Pages that link to "Q27729709"
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The following pages link to Structure determination and analysis of human neutrophil collagenase complexed with a hydroxamate inhibitor (Q27729709):
Displaying 50 items.
- Fractalkine is expressed by smooth muscle cells in response to IFN-gamma and TNF-alpha and is modulated by metalloproteinase activity (Q24292098) (← links)
- Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors (Q27619648) (← links)
- Crystal structure of human MMP9 in complex with a reverse hydroxamate inhibitor (Q27639102) (← links)
- Crystal structures of MMP-9 complexes with five inhibitors: contribution of the flexible Arg424 side-chain to selectivity (Q27646484) (← links)
- Structure of human ADAM-8 catalytic domain complexed with batimastat (Q27681067) (← links)
- Batimastat, a potent matrix mealloproteinase inhibitor, exhibits an unexpected mode of binding (Q27732644) (← links)
- 1.8‐Å Crystal Structure of the Catalytic Domain of Human Neutrophil Collagenase (Matrix Metalloproteinase‐8) Complexed with a Peptidomimetic Hydroxamate Primed‐Side Inhibitor with a Distinct Selectivity Profile (Q27741275) (← links)
- 2 angstrom X-ray structure of adamalysin II complexed with a peptide phosphonate inhibitor adopting a retro-binding mode (Q27748783) (← links)
- Structural differences of matrix metalloproteinases. Homology modeling and energy minimization of enzyme-substrate complexes (Q28144131) (← links)
- Structural basis of matrix metalloproteinases and tissue inhibitors of metalloproteinases (Q28190760) (← links)
- Protease inhibitors. Part 8: synthesis of potent Clostridium histolyticum collagenase inhibitors incorporating sulfonylated L-alanine hydroxamate moieties (Q28374285) (← links)
- Catalytic activities and substrate specificity of the human membrane type 4 matrix metalloproteinase catalytic domain (Q28610274) (← links)
- Protease inhibitors. Part 12. Synthesis of potent matrix metalloproteinase and bacterial collagenase inhibitors incorporating sulfonylated N-4-nitrobenzyl-beta-alanine hydroxamate moieties (Q31416125) (← links)
- Structure of malonic acid-based inhibitors bound to human neutrophil collagenase. A new binding mode explains apparently anomalous data (Q32056848) (← links)
- Matrix metalloproteinase inhibitors (Q33538437) (← links)
- Structural basis of the endoproteinase-protein inhibitor interaction (Q33857500) (← links)
- Matrix metalloproteinase inhibitor batimastat alleviates pathology and improves skeletal muscle function in dystrophin-deficient mdx mice (Q33947243) (← links)
- Critical appraisal of the use of matrix metalloproteinase inhibitors in cancer treatment (Q34293595) (← links)
- Membrane type-matrix metalloproteinases (MT-MMP) (Q35107597) (← links)
- Structural aspects of the metzincin clan of metalloendopeptidases. (Q35127317) (← links)
- Fluorescent Analogue of Batimastat Enables Imaging of α-Secretase in Living Cells (Q36483986) (← links)
- Structure-based organic synthesis of drug prototypes: a personal odyssey (Q36647895) (← links)
- Shedding of discoidin domain receptor 1 by membrane-type matrix metalloproteinases (Q36796884) (← links)
- Matrix metalloproteinase inhibitors: present achievements and future prospects (Q36893821) (← links)
- Specificity of binding with matrix metalloproteinases (Q38014070) (← links)
- Advances in studies on collagenase inhibitors (Q38014072) (← links)
- Hydroxamic acids as matrix metalloproteinase inhibitors (Q38014073) (← links)
- Therapeutic potential of matrix metalloproteinases in Duchenne muscular dystrophy (Q38264461) (← links)
- Experimental and clinical studies on the use of matrix metalloproteinase inhibitors for the treatment of cancer (Q41372764) (← links)
- Collagenolytic and gelatinolytic matrix metalloproteinases and their inhibitors in basal cell carcinoma of skin: comparison with normal skin (Q42483846) (← links)
- Three-dimensional structure of fibrolase, the fibrinolytic enzyme from southern copperhead venom, modeled from the X-ray structure of adamalysin II and atrolysin C. (Q42649098) (← links)
- QM/MM linear response method distinguishes ligand affinities for closely related metalloproteins (Q42739061) (← links)
- A combination of docking, QM/MM methods, and MD simulation for binding affinity estimation of metalloprotein ligands (Q42739068) (← links)
- Structural characterizations of nonpeptidic thiadiazole inhibitors of matrix metalloproteinases reveal the basis for stromelysin selectivity. (Q42846145) (← links)
- Solution structures of stromelysin complexed to thiadiazole inhibitors (Q42846171) (← links)
- Pyrimidine-2,4,6-Triones: a new effective and selective class of matrix metalloproteinase inhibitors (Q43760509) (← links)
- Design and synthesis of dual inhibitors for matrix metalloproteinase and cathepsin. (Q43868983) (← links)
- Tetrahydroisoquinoline-3-carboxylate based matrix-metalloproteinase inhibitors: design, synthesis and structure-activity relationship (Q44126564) (← links)
- Computational study of the catalytic domain of human neutrophil collagenase. specific role of the S3 and S'3 subsites in the interaction with a phosphonate inhibitor. (Q44167541) (← links)
- Inhibition of arginine gingipains (RgpB and HRgpA) with benzamidine inhibitors: zinc increases inhibitory potency (Q44219899) (← links)
- Hydroxyurea is a carbonic anhydrase inhibitor (Q44416611) (← links)
- Effect of species differences on stromelysin-1 (MMP-3) inhibitor potency. An explanation of inhibitor selectivity using homology modeling and chimeric proteins (Q47936331) (← links)
- Hydroxamate derivatives of substrate-analogous peptides containing aminomalonic acid are potent inhibitors of matrix metalloproteinases. (Q54120593) (← links)
- Structural Characterization of the Catalytic Active Site in the Latent and Active Natural Gelatinase B from Human Neutrophils (Q57584591) (← links)
- Protease inhibitors – Part 5. Alkyl/arylsulfonyl- and arylsulfonylureido-/arylureido- glycine hydroxamate inhibitors of Clostridium histolyticum collagenase (Q58863335) (← links)
- Characterization of a metalloproteinase: A late stage specific gelatinase activity in the sea urchin embryo (Q73587455) (← links)
- Matrix metalloproteases: variations on a theme (Q77455726) (← links)
- The constituent tryptophans and bisANS as fluorescent probes of the active site and of a secondary binding site of stromelysin-1 (MMP-3) (Q77684249) (← links)
- Selective inhibition of low affinity IgE receptor (CD23) processing (Q77744141) (← links)
- The design, synthesis, and structure-activity relationships of a series of macrocyclic MMP inhibitors (Q77749176) (← links)