Proteome-wide identification of in vivo targets of DNA damage checkpoint kinases

Proceedings of the National Academy of Sciences of the United States of America

Volumn 104, Issue 25, 2007, Pages 10364-10369

  Smolka, Marcus B ^a   Albuquerque, Claudio P ^a,b   Chen, Sheng Hong ^a,c   Zhou, Huilin ^a,b  

^a LUDWIG INSTITUTE FOR CANCER RESEARCH   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

Author keywords

Mass spectrometry; Mec1; N isotag; Phosphorylation; Rad53

Indexed keywords

ATM PROTEIN; ATR PROTEIN; CHECKPOINT KINASE 2; PHOSPHOTRANSFERASE; PROTEIN MEC1; PROTEIN TEL1; PROTEOME; UNCLASSIFIED DRUG;

ARTICLE; CELL STRESS; DNA DAMAGE; ENZYME ACTIVE SITE; ENZYME PHOSPHORYLATION; ENZYME SUBSTRATE; ENZYME SUBSTRATE COMPLEX; GENOTOXICITY; IN VIVO STUDY; NONHUMAN; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; PROTEIN TARGETING; PROTEOMICS; QUANTITATIVE ANALYSIS; REGULATORY MECHANISM; WILD TYPE; YEAST;

CELL CYCLE PROTEINS; CHROMATOGRAPHY, LIQUID; DNA DAMAGE; FUNGAL PROTEINS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; METHYL METHANESULFONATE; MUTAGENS; PROTEIN KINASES; PROTEIN-SERINE-THREONINE KINASES; PROTEOME; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SUBSTRATE SPECIFICITY; TANDEM MASS SPECTROMETRY;

EID: 34547499407     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0701622104     Document Type: Article

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