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. 2017 Jul 14;7:5475. doi: 10.1038/s41598-017-05806-y

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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A protease-deficient mutant of the 20S proteasome partially suppressed the M288Φ lethal phenotype. PRE4 and pre4-1 cells were transformed with the CUP1 promoter-regulated plasmid expressing wild-type Cdc48 (WT) and mutant Cdc48 with the replacement of E588Q and M288Y. The transformants were grown on media supplemented with 20 µM CuCl₂ at 30 °C for 2 days.