Structural basis for nick recognition by a minimal pluripotent DNA ligase

Nat Struct Mol Biol. 2007 Aug;14(8):770-8. doi: 10.1038/nsmb1266. Epub 2007 Jul 8.

Abstract

Chlorella virus DNA ligase, the smallest eukaryotic ligase known, has pluripotent biological activity and an intrinsic nick-sensing function, despite having none of the accessory domains found in cellular ligases. A 2.3-A crystal structure of the Chlorella virus ligase-AMP intermediate bound to duplex DNA containing a 3'-OH-5'-PO4 nick reveals a new mode of DNA envelopment, in which a short surface loop emanating from the OB domain forms a beta-hairpin 'latch' that inserts into the DNA major groove flanking the nick. A network of interactions with the 3'-OH and 5'-PO4 termini in the active site illuminates the DNA adenylylation mechanism and the crucial roles of AMP in nick sensing and catalysis. Addition of a divalent cation triggered nick sealing in crystallo, establishing that the nick complex is a bona fide intermediate in the DNA repair pathway.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Binding Sites
  • Crystallography, X-Ray
  • DNA Breaks, Single-Stranded*
  • DNA Ligases / chemistry*
  • DNA Ligases / physiology
  • Models, Molecular
  • Nucleotides / chemistry
  • Nucleotides / metabolism
  • Protein Structure, Tertiary
  • Structure-Activity Relationship
  • Viral Proteins / chemistry*
  • Viral Proteins / physiology

Substances

  • Nucleotides
  • Viral Proteins
  • Chlorella virus DNA ligase
  • DNA Ligases

Associated data

  • PDB/2Q2T
  • PDB/2Q2U