Domain within the helicase subunit Mcm4 integrates multiple kinase signals to control DNA replication initiation and fork progression

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

Volumn 111, Issue 18, 2014, Pages

  Sheu, Yi Jun ^a   Kinney, Justin B ^a   Lengronne, Armelle ^b   Pasero, Philippe ^b   Stillman, Bruce ^a  

^a Cold Spring Harbor Laboratory ^*  (United States)

^b INSTITUTE OF HUMAN GENETICS   (France)

Author keywords

Cdc7 Dbf4 kinase; DNA helicase; MCM2 7

Indexed keywords

CHECKPOINT KINASE RAD3; CYCLIN DEPENDENT KINASE; HELICASE; MINICHROMOSOME MAINTENANCE PROTEIN 4;

ANIMAL CELL; ARTICLE; DNA DAMAGE CHECKPOINT; DNA DETERMINATION; DNA REPLICATION; DNA SEQUENCE; ENZYME PHOSPHORYLATION; GENOMIC INSTABILITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN FUNCTION; SIGNAL TRANSDUCTION;

CDC7-DBF4 KINASE; DNA HELICASE; MCM2-7;

CELL CYCLE CHECKPOINTS; CELL CYCLE PROTEINS; CYCLIN-DEPENDENT KINASES; DNA REPLICATION; DNA, FUNGAL; GENOME, FUNGAL; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MINICHROMOSOME MAINTENANCE COMPLEX COMPONENT 4; MUTATION; NUCLEIC ACID CONFORMATION; PHOSPHORYLATION; PROTEIN STRUCTURE, TERTIARY; PROTEIN SUBUNITS; PROTEIN-SERINE-THREONINE KINASES; REPLICATION ORIGIN; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SIGNAL TRANSDUCTION;

EID: 84899846910     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1404063111     Document Type: Article

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