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G8JRY3_ERECY | Endonuclease. (290 aa) | ||||
I6NCV1_ERECY | Uncharacterized protein. (988 aa) | ||||
I6NCR1_ERECY | POLAc domain-containing protein. (1189 aa) | ||||
I6NCQ1_ERECY | DNA repair protein REV1; Deoxycytidyl transferase involved in DNA repair. Transfers a dCMP residue from dCTP to the 3'-end of a DNA primer in a template- dependent reaction. May assist in the first step in the bypass of abasic lesions by the insertion of a nucleotide opposite the lesion. Required for normal induction of mutations by physical and chemical agents; Belongs to the DNA polymerase type-Y family. (873 aa) | ||||
G8JXX5_ERECY | Uncharacterized protein. (722 aa) | ||||
G8JXT1_ERECY | Uncharacterized protein. (370 aa) | ||||
G8JXQ9_ERECY | DNA helicase; Belongs to the MCM family. (882 aa) | ||||
G8JXM6_ERECY | Replication factor C subunit 1. (806 aa) | ||||
G8JXA9_ERECY | DNA_MISMATCH_REPAIR_2 domain-containing protein. (955 aa) | ||||
G8JX68_ERECY | Uncharacterized protein. (199 aa) | ||||
G8JX02_ERECY | DNA_MISMATCH_REPAIR_2 domain-containing protein. (772 aa) | ||||
G8JWQ6_ERECY | AAA domain-containing protein. (356 aa) | ||||
G8JWQ3_ERECY | DNA polymerase alpha subunit B; Accessory subunit of the DNA polymerase alpha complex (also known as the alpha DNA polymerase-primase complex) which plays an essential role in the initiation of DNA synthesis. (652 aa) | ||||
G8JWM3_ERECY | AP_endonuc_2 domain-containing protein. (359 aa) | ||||
FEN1 | Flap endonuclease 1; Structure-specific nuclease with 5'-flap endonuclease and 5'- 3' exonuclease activities involved in DNA replication and repair. During DNA replication, cleaves the 5'-overhanging flap structure that is generated by displacement synthesis when DNA polymerase encounters the 5'-end of a downstream Okazaki fragment. It enters the flap from the 5'-end and then tracks to cleave the flap base, leaving a nick for ligation. Also involved in the long patch base excision repair (LP-BER) pathway, by cleaving within the apurinic/apyrimidinic (AP) site- terminated flap. Acts as [...] (430 aa) | ||||
RRM3 | ATP-dependent DNA helicase RRM3; 5' to 3' DNA replicative helicase recruited to paused replisomes to promote fork progression throughout nonhistone protein- DNA complexes, naturally occurring impediments that are encountered in each S phase where replication forks pauses. Required for timely replication of the telomere and subtelomeric DNA and for wild-type levels of telomeric silencing. Involved in DNA repair during stalled replication fork, regulation of fragile sites expression and essential for genome stability. Plays also a role in mtDNA replication. Has G- quadruplex (G4) unwindi [...] (730 aa) | ||||
G8JWD0_ERECY | DNA_MISMATCH_REPAIR_2 domain-containing protein. (876 aa) | ||||
G8JVN9_ERECY | Uncharacterized protein. (1945 aa) | ||||
G8JVM1_ERECY | Uncharacterized protein. (2019 aa) | ||||
G8JVG1_ERECY | Uncharacterized protein. (1477 aa) | ||||
G8JVF3_ERECY | Double-strand break repair protein; Involved in DNA double-strand break repair (DSBR). Possesses single-strand endonuclease activity and double-strand-specific 3'-5' exonuclease activity. Also involved in meiotic DSB processing. (687 aa) | ||||
G8JV97_ERECY | Endo/exonuclease/phosphatase domain-containing protein. (460 aa) | ||||
G8JV92_ERECY | ENDO3c domain-containing protein. (277 aa) | ||||
G8JV32_ERECY | Uncharacterized protein. (915 aa) | ||||
G8JUZ1_ERECY | DNA_mis_repair domain-containing protein. (718 aa) | ||||
G8JUY1_ERECY | DRMBL domain-containing protein. (585 aa) | ||||
G8JUW4_ERECY | DNA_MISMATCH_REPAIR_2 domain-containing protein; Component of the post-replicative DNA mismatch repair system (MMR). (1038 aa) | ||||
G8JUT3_ERECY | Uncharacterized protein. (1072 aa) | ||||
G8JUQ7_ERECY | Uncharacterized protein. (584 aa) | ||||
G8JUL2_ERECY | KH type-2 domain-containing protein; Belongs to the universal ribosomal protein uS3 family. (328 aa) | ||||
G8JUD9_ERECY | Uncharacterized protein. (1185 aa) | ||||
G8JUB8_ERECY | Structural maintenance of chromosomes protein. (1232 aa) | ||||
G8JU10_ERECY | Uncharacterized protein. (1011 aa) | ||||
G8JTZ7_ERECY | TP6A_N domain-containing protein. (367 aa) | ||||
G8JTK5_ERECY | CBFD_NFYB_HMF domain-containing protein. (181 aa) | ||||
G8JTH1_ERECY | Uncharacterized protein. (624 aa) | ||||
G8JT96_ERECY | RuvB-like helicase; DNA helicase participates in several chromatin remodeling complexes, including the SWR1 and the INO80 complexes. (461 aa) | ||||
G8JT78_ERECY | DNA topoisomerase; Introduces a single-strand break via transesterification at a target site in duplex DNA. Releases the supercoiling and torsional tension of DNA introduced during the DNA replication and transcription by transiently cleaving and rejoining one strand of the DNA duplex. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. Belongs to the type IA topoisomerase family. (638 aa) | ||||
G8JT36_ERECY | Uncharacterized protein. (466 aa) | ||||
UNG1 | Uracil-DNA glycosylase; Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine. (340 aa) | ||||
G8JSV5_ERECY | Uncharacterized protein. (853 aa) | ||||
G8JSQ9_ERECY | Bromo domain-containing protein. (1339 aa) | ||||
G8JSP4_ERECY | Uncharacterized protein. (561 aa) | ||||
G8JSM9_ERECY | Uncharacterized protein. (462 aa) | ||||
G8JSK0_ERECY | Uncharacterized protein. (402 aa) | ||||
G8JSI9_ERECY | DNA repair protein RAD51 homolog; Required both for recombination and for the repair of DNA damage caused by X-rays; Belongs to the RecA family. RAD51 subfamily. (395 aa) | ||||
G8JSC7_ERECY | Ku domain-containing protein. (597 aa) | ||||
G8JS74_ERECY | Uncharacterized protein. (636 aa) | ||||
G8JS66_ERECY | Uncharacterized protein; Belongs to the RecA family. (334 aa) | ||||
G8JS23_ERECY | Uncharacterized protein. (768 aa) | ||||
G8JRW8_ERECY | Ydc2-catalyt domain-containing protein. (389 aa) | ||||
G8JRV8_ERECY | Helicase ATP-binding domain-containing protein. (663 aa) | ||||
G8JRV1_ERECY | DNA_mis_repair domain-containing protein. (742 aa) | ||||
G8JRS4_ERECY | Uncharacterized protein. (1482 aa) | ||||
G8JRC0_ERECY | Uncharacterized protein. (217 aa) | ||||
G8JRA9_ERECY | Uncharacterized protein. (1101 aa) | ||||
G8JR84_ERECY | AAA domain-containing protein. (350 aa) | ||||
G8JR54_ERECY | DNA helicase; Belongs to the MCM family. (774 aa) | ||||
G8JR28_ERECY | Uncharacterized protein. (1618 aa) | ||||
G8JR20_ERECY | UBIQUITIN_CONJUGAT_2 domain-containing protein; Belongs to the ubiquitin-conjugating enzyme family. (170 aa) | ||||
G8JR07_ERECY | Uncharacterized protein. (561 aa) | ||||
SLX1 | Structure-specific endonuclease subunit SLX1; Catalytic subunit of the SLX1-SLX4 structure-specific endonuclease that resolves DNA secondary structures generated during DNA repair and recombination. Has endonuclease activity towards branched DNA substrates, introducing single-strand cuts in duplex DNA close to junctions with ss-DNA. (298 aa) | ||||
G8JQY1_ERECY | DNA topoisomerase I; Releases the supercoiling and torsional tension of DNA introduced during the DNA replication and transcription by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at the specific target site 5'-[CT]CCTTp site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(3'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 5'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand thus r [...] (660 aa) | ||||
G8JQR1_ERECY | MCM domain-containing protein; Belongs to the MCM family. (965 aa) | ||||
G8JQM7_ERECY | AAA domain-containing protein. (332 aa) | ||||
G8JQL3_ERECY | DNA mismatch repair protein; Component of the post-replicative DNA mismatch repair system (MMR). (1233 aa) | ||||
G8JQL1_ERECY | Helicase ATP-binding domain-containing protein. (756 aa) | ||||
G8JQE0_ERECY | DNA_pol_E_B domain-containing protein. (713 aa) | ||||
G8JQC9_ERECY | XPGI domain-containing protein. (758 aa) | ||||
G8JQB5_ERECY | Uncharacterized protein. (273 aa) | ||||
G8JQ58_ERECY | ERCC4 domain-containing protein. (610 aa) | ||||
G8JQ31_ERECY | DNA_MISMATCH_REPAIR_2 domain-containing protein; Component of the post-replicative DNA mismatch repair system (MMR). (954 aa) | ||||
G8JQ27_ERECY | AAA domain-containing protein. (319 aa) | ||||
G8JQ25_ERECY | Uncharacterized protein. (716 aa) | ||||
G8JPV4_ERECY | Uncharacterized protein. (465 aa) | ||||
G8JPU2_ERECY | Ku domain-containing protein. (611 aa) | ||||
G8JPP7_ERECY | Uncharacterized protein. (1058 aa) | ||||
G8JPA1_ERECY | AAA domain-containing protein. (779 aa) | ||||
G8JNW3_ERECY | Uncharacterized protein. (919 aa) | ||||
G8JNT2_ERECY | Uncharacterized protein. (1089 aa) | ||||
NTG1 | Endonuclease III homolog; Bifunctional DNA N-glycosylase with associated apurinic/apyrimidinic (AP) lyase function that catalyzes the first step in base excision repair (BER), the primary repair pathway for the repair of oxidative DNA damage. The DNA N-glycosylase activity releases the damaged DNA base from DNA by cleaving the N-glycosidic bond, leaving an AP site. The AP lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination. Primarily recognizes and repairs oxidative base damage of pyrimidines; Belongs to the Nth/MutY family. (364 aa) | ||||
G8JNP9_ERECY | MutL_C domain-containing protein. (746 aa) | ||||
G8JNP3_ERECY | DNA polymerase. (1469 aa) | ||||
G8JNL8_ERECY | DNA helicase; Belongs to the MCM family. (890 aa) | ||||
G8JNJ0_ERECY | RuvB-like helicase; DNA helicase participates in several chromatin remodeling complexes, including the SWR1 and the INO80 complexes. (467 aa) | ||||
G8JNH4_ERECY | Uncharacterized protein. (1394 aa) | ||||
G8JNE9_ERECY | Uncharacterized protein. (395 aa) | ||||
G8JND8_ERECY | Uncharacterized protein. (1037 aa) | ||||
G8JNB2_ERECY | DNA polymerase; DNA polymerase that functions in several pathways of DNA repair. Involved in base excision repair (BER) responsible for repair of lesions that give rise to abasic (AP) sites in DNA. Also contributes to DNA double-strand break repair by non-homologous end joining and homologous recombination. Has both template-dependent and template- independent (terminal transferase) DNA polymerase activities. Has also a 5'-deoxyribose-5-phosphate lyase (dRP lyase) activity. (531 aa) | ||||
G8JNA2_ERECY | Uncharacterized protein. (681 aa) | ||||
G8JN02_ERECY | DNA helicase; Belongs to the MCM family. (1025 aa) | ||||
G8JMX3_ERECY | Uncharacterized protein. (550 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 [...] (813 aa) | ||||
PIF1 | ATP-dependent DNA helicase PIF1; DNA-dependent ATPase and 5'-3' DNA helicase required for the maintenance of both mitochondrial and nuclear genome stability. Efficiently unwinds G-quadruplex (G4) DNA structures and forked RNA-DNA hybrids. Resolves G4 structures, preventing replication pausing and double-strand breaks (DSBs) at G4 motifs. Involved in the maintenance of telomeric DNA. Inhibits telomere elongation, de novo telomere formation and telomere addition to DSBs via catalytic inhibition of telomerase. Reduces the processivity of telomerase by displacing active telomerase from DNA [...] (884 aa) | ||||
G8JMK8_ERECY | Zinc-hook domain-containing protein. (1298 aa) | ||||
G8JMI9_ERECY | Uncharacterized protein. (1034 aa) | ||||
G8JME6_ERECY | DNA polymerase epsilon catalytic subunit; DNA polymerase II participates in chromosomal DNA replication; Belongs to the DNA polymerase type-B family. (2184 aa) | ||||
G8JM93_ERECY | Telomerase reverse transcriptase; Telomerase is a ribonucleoprotein enzyme essential for the replication of chromosome termini in most eukaryotes. It elongates telomeres. It is a reverse transcriptase that adds simple sequence repeats to chromosome ends by copying a template sequence within the RNA component of the enzyme. (850 aa) | ||||
I6NE88_ERECY | Uncharacterized protein. (206 aa) | ||||
I6NE69_ERECY | DNA polymerase. (1092 aa) | ||||
I6NE21_ERECY | Uncharacterized protein. (1497 aa) | ||||
I6NDZ4_ERECY | RECA_2 domain-containing protein. (450 aa) | ||||
I6NDM1_ERECY | DNA polymerase. (1475 aa) | ||||
I6NDL6_ERECY | Uncharacterized protein. (1331 aa) | ||||
I6NDJ2_ERECY | Uncharacterized protein. (871 aa) | ||||
I6NDJ1_ERECY | HORMA domain-containing protein. (246 aa) | ||||
I6NDI5_ERECY | Uncharacterized protein. (770 aa) | ||||
I6NDC4_ERECY | RECA_2 domain-containing protein. (482 aa) | ||||
I6ND28_ERECY | TRAM domain-containing protein; Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family. (592 aa) | ||||
I6ND06_ERECY | Uncharacterized protein. (1410 aa) |