STRINGSTRING
F4NRM6_BATDJ F4NRM6_BATDJ FEN1 FEN1 F4NRV7_BATDJ F4NRV7_BATDJ F4NSE6_BATDJ F4NSE6_BATDJ F4NTP0_BATDJ F4NTP0_BATDJ F4NTP7_BATDJ F4NTP7_BATDJ F4NTT3_BATDJ F4NTT3_BATDJ F4NUJ4_BATDJ F4NUJ4_BATDJ F4NUQ5_BATDJ F4NUQ5_BATDJ F4NUZ5_BATDJ F4NUZ5_BATDJ F4NV56_BATDJ F4NV56_BATDJ F4NV66_BATDJ F4NV66_BATDJ F4NV73_BATDJ F4NV73_BATDJ F4NVJ0_BATDJ F4NVJ0_BATDJ F4NVK4_BATDJ F4NVK4_BATDJ F4NVP0_BATDJ F4NVP0_BATDJ F4NVZ2_BATDJ F4NVZ2_BATDJ F4NWA6_BATDJ F4NWA6_BATDJ F4NWB6_BATDJ F4NWB6_BATDJ F4NWF8_BATDJ F4NWF8_BATDJ F4NWW9_BATDJ F4NWW9_BATDJ F4NX90_BATDJ F4NX90_BATDJ F4NXH5_BATDJ F4NXH5_BATDJ F4NXZ4_BATDJ F4NXZ4_BATDJ F4NY30_BATDJ F4NY30_BATDJ F4NY32_BATDJ F4NY32_BATDJ MCM7 MCM7 F4NYR6_BATDJ F4NYR6_BATDJ F4NYW3_BATDJ F4NYW3_BATDJ F4NZ43_BATDJ F4NZ43_BATDJ F4NZC8_BATDJ F4NZC8_BATDJ UNG1 UNG1 F4NZP5_BATDJ F4NZP5_BATDJ SLX1 SLX1 BATDEDRAFT_183 BATDEDRAFT_183 NTH1 NTH1 F4P158_BATDJ F4P158_BATDJ F4P1G9_BATDJ F4P1G9_BATDJ F4P1J7_BATDJ F4P1J7_BATDJ BATDEDRAFT_653 BATDEDRAFT_653 F4P2D7_BATDJ F4P2D7_BATDJ F4P2U0_BATDJ F4P2U0_BATDJ F4P2W5_BATDJ F4P2W5_BATDJ F4P382_BATDJ F4P382_BATDJ F4P3N4_BATDJ F4P3N4_BATDJ F4P4H2_BATDJ F4P4H2_BATDJ F4P4Y0_BATDJ F4P4Y0_BATDJ F4P551_BATDJ F4P551_BATDJ F4P553_BATDJ F4P553_BATDJ F4P5J4_BATDJ F4P5J4_BATDJ F4P5P3_BATDJ F4P5P3_BATDJ F4P5T9_BATDJ F4P5T9_BATDJ F4P658_BATDJ F4P658_BATDJ F4P6D4_BATDJ F4P6D4_BATDJ F4P6G8_BATDJ F4P6G8_BATDJ F4P6R2_BATDJ F4P6R2_BATDJ F4P6S8_BATDJ F4P6S8_BATDJ F4P6X8_BATDJ F4P6X8_BATDJ F4P727_BATDJ F4P727_BATDJ F4P7B1_BATDJ F4P7B1_BATDJ F4P7I5_BATDJ F4P7I5_BATDJ F4P7U2_BATDJ F4P7U2_BATDJ F4P8S6_BATDJ F4P8S6_BATDJ F4P902_BATDJ F4P902_BATDJ F4P973_BATDJ F4P973_BATDJ F4P980_BATDJ F4P980_BATDJ F4P9G7_BATDJ F4P9G7_BATDJ F4P9K5_BATDJ F4P9K5_BATDJ F4P9T4_BATDJ F4P9T4_BATDJ F4P9X1_BATDJ F4P9X1_BATDJ F4P9Y1_BATDJ F4P9Y1_BATDJ F4PA52_BATDJ F4PA52_BATDJ F4PB72_BATDJ F4PB72_BATDJ F4PB73_BATDJ F4PB73_BATDJ F4PBE6_BATDJ F4PBE6_BATDJ F4PCC1_BATDJ F4PCC1_BATDJ F4PCF3_BATDJ F4PCF3_BATDJ F4PCH2_BATDJ F4PCH2_BATDJ F4PCX6_BATDJ F4PCX6_BATDJ F4PDL2_BATDJ F4PDL2_BATDJ F4PDU1_BATDJ F4PDU1_BATDJ F4PE31_BATDJ F4PE31_BATDJ F4PE38_BATDJ F4PE38_BATDJ F4PE73_BATDJ F4PE73_BATDJ F4PEI2_BATDJ F4PEI2_BATDJ F4PEQ8_BATDJ F4PEQ8_BATDJ F4PFE7_BATDJ F4PFE7_BATDJ F4PFF0_BATDJ F4PFF0_BATDJ F4PFV2_BATDJ F4PFV2_BATDJ
Nodes:
Network nodes represent proteins
splice isoforms or post-translational modifications are collapsed, i.e. each node represents all the proteins produced by a single, protein-coding gene locus.
Node Color
colored nodes:
query proteins and first shell of interactors
white nodes:
second shell of interactors
Node Content
empty nodes:
proteins of unknown 3D structure
filled nodes:
a 3D structure is known or predicted
Edges:
Edges represent protein-protein associations
associations are meant to be specific and meaningful, i.e. proteins jointly contribute to a shared function; this does not necessarily mean they are physically binding to each other.
Known Interactions
from curated databases
experimentally determined
Predicted Interactions
gene neighborhood
gene fusions
gene co-occurrence
Others
textmining
co-expression
protein homology
Your Input:
F4NRM6_BATDJENDO3c domain-containing protein. (332 aa)
FEN1Flap 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 [...] (388 aa)
F4NRV7_BATDJUncharacterized protein. (1065 aa)
F4NSE6_BATDJUncharacterized protein. (581 aa)
F4NTP0_BATDJDNA topoisomerase 2; Control of topological states of DNA by transient breakage and subsequent rejoining of DNA strands. Topoisomerase II makes double- strand breaks. (1218 aa)
F4NTP7_BATDJUncharacterized protein. (1198 aa)
F4NTT3_BATDJHelicase C-terminal domain-containing protein. (104 aa)
F4NUJ4_BATDJUncharacterized protein. (2388 aa)
F4NUQ5_BATDJUncharacterized protein. (319 aa)
F4NUZ5_BATDJUncharacterized protein. (284 aa)
F4NV56_BATDJATP-dependent DNA helicase; Belongs to the helicase family. RecQ subfamily. (818 aa)
F4NV66_BATDJRECA_2 domain-containing protein. (422 aa)
F4NV73_BATDJMCM domain-containing protein; Belongs to the MCM family. (886 aa)
F4NVJ0_BATDJDNA_MISMATCH_REPAIR_2 domain-containing protein. (952 aa)
F4NVK4_BATDJUncharacterized protein. (825 aa)
F4NVP0_BATDJUncharacterized protein. (823 aa)
F4NVZ2_BATDJHelicase ATP-binding domain-containing protein. (996 aa)
F4NWA6_BATDJUncharacterized protein. (912 aa)
F4NWB6_BATDJUncharacterized protein. (1238 aa)
F4NWF8_BATDJUncharacterized protein. (600 aa)
F4NWW9_BATDJDNA polymerase epsilon catalytic subunit; DNA polymerase II participates in chromosomal DNA replication; Belongs to the DNA polymerase type-B family. (2300 aa)
F4NX90_BATDJRECA_2 domain-containing protein. (354 aa)
F4NXH5_BATDJDNA ligase. (621 aa)
F4NXZ4_BATDJDNA_mis_repair domain-containing protein. (664 aa)
F4NY30_BATDJExpressed protein. (238 aa)
F4NY32_BATDJUncharacterized protein. (101 aa)
MCM7DNA 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 [...] (759 aa)
F4NYR6_BATDJUncharacterized protein. (473 aa)
F4NYW3_BATDJDNA mismatch repair protein; Component of the post-replicative DNA mismatch repair system (MMR). (1194 aa)
F4NZ43_BATDJUncharacterized protein. (914 aa)
F4NZC8_BATDJUncharacterized protein. (480 aa)
UNG1Uracil-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. (286 aa)
F4NZP5_BATDJUncharacterized protein. (704 aa)
SLX1Structure-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. (447 aa)
BATDEDRAFT_183Uncharacterized protein. (1186 aa)
NTH1Endonuclease 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. (266 aa)
F4P158_BATDJATP-dependent DNA helicase; Belongs to the helicase family. (273 aa)
F4P1G9_BATDJUncharacterized protein. (769 aa)
F4P1J7_BATDJHelicase ATP-binding domain-containing protein. (639 aa)
BATDEDRAFT_653BRCT domain-containing protein. (696 aa)
F4P2D7_BATDJHelicase ATP-binding domain-containing protein. (758 aa)
F4P2U0_BATDJStructural maintenance of chromosomes protein. (1192 aa)
F4P2W5_BATDJHelicase ATP-binding domain-containing protein. (359 aa)
F4P382_BATDJHelicase ATP-binding domain-containing protein. (604 aa)
F4P3N4_BATDJDNA polymerase. (1125 aa)
F4P4H2_BATDJDNA 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 [...] (824 aa)
F4P4Y0_BATDJMre11_DNA_bind domain-containing protein; Belongs to the MRE11/RAD32 family. (885 aa)
F4P551_BATDJUncharacterized protein. (2044 aa)
F4P553_BATDJDNA_MISMATCH_REPAIR_2 domain-containing protein. (754 aa)
F4P5J4_BATDJKu domain-containing protein. (840 aa)
F4P5P3_BATDJUncharacterized protein. (613 aa)
F4P5T9_BATDJDRMBL domain-containing protein. (346 aa)
F4P658_BATDJExpressed protein. (467 aa)
F4P6D4_BATDJENDO3c domain-containing protein. (306 aa)
F4P6G8_BATDJTP6A_N domain-containing protein. (423 aa)
F4P6R2_BATDJUncharacterized protein. (114 aa)
F4P6S8_BATDJDNA helicase; Belongs to the MCM family. (854 aa)
F4P6X8_BATDJUncharacterized protein. (988 aa)
F4P727_BATDJUncharacterized protein. (991 aa)
F4P7B1_BATDJUncharacterized protein. (680 aa)
F4P7I5_BATDJUncharacterized protein. (554 aa)
F4P7U2_BATDJDNA helicase; Belongs to the MCM family. (756 aa)
F4P8S6_BATDJUncharacterized protein. (1991 aa)
F4P902_BATDJUmuC domain-containing protein. (604 aa)
F4P973_BATDJRuvB-like helicase; DNA helicase participates in several chromatin remodeling complexes, including the SWR1 and the INO80 complexes. (481 aa)
F4P980_BATDJFanconi-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. (595 aa)
F4P9G7_BATDJUncharacterized protein. (1225 aa)
F4P9K5_BATDJUncharacterized protein. (434 aa)
F4P9T4_BATDJUncharacterized protein. (440 aa)
F4P9X1_BATDJRuvB-like helicase; DNA helicase participates in several chromatin remodeling complexes, including the SWR1 and the INO80 complexes. (456 aa)
F4P9Y1_BATDJUncharacterized protein. (729 aa)
F4PA52_BATDJUncharacterized protein. (1014 aa)
F4PB72_BATDJExpressed protein. (380 aa)
F4PB73_BATDJUncharacterized protein. (641 aa)
F4PBE6_BATDJUncharacterized protein. (777 aa)
F4PCC1_BATDJEndonuclease. (227 aa)
F4PCF3_BATDJDNA_MISMATCH_REPAIR_2 domain-containing protein. (914 aa)
F4PCH2_BATDJDNA-(apurinic or apyrimidinic site) lyase; Belongs to the DNA repair enzymes AP/ExoA family. (394 aa)
F4PCX6_BATDJMCM domain-containing protein; Belongs to the MCM family. (677 aa)
F4PDL2_BATDJRECA_2 domain-containing protein. (54 aa)
F4PDU1_BATDJKu domain-containing protein. (576 aa)
F4PE31_BATDJERCC4 domain-containing protein. (782 aa)
F4PE38_BATDJDNA 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. (612 aa)
F4PE73_BATDJDNA_MISMATCH_REPAIR_2 domain-containing protein; Component of the post-replicative DNA mismatch repair system (MMR). (923 aa)
F4PEI2_BATDJPOLAc domain-containing protein. (1063 aa)
F4PEQ8_BATDJERCC4 domain-containing protein. (942 aa)
F4PFE7_BATDJN6_Mtase domain-containing protein. (153 aa)
F4PFF0_BATDJUncharacterized protein. (411 aa)
F4PFV2_BATDJUncharacterized protein. (1547 aa)
Your Current Organism:
Batrachochytrium dendrobatidis JAM81
NCBI taxonomy Id: 684364
Other names: B. dendrobatidis JAM81
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