The crystal structure of the carbohydrate-recognition domain of the glycoprotein sorting receptor p58/ERGIC-53 reveals an unpredicted metal-binding site and conformational changes associated with calcium ion binding

J Mol Biol. 2003 Dec 12;334(5):845-51. doi: 10.1016/j.jmb.2003.10.031.

Abstract

p58/ERGIC-53 is a calcium-dependent animal lectin that acts as a cargo receptor, binding to a set of glycoproteins in the endoplasmic reticulum (ER) and transporting them to the Golgi complex. It is similar in structure to calcium-dependent leguminous lectins. We have determined the structure of the carbohydrate-recognition domain of p58/ERGIC-53 in its calcium-bound form. The structure reveals localized but large conformational changes in relation to the previously determined metal ion-free structure, mapping mostly to the ligand-binding site. It reveals the presence of two calcium ion-binding sites located 6A apart, one of which has no equivalent in the plant lectins. The second metal ion-binding site present in that class of lectins, binding Mn(2+), is absent from p58/ERGIC-53. The absence of a short loop in the ligand-binding site in this protein suggests that it has adapted to optimally bind the high-mannose Man(8)(GlcNAc)(2) glycan common to glycoproteins at the ER exit stage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Calcium / metabolism*
  • Carbohydrate Metabolism*
  • Crystallography, X-Ray
  • Mannose-Binding Lectins / chemistry*
  • Mannose-Binding Lectins / metabolism
  • Membrane Proteins / chemistry*
  • Membrane Proteins / metabolism
  • Metals / metabolism*
  • Models, Molecular
  • Protein Conformation

Substances

  • Mannose-Binding Lectins
  • Membrane Proteins
  • Metals
  • Calcium

Associated data

  • PDB/1R1Z