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3V6E

Crystal Structure of USP2 and a mutant form of Ubiquitin

Summary for 3V6E
Entry DOI10.2210/pdb3v6e/pdb
DescriptorUbiquitin carboxyl-terminal hydrolase 2, Ubiquitin, ZINC ION, ... (6 entities in total)
Functional Keywordsstructural genomics, structural genomics consortium, sgc, ubiquitin, protease, hydrolase-signaling protein complex, hydrolase/signaling protein
Biological sourceHomo sapiens (human)
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Cellular locationCytoplasm . Isoform 4: Nucleus : O75604
Ubiquitin: Cytoplasm : P0CG48
Total number of polymer chains2
Total formula weight52743.88
Authors
Neculai, M.,Ernst, A.,Sidhu, S.,Arrowsmith, C.H.,Edwards, A.M.,Bountra, C.,Weigelt, J.,Dhe-Paganon, S.,Structural Genomics Consortium (SGC) (deposition date: 2011-12-19, release date: 2012-12-19, Last modification date: 2023-09-13)
Primary citationErnst, A.,Avvakumov, G.,Tong, J.,Fan, Y.,Zhao, Y.,Alberts, P.,Persaud, A.,Walker, J.R.,Neculai, A.M.,Neculai, D.,Vorobyov, A.,Garg, P.,Beatty, L.,Chan, P.K.,Juang, Y.C.,Landry, M.C.,Yeh, C.,Zeqiraj, E.,Karamboulas, K.,Allali-Hassani, A.,Vedadi, M.,Tyers, M.,Moffat, J.,Sicheri, F.,Pelletier, L.,Durocher, D.,Raught, B.,Rotin, D.,Yang, J.,Moran, M.F.,Dhe-Paganon, S.,Sidhu, S.S.
A strategy for modulation of enzymes in the ubiquitin system.
Science, 339:590-595, 2013
Cited by
PubMed Abstract: The ubiquitin system regulates virtually all aspects of cellular function. We report a method to target the myriad enzymes that govern ubiquitination of protein substrates. We used massively diverse combinatorial libraries of ubiquitin variants to develop inhibitors of four deubiquitinases (DUBs) and analyzed the DUB-inhibitor complexes with crystallography. We extended the selection strategy to the ubiquitin conjugating (E2) and ubiquitin ligase (E3) enzymes and found that ubiquitin variants can also enhance enzyme activity. Last, we showed that ubiquitin variants can bind selectively to ubiquitin-binding domains. Ubiquitin variants exhibit selective function in cells and thus enable orthogonal modulation of specific enzymatic steps in the ubiquitin system.
PubMed: 23287719
DOI: 10.1126/science.1230161
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

226707

數據於2024-10-30公開中

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