Structure and mechanism of GDP-mannose glycosyl hydrolase, a Nudix enzyme that cleaves at carbon instead of phosphorus

Structure. 2004 Jun;12(6):927-35. doi: 10.1016/j.str.2004.03.028.

Abstract

GDP-mannose glycosyl hydrolase (GDPMH) catalyzes the hydrolysis of GDP-mannose and GDP-glucose to GDP and sugar by substitution with inversion at C1 of the sugar. The enzyme has a modified Nudix motif and requires one divalent cation for activity. The 1.3 A X-ray structure of the GDPMH-Mg(2+)-GDP complex, together with kinetic, mutational, and NMR data, suggests a mechanism for the GDPMH reaction. Several residues and the divalent cation strongly promote the departure of the GDP leaving group, supporting a dissociative mechanism. Comparison of the GDPMH structure with that of a typical Nudix hydrolase suggests how sequence changes result in the switch of catalytic activity from P-O bond cleavage to C-O bond cleavage. Changes in the Nudix motif result in loss of binding of at least one Mg(2+) ion, and shortening of a loop by 6 residues shifts the catalytic base by approximately 10 A.

Publication types

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

MeSH terms

  • Amino Acid Motifs
  • Amino Acid Sequence
  • Binding Sites
  • Carbon / chemistry
  • Catalysis
  • Cations
  • Crystallography, X-Ray
  • Dimerization
  • Escherichia coli / metabolism
  • Guanosine Diphosphate / chemistry
  • Guanosine Diphosphate Mannose / chemistry*
  • Hydrolysis
  • Ions
  • Kinetics
  • Magnesium / chemistry
  • Magnetic Resonance Spectroscopy
  • Mannose / chemistry
  • Models, Molecular
  • Molecular Sequence Data
  • Mutation
  • N-Glycosyl Hydrolases / chemistry*
  • Phosphorus / chemistry
  • Protein Binding
  • Protein Conformation
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Sequence Homology, Amino Acid
  • Structure-Activity Relationship

Substances

  • Cations
  • Ions
  • Guanosine Diphosphate
  • Phosphorus
  • Guanosine Diphosphate Mannose
  • Carbon
  • N-Glycosyl Hydrolases
  • Magnesium
  • Mannose