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1D5J

CRYSTAL STRUCTURE OF MMP3 COMPLEXED WITH A THIAZEPINE BASED INHIBITOR.

Summary for 1D5J
Entry DOI10.2210/pdb1d5j/pdb
Related1CQR
DescriptorSTROMELYSIN-1, ZINC ION, CALCIUM ION, ... (5 entities in total)
Functional Keywordsmixed alpha beta structure, zinc protease, inhibited, hydrolase
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight40084.11
Authors
Almstead, N.G.,Bradley, R.S.,Pikul, S.,De, B.,Natchus, M.G. (deposition date: 1999-10-07, release date: 2000-10-09, Last modification date: 2024-02-07)
Primary citationAlmstead, 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.
Design, synthesis, and biological evaluation of potent thiazine- and thiazepine-based matrix metalloproteinase inhibitors.
J.Med.Chem., 42:4547-4562, 1999
Cited by
PubMed: 10579818
DOI: 10.1021/jm990330y
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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