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6OCW

Crystal Structure of Mycobacterium tuberculosis Proteasome in Complex with Phenylimidazole-based Inhibitor A85

Summary for 6OCW
Entry DOI10.2210/pdb6ocw/pdb
DescriptorProteasome subunit alpha, Proteasome subunit beta, DIMETHYLFORMAMIDE, ... (6 entities in total)
Functional Keywordsmycobacterium tuberculosis, proteasome inhibitor, phenylimidazole, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceMycobacterium tuberculosis (strain ATCC 25618 / H37Rv)
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Total number of polymer chains28
Total formula weight716902.73
Authors
Hsu, H.C.,Li, H. (deposition date: 2019-03-25, release date: 2019-10-09, Last modification date: 2023-10-11)
Primary citationZhan, W.,Hsu, H.C.,Morgan, T.,Ouellette, T.,Burns-Huang, K.,Hara, R.,Wright, A.G.,Imaeda, T.,Okamoto, R.,Sato, K.,Michino, M.,Ramjee, M.,Aso, K.,Meinke, P.T.,Foley, M.,Nathan, C.F.,Li, H.,Lin, G.
Selective Phenylimidazole-Based Inhibitors of theMycobacterium tuberculosisProteasome.
J.Med.Chem., 62:9246-9253, 2019
Cited by
PubMed: 31560200
DOI: 10.1021/acs.jmedchem.9b01187
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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