Your Input: | |||||
A0A1F5KZL7 | ANK_REP_REGION domain-containing protein. (85 aa) | ||||
A0A1F5L2I4 | Uncharacterized protein. (92 aa) | ||||
A0A1F5L3G9 | MYND-type domain-containing protein. (230 aa) | ||||
A0A1F5L3V0 | Uncharacterized protein. (149 aa) | ||||
A0A1F5L438 | APH domain-containing protein. (278 aa) | ||||
A0A1F5L4I5 | PHD-type domain-containing protein. (841 aa) | ||||
A0A1F5L5C0 | Protein HIR; Required for replication-independent chromatin assembly and for the periodic repression of histone gene transcription during the cell cycle; Belongs to the WD repeat HIR1 family. (1062 aa) | ||||
A0A1F5L5Q2 | Uncharacterized protein. (428 aa) | ||||
A0A1F5L671 | WD_REPEATS_REGION domain-containing protein. (302 aa) | ||||
A0A1F5L718 | 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) | ||||
A0A1F5L7C6 | RFX-type winged-helix domain-containing protein. (857 aa) | ||||
A0A1F5L7X8 | Uncharacterized protein; Belongs to the class V-like SAM-binding methyltransferase superfamily. Histone-lysine methyltransferase family. SET2 subfamily. (886 aa) | ||||
A0A1F5L8A4 | Uncharacterized protein. (1192 aa) | ||||
A0A1F5L8K1 | Helo_like_N domain-containing protein. (539 aa) | ||||
A0A1F5L8S7 | Chromo domain-containing protein. (230 aa) | ||||
A0A1F5L8X9 | Uncharacterized protein. (455 aa) | ||||
A0A1F5LA17 | 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) | ||||
A0A1F5LA33 | Uncharacterized protein. (513 aa) | ||||
A0A1F5LDW9 | Histone domain-containing protein. (161 aa) | ||||
A0A1F5LF14 | ANK_REP_REGION domain-containing protein. (970 aa) | ||||
A0A1F5LFQ0 | HMG box domain-containing protein. (290 aa) | ||||
A0A1F5LFV4 | WD_REPEATS_REGION domain-containing protein. (510 aa) | ||||
A0A1F5LGV4 | MYND-type domain-containing protein. (560 aa) | ||||
A0A1F5LHZ7 | SHNi-TPR domain-containing protein. (452 aa) | ||||
A0A1F5LI05 | SET domain-containing protein. (672 aa) | ||||
A0A1F5LJC1 | Histone chaperone; Histone chaperone that facilitates histone deposition and histone exchange and removal during nucleosome assembly and disassembly. (278 aa) | ||||
A0A1F5LJY2 | Uncharacterized protein. (480 aa) | ||||
A0A1F5LKZ5 | Uncharacterized protein. (174 aa) | ||||
A0A1F5LL49 | Uncharacterized protein. (812 aa) | ||||
A0A1F5LL66 | TPR_REGION domain-containing protein. (860 aa) | ||||
A0A1F5LLD1 | SET domain-containing protein. (453 aa) | ||||
A0A1F5LLN8 | Histone acetyltransferase type B catalytic subunit; Catalytic component of the histone acetylase B (HAT-B) complex. Has intrinsic substrate specificity that modifies lysine in recognition sequence GXGKXG. Involved in DNA double-strand break repair; Belongs to the HAT1 family. (508 aa) | ||||
A0A1F5LLV5 | HUN domain-containing protein. (741 aa) | ||||
A0A1F5LM11 | Histone H2A; Belongs to the histone H2A family. (132 aa) | ||||
A0A1F5LMM3 | Histone H2B; Belongs to the histone H2B family. (141 aa) | ||||
A0A1F5LMX4 | Uncharacterized protein. (809 aa) | ||||
A0A1F5LMZ4 | Uncharacterized protein. (630 aa) | ||||
A0A1F5LP03 | 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) | ||||
A0A1F5LP19 | WD_REPEATS_REGION domain-containing protein. (476 aa) | ||||
A0A1F5LP21 | SPRY domain-containing protein. (618 aa) | ||||
A0A1F5LPG3 | Histone H3; Belongs to the histone H3 family. (136 aa) | ||||
A0A1F5LQG7 | HMG box domain-containing protein. (875 aa) | ||||
A0A1F5LQL7 | Uncharacterized protein. (408 aa) | ||||
A0A1F5LR62 | Uncharacterized protein. (1482 aa) | ||||
A0A1F5LR91 | Uncharacterized protein. (1104 aa) | ||||
A0A1F5LRH7 | SET domain-containing protein. (355 aa) | ||||
A0A1F5LS60 | MYND-type domain-containing protein. (259 aa) | ||||
A0A1F5LTJ7 | Uncharacterized protein. (512 aa) | ||||
A0A1F5LTX8 | Uncharacterized protein. (1372 aa) | ||||
A0A1F5LUC3 | WD_REPEATS_REGION domain-containing protein. (587 aa) | ||||
A0A1F5LUF8 | DUF2236 domain-containing protein. (459 aa) | ||||
A0A1F5LUK8 | Uncharacterized protein; Belongs to the nucleosome assembly protein (NAP) family. (358 aa) | ||||
A0A1F5LV99 | Uncharacterized protein. (169 aa) | ||||
A0A1F5LVA4 | Uncharacterized protein. (163 aa) | ||||
A0A1F5LVD7 | WD_REPEATS_REGION domain-containing protein. (443 aa) | ||||
A0A1F5LVJ5 | Uncharacterized protein. (142 aa) | ||||
A0A1F5LVR2 | Histone acetyltransferase. (532 aa) | ||||
A0A1F5LVU4 | Uncharacterized protein. (642 aa) | ||||
A0A1F5LVX9 | Histone H2A; Belongs to the histone H2A family. (138 aa) | ||||
A0A1F5LW31 | Sialidase domain-containing protein. (578 aa) | ||||
A0A1F5LW56 | Uncharacterized protein. (302 aa) | ||||
A0A1F5LXD8 | PHD-type domain-containing protein. (547 aa) | ||||
A0A1F5LXF0 | Uncharacterized protein. (419 aa) | ||||
A0A1F5LY79 | WD_REPEATS_REGION domain-containing protein. (1110 aa) | ||||
A0A1F5LYP7 | WD_REPEATS_REGION domain-containing protein. (872 aa) | ||||
A0A1F5LZF8 | 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. (505 aa) |