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Crystal structure of the catalytic domain of human ADAM33
Authors:Orth Peter  Reichert Paul  Wang Wenyan  Prosise Winifred W  Yarosh-Tomaine Taisa  Hammond Gerald  Ingram Richard N  Xiao Li  Mirza Urooj A  Zou Jun  Strickland Corey  Taremi S Shane  Le Hung V  Madison Vincent
Institution:Schering-Plough Research Institute, 2015 Galloping Hill Rd, Kenilworth, NJ 07033, USA. peter.orth@spcorp.com
Abstract: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.
Keywords:ADAM33  metalloprotease  asthma  X-ray structure
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