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. 2020 Oct 22;16(10):e1009125. doi: 10.1371/journal.pgen.1009125

Fig 4. Domain architecture of proteins affected by compensatory mutations in I349ΔH2A.Z and I349ΔH2A.Z:H2A.Z.

Fig 4

(A) Essential subunit of Rpd3S complex (FGRAMPH1_01G23597; 1,225 aa). The annotation “Ile673fs” indicates the position of a frameshift starting at position 673 of the protein in I349ΔH2A.Z (an isoleucine in wild-type). (B) Swr1 (FGRAMPH1_01G18675; 1,691 aa). The annotation “His852Pro” indicates the replacement of a histidine at position 852 by a proline in I349ΔH2A.Z:H2A.Z. Domain accession numbers in NCBI CDD/SPARCKLE database: TNG2 superfamily = CL34876, PHD = CL22851, PHD2_PHF12_Rco1 = CD15534, HAS = PFAM07529, DEXQc_SRCAP = CD18003, SF2_C_SNF = CD18793. Architectures are displayed with SnapGene Viewer 5.0.6.