3.4.22.3 alpha2-Macroglobulin - 1068 3.4.22.3 amaranth cystatin Amaranthus hypochondracus cysteine proteinase inhibitor, GenBank accession number DQ792503 81224 3.4.22.3 Benzamidoacetonitrile - 92531 3.4.22.3 Chloroacetamide - 10612 3.4.22.3 cystatin from egg white, strong inhibition 1600 3.4.22.3 cystatin from chicken egg 1600 3.4.22.3 cysteine proteinase inhibitor in human seminal plasma - 100400 3.4.22.3 diisopropyl fluorophosphate - 244 3.4.22.3 E-64 complete inhibition of all five ficin isoforms at 0.1 mM 559 3.4.22.3 E-64 0.01 mM, complete inhibition 559 3.4.22.3 H2O2 - 22 3.4.22.3 HgCl2 1 mM, complete inhibition 110 3.4.22.3 HgCl2 - 110 3.4.22.3 I2 - 2846 3.4.22.3 inhibitors from rat and serum liver - 100748 3.4.22.3 iodoacetamide activity is completely inhibited, cysteine-group specific inhibitor, confirms the participation of the cysteine residue at the active site of the enzyme 67 3.4.22.3 iodoacetamide complete inhibition of all five ficin isoforms at 5 mM 67 3.4.22.3 iodoacetamide - 67 3.4.22.3 iodoacetamide 3 mM, complete inhibition 67 3.4.22.3 iodoacetic acid - 213 3.4.22.3 methylmethanethiol sulfonate complete inhibition of all five ficin isoforms at 3 mM 167857 3.4.22.3 additional information all five ficin isoforms are not inhibited by pepstatin A, Pafabloc SC, and EDTA 2 3.4.22.3 additional information ficin E is not affected by Mg2+, Ca2+ and Mn2+ at a concentration up to 10 mM. It is unaffected by synthetic (Pefabloc SC, benzamidine) and by natural proteinaceous (aprotinin) serine proteases inhibitors, by aspartic proteases inhibitors (pepstatin A) and by metallo-proteases inhibitors (EDTA, EGTA) 2 3.4.22.3 Na2S4O6 - 21185 3.4.22.3 Nalpha-tosyl-L-lysine chloromethyl ketone complete inhibition of all five ficin isoforms at 0.1 mM 9364 3.4.22.3 Nalpha-tosyl-L-phenylalanine chloromethylketone complete inhibition of all five ficin isoforms at 0.1 mM 167858 3.4.22.3 naturally occuring protein crystal in potato - 101179 3.4.22.3 NEM - 89 3.4.22.3 o-phenanthroline - 239 3.4.22.3 p-chloromercuribenzoate activity is completely inhibited by the cysteine-group specific inhibitor 43 3.4.22.3 PCMB - 78 3.4.22.3 phenylmethane sulfonyl fluoride - 44690 3.4.22.3 potassium tetrathionate - 109460 3.4.22.3 Proflavine - 6016 3.4.22.3 Proflavine the inhibitor increases the noncovalent reversible binding affinity of ficin towards the maleimides without affecting the nucleophilic reactivity of the catalytically essential thiol groups which are alkylated in the inactivation reaction 6016 3.4.22.3 Sodium tetrathionate activity is completely inhibited by the cysteine-group specific inhibitor 6592 3.4.22.3 TLCK 0.1 mM, complete inhibition 4621 3.4.22.3 TPCK 0.1 mM, complete inhibition 7403 3.4.22.3 Zn2+ 1 mM, complete inhibition 14