High-resolution crystal structures of factor XIa coagulation factor in complex with nonbasic high-affinity synthetic inhibitors

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2012 Apr 1;68(Pt 4):404-8. doi: 10.1107/S1744309112009037. Epub 2012 Mar 27.

Abstract

Factor XI (FXI) is a key enzyme in the coagulation pathway and an attractive target for the development of anticoagulant drugs. A small number of high-resolution crystal structures of FXIa in complex with small synthetic inhibitors have been published to date. All of these ligands have a basic P1 group and bind exclusively in the nonprime side of the active site of FXIa. Here, two structures of FXIa in complex with nonbasic inhibitors that occupy both the prime and nonprime sides of the active site are presented. These new structures could be valuable in the design and optimization of new FXIa synthethic inhibitors.

MeSH terms

  • Crystallography, X-Ray
  • Enzyme Inhibitors / chemistry*
  • Enzyme Inhibitors / metabolism
  • Factor XIa / antagonists & inhibitors
  • Factor XIa / chemistry*
  • Factor XIa / metabolism
  • Humans
  • Ligands
  • Models, Molecular
  • Protein Binding
  • Protein Interaction Domains and Motifs*
  • Structural Homology, Protein

Substances

  • Enzyme Inhibitors
  • Ligands
  • Factor XIa

Associated data

  • PDB/3SOR
  • PDB/3SOS