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5WDJ

CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH COMPOUND-6 AKA 7-(BENZYLOXY)-1H-[1,2, 3]TRIAZOLO[4,5-D]PYRIMIDIN-5-AMINE

Summary for 5WDJ
Entry DOI10.2210/pdb5wdj/pdb
DescriptorMyeloperoxidase, alpha-L-fucopyranose, alpha-D-mannopyranose, ... (12 entities in total)
Functional Keywordsmyeloperoxidase, metal binding protein
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains4
Total formula weight135605.64
Authors
Khan, J.A. (deposition date: 2017-07-05, release date: 2018-04-18, Last modification date: 2024-10-23)
Primary citationDuclos, F.,Abell, L.M.,Harden, D.G.,Pike, K.,Nowak, K.,Locke, G.A.,Duke, G.J.,Liu, X.,Fernando, G.,Shaw, S.A.,Vokits, B.P.,Wurtz, N.R.,Viet, A.,Valente, M.N.,Stachura, S.,Sleph, P.,Khan, J.A.,Gao, J.,Dongre, A.R.,Zhao, L.,Wexler, R.R.,Gordon, D.A.,Kick, E.K.
Triazolopyrimidines identified as reversible myeloperoxidase inhibitors.
Medchemcomm, 8:2093-2099, 2017
Cited by
PubMed Abstract: Myeloperoxidase, a mammalian peroxidase involved in the immune system as an anti-microbial first responder, can produce hypochlorous acid in response to invading pathogens. Myeloperoxidase has been implicated in several chronic pathological diseases due to the chronic production of hypochlorous acid, as well as other reactive radical species. A high throughput screen and triaging protocol was developed to identify a reversible inhibitor of myeloperoxidase toward the potential treatment of chronic diseases such as atherosclerosis. The identification and characterization of a reversible myeloperoxidase inhibitor, 7-(benzyloxy)-3-[1,2,3]triazolo[4,5-]pyrimidin-5-amine is described.
PubMed: 30108726
DOI: 10.1039/c7md00268h
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.4 Å)
Structure validation

229183

数据于2024-12-18公开中

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