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Journal Abstract Search

375 related items for PubMed ID: 8993332

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  • 3. Proteolysis of factor V by cathepsin G and elastase indicates that cleavage at Arg1545 optimizes cofactor function by facilitating factor Xa binding.
    Camire RM, Kalafatis M, Tracy PB.
    Biochemistry; 1998 Aug 25; 37(34):11896-906. PubMed ID: 9718313
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  • 7. Kinetics of factor Xa inhibition by recombinant tick anticoagulant peptide: both active site and exosite interactions are required for a slow- and tight-binding inhibition mechanism.
    Rezaie AR.
    Biochemistry; 2004 Mar 30; 43(12):3368-75. PubMed ID: 15035608
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  • 9. Trp2063 and Trp2064 in the factor Va C2 domain are required for high-affinity binding to phospholipid membranes but not for assembly of the prothrombinase complex.
    Peng W, Quinn-Allen MA, Kim SW, Alexander KA, Kane WH.
    Biochemistry; 2004 Apr 13; 43(14):4385-93. PubMed ID: 15065883
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  • 12. Nematode anticoagulant protein c2 reveals a site on factor Xa that is important for macromolecular substrate binding to human prothrombinase.
    Buddai SK, Toulokhonova L, Bergum PW, Vlasuk GP, Krishnaswamy S.
    J Biol Chem; 2002 Jul 19; 277(29):26689-98. PubMed ID: 12011050
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  • 19. Exosite binding tethers the macromolecular substrate to the prothrombinase complex and directs cleavage at two spatially distinct sites.
    Boskovic DS, Krishnaswamy S.
    J Biol Chem; 2000 Dec 08; 275(49):38561-70. PubMed ID: 10984491
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  • 20. Prothrombinase complex assembly. Contributions of protein-protein and protein-membrane interactions toward complex formation.
    Krishnaswamy S.
    J Biol Chem; 1990 Mar 05; 265(7):3708-18. PubMed ID: 2303476
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