Structure analysis of endosialidase NF at 0.98 A resolution

Acta Crystallogr D Biol Crystallogr. 2010 Feb;66(Pt 2):176-80. doi: 10.1107/S0907444909048720. Epub 2010 Jan 22.

Abstract

Endosialidase NF (endoNF) is a bacteriophage-derived endosialidase that specifically degrades alpha-2,8-linked polysialic acid. The structure of a new crystal form of endoNF in complex with sialic acid has been refined at 0.98 A resolution. The 210 kDa homotrimeric multi-domain enzyme displays outstanding stability and resistance to SDS. Even at atomic resolution, only a minor fraction of side chains possess alternative conformations. However, multiple conformations of an active-site residue imply that it has an important catalytic function in the cleavage mechanism of polysialic acid.

MeSH terms

  • Bacteriophages / enzymology*
  • Catalytic Domain
  • Crystallography, X-Ray
  • Enzyme Stability
  • Models, Molecular
  • N-Acetylneuraminic Acid / chemistry
  • N-Acetylneuraminic Acid / metabolism
  • Neuraminidase / chemistry*
  • Neuraminidase / metabolism
  • Protein Multimerization
  • Protein Structure, Quaternary
  • Protein Structure, Tertiary

Substances

  • endo-N-acetylneuraminidase
  • Neuraminidase
  • N-Acetylneuraminic Acid