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. 2020 Nov 4;11:5564. doi: 10.1038/s41467-020-19390-9

Table 2.

Saccharomyces cerevisiae strains used in this study.

Name Genotype, plasmids Notes Origin
CEN.PK 113-5D MATa; ura3-52 Haploid laboratory strain with uracil auxotrophy, mating type ‘a’ Euroscarf57
CEN01 CEN.PK 113-5D, pRS416 Prototrophic strain with empty URA3 vector This study
REC. EC CEN.PK 113-5D with modified YGR067CY392*, pRS416 Strain expressing a truncated Ygr067cp where Tyrosine at position 392 is replaced with a stop codon This study
REC. EC adh2Δ CEN.PK 113-5D with modified YGR067CY392*, pRS416 Strain expressing a truncated Ygr067cp where Tyrosine at position 392 is replaced with a stop codon, and Adh2p deletion This study
REC. EC shm1Δ CEN.PK 113-5D with modified YGR067CY392*, pRS416 Strain expressing a truncated Ygr067cp where Tyrosine at position 392 is replaced with a stop codon, and Shm1p deletion This study
REC. EC cat8Δ CEN.PK 113-5D with modified YGR067CY392*, pRS416 Strain expressing a truncated Ygr067cp where Tyrosine at position 392 is replaced with a stop codon, and Cat8p deletion This study
REC. EC acs1Δ CEN.PK 113-5D with modified YGR067CY392*, pRS416 Strain expressing a truncated Ygr067cp where Tyrosine at position 392 is replaced with a stop codon, and Acs1p deletion This study