Crystal structure of the catalytic domain of human ADAM33

P Orth, P Reichert, W Wang, WW Prosise… - Journal of molecular …, 2004 - Elsevier
P Orth, P Reichert, W Wang, WW Prosise, T Yarosh-Tomaine, G Hammond, RN Ingram…
Journal of molecular biology, 2004Elsevier
Adam33 is a putative asthma susceptibility gene encoding for a membrane-anchored
metalloprotease belonging to the ADAM family. The ADAMs (a disintegrin and
metalloprotease) are a family of glycoproteins implicated in cell-cell interactions, cell fusion,
and cell signaling. We have determined the crystal structure of the Adam33 catalytic domain
in complex with the inhibitor marimastat and the inhibitor-free form. The structures reveal the
polypeptide fold and active site environment resembling that of other metalloproteases. The …
Adam33 is a putative asthma susceptibility gene encoding for a membrane-anchored metalloprotease belonging to the ADAM family. The ADAMs (a disintegrin and metalloprotease) are a family of glycoproteins implicated in cell-cell interactions, cell fusion, and cell signaling. We have determined the crystal structure of the Adam33 catalytic domain in complex with the inhibitor marimastat and the inhibitor-free form. The structures reveal the polypeptide fold and active site environment resembling that of other metalloproteases. The substrate-binding site contains unique features that allow the structure-based design of specific inhibitors of this enzyme.
Elsevier