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Structure paper

TitleDesign, synthesis, and biological evaluation of potent thiazine- and thiazepine-based matrix metalloproteinase inhibitors.
Journal, issue, pagesJ. Med. Chem., Vol. 42, Page 4547-4562, Year 1999
Publish dateOct 7, 1999 (structure data deposition date)
AuthorsAlmstead, N.G. / Bradley, R.S. / Pikul, S. / De, B. / Natchus, M.G. / Taiwo, Y.O. / Gu, F. / Williams, L.E. / Hynd, B.A. / Janusz, M.J. ...Almstead, N.G. / Bradley, R.S. / Pikul, S. / De, B. / Natchus, M.G. / Taiwo, Y.O. / Gu, F. / Williams, L.E. / Hynd, B.A. / Janusz, M.J. / Dunaway, C.M. / Mieling, G.E.
External linksJ. Med. Chem. / PubMed:10579818
MethodsX-ray diffraction
Resolution2.6 Å
Structure data

PDB-1d5j:
CRYSTAL STRUCTURE OF MMP3 COMPLEXED WITH A THIAZEPINE BASED INHIBITOR.
Method: X-RAY DIFFRACTION / Resolution: 2.6 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-CA:
Unknown entry

ChemComp-MM3:
N-HYDROXY-4-[(4-METHOXYLPHENYL)SULFONYL]-2,2-DIMETHYL-HEXAHYDRO-1,4-THIAZEPINE-3(S)-CARBOXAMIDE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE / MIXED ALPHA BETA STRUCTURE / ZINC PROTEASE / INHIBITED

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