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1G05

HETEROCYCLE-BASED MMP INHIBITOR WITH P2'SUBSTITUENTS

Summary for 1G05
Entry DOI10.2210/pdb1g05/pdb
Related1CQR 1D5J 1D7X 1D8F 1D8M
DescriptorSTROMELYSIN-1 PRECURSOR, ZINC ION, CALCIUM ION, ... (5 entities in total)
Functional Keywordsmixed alpha beta structure, zinc protease, inhibited, hydrolase
Biological sourceHomo sapiens (human)
Cellular locationSecreted, extracellular space, extracellular matrix (Probable): P08254
Total number of polymer chains2
Total formula weight39754.61
Authors
Pikul, S.,Dunham, K.M.,Almstead, N.G.,De, B.,Natchus, M.G.,Taiwo, Y.O.,Williams, L.E.,Hynd, B.A.,Hsieh, L.C.,Janusz, M.J. (deposition date: 2000-10-05, release date: 2001-10-05, Last modification date: 2024-02-07)
Primary citationPikul, S.,Dunham, K.M.,Almstead, N.G.,De, B.,Natchus, M.G.,Taiwo, Y.O.,Williams, L.E.,Hynd, B.A.,Hsieh, L.C.,Janusz, M.J.,Gu, F.,Mieling, G.E.
Heterocycle-based MMP inhibitors with P2' substituents.
Bioorg.Med.Chem.Lett., 11:1009-1013, 2001
Cited by
PubMed: 11327577
DOI: 10.1016/S0960-894X(01)00137-8
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.45 Å)
Structure validation

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