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Structure paper

TitleStructural Elucidation of a Nonpeptidic Inhibitor Specific for the Human Immunoproteasome.
Journal, issue, pagesChembiochem, Vol. 18, Page 523-526, Year 2017
Publish dateOct 12, 2016 (structure data deposition date)
AuthorsCui, H. / Baur, R. / Le Chapelain, C. / Dubiella, C. / Heinemeyer, W. / Huber, E.M. / Groll, M.
External linksChembiochem / PubMed:28098422
MethodsX-ray diffraction
Resolution2.7 Å
Structure data

PDB-5m2b:
Yeast 20S proteasome with human beta5i (1-138) and human beta6 (97-111; 118-133) in complex with thiazole based inhibitor Ro19
Method: X-RAY DIFFRACTION / Resolution: 2.7 Å

Chemicals

ChemComp-MG:
Unknown entry

ChemComp-CL:
Unknown entry

ChemComp-7DX:
(2~{S})-2-cyclohexyl-4-oxidanylidene-4-[[7-(4-phenyl-1,3-thiazol-2-yl)quinolin-2-yl]amino]butanoic acid

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
  • saccharomyces cerevisiae s288c (yeast)
  • saccharomyces cerevisiae (strain atcc 204508 / s288c) (yeast)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / HYDROLASE-HYDROLASE INHIBITOR complex / Proteasome / Mutant / Inhibitor / Binding Analysis

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