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资源简介：
Human retinal pigment epithelial cell, Plk1 wild-type, silac
应用场景：
创建时间：
2012-12-31
相关数据集
D6_T30
To examine the signaling pathways active downstream ACKR2, both in constitutive and ligand-stimulated conditions, we carried out a large-scale mass spec-based quantitative phosphoproteomic analysis by
NIAID Data Ecosystem70
Additional file 3 of Multi-omics analysis identifies drivers of protein phosphorylation
Additional file 3: Table S2. Sex effect for proteins and phosphorylation sites in three tissues in CC strains.
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Comparison between our phosphoproteomics dataset and published rhythmic phosphoproteome.
(Table 1) Newly identified rhythmic phosphosites in our study. (Table 2) Common rhythmic phosphosites in our and published studies. (XLSX)
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Table4_Chemical Genetic Validation of CSNK2 Substrates Using an Inhibitor-Resistant Mutant in Combination with Triple SILAC Quantitative Phosphoproteomics.XLSX
Casein Kinase 2 (CSNK2) is an extremely pleiotropic, ubiquitously expressed protein kinase involved in the regulation of numerous key biological processes. Mapping the CSNK2-dependent phosphoproteome
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