STRINGSTRING
B0XFE1_CULQU B0XFE1_CULQU B0XF55_CULQU B0XF55_CULQU B0XCK9_CULQU B0XCK9_CULQU B0XB82_CULQU B0XB82_CULQU B0XB31_CULQU B0XB31_CULQU B0XAL3_CULQU B0XAL3_CULQU B0XAB7_CULQU B0XAB7_CULQU B0X912_CULQU B0X912_CULQU B0X813_CULQU B0X813_CULQU B0X7G0_CULQU B0X7G0_CULQU B0X777_CULQU B0X777_CULQU B0X776_CULQU B0X776_CULQU B0X696_CULQU B0X696_CULQU B0X672_CULQU B0X672_CULQU B0X5W2_CULQU B0X5W2_CULQU B0X3N5_CULQU B0X3N5_CULQU B0X3N4_CULQU B0X3N4_CULQU B0X3C4_CULQU B0X3C4_CULQU B0W8I7_CULQU B0W8I7_CULQU B0W6X7_CULQU B0W6X7_CULQU B0W784_CULQU B0W784_CULQU B0W7M0_CULQU B0W7M0_CULQU B0W874_CULQU B0W874_CULQU B0WYA5_CULQU B0WYA5_CULQU B0WYG9_CULQU B0WYG9_CULQU B0WYS5_CULQU B0WYS5_CULQU B0WYV1_CULQU B0WYV1_CULQU B0WZ32_CULQU B0WZ32_CULQU B0WZK0_CULQU B0WZK0_CULQU B0X0B6_CULQU B0X0B6_CULQU B0X0D2_CULQU B0X0D2_CULQU B0X0Q9_CULQU B0X0Q9_CULQU B0X0Y6_CULQU B0X0Y6_CULQU B0X0Y7_CULQU B0X0Y7_CULQU B0X122_CULQU B0X122_CULQU B0X1I3_CULQU B0X1I3_CULQU B0X2Z9_CULQU B0X2Z9_CULQU B0WXB6_CULQU B0WXB6_CULQU B0WX78_CULQU B0WX78_CULQU B0WX77_CULQU B0WX77_CULQU B0WWB3_CULQU B0WWB3_CULQU B0WWB1_CULQU B0WWB1_CULQU B0WVS5_CULQU B0WVS5_CULQU B0WVL3_CULQU B0WVL3_CULQU B0WV82_CULQU B0WV82_CULQU B0WV80_CULQU B0WV80_CULQU B0WV77_CULQU B0WV77_CULQU B0WUX9_CULQU B0WUX9_CULQU B0WU43_CULQU B0WU43_CULQU B0WTR3_CULQU B0WTR3_CULQU B0WTK9_CULQU B0WTK9_CULQU B0WTA6_CULQU B0WTA6_CULQU B0WT70_CULQU B0WT70_CULQU B0WSS7_CULQU B0WSS7_CULQU B0WSQ0_CULQU B0WSQ0_CULQU B0WSH3_CULQU B0WSH3_CULQU B0VZA3_CULQU B0VZA3_CULQU B0VZU0_CULQU B0VZU0_CULQU B0W0A9_CULQU B0W0A9_CULQU B0W0J0_CULQU B0W0J0_CULQU B0W0J1_CULQU B0W0J1_CULQU B0W1B0_CULQU B0W1B0_CULQU B0W2A3_CULQU B0W2A3_CULQU B0W335_CULQU B0W335_CULQU B0W3I5_CULQU B0W3I5_CULQU B0W412_CULQU B0W412_CULQU B0W417_CULQU B0W417_CULQU B0W5E3_CULQU B0W5E3_CULQU B0WSD8_CULQU B0WSD8_CULQU B0WQ25_CULQU B0WQ25_CULQU B0WP18_CULQU B0WP18_CULQU B0WMX3_CULQU B0WMX3_CULQU B0WMV3_CULQU B0WMV3_CULQU B0WMU0_CULQU B0WMU0_CULQU B0WMC6_CULQU B0WMC6_CULQU B0WLC6_CULQU B0WLC6_CULQU B0WLC5_CULQU B0WLC5_CULQU B0WLB5_CULQU B0WLB5_CULQU B0WKF2_CULQU B0WKF2_CULQU B0WK67_CULQU B0WK67_CULQU B0WK66_CULQU B0WK66_CULQU B0WK00_CULQU B0WK00_CULQU B0X300_CULQU B0X300_CULQU B0WJM0_CULQU B0WJM0_CULQU B0WJB2_CULQU B0WJB2_CULQU B0WJB1_CULQU B0WJB1_CULQU B0WJB0_CULQU B0WJB0_CULQU B0WIV2_CULQU B0WIV2_CULQU B0WIS7_CULQU B0WIS7_CULQU B0WID5_CULQU B0WID5_CULQU B0WH36_CULQU B0WH36_CULQU B0WGW2_CULQU B0WGW2_CULQU B0WGT6_CULQU B0WGT6_CULQU B0WGC0_CULQU B0WGC0_CULQU B0WG64_CULQU B0WG64_CULQU B0WFR1_CULQU B0WFR1_CULQU B0WF32_CULQU B0WF32_CULQU B0WE07_CULQU B0WE07_CULQU B0WDA0_CULQU B0WDA0_CULQU B0WCK1_CULQU B0WCK1_CULQU B0WCK0_CULQU B0WCK0_CULQU B0WC67_CULQU B0WC67_CULQU B0WB50_CULQU B0WB50_CULQU B0WAT3_CULQU B0WAT3_CULQU B0WAP9_CULQU B0WAP9_CULQU B0WAD3_CULQU B0WAD3_CULQU B0WA29_CULQU B0WA29_CULQU B0W9S4_CULQU B0W9S4_CULQU B0X397_CULQU B0X397_CULQU B0X3A0_CULQU B0X3A0_CULQU B0W5Z1_CULQU B0W5Z1_CULQU B0W6K4_CULQU B0W6K4_CULQU B0W6K5_CULQU B0W6K5_CULQU B0W6K6_CULQU B0W6K6_CULQU B0W6K7_CULQU B0W6K7_CULQU B0W6L3_CULQU B0W6L3_CULQU B0W9K3_CULQU B0W9K3_CULQU B0W9J9_CULQU B0W9J9_CULQU B0W982_CULQU B0W982_CULQU B0W973_CULQU B0W973_CULQU B0XLV8_CULQU B0XLV8_CULQU B0XLN1_CULQU B0XLN1_CULQU B0XLJ7_CULQU B0XLJ7_CULQU B0XLI3_CULQU B0XLI3_CULQU B0XLF0_CULQU B0XLF0_CULQU B0XLA0_CULQU B0XLA0_CULQU B0XL76_CULQU B0XL76_CULQU B0XKQ0_CULQU B0XKQ0_CULQU B0XK02_CULQU B0XK02_CULQU B0XJH0_CULQU B0XJH0_CULQU B0XIT8_CULQU B0XIT8_CULQU B0XH16_CULQU B0XH16_CULQU B0XGX6_CULQU B0XGX6_CULQU B0XFM3_CULQU B0XFM3_CULQU B0XFG1_CULQU B0XFG1_CULQU B0XF83_CULQU B0XF83_CULQU
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:
B0XFE1_CULQUANK_REP_REGION domain-containing protein. (203 aa)
B0XF55_CULQUUncharacterized protein. (683 aa)
B0XCK9_CULQUTIMELESS-interacting protein; Plays an important role in the control of DNA replication and the maintenance of replication fork stability. Belongs to the CSM3 family. (274 aa)
B0XB82_CULQUChromatin regulatory protein sir2. (339 aa)
B0XB31_CULQUSerine/threonine-protein kinase chk2. (132 aa)
B0XAL3_CULQUPredicted protein. (298 aa)
B0XAB7_CULQUUncharacterized protein. (756 aa)
B0X912_CULQUUncharacterized protein. (755 aa)
B0X813_CULQUUncharacterized protein. (253 aa)
B0X7G0_CULQUAspartyl-tRNA synthetase. (550 aa)
B0X777_CULQUHistone H4; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. (110 aa)
B0X776_CULQUHistone H4; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. (104 aa)
B0X696_CULQUHistone H4; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. (117 aa)
B0X672_CULQUUncharacterized protein. (321 aa)
B0X5W2_CULQUMeiotic recombination repair protein 11. (306 aa)
B0X3N5_CULQUCyclin a; Belongs to the cyclin family. (376 aa)
B0X3N4_CULQUCyclin a; Belongs to the cyclin family. (160 aa)
B0X3C4_CULQUArtemis protein. (397 aa)
B0W8I7_CULQUXRCC1_N domain-containing protein. (500 aa)
B0W6X7_CULQUMeiotic recombination repair protein 11. (311 aa)
B0W784_CULQUUncharacterized protein. (436 aa)
B0W7M0_CULQUUncharacterized protein. (292 aa)
B0W874_CULQUUncharacterized protein. (701 aa)
B0WYA5_CULQUUncharacterized protein. (277 aa)
B0WYG9_CULQUPol-like protein. (315 aa)
B0WYS5_CULQUPoly [ADP-ribose] polymerase. (1000 aa)
B0WYV1_CULQUBRCT domain-containing protein. (358 aa)
B0WZ32_CULQUHistone H4; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. (124 aa)
B0WZK0_CULQUDNA-repair protein XRCC1. (665 aa)
B0X0B6_CULQUBRCT domain-containing protein. (615 aa)
B0X0D2_CULQUUncharacterized protein. (1747 aa)
B0X0Q9_CULQUPoly. (531 aa)
B0X0Y6_CULQURING-type domain-containing protein. (190 aa)
B0X0Y7_CULQUUncharacterized protein. (607 aa)
B0X122_CULQUDNA repair protein rad9. (453 aa)
B0X1I3_CULQUPolyubiquitin. (533 aa)
B0X2Z9_CULQUGIY-YIG domain-containing protein. (66 aa)
B0WXB6_CULQUUncharacterized protein. (484 aa)
B0WX78_CULQUPoly. (139 aa)
B0WX77_CULQUPoly. (315 aa)
B0WWB3_CULQUPoly. (190 aa)
B0WWB1_CULQUPoly. (110 aa)
B0WVS5_CULQUKu P80 DNA helicase. (722 aa)
B0WVL3_CULQUCell division control protein 2 cognate; Belongs to the protein kinase superfamily. (296 aa)
B0WV82_CULQUHelicase. (1024 aa)
B0WV80_CULQUHelicase. (105 aa)
B0WV77_CULQUChromatin remodelling complex ATPase chain Iswi. (730 aa)
B0WUX9_CULQUPoly. (327 aa)
B0WU43_CULQUUncharacterized protein. (359 aa)
B0WTR3_CULQU3'-5' exonuclease. (489 aa)
B0WTK9_CULQUUncharacterized protein. (277 aa)
B0WTA6_CULQU3'-5' exonuclease. (755 aa)
B0WT70_CULQUMSTP096. (244 aa)
B0WSS7_CULQUDNA topoisomerase 2-binding protein 1. (1363 aa)
B0WSQ0_CULQUProtein phosphatase 4. (148 aa)
B0WSH3_CULQUTyrosine-protein kinase. (377 aa)
B0VZA3_CULQUDNA repair protein rad50. (146 aa)
B0VZU0_CULQUUncharacterized protein. (540 aa)
B0W0A9_CULQUUncharacterized protein. (164 aa)
B0W0J0_CULQUTimeout/timeless-2. (1412 aa)
B0W0J1_CULQUTimeout/timeless-2. (683 aa)
B0W1B0_CULQUCrossover junction endonuclease MUS81. (450 aa)
B0W2A3_CULQUHistone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. (458 aa)
B0W335_CULQURAD51C protein, putative. (274 aa)
B0W3I5_CULQUSerine/threonine-protein phosphatase. (307 aa)
B0W412_CULQUAtaxia telangiectasia mutated, putative; Belongs to the PI3/PI4-kinase family. (370 aa)
B0W417_CULQUAtaxia telangiectasia mutated, putative. (1315 aa)
B0W5E3_CULQUTyrosyl-dna phosphodiesterase. (142 aa)
B0WSD8_CULQUUncharacterized protein. (1034 aa)
B0WQ25_CULQUSerine/threonine-protein kinase chk2. (494 aa)
B0WP18_CULQUUncharacterized protein. (192 aa)
B0WMX3_CULQUUncharacterized protein. (198 aa)
B0WMV3_CULQUDNA-repair protein XRCC3. (281 aa)
B0WMU0_CULQUUncharacterized protein. (1673 aa)
B0WMC6_CULQUUncharacterized protein. (280 aa)
B0WLC6_CULQUCDC24_OB3 domain-containing protein. (471 aa)
B0WLC5_CULQUUncharacterized protein. (288 aa)
B0WLB5_CULQURad51 domain-containing protein. (296 aa)
B0WKF2_CULQUWerner syndrome helicase. (1079 aa)
B0WK67_CULQUChromatin regulatory protein sir2. (1126 aa)
B0WK66_CULQUChromatin regulatory protein sir2. (260 aa)
B0WK00_CULQURothmund-thomson syndrome DNA helicase recq4, putative. (1527 aa)
B0X300_CULQUUncharacterized protein. (289 aa)
B0WJM0_CULQUMeiotic recombination repair protein 11. (145 aa)
B0WJB2_CULQUUncharacterized protein. (974 aa)
B0WJB1_CULQUUncharacterized protein; Belongs to the PI3/PI4-kinase family. (2909 aa)
B0WJB0_CULQUUncharacterized protein; Belongs to the PI3/PI4-kinase family. (272 aa)
B0WIV2_CULQUUncharacterized protein. (724 aa)
B0WIS7_CULQUTimeless protein. (996 aa)
B0WID5_CULQUUncharacterized protein. (371 aa)
B0WH36_CULQU3'-5' exonuclease domain-containing protein. (302 aa)
B0WGW2_CULQUTyrosyl-dna phosphodiesterase. (615 aa)
B0WGT6_CULQUImportin subunit alpha; Belongs to the importin alpha family. (459 aa)
B0WGC0_CULQUDNA 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. (992 aa)
B0WG64_CULQUHistone H4; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. (103 aa)
B0WFR1_CULQUCyclin a, putative; Belongs to the cyclin family. (295 aa)
B0WF32_CULQUUncharacterized protein. (337 aa)
B0WE07_CULQUDNA ligase 4; Belongs to the ATP-dependent DNA ligase family. (875 aa)
B0WDA0_CULQUNon-specific serine/threonine protein kinase. (459 aa)
B0WCK1_CULQUEyes absent homolog; Belongs to the HAD-like hydrolase superfamily. EYA family. (489 aa)
B0WCK0_CULQUEyes absent homolog; Belongs to the HAD-like hydrolase superfamily. EYA family. (227 aa)
B0WC67_CULQUDouble-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. (640 aa)
B0WB50_CULQUUncharacterized protein. (146 aa)
B0WAT3_CULQUDUF1767 domain-containing protein. (618 aa)
B0WAP9_CULQUDNA repair protein RAD50. (1292 aa)
B0WAD3_CULQUTyrosine-protein kinase Abl. (1521 aa)
B0WA29_CULQUERCC4 domain-containing protein. (316 aa)
B0W9S4_CULQUDNA repair protein RAD51 homolog; Binds to single and double-stranded DNA and exhibits DNA- dependent ATPase activity. Underwinds duplex DNA. Belongs to the RecA family. RAD51 subfamily. (349 aa)
B0X397_CULQUDNA polymerase theta. (482 aa)
B0X3A0_CULQUDNA polymerase theta. (1177 aa)
B0W5Z1_CULQUReplication protein A subunit; As part of the heterotrimeric replication protein A complex (RPA/RP-A), binds and stabilizes single-stranded DNA intermediates, that form during DNA replication or upon DNA stress. It prevents their reannealing and in parallel, recruits and activates different proteins and complexes involved in DNA metabolism. Thereby, it plays an essential role both in DNA replication and the cellular response to DNA damage. (615 aa)
B0W6K4_CULQUP53 domain-containing protein. (364 aa)
B0W6K5_CULQUP53 domain-containing protein. (344 aa)
B0W6K6_CULQUP53 domain-containing protein. (391 aa)
B0W6K7_CULQUCellular tumor antigen p53. (431 aa)
B0W6L3_CULQUP53 domain-containing protein. (436 aa)
B0W9K3_CULQUCell cycle checkpoint protein rad17, putative. (530 aa)
B0W9J9_CULQUUncharacterized protein. (297 aa)
B0W982_CULQUUbiquitin. (323 aa)
B0W973_CULQUUncharacterized protein. (1065 aa)
B0XLV8_CULQUUncharacterized protein. (292 aa)
B0XLN1_CULQUUncharacterized protein. (284 aa)
B0XLJ7_CULQUCrossover junction endonuclease MUS81. (450 aa)
B0XLI3_CULQUHistone H4; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. (92 aa)
B0XLF0_CULQUXRCC1_N domain-containing protein. (391 aa)
B0XLA0_CULQUMre11_DNA_bind domain-containing protein. (1391 aa)
B0XL76_CULQUUncharacterized protein. (278 aa)
B0XKQ0_CULQURMI1_C domain-containing protein. (134 aa)
B0XK02_CULQURAD51D. (323 aa)
B0XJH0_CULQUDNA ligase 4. (805 aa)
B0XIT8_CULQUUncharacterized protein. (298 aa)
B0XH16_CULQURothmund-thomson syndrome DNA helicase recq4, putative. (1093 aa)
B0XGX6_CULQURAD51C protein, putative. (275 aa)
B0XFM3_CULQUMre11_DNA_bind domain-containing protein. (286 aa)
B0XFG1_CULQUCraniofacial development protein 2. (121 aa)
B0XF83_CULQUUncharacterized protein. (778 aa)
Your Current Organism:
Culex quinquefasciatus
NCBI taxonomy Id: 7176
Other names: C. quinquefasciatus, Culex fatigans, Culex pipiens fatigans, Culex pipiens quinquefasciatus, southern house mosquito
Server load: low (20%) [HD]
STRING is a Core Data Resource as designated by Global Biodata Coalition and ELIXIR.