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Solution Structure of Matrilysin (MMP-7) Complexed to Constraint Conformational Sulfonamide Inhibitor[HYDROLASE]
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The Discovery of MMP7 Inhibitors Exploiting a Novel Selectivity Trigger[HYDROLASE]
MATRILYSIN COMPLEXED WITH SULFODIIMINE INHIBITOR[METALLOPROTEASE]
MATRILYSIN COMPLEXED WITH HYDROXAMATE INHIBITOR[METALLOPROTEASE]
MATRILYSIN COMPLEXED WITH CARBOXYLATE INHIBITOR[METALLOPROTEASE]
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The Discovery of MMP7 inhibitors Exploiting a Novel Selectivity Trigger[HYDROLASE]
CRYSTAL STRUCTURE OF FIBROBLAST STROMELYSIN-1: THE C-TRUNCATED HUMAN PROENZYME[HYDROLASE]
X-Ray Structure Of Human Prommp-1: New Insights Into Collagenase Action[Hydrolase, EC: 3.4.24.7]
Catalytic domain of proMMP-2 E404Q mutant[HYDROLASE/HYDROLASE INHIBITOR]
proMMP-2/TIMP-2 complex[HYDROLASE]
GELATINASE A (FULL-LENGTH)[HYDROLASE]
CATALYTIC DOMAIN OF HUMAN STROMELYSIN-1 AT PH 5.5 AND 40OC COMPLEXED WITH INHIBITOR[HYDROLASE/HYDROLASE INHIBITOR]
SOLUTION STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN STROMELYSIN-1 COMPLEXED TO A POTENT NON-PEPTIDIC INHIBITOR, NMR, 20 STRUCTURES[METALLOPROTEASE]
Stromelysin-1 catalytic domain with hydrophobic inhibitor bound, ph 7.0, 32oc, 20 mm cacl2, 15% acetonitrile; nmr average of 20 structures minimized with restraints[HYDROLASE/HYDROLASE INHIBITOR]
CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN FIBROBLAST STROMELYSIN-1 INHIBITED WITH THE N-CARBOXY-ALKYL INHIBITOR L-702,842[HYDROLASE]
Stromelysin-1 (MMP-3) complexed to a hydroxamic acid inhibitor[HYDROLASE]
Crystal Structure Analysis of human Macrophage Elastase MMP-12[HYDROLASE]
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