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3SDI

Structure of yeast 20S open-gate proteasome with Compound 20

Summary for 3SDI
Entry DOI10.2210/pdb3sdi/pdb
Related3MG4 3MG6 3MG7 3MG8 3OEU 3OEV 3SDK
Related PRD IDPRD_001071
DescriptorProteasome component Y7, Proteasome component C11, Proteasome component PRE2, ... (18 entities in total)
Functional Keywords20s proteasome, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceSaccharomyces cerevisiae (Baker's yeast)
More
Cellular locationCytoplasm: P23639 P22141 P30656 P23724 P30657 P38624 P23638 P40303 P32379 P40302 P21242 P21243 P25043 P25451
Total number of polymer chains28
Total formula weight707777.99
Authors
Sintchak, M.D. (deposition date: 2011-06-09, release date: 2012-06-13, Last modification date: 2023-09-13)
Primary citationBlackburn, C.,Barrett, C.,Blank, J.L.,Bruzzese, F.J.,Bump, N.,Dick, L.R.,Fleming, P.,Garcia, K.,Hales, P.,Hu, Z.,Jones, M.,Liu, J.X.,Sappal, D.S.,Sintchak, M.D.,Tsu, C.,Gigstad, K.M.
Optimization of a series of dipeptides with a P3 threonine residue as non-covalent inhibitors of the chymotrypsin-like activity of the human 20S proteasome.
Bioorg.Med.Chem.Lett., 20:6581-6586, 2010
Cited by
PubMed: 20875739
DOI: 10.1016/j.bmcl.2010.09.032
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.65 Å)
Structure validation

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数据于2024-04-17公开中

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