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6YJM

Crystal Structure of the Catalytic Domain of ADAMTS-5 in Complex with the Inhibitor GLPG1972

Summary for 6YJM
Entry DOI10.2210/pdb6yjm/pdb
DescriptorA disintegrin and metalloproteinase with thrombospondin motifs 5, ZINC ION, CALCIUM ION, ... (5 entities in total)
Functional Keywordszinc metalloproteinase, aggrecanase, hydrolase
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight50586.08
Authors
Goepfert, A.,Leonard, P.,Triballeau, N.,Fleury, D.,Mollat, P.,Lamers, M. (deposition date: 2020-04-03, release date: 2021-04-14, Last modification date: 2024-01-24)
Primary citationBrebion, F.,Gosmini, R.,Deprez, P.,Varin, M.,Peixoto, C.,Alvey, L.,Jary, H.,Bienvenu, N.,Triballeau, N.,Blanque, R.,Cottereaux, C.,Christophe, T.,Vandervoort, N.,Mollat, P.,Touitou, R.,Leonard, P.,De Ceuninck, F.,Botez, I.,Monjardet, A.,van der Aar, E.,Amantini, D.
Discovery of GLPG1972/S201086, a Potent, Selective, and Orally Bioavailable ADAMTS-5 Inhibitor for the Treatment of Osteoarthritis.
J.Med.Chem., 64:2937-2952, 2021
Cited by
PubMed: 33719441
DOI: 10.1021/acs.jmedchem.0c02008
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.25 Å)
Structure validation

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