EC Number   |
Title |
Organism |
|---|
   3.4.24.46 | 2 angstrom X-ray structure of adamalysin II complexed with a peptide phosphonate inhibitor adopting a retro-binding mode |
Crotalus adamanteus |
| 3.4.24.46 | Activation of snake venom metalloproteinases by a cysteine switch-like mechanism |
Crotalus adamanteus |
| 3.4.24.46 | Astacins, serralysins, snake venom and matrix metalloproteinases exhibit identical zinc-binding environments (HEXXHXXGXXH and Met-turn) and topologies and should be grouped into a common family, the metzincins |
Crotalus adamanteus |
| 3.4.24.46 | Crystallization and preliminary x-ray diffraction data of proteinase II from Crotalus adamanteus (eastern diamond rattlesnake) |
Crotalus adamanteus |
| 3.4.24.46 | Evidence of antiangiogenic and antimetastatic activities of the recombinant disintegrin domain of metargidin |
Homo sapiens |
| 3.4.24.46 | Identification of the cleavage sites resulting from enzymatic inactivation of human antithrombin III by Crotalus adamanteus proteinase II in the the presence and absence of heparin |
Crotalus adamanteus |
| 3.4.24.46 | Inhibition of adamalysin II and MMPs by phosphonate analogues of snake venom peptides |
Crotalus adamanteus |
| 3.4.24.46 | Purification and some properties of two proteinases from Crotalus adamanteus venom that inactivate human alpha 1-proteinase inhibitor |
Crotalus adamanteus |
| 3.4.24.46 | Refined 2.0 A X-ray crystal structure of the snake venom zinc-endopeptidase adamalysin II. Primary and tertiary structure determination, refinement, molecular structure and comparison with astacin, collagenase and thermolysin |
Crotalus adamanteus |
| 3.4.24.46 | Structures of adamalysin II with peptidic inhibitors. Implications for the design of tumor necrosis factor alpha convertase inhibitors |
Crotalus adamanteus |
