Matrix metalloproteases: Structure-based drug discovery targets
- 1 July 1995
- journal article
- Published by Springer Nature in Perspectives in Drug Discovery and Design
- Vol. 2 (3) , 343-351
- https://doi.org/10.1007/bf02172028
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Families of zinc metalloproteasesPublished by Wiley ,2001
- Crystal structures of matrilysin-inhibitor complexesBiochemistry, 1995
- Metalloproteinase super–families and drug designNature Structural & Molecular Biology, 1994
- Structural implications for the role of the N terminus in the ‘superactivation’ of collagenasesFEBS Letters, 1994
- Tumor Cell Interactions with the Extracellular Matrix During Invasion and MetastasisAnnual Review of Cell Biology, 1993
- 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’FEBS Letters, 1993
- Comparative sequence specificities of human 72- and 92-kDa gelatinases (type IV collagenases) and PUMP (matrilysin)Biochemistry, 1993
- A novel coumarin‐labelled peptide for sensitive continuous assays of the matrix metalloproteinasesFEBS Letters, 1992
- An internal cysteine plays a role in the maintenance of the latency of human fibroblast collagenaseBiochemistry, 1991
- Binding of N-carboxymethyl dipeptide inhibitors to thermolysin determined by x-ray crystallography: a novel class of transition-state analogs for zinc peptidasesBiochemistry, 1984