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2. Molecular basis for the inhibition of human alpha-thrombin by the macrocyclic peptide cyclotheonamide A. Maryanoff BE, Qiu X, Padmanabhan KP, Tulinsky A, Almond HR, Andrade-Gordon P, Greco MN, Kauffman JA, Nicolaou KC, Liu A. Proc Natl Acad Sci U S A; 1993 Sep 01; 90(17):8048-52. PubMed ID: 8367461 [Abstract] [Full Text] [Related]
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7. The isomorphous structures of prethrombin2, hirugen-, and PPACK-thrombin: changes accompanying activation and exosite binding to thrombin. Vijayalakshmi J, Padmanabhan KP, Mann KG, Tulinsky A. Protein Sci; 1994 Dec 04; 3(12):2254-71. PubMed ID: 7756983 [Abstract] [Full Text] [Related]
8. Crystal structure of two new bifunctional nonsubstrate type thrombin inhibitors complexed with human alpha-thrombin. Féthière J, Tsuda Y, Coulombe R, Konishi Y, Cygler M. Protein Sci; 1996 Jun 04; 5(6):1174-83. PubMed ID: 8762149 [Abstract] [Full Text] [Related]
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17. Inhibition of thrombin and other trypsin-like serine proteinases by cyclotheonamide A. Lewis SD, Ng AS, Baldwin JJ, Fusetani N, Naylor AM, Shafer JA. Thromb Res; 1993 Apr 15; 70(2):173-90. PubMed ID: 8322286 [Abstract] [Full Text] [Related]
20. Nonpolar interactions of thrombin and its inhibitors at the fibrinogen recognition exosite: thermodynamic analysis. Cheng Y, Slon-Usakiewicz JJ, Wang J, Purisima EO, Konishi Y. Biochemistry; 1996 Oct 08; 35(40):13021-9. PubMed ID: 8855937 [Abstract] [Full Text] [Related] Page: [Next] [New Search]