Title of article :
Crystals of Urokinase Type Plasminogen Activator Complexes Reveal the Binding Mode of Peptidomimetic Inhibitors
Author/Authors :
Ewa Zeslawska، نويسنده , , Uwe Jacob، نويسنده , , Andrea Schweinitz، نويسنده , , Gary Coombs، نويسنده , , Wolfram Bode، نويسنده , , Edwin Madison، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2003
Pages :
10
From page :
109
To page :
118
Abstract :
Urokinase type plasminogen activator (uPA), a trypsin-like serine proteinase, plays an important role in normal tissue re-modelling, cell adhesion, and cell motility. In addition, studies utilizing normal animals and potent, selective uPA inhibitors or genetically modified mice that lack functional uPA genes have demonstrated that uPA can significantly enhance tumor initiation, growth, progression and metastasis, strongly suggesting that this enzyme may be a promising anti-cancer target.
Keywords :
Urokinase , Proteinase , Inhibitor , Structure–activity relation , cancer
Journal title :
Journal of Molecular Biology
Serial Year :
2003
Journal title :
Journal of Molecular Biology
Record number :
1242588
Link To Document :
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