Multimerization of the adenovirus DNA-binding protein is the driving force for ATP-independent DNA unwinding during strand displacement synthesis

EMBO Journal

Volumn 16, Issue 6, 1997, Pages 1455-1463

  Dekker, Job ^a   Kanellopoulos, Panagiotis N ^b   Loonstra, Ate K ^a   Van Oosterhout, Joost A W M ^a   Leonard, Kevin ^b   Tucker, Paul A ^b   Van Der Vliet, Peter C ^a  

^a UTRECHT UNIVERSITY   (Netherlands)

^b EUROPEAN MOLECULAR BIOLOGY LABORATORY   (Germany)

Author keywords

Adenovirus; DNA replication; DNA unwinding; Helix destabilizing proteins

Indexed keywords

ADENOSINE TRIPHOSPHATE; DNA BINDING PROTEIN; HELICASE; SINGLE STRANDED DNA;

ADENOVIRUS; ANIMAL CELL; ARTICLE; CARBOXY TERMINAL SEQUENCE; CRYSTAL STRUCTURE; DNA DENATURATION; DNA REPLICATION; DNA TEMPLATE; NONHUMAN; PRIORITY JOURNAL; PROTEIN SYNTHESIS;

ADENOSINE TRIPHOSPHATE; ADENOVIRIDAE; ANIMALS; BACULOVIRIDAE; BASE SEQUENCE; CELL LINE; DNA PRIMERS; DNA REPLICATION; DNA, SINGLE-STRANDED; DNA, VIRAL; DNA-BINDING PROTEINS; MODELS, MOLECULAR; MOLECULAR STRUCTURE; MUTATION; NUCLEIC ACID CONFORMATION; PROTEIN CONFORMATION; SEQUENCE DELETION; SPODOPTERA; VIRAL PROTEINS;

ADENOVIRIDAE; ANIMALIA;

EID: 0031003554     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: 10.1093/emboj/16.6.1455     Document Type: Article

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