Crystal structure of the Zalpha domain of the human editing enzyme ADAR1 bound to left-handed Z-DNA

Science. 1999 Jun 11;284(5421):1841-5. doi: 10.1126/science.284.5421.1841.

Abstract

The editing enzyme double-stranded RNA adenosine deaminase includes a DNA binding domain, Zalpha, which is specific for left-handed Z-DNA. The 2.1 angstrom crystal structure of Zalpha complexed to DNA reveals that the substrate is in the left-handed Z conformation. The contacts between Zalpha and Z-DNA are made primarily with the "zigzag" sugar-phosphate backbone, which provides a basis for the specificity for the Z conformation. A single base contact is observed to guanine in the syn conformation, characteristic of Z-DNA. Intriguingly, the helix-turn-helix motif, frequently used to recognize B-DNA, is used by Zalpha to contact Z-DNA.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Deaminase / chemistry*
  • Adenosine Deaminase / metabolism
  • Amino Acid Sequence
  • Binding Sites
  • Crystallography, X-Ray
  • DNA / chemistry
  • DNA / metabolism*
  • Helix-Turn-Helix Motifs
  • Humans
  • Hydrogen Bonding
  • Models, Molecular
  • Molecular Sequence Data
  • Nucleic Acid Conformation
  • Protein Conformation
  • Protein Structure, Secondary
  • RNA-Binding Proteins
  • Substrate Specificity
  • Water / metabolism

Substances

  • RNA-Binding Proteins
  • Water
  • DNA
  • ADARB1 protein, human
  • Adenosine Deaminase

Associated data

  • PDB/1QBJ