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spo11 | Meiosis-specific topoisomerase Spo11. (466 aa) | ||||
msh1 | DNA mismatch repair protein; Component of the post-replicative DNA mismatch repair system (MMR). (1249 aa) | ||||
NCU07554 | Structural maintenance of chromosomes protein. (1204 aa) | ||||
NCU04445 | Uncharacterized protein. (1217 aa) | ||||
NCU06438 | DNA repair helicase RAD25. (862 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 [...] (824 aa) | ||||
msh-3 | DNA mismatch repair protein msh-3; Component of the post-replicative DNA mismatch repair system (MMR). Heterodimerizes with msh-2 to form MutS beta, which binds to DNA mismatches thereby initiating DNA repair. Msh-3 provides substrate- binding and substrate specificity to the complex. When bound, the MutS beta heterodimer bends the DNA helix and shields approximately 20 base pairs. Acts mainly to repair insertion-deletion loops (IDLs) from 2 to 13 nucleotides in size, but can also repair base-base and single insertion-deletion mismatches that occur during replication. After mismatch bi [...] (1145 aa) | ||||
mph1 | ATP-dependent DNA helicase mph1; ATP-dependent DNA helicase involved in DNA damage repair by homologous recombination and in genome maintenance. Capable of unwinding D-loops. Plays a role in limiting crossover recombinants during mitotic DNA double-strand break (DSB) repair. Component of a FANCM-MHF complex which promotes gene conversion at blocked replication forks, probably by reversal of the stalled fork. Belongs to the DEAD box helicase family. DEAH subfamily. FANCM sub-subfamily. (1168 aa) | ||||
qde-3 | RecQ family helicase. (2330 aa) | ||||
NCU00517 | Cell cycle checkpoint protein RAD17. (944 aa) | ||||
NCU00832 | Uncharacterized protein. (402 aa) | ||||
NCU02539 | DNA helicase; Belongs to the MCM family. (1013 aa) | ||||
crf9-1 | RING-13 protein. (1214 aa) | ||||
crf2-1 | Chromatin-remodeling ATPase INO80; ATPase component of the INO80 complex which remodels chromatin by shifting nucleosomes and is involved in DNA repair. (1997 aa) | ||||
hel-2 | RuvB-like helicase 2; DNA helicase which participates in several chromatin remodeling complexes, including the SWR1 and the INO80 complexes. The SWR1 complex mediates the ATP-dependent exchange of histone H2A for the H2A variant H2A.Z leading to transcriptional regulation of selected genes by chromatin remodeling. The INO80 complex remodels chromatin by shifting nucleosomes and is involved in DNA repair. Also involved in pre-rRNA processing (By similarity); Belongs to the RuvB family. (481 aa) | ||||
hel-1 | RuvB-like helicase 1; DNA helicase which participates in several chromatin remodeling complexes, including the SWR1 and the INO80 complexes. The SWR1 complex mediates the ATP-dependent exchange of histone H2A for the H2A variant H2A.Z leading to transcriptional regulation of selected genes by chromatin remodeling. The INO80 complex remodels chromatin by shifting nucleosomes and is involved in DNA repair. Also involved in pre-rRNA processing (By similarity); Belongs to the RuvB family. (458 aa) | ||||
Prd-6 | Regulator of nonsense transcripts 1 homolog; Eliminates the production of nonsense-containing RNAs. Belongs to the DNA2/NAM7 helicase family. (1093 aa) | ||||
crf8-1 | TBP associated factor, variant. (1893 aa) | ||||
NCU00401 | Uncharacterized protein. (458 aa) | ||||
NCU07519 | ATP-dependent DNA helicase; Belongs to the helicase family. (813 aa) | ||||
NCU04749 | DNA replication helicase Dna2. (1727 aa) | ||||
NCU06338 | DNA topoisomerase 2. (1994 aa) | ||||
mlh-1 | DNA mismatch repair protein mutL, variant. (751 aa) | ||||
NCU03337 | ATP-dependent DNA helicase; Belongs to the helicase family. RecQ subfamily. (483 aa) | ||||
crf6-1 | Chromodomain helicase, variant. (1664 aa) | ||||
NCU07395 | DNA-binding protein SMUBP-2. (736 aa) | ||||
crf3-1 | SNF2-family ATP dependent chromatin remodeling factor snf21. (1482 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. (931 aa) | ||||
NCU09384 | DNA_MISMATCH_REPAIR_2 domain-containing protein. (872 aa) | ||||
mlh-2 | MUTL-2. (772 aa) | ||||
NCU06767 | Replication factor C subunit 1. (1086 aa) | ||||
eaf-1 | Chromatin modification-related protein eaf-1; Component of the NuA4 histone acetyltransferase complex which is involved in transcriptional activation of selected genes principally by acetylation of nucleosomal histone H4 and H2A. The NuA4 complex is also involved in DNA repair (By similarity). (2189 aa) | ||||
atrx | ATRX. (1869 aa) | ||||
csb | DNA repair protein Rhp26/Rad26. (1173 aa) | ||||
pms-1 | DNA mismatch repair protein. (1157 aa) | ||||
crf5-1 | Chromatin remodeling factor 5-1. (907 aa) | ||||
mus-51 | ATP-dependent DNA helicase II subunit 1; Single-stranded DNA-dependent ATP-dependent helicase. Involved in non-homologous end joining (NHEJ) DNA double strand break repair. DNA-binding is sequence-independent but has a high affinity to nicks in double-stranded DNA and to the ends of duplex DNA. Binds to naturally occurring chromosomal ends, and therefore provides chromosomal end protection. Required also for telomere recombination to repair telomeric ends in the absence of telomerase. ku70, of the ku70/ku80 heterodimer, binds to the stem loop of tlc1, the RNA component of telomerase. I [...] (645 aa) | ||||
NCU06365 | DEAD/DEAH box helicase. (1175 aa) | ||||
NCU05194 | DNA helicase; Belongs to the MCM family. (972 aa) | ||||
NCU08806 | RECA_2 domain-containing protein. (442 aa) | ||||
NCU06627 | Uncharacterized protein. (1190 aa) | ||||
NCU03091 | Uncharacterized protein. (441 aa) | ||||
csa | DNA excision repair protein. (1269 aa) | ||||
crf7-1 | Chromodomain-helicase-DNA-binding protein 4. (1726 aa) | ||||
NCU04786 | SNF2 family helicase/ATPase. (1197 aa) | ||||
mus-50 | UvrD/REP helicase. (1105 aa) | ||||
dbp-9 | ATP-dependent RNA helicase dbp-9; ATP-binding RNA helicase involved in the biogenesis of 60S ribosomal subunits and is required for the normal formation of 25S and 5.8S rRNAs; Belongs to the DEAD box helicase family. DDX56/DBP9 subfamily. (676 aa) | ||||
NCU09793 | DEAD/DEAH box DNA helicase. (1563 aa) | ||||
col-25 | Fungal specific transcription factor. (1194 aa) | ||||
NCU05756 | Peptidase M4. (449 aa) | ||||
NCU02402 | SMC_N domain-containing protein. (1167 aa) | ||||
msh6 | DNA mismatch repair protein; Component of the post-replicative DNA mismatch repair system (MMR). (1246 aa) | ||||
NCU08883 | SNF2_N domain-containing protein. (355 aa) | ||||
mus-41 | DNA repair protein rad5; Probable helicase, member of the UBC2/RAD6 epistasis group. Functions with DNA repair protein uvs-2/rad18 in error-free postreplication DNA repair. Involved in the maintenance of wild-type rates of instability of simple repetitive sequences such as poly(GT) repeats. Seems to be involved in maintaining a balance which acts in favor of error-prone non-homologous joining during DNA double-strand breaks repairs (By similarity). (1228 aa) | ||||
crf10-1 | Clockswitch protein CSW-1. (1011 aa) | ||||
crf1-1 | Helicase swr-1; Catalytic component of the SWR1 complex which mediates the ATP-dependent exchange of histone H2A for the H2A variant H2A.Z leading to transcriptional regulation of selected genes by chromatin remodeling; Belongs to the SNF2/RAD54 helicase family. SWR1 subfamily. (1845 aa) | ||||
crf4-1 | Chromatin remodelling complex ATPase chain ISW1. (1126 aa) | ||||
NCU01625 | DNA repair helicase RAD3. (806 aa) | ||||
mus-52 | ATP-dependent DNA helicase II subunit 2; Single-stranded DNA-dependent ATP-dependent helicase. Involved in non-homologous end joining (NHEJ) DNA double strand break repair. DNA-binding is sequence-independent but has a high affinity to nicks in double-stranded DNA and to the ends of duplex DNA. Binds to naturally occurring chromosomal ends, and therefore provides chromosomal end protection. Required also for telomere recombination to repair telomeric ends in the absence of telomerase. ku70, of the ku70/ku80 heterodimer, binds to the stem loop of tlc1, the RNA component of telomerase. I [...] (725 aa) | ||||
uvs-6 | UVS6. (1314 aa) | ||||
mus-25 | DNA repair and recombination protein RAD54. (835 aa) | ||||
NCU06833 | UvrD_C_2 domain-containing protein. (722 aa) | ||||
mei-3 | 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. (353 aa) | ||||
NCU08706 | AAA family ATPase. (622 aa) | ||||
NCU05385 | MutL_C domain-containing protein. (937 aa) | ||||
NCU01340 | Uncharacterized protein. (215 aa) | ||||
NCU03649 | Uncharacterized protein. (608 aa) | ||||
rad16 | DNA repair protein RAD16. (1079 aa) | ||||
NCU03652 | SNF2 family helicase/ATPase. (1548 aa) | ||||
mus-8 | Ubiquitin-conjugating enzyme E2 2; Catalyzes the covalent attachment of ubiquitin to other proteins. Plays a role in transcription regulation by catalyzing the monoubiquitination of histone H2B to form H2BK123ub1. H2BK123ub1 gives a specific tag for epigenetic transcriptional activation and is also a prerequisite for H3K4me and H3K79me formation. Also involved in postreplication repair of UV-damaged DNA, in N-end rule-dependent protein degradation and in sporulation; Belongs to the ubiquitin-conjugating enzyme family. (151 aa) | ||||
msh-2 | DNA mismatch repair protein msh-2; Involved in post-replicative DNA-mismatch repair. Binds to mismatch-containing DNA (By similarity). (937 aa) | ||||
NCU01771 | DNA repair protein rhp57. (510 aa) | ||||
chl1 | ATP-dependent DNA helicase chl1; ATP-dependent DNA helicase important for chromosome transmission and normal cell cycle progression in G(2)/M (By similarity). May have a role in changing DNA topology to allow the loading of proteins involved in maintaining sister chromatid cohesion in the vicinity of the centromeres (By similarity). Has a specific role in chromosome segregation during meiosis II (By similarity). (1068 aa) | ||||
msh4 | MutS ortholog 4 protein. (1318 aa) |