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A0A3F3Q5Y8 | Muts domain V-domain-containing protein. (1653 aa) | ||||
A0A3F3QIA2 | Kinase-like domain-containing protein. (376 aa) | ||||
A0A3F3QIF4 | SIR2 family histone deacetylase. (612 aa) | ||||
A0A3F3QIM6 | DSS1/SEM1 family-domain-containing protein. (88 aa) | ||||
A0A3F3QIR2 | Uncharacterized protein. (363 aa) | ||||
A0A3F3QIW4 | 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. (629 aa) | ||||
A0A3F3QJ09 | Uncharacterized protein. (275 aa) | ||||
A0A3F3QJ19 | P-loop containing nucleoside triphosphate hydrolase protein. (577 aa) | ||||
SLX4 | Structure-specific endonuclease subunit SLX4; Regulatory 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. (830 aa) | ||||
A0A3F3QJK8 | ATP-dependent DNA helicase II subunit 2; Single-stranded DNA-dependent ATP-dependent helicase. (714 aa) | ||||
A0A3F3QKM2 | Uncharacterized protein. (403 aa) | ||||
A0A3F3QKS1 | Non-structural maintenance of chromosomes element 4; Component of the SMC5-SMC6 complex, that promotes sister chromatid alignment after DNA damage and facilitates double-stranded DNA breaks (DSBs) repair via homologous recombination between sister chromatids. (444 aa) | ||||
A0A3F3QLC7 | Sld5 domain-containing protein. (178 aa) | ||||
A0A3F3QI67 | DNA mismatch repair protein Msh5. (920 aa) | ||||
A0A3F3QFT7 | Transcriptional regulation of mitochondrial recombination-domain-containing protein. (350 aa) | ||||
A0A3F3QGM4 | Kinetochore component CENP-S-domain-containing protein. (102 aa) | ||||
A0A3F3QI36 | 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. (347 aa) | ||||
A0A3F3QHM3 | DNA topoisomerase 2; Control of topological states of DNA by transient breakage and subsequent rejoining of DNA strands. Topoisomerase II makes double- strand breaks. (1708 aa) | ||||
A0A3F3QHD8 | DNA helicase; Belongs to the MCM family. (961 aa) | ||||
A0A3F3QH94 | 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. (797 aa) | ||||
A0A3F3QH71 | RPA_C domain-containing protein. (288 aa) | ||||
A0A3F3QH54 | SNF2 family N-terminal domain-domain-containing protein. (892 aa) | ||||
A0A3F3PHV2 | Uncharacterized protein. (226 aa) | ||||
A0A3F3PKH7 | Uncharacterized protein. (197 aa) | ||||
A0A3F3PL36 | Uncharacterized protein. (200 aa) | ||||
A0A3F3PL38 | Kinase-like domain-containing protein. (491 aa) | ||||
A0A3F3PLP1 | DNA ligase. (1009 aa) | ||||
A0A3F3PMT7 | Uncharacterized protein. (555 aa) | ||||
A0A3F3PN32 | DUF1767 domain-containing protein. (237 aa) | ||||
A0A3F3PNZ9 | Ribonuclease H-like domain-containing protein. (458 aa) | ||||
A0A3F3PQA1 | DNA mismatch repair protein; Component of the post-replicative DNA mismatch repair system (MMR). (1118 aa) | ||||
A0A3F3PQZ5 | Uncharacterized protein. (1024 aa) | ||||
A0A3F3PR65 | WD domain protein. (409 aa) | ||||
A0A3F3PSU9 | Rec8 like protein-domain-containing protein. (589 aa) | ||||
A0A3F3PSW9 | 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. (606 aa) | ||||
A0A3F3PT54 | Mitochondrial genome maintenance MGM101. (265 aa) | ||||
A0A3F3PT93 | Kinase-like domain-containing protein. (365 aa) | ||||
A0A3F3PTY6 | ERCC4 domain-containing protein. (977 aa) | ||||
A0A3F3PTY8 | AAA_23 domain-containing protein. (339 aa) | ||||
A0A3F3PU45 | DNA_LIGASE_A3 domain-containing protein. (1063 aa) | ||||
A0A3F3PU55 | DNA helicase; Belongs to the MCM family. (720 aa) | ||||
A0A3F3PUB6 | DNA ligase. (834 aa) | ||||
A0A3F3PUG0 | Transcriptional adapter 2; Functions as component of the transcription regulatory histone acetylation (HAT) complexes SAGA, SALSA and ADA. SAGA is involved in RNA polymerase II-dependent transcriptional regulation. (520 aa) | ||||
A0A3F3PUI8 | Cenp-O kinetochore centromere component-domain-containing protein. (356 aa) | ||||
A0A3F3PUM8 | CDC45 family. (860 aa) | ||||
A0A3F3PVK7 | Uncharacterized protein. (374 aa) | ||||
A0A3F3PWP6 | Sister chromatid cohesion protein. (1772 aa) | ||||
A0A3F3PWZ3 | P-loop containing nucleoside triphosphate hydrolase protein. (1441 aa) | ||||
A0A3F3PX30 | Vacuolar protein 14 C-terminal Fig4p binding-domain-containing protein. (1756 aa) | ||||
A0A3F3PYB0 | MAGE-domain-containing protein. (344 aa) | ||||
A0A3F3PYC6 | DNA polymerase. (1668 aa) | ||||
A0A3F3PYN2 | Uncharacterized protein. (712 aa) | ||||
A0A3F3PZ42 | Mus7/MMS22 family-domain-containing protein. (2391 aa) | ||||
A0A3F3Q0D7 | Uncharacterized protein. (240 aa) | ||||
A0A3F3Q0Q7 | DNA helicase; Belongs to the MCM family. (898 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. (424 aa) | ||||
A0A3F3Q175 | Nse1 non-SMC component of SMC5-6 complex-domain-containing protein. (394 aa) | ||||
A0A3F3Q1V4 | Spo11/DNA topoisomerase VI subunit A. (395 aa) | ||||
A0A3F3Q290 | Mono-functional DNA-alkylating methyl methanesulfonate N-term-domain-containing protein. (1278 aa) | ||||
A0A3F3Q294 | DNA helicase; Belongs to the MCM family. (887 aa) | ||||
A0A3F3Q2C7 | SNF2 family N-terminal domain-domain-containing protein. (1008 aa) | ||||
A0A3F3Q2X5 | Meiotic nuclear division protein 1; Required for proper homologous chromosome pairing and efficient cross-over and intragenic recombination during meiosis. Belongs to the MND1 family. (231 aa) | ||||
A0A3F3Q3E1 | Uncharacterized protein. (234 aa) | ||||
A0A3F3Q3W6 | Crossover junction endonuclease mus81. (583 aa) | ||||
A0A3F3Q403 | Rad2-like endonuclease. (875 aa) | ||||
A0A3F3Q4C6 | DNA polymerase subunit Cdc27. (447 aa) | ||||
A0A3F3Q4Q9 | Fanconi-associated nuclease; Nuclease required for the repair of DNA interstrand cross- links (ICL). Acts as a 5'-3' exonuclease that anchors at a cut end of DNA and cleaves DNA successively at every third nucleotide, allowing to excise an ICL from one strand through flanking incisions. Belongs to the FAN1 family. (851 aa) | ||||
A0A3F3Q4U5 | Uncharacterized protein. (577 aa) | ||||
A0A3F3Q4V1 | ATP-dependent DNA helicase; Belongs to the helicase family. RecQ subfamily. (541 aa) | ||||
A0A3F3Q501 | Mating-type switching protein Swi10. (327 aa) | ||||
A0A3F3QFI6 | Pkinase-domain-containing protein. (1141 aa) | ||||
A0A3F3QF50 | SPOC like C-terminal domain-containing protein. (653 aa) | ||||
A0A3F3QEW0 | Replication factor A protein 3. (122 aa) | ||||
A0A3F3QEC4 | Uncharacterized protein. (751 aa) | ||||
KAE1 | tRNA N6-adenosine threonylcarbamoyltransferase; Component of the EKC/KEOPS complex that is required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. The complex is probably involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37. KAE1 likely plays a direct catalytic role in this reaction, but requires other protein(s) of the complex to fulfill this activity. The EKC/KEOPS complex also promotes both telomere uncapping and telomere elongation. Th [...] (361 aa) | ||||
A0A3F3QDW8 | Aldehyde/histidinol dehydrogenase; Belongs to the aldehyde dehydrogenase family. (631 aa) | ||||
A0A3F3QDS4 | Pachytene checkpoint component Pch2; Belongs to the AAA ATPase family. (486 aa) | ||||
A0A3F3QDQ6 | Checkpoint protein; Belongs to the HUS1 family. (363 aa) | ||||
A0A3F3QD28 | RING-type domain-containing protein. (272 aa) | ||||
A0A3F3QD16 | Muts domain V-domain-containing protein. (920 aa) | ||||
A0A3F3QD11 | Rad1/Rec1/Rad17. (376 aa) | ||||
A0A3F3QCV8 | Sld5 domain-containing protein. (223 aa) | ||||
A0A3F3QCT0 | Uncharacterized protein. (77 aa) | ||||
A0A3F3QCH3 | Uncharacterized protein. (156 aa) | ||||
A0A3F3QBW0 | Zinc-finger of the MIZ type in Nse subunit-domain-containing protein. (541 aa) | ||||
A0A3F3QA68 | ATP-dependent DNA helicase. (1568 aa) | ||||
A0A3F3Q9G0 | Rad51-domain-containing protein; Belongs to the RecA family. (337 aa) | ||||
A0A3F3Q8T4 | Endonuclease. (334 aa) | ||||
A0A3F3Q8N1 | DNA ligase. (884 aa) | ||||
A0A3F3Q8L9 | DNA helicase; Belongs to the MCM family. (958 aa) | ||||
A0A3F3Q8B8 | Thermolysin metallopeptidase. (369 aa) | ||||
A0A3F3Q7Y4 | Putative DNA helicase ino80. (1697 aa) | ||||
A0A3F3Q7W6 | S-adenosyl-L-methionine-dependent methyltransferase. (346 aa) | ||||
A0A3F3Q7W3 | Swi5-domain-containing protein. (107 aa) | ||||
A0A3F3Q6S5 | Histidine kinase-like ATPase. (730 aa) | ||||
A0A3F3Q6R1 | Pkinase-domain-containing protein; Belongs to the mitochondrial carrier (TC 2.A.29) family. (2165 aa) | ||||
A0A3F3Q6I7 | Serine/threonine-protein phosphatase. (426 aa) | ||||
A0A3F3Q622 | Uncharacterized protein. (759 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 [...] (807 aa) |