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A0A090LXI4 | Chromosome segregation protein Spc25. (261 aa) | ||||
A0A090LXS2 | Unnamed product. (465 aa) | ||||
A0A090LY11 | Rad21/Rec8-like protein, N-terminal. (594 aa) | ||||
A0A090LY49 | DNA-binding domain. (433 aa) | ||||
A0A090LYX4 | Origin recognition complex, subunit 5. (512 aa) | ||||
A0A090LYY2 | Structural maintenance of chromosomes protein. (1232 aa) | ||||
A0A090LZ15 | Unnamed product. (1037 aa) | ||||
A0A090LZ31 | BRCT domain. (433 aa) | ||||
A0A090LZL2 | Structural maintenance of chromosomes protein. (1204 aa) | ||||
A0A090M0Y2 | ATP-dependent DNA helicase; Belongs to the helicase family. RecQ subfamily. (736 aa) | ||||
A0A090M1A1 | Serine/threonine-protein kinase, active site. (728 aa) | ||||
A0A090M1K2 | Checkpoint protein Hus1/Mec3. (315 aa) | ||||
A0A090M1P8 | Helicase, C-terminal. (1099 aa) | ||||
A0A090M1T7 | Fibronectin, type III. (2452 aa) | ||||
A0A090M1U8 | DNA mismatch repair protein MutS-like,N-terminal. (1042 aa) | ||||
A0A090M1X2 | 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. (336 aa) | ||||
A0A090M219 | Piezo family. (2430 aa) | ||||
A0A090M290 | DNA topoisomerase, type IA, central region,subdomain 2. (1046 aa) | ||||
A0A090M2I9 | Polynucleotide 3'-phosphatase. (236 aa) | ||||
A0A090M2L8 | DNA mismatch repair protein Pms1/Mlh2. (829 aa) | ||||
A0A090M2L9 | 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. (850 aa) | ||||
A0A090M376 | DNA-(apurinic or apyrimidinic site) lyase; Belongs to the DNA repair enzymes AP/ExoA family. (351 aa) | ||||
A0A090M3G2 | Structural maintenance of chromosomes protein 6. (1058 aa) | ||||
A0A090M3J2 | Transcription factor CBF/NF-Y/archaeal histone. (148 aa) | ||||
A0A090M3U8 | Phox/Bem1p. (628 aa) | ||||
A0A090M434 | DNA helicase; Belongs to the MCM family. (758 aa) | ||||
A0A090M4B1 | P-loop containing nucleoside triphosphate hydrolase. (837 aa) | ||||
A0A090M4F0 | Armadillo-type fold. (1302 aa) | ||||
A0A090M4W1 | DNA replication factor Dna2, N-terminal. (1417 aa) | ||||
A0A090M4X5 | IQ motif, EF-hand binding site. (1483 aa) | ||||
A0A090M500 | DNA-(apurinic or apyrimidinic site) lyase; Belongs to the DNA repair enzymes AP/ExoA family. (372 aa) | ||||
A0A090M513 | Zinc finger, GRF-type. (420 aa) | ||||
A0A090M5D6 | Rad9. (407 aa) | ||||
A0A090M5H5 | P-loop containing nucleoside triphosphate hydrolase. (927 aa) | ||||
A0A090M5K8 | Haemerythrin/HHE cation-binding motif. (888 aa) | ||||
A0A090M5L0 | DNA repair nuclease, XPF-type/Helicase. (695 aa) | ||||
A0A090M5N0 | Unnamed product. (427 aa) | ||||
A0A090M5P7 | DNA primase large subunit, eukaryotic/archaeal. (511 aa) | ||||
A0A090M5Q4 | DNA replication complex GINS protein SLD5; The GINS complex plays an essential role in the initiation of DNA replication; Belongs to the GINS4/SLD5 family. (265 aa) | ||||
A0A090M625 | Mini-chromosome maintenance complex protein 4; Belongs to the MCM family. (625 aa) | ||||
A0A090M630 | P-loop containing nucleoside triphosphate hydrolase. (744 aa) | ||||
A0A090M6F5 | P-loop containing nucleoside triphosphate hydrolase; Belongs to the MCM family. (881 aa) | ||||
A0A090M6H1 | CDC45 family. (582 aa) | ||||
A0A090M6H5 | Structural maintenance of chromosomes protein. (1251 aa) | ||||
A0A090M6Q2 | P-loop containing nucleoside triphosphate hydrolase. (611 aa) | ||||
A0A090M6R3 | Breast cancer type 1 susceptibility protein (BRCA1). (589 aa) | ||||
A0A090M773 | P-loop containing nucleoside triphosphate hydrolase; Belongs to the MCM family. (770 aa) | ||||
A0A090M783 | 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. (751 aa) | ||||
A0A090M7A5 | GINS complex, subunit Psf2. (184 aa) | ||||
A0A090M7B5 | NADH-ubiquinone oxidoreductase, 21kDa subunit,N-terminal. (92 aa) | ||||
A0A090M7R9 | MAGE protein. (322 aa) | ||||
A0A090M7S5 | DNA polymerase. (1175 aa) | ||||
A0A090M861 | ATP-dependent helicase, C-terminal. (1100 aa) | ||||
A0A090M894 | Pyruvate phosphate dikinase,PEP/pyruvate-binding. (1303 aa) | ||||
A0A090M8X2 | DNA-repair protein, UmuC-like, N-terminal. (523 aa) | ||||
A0A090M9A2 | BRCT domain. (1032 aa) | ||||
A0A090M9A7 | DNA polymerase delta, subunit 4. (116 aa) | ||||
A0A090M9A8 | DNA ligase. (778 aa) | ||||
A0A090M9F5 | Helicase, C-terminal. (1352 aa) | ||||
A0A090M9G2 | Breast cancer type 1 susceptibility protein (BRCA1). (517 aa) | ||||
A0A090M9H8 | PIK-related kinase, FATC; Belongs to the PI3/PI4-kinase family. (2855 aa) | ||||
A0A090M9L0 | DNA mismatch repair protein, MSH2; Component of the post-replicative DNA mismatch repair system (MMR). (926 aa) | ||||
A0A090MA11 | DNA helicase; Belongs to the MCM family. (839 aa) | ||||
A0A090MA71 | DNA ligase, ATP-dependent, N-terminal. (993 aa) | ||||
A0A090MAZ7 | Uncharacterized protein. (297 aa) | ||||
A0A090MB94 | DNA topoisomerase 2; Control of topological states of DNA by transient breakage and subsequent rejoining of DNA strands. Topoisomerase II makes double- strand breaks. (1413 aa) | ||||
A0A090MBJ3 | XPG/Rad2 endonuclease. (231 aa) | ||||
A0A090MBP1 | Sister chromatid cohesion protein. (1713 aa) | ||||
A0A090MCI5 | Cyclophilin-like peptidyl-prolyl cis-trans isomerase domain. (305 aa) | ||||
A0A090MCU8 | DNA recombination and repair protein Rad51,C-terminal. (363 aa) | ||||
A0A090MCZ2 | DNA recombination and repair protein Rad51,C-terminal. (363 aa) | ||||
A0A090MD02 | Von Willebrand factor, type A. (655 aa) | ||||
A0A090MD09 | Ribonuclease; Endonuclease that specifically degrades the RNA of RNA-DNA hybrids; Belongs to the RNase HII family. (309 aa) | ||||
A0A090N2T6 | Helix-hairpin-helix motif, class 2. (328 aa) | ||||
A0A090N2X1 | Kinetochore protein Nuf2. (450 aa) | ||||
A0A090N311 | DNA recombination and repair protein Rad51,C-terminal. (299 aa) | ||||
A0A090N314 | Peptidase M3B, oligopeptidase F, N-terminal. (615 aa) | ||||
A0A090N354 | BRCT domain. (810 aa) | ||||
A0A090N363 | Unnamed product. (445 aa) | ||||
A0A090N399 | Zinc finger, CCHC-type; Plays an important role in the control of DNA replication and the maintenance of replication fork stability. Belongs to the CSM3 family. (351 aa) | ||||
A0A090N3A3 | Origin recognition complex subunit 1; Component of the origin recognition complex (ORC) that binds origins of replication. DNA-binding is ATP-dependent, however specific DNA sequences that define origins of replication have not been identified so far. ORC is required to assemble the pre-replication complex necessary to initiate DNA replication. (848 aa) | ||||
A0A090N3B1 | P-loop containing nucleoside triphosphate hydrolase. (358 aa) | ||||
A0A090N3J5 | P-loop containing nucleoside triphosphate hydrolase. (931 aa) | ||||
A0A090N3M7 | DNA mismatch repair protein; Component of the post-replicative DNA mismatch repair system (MMR). (1211 aa) | ||||
A0A090N3N1 | Proliferating cell nuclear antigen; This protein is an auxiliary protein of DNA polymerase delta and is involved in the control of eukaryotic DNA replication by increasing the polymerase's processibility during elongation of the leading strand; Belongs to the PCNA family. (261 aa) | ||||
A0A090N3N2 | Rad21/Rec8-like protein, N-terminal. (500 aa) | ||||
A0A090N3U7 | Non-structural maintenance of chromosomes element 1. (241 aa) | ||||
A0A090N3X8 | Von Willebrand factor, type A. (636 aa) | ||||
A0A090N410 | Structural maintenance of chromosomes protein. (1207 aa) | ||||
A0A090N433 | DNA recombination and repair protein Rad51,C-terminal. (337 aa) | ||||
A0A090N445 | 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. (668 aa) | ||||
A0A090N458 | DNA-repair protein, UmuC-like, N-terminal. (553 aa) | ||||
A0A090N488 | DNA recombination/repair protein RecA,monomer-monomer interface; Belongs to the RecA family. (382 aa) | ||||
A0A090N493 | BRCT domain. (221 aa) | ||||
A0A090N4C2 | Unnamed product. (906 aa) | ||||
A0A090N4C7 | DNA recombination and repair protein Rad51,C-terminal; Belongs to the RecA family. (289 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 [...] (710 aa) | ||||
A0A090N4U1 | DNA primase large subunit, eukaryotic/archaeal. (517 aa) | ||||
A0A090N4V2 | DNA repair protein RAD51 homolog; Binds to single and double-stranded DNA and exhibits DNA- dependent ATPase activity. Unwinds duplex DNA. Component of the meiotic recombination pathway. Seems to play a role in mediating chromosome homology search, chromosome pairing and synapsis at early stages and probably chromosome crossing-over at later stages in meiosis. Probably is involved in the repair of meiotic double strand breaks (DBSs) and in homologous recombination; Belongs to the RecA family. RAD51 subfamily. (340 aa) | ||||
A0A090N4V3 | Ribosomal protein S5 domain 2-type fold,subgroup. (671 aa) | ||||
A0A090N4Y0 | DNA polymerase epsilon subunit; Participates in DNA repair and in chromosomal DNA replication; Belongs to the DNA polymerase epsilon subunit B family. (552 aa) | ||||
A0A096P770 | P-loop containing nucleoside triphosphate hydrolase. (1233 aa) | ||||
A0A096P7A8 | Helicase, C-terminal. (1140 aa) | ||||
A0A096P7C3 | DNA topoisomerase 2; Control of topological states of DNA by transient breakage and subsequent rejoining of DNA strands. Topoisomerase II makes double- strand breaks. (693 aa) | ||||
A0A096P7D7 | Pyruvate phosphate dikinase,PEP/pyruvate-binding. (1522 aa) | ||||
A0A096P7F3 | Donson. (419 aa) | ||||
A0A096P7I3 | Thioredoxin-like fold. (243 aa) | ||||
A0A096P7L9 | Unnamed product. (443 aa) | ||||
A0A096P7W1 | Origin recognition complex, subunit 3. (967 aa) | ||||
A0A096P845 | Serine/threonine-protein kinase, active site. (575 aa) | ||||
A0A096P860 | DNA mismatch repair protein MutS-homologue MSH6. (383 aa) | ||||
A0A096P8D7 | Condensin complex subunit 2; Regulatory subunit of the condensin complex, a complex required for conversion of interphase chromatin into mitotic-like condense chromosomes. (679 aa) | ||||
A0A096P8E6 | Ribosomal protein S5 domain 2-type fold,subgroup. (712 aa) | ||||
A0A096P8F0 | Structure-specific endonuclease subunit SLX1 homolog; Catalytic subunit of a heterodimeric 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; Belongs to the SLX1 family. (386 aa) | ||||
A0A096P8M7 | 5'-3' exonuclease, C-terminal domain. (514 aa) | ||||
A0A096P8N0 | Unnamed product. (549 aa) | ||||
A0A096P8U0 | Helix-turn-helix, base-excision DNA repair,C-terminal. (404 aa) | ||||
A0A096P8W6 | Double-stranded RNA-binding domain. (397 aa) | ||||
A0A096P8W9 | Pseudouridine synthase I, TruA, N-terminal. (632 aa) | ||||
A0A096P8Y1 | P-loop containing nucleoside triphosphate hydrolase. (888 aa) | ||||
A0A096P972 | DNA gyrase/topoisomerase IV, subunit A,C-terminal beta-pinwheel. (911 aa) | ||||
A0A096P995 | WD40 repeat. (858 aa) | ||||
A0A096P9K4 | Pentapeptide repeat. (232 aa) | ||||
A0A096P9S7 | P-loop containing nucleoside triphosphate hydrolase. (348 aa) | ||||
A0A096P9U7 | DNA-(apurinic or apyrimidinic site) lyase; Belongs to the DNA repair enzymes AP/ExoA family. (236 aa) | ||||
A0A096P9V5 | Replication protein A subunit; Component of the replication protein A complex (RPA) required for DNA recombination, repair and replication. The activity of RPA is mediated by single-stranded DNA binding and protein interactions. Probably involved in repair of double-strand DNA breaks (DSBs) induced by genotoxic stresses. (576 aa) | ||||
A0A096PAL4 | Sister chromatid cohesion protein Dcc1. (407 aa) | ||||
NTH1 | 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. (355 aa) | ||||
A0A096PAV9 | Replication protein A subunit; Component of the replication protein A complex (RPA) required for DNA recombination, repair and replication. The activity of RPA is mediated by single-stranded DNA binding and protein interactions. Probably involved in repair of double-strand DNA breaks (DSBs) induced by genotoxic stresses. (808 aa) | ||||
A0A096PAW2 | Integral membrane protein TerC,riboswitch-linked. (281 aa) | ||||
A0A096PB20 | Origin recognition complex, subunit 2. (478 aa) | ||||
A0A096PB81 | Nuclear condensin complex subunit 3, C-terminal domain. (984 aa) | ||||
A0A096PBM0 | DNA helicase; Belongs to the MCM family. (969 aa) | ||||
A0A096PBR4 | GINS complex, subunit Psf1. (198 aa) | ||||
A0A096PBR9 | NAD-dependent DNA ligase, N-terminal. (832 aa) | ||||
A0A096PBS1 | Unnamed product. (264 aa) | ||||
A0A1Y5I503 | DNA topoisomerase I, DNA binding, mixed alpha/beta motif, eukaryotic-type. (783 aa) | ||||
Q00S32_OSTTA | C-5 cytosine methyltransferase; Belongs to the class I-like SAM-binding methyltransferase superfamily. C5-methyltransferase family. (625 aa) | ||||
Q00SU5_OSTTA | Unnamed product. (248 aa) | ||||
Q00SZ4_OSTTA | Restriction endonuclease type II-like. (204 aa) | ||||
Q00TC0_OSTTA | Unnamed product. (197 aa) | ||||
Q00TY0_OSTTA | GINS complex, subunit Psf3. (220 aa) | ||||
Q00UC7_OSTTA | DNA helicase (DNA repair), Rad3 type. (1048 aa) | ||||
Q00UQ6_OSTTA | Endonuclease III-like, iron-sulphur cluster loop motif. (296 aa) | ||||
Q00WX0_OSTTA | DNA primase; Belongs to the eukaryotic-type primase small subunit family. (452 aa) | ||||
Q00X67_OSTTA | Replication protein A, C-terminal. (262 aa) | ||||
Q00XQ6_OSTTA | P-loop containing nucleoside triphosphate hydrolase. (354 aa) | ||||
Q00XT2_OSTTA | Helix-hairpin-helix motif, class 2. (987 aa) | ||||
Q00XW5_OSTTA | PIK-related kinase, FATC; Belongs to the PI3/PI4-kinase family. (3010 aa) | ||||
Q00Y71_OSTTA | Cohesin loading factor. (687 aa) | ||||
Q00YE0_OSTTA | DNA polymerase alpha/epsilon, subunit B. (453 aa) | ||||
Q00YR2_OSTTA | DNA repair metallo-beta-lactamase. (607 aa) | ||||
Q00YV3_OSTTA | DNA polymerase epsilon catalytic subunit; DNA polymerase II participates in chromosomal DNA replication; Belongs to the DNA polymerase type-B family. (2339 aa) | ||||
Q00YX1_OSTTA | DNA-repair protein, UmuC-like, N-terminal. (595 aa) | ||||
Q00Z03_OSTTA | 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. (650 aa) | ||||
Q00Z11_OSTTA | Ribonuclease H-like domain. (455 aa) | ||||
Q00ZM8_OSTTA | Acyl-CoA N-acyltransferase. (363 aa) | ||||
Q010G9_OSTTA | Serine/threonine-protein kinase, active site; Belongs to the protein kinase superfamily. (333 aa) | ||||
Q010V0_OSTTA | Replication factor Mcm10. (594 aa) | ||||
Q011U8_OSTTA | Restriction endonuclease type II-like. (369 aa) | ||||
Q011Z0_OSTTA | SNF2-related. (730 aa) | ||||
Q012B7_OSTTA | P-loop containing nucleoside triphosphate hydrolase. (342 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 [...] (389 aa) | ||||
Q013S3_OSTTA | Restriction endonuclease type II-like. (987 aa) | ||||
Q013X2_OSTTA | DNA polymerase. (1530 aa) | ||||
Q015N2_OSTTA | DNA-repair protein, UmuC-like, N-terminal. (605 aa) | ||||
Q015S8_OSTTA | Endonuclease/exonuclease/phosphatase. (387 aa) | ||||
Q015V4_OSTTA | Integral membrane protein TerC. (358 aa) | ||||
Q016H0_OSTTA | Beta-lactamase-like. (517 aa) | ||||
Q016K9_OSTTA | Polynucleotide kinase 3-phosphatase, eukaryota. (202 aa) | ||||
Q018Q3_OSTTA | Kinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (500 aa) | ||||
Q018W6_OSTTA | Unnamed product. (246 aa) | ||||
Q01B29_OSTTA | DNA mismatch repair protein MutS-like,N-terminal. (1062 aa) | ||||
Q01BC5_OSTTA | Methyl-CpG DNA binding. (813 aa) | ||||
Q01BG6_OSTTA | DEAD2. (970 aa) | ||||
Q01BJ4_OSTTA | Kinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (771 aa) | ||||
Q01C10_OSTTA | DNA mismatch repair protein MutS-like,N-terminal. (1077 aa) | ||||
Q01CA7_OSTTA | 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. (842 aa) | ||||
Q01CG6_OSTTA | Unnamed product. (940 aa) | ||||
Q01DB1_OSTTA | HD/PDEase domain. (229 aa) | ||||
Q01DX9_OSTTA | 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. (1284 aa) | ||||
Q01EF3_OSTTA | Timeless protein. (614 aa) | ||||
Q01F26_OSTTA | DNA helicase; Belongs to the MCM family. (707 aa) | ||||
Q01F45_OSTTA | P-loop containing nucleoside triphosphate hydrolase. (341 aa) | ||||
Q01F52_OSTTA | P-loop containing nucleoside triphosphate hydrolase. (553 aa) | ||||
Q01FG0_OSTTA | RecF/RecN/SMC, N-terminal. (1075 aa) | ||||
Q01FP0_OSTTA | EGF-like, conserved site. (524 aa) | ||||
Q01FV9_OSTTA | STAG. (1097 aa) | ||||
Q01GB6_OSTTA | Nuclear transport factor 2, Eukaryote. (141 aa) | ||||
Q01GH7_OSTTA | Mini-chromosome maintenance complex-binding protein. (624 aa) | ||||
Q01GI0_OSTTA | DNA helicase; Belongs to the MCM family. (873 aa) | ||||
Q01GV4_OSTTA | DNA repair protein Rad50, eukaryotes. (1313 aa) |