Your Input: | |||||
A0A1L9XA74 | Uncharacterized protein. (425 aa) | ||||
A0A1L9WKV2 | Uncharacterized protein. (1702 aa) | ||||
A0A1L9WKY0 | Transcription elongation factor SPT4; The SPT4-SPT5 complex mediates both activation and inhibition of transcription elongation, and plays a role in pre-mRNA processing. This complex seems to be important for the stability of the RNA polymerase II elongation machinery on the chromatin template but not for the inherent ability of this machinery to translocate down the gene. (120 aa) | ||||
A0A1L9WLR0 | Uncharacterized protein. (390 aa) | ||||
A0A1L9WLS2 | Telo_bind domain-containing protein. (621 aa) | ||||
A0A1L9WM34 | Checkpoint protein; Belongs to the HUS1 family. (381 aa) | ||||
A0A1L9WM77 | Uncharacterized protein. (634 aa) | ||||
A0A1L9WM91 | Uncharacterized protein. (596 aa) | ||||
A0A1L9WN95 | Uncharacterized protein. (423 aa) | ||||
A0A1L9WNT2 | Deacetylase sirtuin-type domain-containing protein. (492 aa) | ||||
A0A1L9WNV1 | Uncharacterized protein. (362 aa) | ||||
A0A1L9WP30 | Uncharacterized protein. (1449 aa) | ||||
A0A1L9WPC3 | Uncharacterized protein. (904 aa) | ||||
A0A1L9WPE6 | Uncharacterized protein. (214 aa) | ||||
A0A1L9WPZ3 | Serine/threonine-protein kinase. (1135 aa) | ||||
A0A1L9WQ37 | Uncharacterized protein. (258 aa) | ||||
A0A1L9WQS1 | GFA domain-containing protein. (154 aa) | ||||
A0A1L9WRB4 | DHR10 domain-containing protein. (464 aa) | ||||
A0A1L9WRC9 | Uncharacterized protein. (178 aa) | ||||
A0A1L9WRI3 | 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. (516 aa) | ||||
A0A1L9WRX3 | HTH myb-type domain-containing protein. (881 aa) | ||||
A0A1L9WSW1 | Histone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. (359 aa) | ||||
A0A1L9WSX4 | Uncharacterized protein. (346 aa) | ||||
A0A1L9WTA8 | Protein kinase domain-containing protein. (812 aa) | ||||
A0A1L9WTQ0 | G-patch domain-containing protein. (372 aa) | ||||
A0A1L9WTS6 | Uncharacterized protein. (774 aa) | ||||
A0A1L9WUP2 | Uncharacterized protein. (1066 aa) | ||||
A0A1L9WUQ2 | Uncharacterized protein. (287 aa) | ||||
A0A1L9WV05 | Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit; The B regulatory subunit might modulate substrate selectivity and catalytic activity, and also might direct the localization of the catalytic enzyme to a particular subcellular compartment. (679 aa) | ||||
A0A1L9WV26 | Uncharacterized protein. (377 aa) | ||||
A0A1L9WV73 | TPR_REGION domain-containing protein. (766 aa) | ||||
A0A1L9WVM9 | Uncharacterized protein. (308 aa) | ||||
A0A1L9WW09 | Uncharacterized protein. (667 aa) | ||||
A0A1L9WW34 | DNA helicase; Belongs to the MCM family. (720 aa) | ||||
A0A1L9WWB6 | GFA domain-containing protein. (163 aa) | ||||
A0A1L9WWL3 | Ima1_N domain-containing protein. (871 aa) | ||||
A0A1L9WWR5 | Transcription elongation factor Spt6; Plays a role in maintenance of chromatin structure during RNA polymerase II transcription elongation thereby repressing transcription initiation from cryptic promoters. Mediates the reassembly of nucleosomes onto the promoters of at least a selected set of genes during repression; the nucleosome reassembly is essential for transcriptional repression; Belongs to the SPT6 family. (1417 aa) | ||||
A0A1L9WWT9 | Protein kinase domain-containing protein. (496 aa) | ||||
A0A1L9WWW9 | CENP-T_C domain-containing protein. (428 aa) | ||||
A0A1L9WX56 | Stc1 domain-containing protein. (275 aa) | ||||
A0A1L9WX71 | RNA-dependent RNA polymerase. (1331 aa) | ||||
A0A1L9WX97 | Uncharacterized protein. (679 aa) | ||||
A0A1L9WXC1 | J domain-containing protein. (324 aa) | ||||
A0A1L9WXJ8 | Condensin complex subunit 1; Regulatory subunit of the condensin complex, a complex required for conversion of interphase chromatin into mitotic-like condense chromosomes. The condensin complex probably introduces positive supercoils into relaxed DNA in the presence of type I topoisomerases and converts nicked DNA into positive knotted forms in the presence of type II topoisomerases. (1187 aa) | ||||
A0A1L9WXL5 | 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. (533 aa) | ||||
A0A1L9WXU0 | Serine/threonine-protein phosphatase; Belongs to the PPP phosphatase family. (324 aa) | ||||
A0A1L9WY17 | Stn1 domain-containing protein. (303 aa) | ||||
A0A1L9WYH5 | Chromo domain-containing protein. (854 aa) | ||||
A0A1L9WZ89 | Uncharacterized protein. (109 aa) | ||||
A0A1L9WZB6 | PAT1 domain-containing protein. (826 aa) | ||||
A0A1L9WZH3 | Uncharacterized protein. (83 aa) | ||||
A0A1L9WZN4 | Serine/threonine-protein kinase Tel1; Serine/threonine protein kinase which activates checkpoint signaling upon genotoxic stresses such as ionizing radiation (IR), ultraviolet light (UV), or DNA replication stalling, thereby acting as a DNA damage sensor. Recognizes the substrate consensus sequence [ST]- Q. Phosphorylates histone H2A to form H2AS128ph (gamma-H2A) at sites of DNA damage, involved in the regulation of DNA damage response mechanism. Required for the control of telomere length and genome stability; Belongs to the PI3/PI4-kinase family. ATM subfamily. (2897 aa) | ||||
A0A1L9WZT7 | Uncharacterized protein. (1169 aa) | ||||
A0A1L9X0N1 | CULLIN_2 domain-containing protein; Belongs to the cullin family. (894 aa) | ||||
A0A1L9X0V0 | Uncharacterized protein; Belongs to the short-chain dehydrogenases/reductases (SDR) family. (265 aa) | ||||
A0A1L9WEL1 | Uncharacterized protein. (129 aa) | ||||
A0A1L9WEM1 | Uncharacterized protein. (718 aa) | ||||
A0A1L9WEP1 | Replication protein A subunit; As part of the replication protein A (RPA/RP-A), a single- stranded DNA-binding heterotrimeric complex, may play an essential role in DNA replication, recombination and repair. Binds and stabilizes single-stranded DNA intermediates, preventing complementary DNA reannealing and recruiting different proteins involved in DNA metabolism. (605 aa) | ||||
A0A1L9WGG1 | SAP domain-containing protein. (654 aa) | ||||
A0A1L9WGH9 | Uncharacterized protein. (362 aa) | ||||
A0A1L9WGS1 | Protein kinase domain-containing protein. (341 aa) | ||||
A0A1L9WGT9 | HORMA domain-containing protein. (225 aa) | ||||
A0A1L9WGX3 | Uncharacterized protein. (686 aa) | ||||
A0A1L9WH99 | Uncharacterized protein. (226 aa) | ||||
A0A1L9WHK4 | Uncharacterized protein. (1054 aa) | ||||
A0A1L9WKC1 | Kinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (910 aa) | ||||
A0A1L9WJZ5 | Uncharacterized protein. (200 aa) | ||||
A0A1L9X1D1 | Csm1 domain-containing protein. (535 aa) | ||||
A0A1L9X1L0 | GFA domain-containing protein. (150 aa) | ||||
A0A1L9X202 | Chromo domain-containing protein. (227 aa) | ||||
A0A1L9X270 | Uncharacterized protein. (488 aa) | ||||
A0A1L9X2D3 | Uncharacterized protein. (1240 aa) | ||||
A0A1L9X2Q7 | DNA helicase; Belongs to the MCM family. (883 aa) | ||||
A0A1L9X3H8 | Spc7 domain-containing protein. (1572 aa) | ||||
A0A1L9X3M5 | Uncharacterized protein. (440 aa) | ||||
A0A1L9X3T0 | Uncharacterized protein; Belongs to the CGI121/TPRKB family. (199 aa) | ||||
A0A1L9X3W7 | ATP-dependent DNA helicase II subunit 2; Single-stranded DNA-dependent ATP-dependent helicase. (723 aa) | ||||
A0A1L9X422 | Uncharacterized protein. (182 aa) | ||||
A0A1L9X4B7 | Uncharacterized protein. (629 aa) | ||||
A0A1L9X4F5 | Protein kinase domain-containing protein; Belongs to the protein kinase superfamily. (389 aa) | ||||
A0A1L9X4N7 | NUDE_C domain-containing protein. (598 aa) | ||||
MCM7 | DNA replication licensing factor MCM7; Acts as component of the mcm2-7 complex (mcm complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the mcm2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differential [...] (805 aa) | ||||
A0A1L9X5T5 | Uncharacterized protein. (831 aa) | ||||
A0A1L9X616 | Zn(2)-C6 fungal-type domain-containing protein. (710 aa) | ||||
A0A1L9X659 | Rif1_N domain-containing protein. (1800 aa) | ||||
A0A1L9X6V8 | Uncharacterized protein. (247 aa) | ||||
A0A1L9X7C6 | Uncharacterized protein. (357 aa) | ||||
A0A1L9X891 | RPA_C domain-containing protein. (268 aa) | ||||
A0A1L9X8H2 | Uncharacterized protein. (622 aa) | ||||
A0A1L9X8Q4 | Spindle pole body component. (987 aa) | ||||
A0A1L9X8S2 | Uncharacterized protein. (502 aa) | ||||
A0A1L9X8V2 | Histone deacetylase; Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. (775 aa) | ||||
A0A1L9X937 | ATP-grasp domain-containing protein. (471 aa) | ||||
A0A1L9X9G2 | TYR_PHOSPHATASE_2 domain-containing protein. (601 aa) | ||||
A0A1L9X9I0 | PHD-type domain-containing protein. (900 aa) | ||||
A0A1L9X9T8 | Uncharacterized protein. (897 aa) | ||||
A0A1L9XAB2 | Uncharacterized protein. (728 aa) |