PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 1310045-7 1992 Nearly identical binding to thrombin and elTM is observed when active-site-blocked activated bovine protein C is substituted for protein C. Thrombin inhibited by diisopropyl fluorophosphate and thrombin inhibited by a tripeptide chloromethyl ketone exhibited identical behavior in binding experiments, suggesting that the accessibility of protein C to the substrate recognition cleft of these two forms of thrombin is nearly equal. Isoflurophate 162-189 coagulation factor II, thrombin Bos taurus 28-36 1310045-7 1992 Nearly identical binding to thrombin and elTM is observed when active-site-blocked activated bovine protein C is substituted for protein C. Thrombin inhibited by diisopropyl fluorophosphate and thrombin inhibited by a tripeptide chloromethyl ketone exhibited identical behavior in binding experiments, suggesting that the accessibility of protein C to the substrate recognition cleft of these two forms of thrombin is nearly equal. Isoflurophate 162-189 coagulation factor II, thrombin Bos taurus 140-148 6725279-6 1984 Similar values for Ki were obtained when fibrinogen was used to inhibit the inactivation of bovine alpha- and beta-thrombin by diisopropylphosphorofluoridate. Isoflurophate 127-157 coagulation factor II, thrombin Bos taurus 115-123 6896460-12 1982 The active site directed irreversible thrombin inhibitors diisopropyl phosphorofluoridate and D-phenylalanylprolylarginyl chloromethyl ketone displace DAPA from thrombin but not from prethrombin 2. Isoflurophate 58-89 coagulation factor II, thrombin Bos taurus 38-46 6896460-12 1982 The active site directed irreversible thrombin inhibitors diisopropyl phosphorofluoridate and D-phenylalanylprolylarginyl chloromethyl ketone displace DAPA from thrombin but not from prethrombin 2. Isoflurophate 58-89 coagulation factor II, thrombin Bos taurus 161-169 718867-8 1978 Displacement of factor Xa from the platelet receptor by diisopropyl fluorophosphate-factor Xa effectively blocked thrombin formation. Isoflurophate 56-83 coagulation factor II, thrombin Bos taurus 114-122 11991818-2 2002 Bovine thrombin was treated with diisopropyl fluorophosphate, and prepared diisopropylphosphoryl-thrombin was used for the immunization to BALB/c mice. Isoflurophate 33-60 coagulation factor II, thrombin Bos taurus 7-15 1964457-6 1990 The esterase activity was strongly inhibited by diisopropylfluorophosphate and phenylmethanesulfonyl fluoride, and to a lesser extent by tosyl-L-lysine chloromethyl ketone, indicating that the enzyme is a serine protease like thrombin. Isoflurophate 48-74 coagulation factor II, thrombin Bos taurus 226-234 2501229-10 1989 Thrombin inactivated with diisopropylfluorophosphate (DFP) did not induce an increase in t-PA levels. Isoflurophate 26-52 coagulation factor II, thrombin Bos taurus 0-8 2501229-10 1989 Thrombin inactivated with diisopropylfluorophosphate (DFP) did not induce an increase in t-PA levels. Isoflurophate 54-57 coagulation factor II, thrombin Bos taurus 0-8 943183-2 1976 Upon incubation of the prothrombin for 30 h with a combination of neuraminidase, alpha- and beta-galactosidase and beta-N-acetylglucosaminidase in 4 mM diisopropylfluorophosphate at pH 5.3 and 30 degrees C, about 70% of the carbohydrates were removed without affecting the coagulation activity. Isoflurophate 152-178 coagulation factor II, thrombin Bos taurus 23-34