The CDC13-STN1-TEN1 complex stimulates Pol α activity by promoting RNA priming and primase-to-polymerase switch

Nature Communications

Volumn 5, Issue , 2014, Pages

  Lue, Neal F ^a   Chan, Jamie ^a   Wright, Woodring E ^b   Hurwitz, Jerard ^c  

^a WEILL CORNELL MEDICAL COLLEGE   (United States)

^b UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^c MEMORIAL SLOAN KETTERING CANCER CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA POLYMERASE; DNA PRIMASE; POL ALPHA PROTEIN; PRIMER RNA; RNA POLYMERASE; UNCLASSIFIED DRUG; CELL CYCLE PROTEIN; DNA DIRECTED DNA POLYMERASE BETA; FUNGAL DNA; FUNGAL PROTEIN; FUNGAL RNA; NONHISTONE PROTEIN; PROTEIN BINDING; SINGLE STRANDED DNA; TELOMERE BINDING PROTEIN;

COMPLEXATION; ENZYME ACTIVITY; GENETIC VARIATION; GENOME; RNA; YEAST;

AMINO TERMINAL SEQUENCE; ARTICLE; CANDIDA GLABRATA; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; GENOMIC INSTABILITY; NONHUMAN; OPHTHALMIC FEMTOSECOND LASER; REGULATORY MECHANISM; RNA STRUCTURE; STIMULATION; TELOMERE; BINDING SITE; CHEMISTRY; FUNGAL GENOME; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; PROTEIN SECONDARY STRUCTURE; PROTEIN TERTIARY STRUCTURE;

CANDIDA GLABRATA;

BINDING SITES; CANDIDA GLABRATA; CELL CYCLE PROTEINS; CHROMOSOMAL PROTEINS, NON-HISTONE; DNA POLYMERASE I; DNA PRIMASE; DNA, FUNGAL; DNA, SINGLE-STRANDED; FUNGAL PROTEINS; GENE EXPRESSION REGULATION, FUNGAL; GENOME, FUNGAL; GENOMIC INSTABILITY; PROTEIN BINDING; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; RNA, FUNGAL; TELOMERE; TELOMERE-BINDING PROTEINS;

EID: 84923379956     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms6762     Document Type: Article

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