Crystal Structure of the Catalytic Domain of Human ADAM33

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 cry...

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Veröffentlicht in:Journal of molecular biology 2004-01, Vol.335 (1), p.129-137
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung: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.
ISSN:0022-2836
1089-8638
DOI:10.1016/j.jmb.2003.10.037