Your Input: | |||||
PF3D7_0630300 | DNA polymerase epsilon catalytic subunit A, putative. (2907 aa) | ||||
PF3D7_0107800 | Double-strand break repair protein MRE11. (1233 aa) | ||||
PF3D7_1129500 | A/G-specific adenine glycosylase, putative. (611 aa) | ||||
PF3D7_1037000 | DNA polymerase zeta catalytic subunit, putative. (2226 aa) | ||||
A0A143ZZR0 | Meiotic recombination protein SPO11, putative. (307 aa) | ||||
PF3D7_1337500 | Uncharacterized protein. (3334 aa) | ||||
PF3D7_0408400 | Uncharacterized protein. (471 aa) | ||||
PF3D7_0706700 | DNA mismatch repair protein MSH2, putative. (873 aa) | ||||
PF3D7_0818700 | DNA helicase, putative. (1223 aa) | ||||
PF08_0048 | Probable ATP-dependent helicase PF08_0048; Catalytic component of a chromatin remodeling complex. Belongs to the SNF2/RAD54 helicase family. SWR1 subfamily. (2082 aa) | ||||
PF3D7_1331100 | DNA polymerase theta, putative. (1244 aa) | ||||
PF3D7_0604600 | DNA helicase, putative. (1712 aa) | ||||
PFF0285c | Probable DNA repair protein RAD50; Essential component of the MRN complex, a complex that possesses single-stranded DNA endonuclease and 3' to 5' exonuclease activities, and plays a central role in double-strand break (DSB) repair, chromosome morphogenesis, DNA repair and meiosis. In the complex, it mediates the ATP-binding and is probably required to bind DNA ends and hold them in close proximity (By similarity). Belongs to the SMC family. RAD50 subfamily. (2236 aa) | ||||
PF3D7_1343400 | DNA repair protein RAD5, putative. (1452 aa) | ||||
PF3D7_1332600 | DNA-(Apurinic or apyrimidinic site) lyase 1, putative. (597 aa) | ||||
PF3D7_1324500 | DEAD box helicase, putative. (1099 aa) | ||||
PF3D7_1317100 | DNA replication licensing factor MCM4; Belongs to the MCM family. (1005 aa) | ||||
PF3D7_1314200 | 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. (2518 aa) | ||||
PF3D7_1304100 | DNA ligase. (912 aa) | ||||
PF3D7_1117800 | DNA mismatch repair protein MLH. (1016 aa) | ||||
PF3D7_1112600 | ATPase, putative. (707 aa) | ||||
PF3D7_1106700 | DNA replication ATP-dependent helicase/nuclease DNA2, putative. (1024 aa) | ||||
PF3D7_1106000 | RuvB-like helicase; Belongs to the RuvB family. (475 aa) | ||||
PF3D7_1104200 | Chromatin remodeling protein. (1426 aa) | ||||
PF3D7_1037600 | TFIIH basal transcription factor complex helicase XPB subunit, putative. (886 aa) | ||||
PF3D7_1008200 | Endonuclease, putative. (388 aa) | ||||
PF3D7_1474300 | DNA repair metallo-beta-lactamase protein, putative. (860 aa) | ||||
PF3D7_1467100 | DNA-3-methyladenine glycosylase, putative. (501 aa) | ||||
PF3D7_1458700 | Exonuclease V, mitochondrial, putative. (353 aa) | ||||
PF3D7_1449400 | Crossover junction endonuclease MUS81, putative. (1271 aa) | ||||
PF3D7_1439100 | DEAD/DEAH box helicase, putative. (2472 aa) | ||||
PF3D7_1433500 | DNA topoisomerase 2; Control of topological states of DNA by transient breakage and subsequent rejoining of DNA strands. Topoisomerase II makes double- strand breaks. (1472 aa) | ||||
PF3D7_1430600 | Endonuclease/exonuclease/phosphatase family protein, putative. (876 aa) | ||||
PF3D7_1429900 | ADP-dependent DNA helicase RecQ. (1440 aa) | ||||
PF3D7_1427500 | DNA mismatch repair protein MSH2, putative. (811 aa) | ||||
PF3D7_1425400 | DEAD/DEAH box helicase, putative. (1236 aa) | ||||
PF3D7_1417800 | DNA helicase. (971 aa) | ||||
PF3D7_1415000 | 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. (322 aa) | ||||
PF3D7_1411400 | Plastid replication-repair enzyme. (2016 aa) | ||||
PF3D7_1408400 | FANCJ-like helicase, putative. (1160 aa) | ||||
PF3D7_1405400 | DNA mismatch repair protein, putative. (1515 aa) | ||||
PF3D7_0411900 | DNA polymerase. (1912 aa) | ||||
PF3D7_1250800 | DNA repair protein rhp16, putative. (1647 aa) | ||||
PF3D7_1239500 | DNA topoisomerase 2; Control of topological states of DNA by transient breakage and subsequent rejoining of DNA strands. Topoisomerase II makes double- strand breaks. (1006 aa) | ||||
Q8I5N7_PLAF7 | Meiotic recombination protein SPO11, putative. (327 aa) | ||||
PF3D7_1211700 | DNA replication licensing factor MCM5, putative; Belongs to the MCM family. (758 aa) | ||||
PF3D7_1211300 | DNA helicase MCM8, putative; Belongs to the MCM family. (1135 aa) | ||||
PF3D7_0803400 | DNA repair and recombination protein RAD54, putative. (1239 aa) | ||||
PF3D7_0809700 | RuvB-like helicase; Belongs to the RuvB family. (520 aa) | ||||
PF3D7_0816800 | Meiotic recombination protein DMC1, putative; Belongs to the RecA family. (347 aa) | ||||
PF3D7_0726300 | DNA mismatch repair protein PMS1, putative. (1330 aa) | ||||
PF3D7_0725000 | Exonuclease I, putative. (1347 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 [...] (821 aa) | ||||
PF3D7_1368800 | DNA repair endonuclease XPF, putative. (1700 aa) | ||||
PF3D7_1362200 | RuvB-like helicase; Belongs to the RuvB family. (483 aa) | ||||
PF3D7_1357500 | DNA helicase, putative. (906 aa) | ||||
PF3D7_1355100 | DNA helicase; Belongs to the MCM family. (929 aa) | ||||
PF3D7_1347100 | 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. (710 aa) | ||||
PF3D7_0505500 | DNA mismatch repair protein; Component of the post-replicative DNA mismatch repair system (MMR). (1350 aa) | ||||
PF3D7_1223300 | DNA gyrase subunit A. (1222 aa) | ||||
PF3D7_1017000 | DNA polymerase. (1094 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 [...] (672 aa) | ||||
PF3D7_0305600 | DNA-(apurinic or apyrimidinic site) lyase; Belongs to the DNA repair enzymes AP/ExoA family. (617 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; Belongs to the Nth/MutY family. (437 aa) | ||||
PF3D7_0419300 | Rad51 domain-containing protein. (346 aa) | ||||
PF3D7_0416300 | DNA helicase MCM9, putative; Belongs to the MCM family. (1465 aa) | ||||
PFD0685c | Structural maintenance of chromosomes protein 3 homolog; Central component of cohesin, a complex required for chromosome cohesion during the cell cycle. The cohesin complex may form a large proteinaceous ring within which sister chromatids can be trapped. At anaphase, the complex is cleaved and dissociates from chromatin, allowing sister chromatids to segregate. Cohesion is coupled to DNA replication and is involved in DNA repair. The cohesin complex plays also an important role in spindle pole assembly during mitosis and in chromosomes movement (By similarity); Belongs to the SMC fami [...] (1193 aa) | ||||
PF3D7_0934100 | TFIIH basal transcription factor complex helicase XPD subunit. (1056 aa) | ||||
PF3D7_0918600 | ATP-dependent DNA helicase Q1. (728 aa) | ||||
PF3D7_0917100 | N-glycosylase/DNA lyase, putative. (757 aa) | ||||
PF3D7_0910500 | DNA repair protein REV1, putative. (1697 aa) | ||||
PF3D7_0527000 | DNA replication licensing factor MCM3, putative; Belongs to the MCM family. (962 aa) | ||||
PF3D7_0514100 | ATP-dependent DNA helicase UvrD. (1441 aa) | ||||
PF3D7_0510500 | Topoisomerase I. (839 aa) | ||||
PF3D7_0624600 | SNF2 helicase, putative. (2719 aa) | ||||
PF3D7_0625300 | DNA polymerase 1, putative. (1444 aa) | ||||
PF3D7_1027600 | Meiotic recombination protein SPO11-2, putative. (336 aa) | ||||
PF3D7_0203900 | 5'-3' exonuclease, N-terminal resolvase-like domain, putative. (577 aa) | ||||
PF3D7_0206000 | DNA repair protein RAD2, putative. (1516 aa) | ||||
PF3D7_0219600 | Replication factor C subunit 1. (904 aa) |