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Structure paper

TitleSelective inhibition of the immunoproteasome by ligand-induced crosslinking of the active site.
Journal, issue, pagesAngew. Chem. Int. Ed. Engl., Vol. 53, Page 11969-11973, Year 2014
Publish dateAug 4, 2014 (structure data deposition date)
AuthorsDubiella, C. / Cui, H. / Gersch, M. / Brouwer, A.J. / Sieber, S.A. / Kruger, A. / Liskamp, R.M. / Groll, M.
External linksAngew. Chem. Int. Ed. Engl. / PubMed:25244435
MethodsX-ray diffraction
Resolution2.1 - 2.4 Å
Structure data

PDB-4r17:
Ligand-induced aziridine-formation at subunit beta5 of the yeast 20S proteasome
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

PDB-4r18:
Ligand-induced Lys33-Thr1 crosslinking at subunit beta5 of the yeast 20S proteasome
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

Chemicals

ChemComp-MG:
Unknown entry

ChemComp-3K4:
(2S,3S)-3-methylaziridine-2-carboxylic acid

ChemComp-HOH:
WATER

ChemComp-ABA:
ALPHA-AMINOBUTYRIC ACID

Source
  • saccharomyces cerevisiae s288c (yeast)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / Proteasome / Drug Development / Binding Analysis / Umpolung / Crosslink / HYDROLASE-HYDROLASE INHIBITOR complex

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