y187‑p, ERK2 (mouse): Y185‑p, ERK2 (rat): Y185‑p, ERK2 (chicken): Y195‑p
Characterization
 Methods used to characterize site in vivo:  phospho-antibody, western blotting
 Disease tissue studied:  melanoma skin cancer
 Relevant cell lines - cell types - tissues:  NHEM (melanocyte), SK-MEL24 (melanocyte), WM35 (melanocyte)
 Cellular systems studied:  cell lines
 Species studied:  human
 Comments:  UACC-903 cells
Upstream Regulation
 Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
siRNA Akt3 (human) no change compared to control normal melanocytes
siRNA Akt3 (human) increase melanoma cells
LY294002 increase melanoma cells
Akt3 (human) decrease activated, melanoma cells


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