Structural basis for the highly selective inhibition of MMP-13

Chem Biol. 2005 Feb;12(2):181-9. doi: 10.1016/j.chembiol.2004.11.014.

Abstract

Inhibitors for matrix metalloproteinases (MMPs) are under investigation for the treatment of cancer, arthritis, and cardiovascular disease. Here, we report a class of highly selective MMP-13 inhibitors (pyrimidine dicarboxamides) that exhibit no detectable activity against other MMPs. The high-resolution X-ray structures of three molecules of this series bound to MMP-13 reveal a novel binding mode characterized by the absence of interactions between the inhibitors and the catalytic zinc. The inhibitors bind in the S1' pocket and extend into an additional S1' side pocket, which is unique to MMP-13. We analyze the determinants for selectivity and describe the rational design of improved compounds with low nanomolar affinity.

MeSH terms

  • Amino Acid Sequence
  • Binding Sites
  • Collagenases / chemistry*
  • Crystallography, X-Ray
  • Drug Design
  • Matrix Metalloproteinase 13
  • Matrix Metalloproteinase Inhibitors*
  • Models, Molecular
  • Molecular Sequence Data
  • Protease Inhibitors / chemical synthesis*
  • Protease Inhibitors / chemistry*
  • Protease Inhibitors / pharmacology
  • Protein Structure, Secondary
  • Water

Substances

  • Matrix Metalloproteinase Inhibitors
  • Protease Inhibitors
  • Water
  • Collagenases
  • Matrix Metalloproteinase 13

Associated data

  • PDB/1XUC
  • PDB/1XUD
  • PDB/1XUR