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D5G4G8_TUBMM | Uncharacterized protein. (146 aa) | ||||
D5G561_TUBMM | Histone H2A; Belongs to the histone H2A family. (134 aa) | ||||
D5G562_TUBMM | Histone H2B; Belongs to the histone H2B family. (138 aa) | ||||
D5G566_TUBMM | H15 domain-containing protein. (228 aa) | ||||
D5G6N7_TUBMM | PH domain-containing protein. (685 aa) | ||||
D5G7G8_TUBMM | Uncharacterized protein. (1134 aa) | ||||
D5G7U3_TUBMM | Uncharacterized protein. (901 aa) | ||||
D5G9C4_TUBMM | SET domain-containing protein. (355 aa) | ||||
D5G9H9_TUBMM | Uncharacterized protein. (586 aa) | ||||
D5GAU8_TUBMM | PHD domain-containing protein. (673 aa) | ||||
D5GBC0_TUBMM | Histone H4; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. (103 aa) | ||||
D5GCV3_TUBMM | Histone H4; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. (143 aa) | ||||
D5GDB9_TUBMM | Histone domain-containing protein. (152 aa) | ||||
D5GEI8_TUBMM | Uncharacterized protein; Belongs to the class V-like SAM-binding methyltransferase superfamily. Histone-lysine methyltransferase family. SET2 subfamily. (892 aa) | ||||
D5GF07_TUBMM | Histone domain-containing protein. (136 aa) | ||||
D5GFN9_TUBMM | SET domain-containing protein. (593 aa) | ||||
D5GHA6_TUBMM | Histone-lysine N-methyltransferase, H3 lysine-79 specific; Histone methyltransferase that specifically methylates histone H3 to form H3K79me. This methylation is required for telomere silencing and for the pachytene checkpoint during the meiotic cell cycle by allowing the recruitment of RAD9 to double strand breaks. Nucleosomes are preferred as substrate compared to free histones. (377 aa) | ||||
D5GHJ7_TUBMM | B30.2/SPRY domain-containing protein. (376 aa) | ||||
D5GI24_TUBMM | WD_REPEATS_REGION domain-containing protein. (334 aa) | ||||
D5GIC1_TUBMM | BAH domain-containing protein. (411 aa) | ||||
D5GID0_TUBMM | Uncharacterized protein. (846 aa) | ||||
D5GIN5_TUBMM | WD_REPEATS_REGION domain-containing protein. (460 aa) | ||||
D5GJS2_TUBMM | PHD-type domain-containing protein. (534 aa) | ||||
D5GKI6_TUBMM | Histone-lysine N-methyltransferase, H3 lysine-4 specific; Catalytic component of the COMPASS (Set1C) complex that specifically mono-, di- and trimethylates histone H3 to form H3K4me1/2/3, which subsequently plays a role in telomere length maintenance and transcription elongation regulation. (1200 aa) | ||||
D5GKT7_TUBMM | WD_REPEATS_REGION domain-containing protein. (472 aa) | ||||
D5GM40_TUBMM | Uncharacterized protein. (489 aa) | ||||
D5GNG2_TUBMM | Uncharacterized protein. (258 aa) | ||||
D5GP65_TUBMM | Uncharacterized protein. (1697 aa) |