Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle.

Daub, Henrik; Olsen, Jesper V; Bairlein, Michaela; Gnad, Florian; Oppermann, Felix S; Körner, Roman; Greff, Zoltán; Kéri, György; Stemmann, Olaf; Mann, Matthias

Daub, Henrik; Olsen, Jesper V; Bairlein, Michaela; Gnad, Florian; Oppermann, Felix S; Körner, Roman; Greff, Zoltán; Kéri, György; Stemmann, Olaf; Mann, Matthias.

Affiliation

Daub H; Cell Signaling Group, Department of Molecular Biology, Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152 Martinsried, Germany. daub@biochem.mpg.de

Mol Cell ; 31(3): 438-48, 2008 Aug 08.

Article in En | MEDLINE | ID: mdl-18691976

Subject(s)

Cell Cycle; Phosphoproteins/analysis; Phosphotransferases/metabolism; Proteomics; Amino Acid Sequence; Enzyme Activation; HeLa Cells; Humans; Mitosis; Molecular Sequence Data; Phosphopeptides/analysis; Phosphorylation; Phosphotransferases/chemistry; S Phase; Substrate Specificity

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Full text: 1 Database: MEDLINE Main subject: Phosphoproteins / Phosphotransferases / Cell Cycle / Proteomics Limits: Humans Language: En Journal: Mol Cell Journal subject: BIOLOGIA MOLECULAR Year: 2008 Type: Article Affiliation country: Germany

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