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. Author manuscript; available in PMC: 2018 Jun 1.
Published in final edited form as: J Proteome Res. 2018 May 4;17(6):2102–2111. doi: 10.1021/acs.jproteome.8b00057

Table 4.

Cluster analysis of the proteins hyper-phosphorylated by IL-3 (q<0.01 and log 2 fold change > 0.25)

DAVID 6.8 Functional Annotating Clustering

Cluster Functional annotation
Signaling Kinases (72; p=1.6 ×10−15)
Serine/threonine-protein kinase (46, p=1.2 ×10−11)
Regulation of Ras protein signal transduction (25, p=3.9 ×10−4)
MAPKKK cascade (21, p=3.4 ×10−3)
Transmembrane receptor protein tyrosine kinase signaling pathway (21, p=2.2 ×10−2)
Cytoskeleton Cytoskeleton (96; p=1.3×10−9)
Actin cytoskeleton (29; p=8.9×10−6)
RNA/translation RNA-binding (41, p=5.1×10−5)
mRNA transport (13, p=9.6×10−5)
Ubiquitin-associated/translation elongation factor EF1B (11, p=1.3×10−4)
Posttranscriptional regulation of gene expression (21, p=1.2×10−2)
Translation regulation (9, p=1.5×10−2)
mTOR signaling pathway (9, p=3.4×10−2)
Golgi apparatus (47, p=2.7×10−2)
Intracellular movement Vesicle-mediated transport (50, p=3.4×10−5)
Nucleocytoplasmic transport (19, p=3.6×10−3)
Membrane-bounded vesicle (36, p=8.0×10−3)
Other cell responses Focal adhesion (16, p=6.0×10−5)
Positive regulation of apoptosis (33, p=1.5×10−2)

In parentheses: number of proteins hyper-phosphorylated by IL-3 (q<0.01 and log 2 fold change > 0.25) for each functional annotation; p values (Benjamini correction)

Underlined are clusters for which a list of proteins is shown in Supplemental Tables 5, 6, 7 and 8