Ser1042
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Phosphorylation Site Page:
Ser1042 - NUP98 (mouse)

Site Information
SHSSKSRsIVGGLLQ   SwissProt Entrez-Gene
Predicted information:  Scansite
Orthologous residues: NUP98 (human): S1043, NUP98 iso6 (human): (S1043), NUP98 (rat): (S1042), NUP98 iso2 (human): (S1026)
Blast this site against: NCBI  SwissProt  PDB 
Site Group ID: 3191797

In vivo Characterization
Methods used to characterize site in vivo: mass spectrometry (1, 2, 3, 4, 5, 6, 7)
Relevant cell line - cell type - tissue: '3T3-L1, differentiated' (adipocyte) (1, 2), brain (6), Hepa 1-6 (epithelial) (7), kidney (5), lung (5), macrophage-peritoneum [RIP3 (mouse), homozygous knockout] (3), MEF (fibroblast) [p53 (mouse), homozygous knockout] (4), spleen (5)




References

1

Parker BL, et al. (2015) Targeted phosphoproteomics of insulin signaling using data-independent acquisition mass spectrometry. Sci Signal 8, rs6
26060331   Curated Info

2

Humphrey SJ, et al. (2013) Dynamic Adipocyte Phosphoproteome Reveals that Akt Directly Regulates mTORC2. Cell Metab 17, 1009-20
23684622   Curated Info

3

Wu X, et al. (2012) Investigation of receptor interacting protein (RIP3)-dependent protein phosphorylation by quantitative phosphoproteomics. Mol Cell Proteomics 11, 1640-51
22942356   Curated Info

4

Hsu PP, et al. (2011) The mTOR-regulated phosphoproteome reveals a mechanism of mTORC1-mediated inhibition of growth factor signaling. Science 332, 1317-22
21659604   Curated Info

5

Huttlin EL, et al. (2010) A tissue-specific atlas of mouse protein phosphorylation and expression. Cell 143, 1174-89
21183079   Curated Info

6

Wiƛniewski JR, et al. (2010) Brain phosphoproteome obtained by a FASP-based method reveals plasma membrane protein topology. J Proteome Res 9, 3280-9
20415495   Curated Info

7

Pan C, Gnad F, Olsen JV, Mann M (2008) Quantitative phosphoproteome analysis of a mouse liver cell line reveals specificity of phosphatase inhibitors. Proteomics 8, 4534-46
18846507   Curated Info

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