Matrix_104 | PI | Not Available | | 72.52% |
Matrix_443 | AGL15 | Not Available | | 72.23% |
Matrix_55 | PIF3 | Not Available | | 70.10% |
Matrix_403 | BZR1 | Not Available | | 69.87% |
Matrix_214 | AP1 | Not Available | | 69.51% |
Matrix_108 | PIF4 | Interaction between BZR1 and PIF4 integrates brassinosteroid and environmental responses | | 68.81% |
Matrix_359 | FLC | Not Available | | 68.30% |
Matrix_19 | PIF5 | Phytochrome interacting factors 4 and 5 control seedling growth in changing light conditions by directly controlling auxin signaling | | 67.96% |
Matrix_498 | AT2G28710; AT3G46070; AT3G46080; ZAT7 | Not Available | | 67.70% |
Matrix_257 | NAC050; ANAC051; anac057; NAC2 | Not Available | | 67.20% |
Matrix_305 | PIF4 | Interaction between BZR1 and PIF4 integrates brassinosteroid and environmental responses | | 66.49% |
Matrix_191 | PIF5 | Phytochrome interacting factors 4 and 5 control seedling growth in changing light conditions by directly controlling auxin signaling | | 66.29% |
Matrix_153 | AP2 | Not Available | | 66.26% |
Matrix_122 | ABF1; AREB2 | Not Available | | 65.07% |
Matrix_449 | BIM2 | Not Available | | 64.91% |
Matrix_158 | AT1G03040; LRL1; UNE12; LRL2; LRL3 | Not Available | | 64.68% |
Matrix_514 | DYT1 | Regulation of the Arabidopsis anther transcriptome by DYT1 for pollen development | | 64.58% |
Matrix_200 | PIL5; AT4G28790; AT4G28800; AT4G28811; AT4G28815 | Not Available | | 64.53% |
Matrix_323 | BIM3 | Not Available | | 64.49% |
Matrix_330 | MYC2; TT8 | Not Available | | 64.20% |
Matrix_480 | BES1 | Not Available | | 64.18% |
Matrix_465 | MYC4 | Not Available | | 63.76% |
Matrix_120 | BEE2 | Not Available | | 63.20% |
Matrix_389 | ILR3 | Not Available | | 62.80% |
Matrix_77 | PRR5 | Not Available | | 62.46% |
Matrix_338 | AP2 | Not Available | | 62.28% |
Motif_154 | ABREBNNAPA | ABRE of napA storage-protein gene of Brassica napus; ABA responsive element; dist B ABRE mediated transactivation by ABI3 adn ABI3-dependent response to ABA; a tetramer of the composite RY/G complex mediated only ABA-independent transactivation by ABI3; B2 domain of ABI3 is necessary for ABA-independent and ABA-dependent activation through the dist B ABRE; B3 domain of ABI3 interacts with the RY/G complex | | 61.86% |
Matrix_194 | HYH; HY5 | Not Available | | 60.88% |
Matrix_331 | GBF1 | Not Available | | 60.85% |
Matrix_113 | ABI5 | Not Available | | 60.66% |
Matrix_80 | BIM1 | Not Available | | 60.42% |
Matrix_156 | POC1 | Not Available | | 60.25% |
Matrix_213 | ATHB22 | Not Available | | 59.61% |
Matrix_109 | GBF3 | Not Available | | 59.56% |
Matrix_404 | OBP4 | Not Available | | 59.31% |
Matrix_369 | AT2G18300 | Not Available | | 59.24% |
Matrix_424 | MYB59 | Not Available | | 59.24% |
Motif_498 | SGBFGMGMAUX28 | bZIP proteins SGBF-1 and SGBF-2 binding site in soybean GmAux28 gene promoter | | 59.21% |
Matrix_129 | ABF1 | Not Available | | 59.06% |
Matrix_229 | CDC5 | A cdc5+ homolog of a higher plant, Arabidopsis thaliana | | 58.93% |
Matrix_301 | PIL5 | Not Available | | 58.38% |
Matrix_306 | TGA1 | TGA1 and G-box binding factors: two distinct classes of Arabidopsis leucine zipper proteins compete for the G-box-like element TGACGTGG | | 58.26% |
Matrix_313 | ATMYB65; MYB33 | Not Available | | 58.25% |
Matrix_299 | PFG3 | Not Available | | 57.83% |
Matrix_315 | MYB111 | Not Available | | 57.81% |
Matrix_36 | RAV1_1 | RAV1, a novel DNA-binding protein, binds to bipartite recognition sequence through two distinct DNA-binding domains uniquely found in higher plants | | 57.62% |
Matrix_211 | MYB3 | Not Available | | 57.47% |
Matrix_469 | NAC041; NAC083 | Not Available | | 57.39% |
Matrix_85 | SPL5 | Not Available | | 57.15% |
Matrix_41 | anac058 | Not Available | | 57.10% |
Matrix_186 | FHY3 | Not Available | | 56.92% |
Matrix_33 | SPL11; SPL10; SPL2 | Not Available | | 56.89% |
Matrix_440 | LFY | Not Available | | 56.88% |
Matrix_225 | MYB52 | Not Available | | 56.87% |
Matrix_450 | SPL7 | Not Available | | 56.83% |
Matrix_337 | MYB46 | Not Available | | 56.74% |
Matrix_14 | ZCW32; AT5G62610 | Not Available | | 56.70% |
Matrix_68 | AtMYB77 | More than 80 R2R3-MYB regulatory genes in the genome of Arabidopsis thaliana. Plant J 14: 273-84 | | 56.68% |
Matrix_47 | AtMYB77 | Not Available | | 56.68% |
Matrix_183 | BES1 | A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana | | 56.53% |
Matrix_307 | RGL2; RGL3 | Not Available | | 56.28% |
Motif_418 | ABRE2HVA22 | ABRE2 of barley HVA22 gene; G-box; component of ABA response complex in HVA22 gene; see ABRE3 of HVA22 gene; see CE1 (coupling element 1 = TGCCACCGG) | | 56.15% |
Matrix_31 | SPL1 | Not Available | | 56.08% |
Matrix_151 | ASIL1 | Not Available | | 56.07% |
Motif_507 | ABASEED1 | ABA regulation; seed expression; Gene: carrot Dc3; Transacting factor: bZIP; Contains ACGT motif | | 55.75% |
Matrix_206 | CUC1; ANAC100 | Not Available | | 55.69% |
Matrix_339 | bHLH104 | Not Available | | 55.58% |
Matrix_466 | PRR5 | Not Available | | 55.50% |
Matrix_199 | AT1G69170; SPL9; SPL15; SPL13A; SPL13B | Not Available | | 55.48% |
Matrix_247 | PIF3 | Not Available | | 55.33% |
Matrix_438 | AtbZIP63 | Not Available | | 54.95% |
Matrix_254 | MYB52 | Not Available | | 54.91% |
Matrix_332 | SPT; ALC | Not Available | | 54.89% |
Matrix_273 | ANAC55 | Not Available | | 54.89% |
Motif_197 | HY5 | Arabidopsis bZIP protein HY5 directly interacts with light-responsive promoters in mediating light control of gene expression | | 54.87% |
Matrix_59 | AT4G00238; AT4G00250 | Not Available | | 54.80% |
Matrix_52 | ZAT18 | Not Available | | 54.76% |
Matrix_264 | ATAREB1 | Not Available | | 54.62% |
Matrix_188 | SPL4 | Not Available | | 54.56% |
Matrix_12 | EIN3; EIL2 | Not Available | | 54.46% |
Matrix_433 | ATERF1 | Not Available | | 54.44% |
Matrix_326 | AT5G07310; Rap2.6L; AT5G61890 | Not Available | | 54.41% |
Motif_499 | AtMYC2 | A basic helix-loop-helix transcription factor in Arabidopsis, MYC2, acts as a repressor of blue light-mediated photomorphogenic growth | | 54.41% |
Motif_566 | AREB1; AREB2 | Interaction between two cis-acting elements, ABRE and DRE, in ABA-dependent expression of Arabidopsis rd29A gene in response to dehydration and high-salinity stresses | | 54.34% |
Motif_314 | HY5AT | G box; Binding site of Arabidopsis bZIP protein HY5; HY5 is constitutively nuclear localized and is involved in light regulation of transcriptional activity of the promoters containing the G-box;HY5 abundance peaks in early seedling development, consistent with its role in promoting photomorphogenesis; HY5 stability and activity is regulated by phosphorylation in its COP1 binding domain; HY5 regulates stimulus-induced development of root and hypocotyl | | 54.11% |
Matrix_499 | ARR18 | Not Available | | 54.01% |
Matrix_355 | ERF10; ERF11 | Not Available | | 53.96% |
Matrix_351 | HAT9; ATHB-4; ATHB2; HAT22; HAT14 | Not Available | | 53.92% |
Matrix_495 | HD-GL2-1; ANL2 | Not Available | | 53.81% |
Matrix_287 | ERF2 | Not Available | | 53.74% |
Motif_92 | ABREATRD22 | ABRE (ABA responsive element) in Arabidopsis dehydration-responsive gene rd22 | | 53.50% |
Matrix_456 | bZIP60 | Not Available | | 53.48% |
Matrix_171 | LBD3; LBD4 | Not Available | | 53.46% |
Matrix_249 | WRKY11 | Not Available | | 53.40% |
Motif_560 | GLUTECOREOS | Core site required for binding of the trans-acting factor in the promoter region of rice glutelin (type 2 glutelin gene family) | | 53.37% |
Motif_571 | GBOXSORBCS1 | G-box found in the spinach RBCS-1 gene promoter; Located between -219 and -212; G-box trimer confers relatively high level expression in roots | | 53.35% |
Matrix_416 | ASL5 | Not Available | | 53.27% |
Motif_406 | ABREBZMRAB28 | ABA-responsive element (ABRE B) found at -105 to -96 in maize rab28; Maize rab28 is ABA-inducible in embryos and vegetative tissues | | 53.24% |
Matrix_322 | NST3; ANAC015; BRN2 | Not Available | | 53.23% |
Matrix_278 | AtbZIP44 | Not Available | | 53.22% |
Matrix_448 | ATERF6 | Not Available | | 53.20% |
Matrix_427 | ZAT14 | Not Available | | 53.18% |
Matrix_304 | AtSPL3 | Functional dissection of the plant-specific SBP-domain: overlap of the DNA-binding and nuclear localization domains | | 53.16% |
Matrix_231 | HDG2; HDG3; ATML1; HB-7 | Not Available | | 53.14% |
Matrix_377 | AT1G75490; DREB2C; AT2G40350; AT5G18450 | Not Available | | 53.13% |
Matrix_118 | PIF3_2 | Direct targeting of light signals to a promoter element-bound transcription factor | | 53.10% |
Matrix_345 | POC1 | Not Available | | 53.10% |
Matrix_502 | AT3G13040 | Not Available | | 53.07% |
Matrix_458 | MGP; AT1G14580; AtIDD7; AtIDD5; AtIDD4; AtIDD12; JKD; AT5G66730 | Not Available | | 53.06% |
Matrix_97 | APRR2 | Not Available | | 53.04% |
Matrix_209 | RAP2.6 | Not Available | | 52.99% |
Matrix_316 | WRKY15; WRKY39; WRKY7; WRKY74 | Not Available | | 52.91% |
Motif_599 | LREBOXIIPCCHS1; HY5 | BoxII; Light responsive element (LRE) found in the parsley CHS-1 (chalcone synthase-1) gene promoter; Required for light responsiveness; nuclear protein binding site; Highly conserved in various light inducible gene promoters; Arabidopsis bZIP protein HY5 directly interacts with light-responsive promoters in mediating light control of gene expression | | 52.88% |
Matrix_500 | WRKY43 | Not Available | | 52.82% |
Matrix_107 | AtSPL3 | Not Available | | 52.80% |
Matrix_58 | WRKY55; ATWRKY54; WRKY46; WRKY70; AtWRKY41; WRKY53; WRKY30 | Not Available | | 52.79% |
Matrix_140 | ATHB5 | DNA-binding and dimerization preferences of Arabidopsis homeodomain-leucine zipper transcription factors in vitro | | 52.74% |
Matrix_415 | WRKY27 | Not Available | | 52.72% |
Matrix_300 | bZIP68; bZIP16 | Not Available | | 52.70% |
Matrix_56 | BZIP17; BZIP28; BZIP49 | Not Available | | 52.69% |
Matrix_221 | SPL7 | Not Available | | 52.67% |
Matrix_418 | KNAT6; KNAT2 | Not Available | | 52.61% |
Motif_338 | HY5 | Arabidopsis bZIP protein HY5 directly interacts with light-responsive promoters in mediating light control of gene expression | | 52.61% |
Matrix_321 | HRD | Not Available | | 52.53% |
Matrix_455 | MYB111 | Not Available | | 52.52% |
Matrix_101 | ERF5 | Not Available | | 52.47% |
Matrix_494 | OBP4 | Not Available | | 52.47% |
Matrix_8 | KAN1 | Not Available | | 52.44% |
Matrix_226 | GATA1 | Not Available | | 52.44% |
Matrix_280 | TCP24; TCP1; BRC2; ATTCP18 | Not Available | | 52.43% |
Matrix_3 | WRKY48 | Not Available | | 52.43% |
Motif_232 | ABADESI1 | Responsive to ABA and desiccation; Motif I of rice rab16A-D (initially called rab-21); Expressed in seeds late during embryogenesis; Induced by ABA and osmotic stress in vegetative tissues; Contains ACGT motif; transacting factor: TAF-1 | | 52.41% |
Matrix_461 | ATHB12 | Not Available | | 52.39% |
Matrix_193 | RAV1 | Not Available | | 52.34% |
Matrix_265 | NGA3 | Not Available | | 52.34% |
Matrix_296 | GBF2 | Not Available | | 52.32% |
Matrix_202 | WRKY71; WRKY28; WRKY8 | Not Available | | 52.23% |
Matrix_317 | AT1G06070; AT2G31370; AT2G40620 | Not Available | | 52.23% |
Matrix_91 | CRF3 | Not Available | | 52.21% |
Matrix_492 | ETT | Not Available | | 52.15% |
Motif_689 | ANAC092 | NAC Transcription Factor ORE1 and Senescence-Induced BIFUNCTIONAL NUCLEASE1 (BFN1) Constitute a Regulatory Cascade in Arabidopsis | | 52.11% |
Motif_112 | GBOX10NT | One of 11 G-box sequences in tobacco; Required for high-level constitutive expression in seed, leaf, root, axillary bud, almost all parts of flower buds and pollen | | 52.09% |
Matrix_435 | ATHB51 | Not Available | | 52.09% |
Matrix_314 | WRKY65; WRKY14; WRKY35; WRKY69; WRKY16; ATWRKY52 | Not Available | | 52.08% |
Matrix_493 | AT1G22985; AT1G71130 | Not Available | | 52.08% |
Matrix_343 | AT2G33710 | Not Available | | 52.08% |
Matrix_409 | DEAR3 | Not Available | | 52.07% |
Matrix_293 | WRKY38 | Not Available | | 52.06% |
Matrix_263 | WRKY33; WRKY19; WRKY32 | Not Available | | 52.06% |
Matrix_256 | IXR11; KNAT5; KNAT4; KNAT3 | Not Available | | 51.89% |
Matrix_75 | WRKY29 | Not Available | | 51.85% |
Matrix_50 | ATERF14; AT5G43410 | Not Available | | 51.84% |
Matrix_328 | AT1G76580 | Not Available | | 51.81% |
Matrix_17 | WRKY22 | Not Available | | 51.76% |
Matrix_131 | HDG12; EDT1; GL2; HDG8 | Not Available | | 51.74% |
Motif_644 | ABREDISTBBNNAPA | dist B (distal portion of B-box) found in napA gene of Brassica napus; Shows similarity to ABRE; Found between -148 and -124; Required for seed specific expression and ABA responsiveness;dist B ABRE mediated transactivation by ABI3 adn ABI3-dependent response to ABA; a tetramer of the composite RY/G complex mediated only ABA-independent transactivation by ABI3; B2 domain of ABI3 is necessary for ABA-independent and ABA-dependent activation through the dist B ABRE | | 51.68% |
Matrix_446 | LBD16 | Not Available | | 51.62% |
Matrix_93 | YAB5 | Not Available | | 51.56% |
Matrix_518 | AT2G21230 | Not Available | | 51.55% |
Motif_120 | ABRETAEM | ABRE (ABA responsive element) found in wheat Em gene; transacting factor: EMBP-1; EMBP-1 binds to CACGTGGC | | 51.45% |
Matrix_71 | ATHB7 | Not Available | | 51.35% |
Matrix_286 | GATA7 | Not Available | | 51.32% |
Matrix_467 | RAV1 | Not Available | | 51.32% |
Matrix_34 | RAV1_2 | RAV1, a novel DNA-binding protein, binds to bipartite recognition sequence through two distinct DNA-binding domains uniquely found in higher plants | | 51.32% |
Matrix_477 | RAV1 | Not Available | | 51.32% |
Matrix_268 | EMB2749; VND5; SMB; VND1; ANAC076; NAC101; ANAC105 | Not Available | | 51.28% |
Matrix_196 | TCP20; AT5G41030 | Not Available | | 51.26% |
Matrix_374 | AT5G07580; AT5G61590 | Not Available | | 51.26% |
Matrix_508 | APL; AT3G12730; AT3G24120; UNE16 | Not Available | | 51.23% |
Motif_617 | ABRE3HVA1 | ABA responsive element, ABRE3, found in barley HVA1 gene encoding a class 3 late embryogenesis-abundant protein; stress response | | 51.22% |
Matrix_463 | HAT3.1 | Not Available | | 51.20% |
Matrix_227 | AT1G64620 | Not Available | | 51.14% |
Matrix_233 | MYC3 | Not Available | | 51.13% |
Matrix_437 | MYC2 | Not Available | | 51.09% |
Matrix_182 | ATHB6 | Not Available | | 51.02% |
Matrix_302 | HAT1; HAT2 | Not Available | | 51.00% |
Matrix_392 | ARR2 | Not Available | | 50.99% |
Motif_616 | BZIP12; ABI5 | The homologous ABI5 and EEL transcription factors function antagonistically to fine-tune gene expression during late embryogenesis | | 50.98% |
Matrix_9 | AT5G04760 | Not Available | | 50.94% |
Matrix_259 | AT1G50680; AT1G51120 | Not Available | | 50.94% |
Matrix_197 | NAP | Not Available | | 50.83% |
Matrix_370 | WRKY50; WRKY51 | Not Available | | 50.83% |
Matrix_475 | AT5G64220 | Not Available | | 50.80% |
Matrix_491 | AT1G68670; AT3G25790 | Not Available | | 50.77% |
Matrix_161 | MYBC1; AT3G10760; LUX; AT5G05090; AT5G59570 | Not Available | | 50.77% |
Matrix_271 | AT3G16350 | Not Available | | 50.71% |
Matrix_284 | KAN2; KAN3; KAN; KAN4 | Not Available | | 50.70% |
Matrix_308 | INO | Not Available | | 50.70% |
Matrix_406 | ATERF-7 | Not Available | | 50.68% |
Matrix_329 | WRKY12 | Not Available | | 50.67% |
Matrix_380 | ATMYR1 | Not Available | | 50.67% |
Matrix_511 | AT1G05805; AT1G35460; AT1G51140; AT2G42280; AT2G43140; AT4G09180 | Not Available | | 50.63% |
Motif_211 | ABREMOTIFIOSRAB16B | Motif I found in the promoter of rice rab16B gene; Motif I and motif III are both required for ABA responsiveness; However, each can substitute for the other | | 50.61% |
Matrix_420 | ANAC58 | Not Available | | 50.60% |
Matrix_261 | ATERF-1 | Not Available | | 50.60% |
Matrix_472 | ZN_C2_H2 | Not Available | | 50.57% |
Motif_527 | LFY | Structural basis for LEAFY floral switch function and similarity with helix-turn-helix proteins | | 50.54% |
Motif_159 | LFY | Structural basis for LEAFY floral switch function and similarity with helix-turn-helix proteins | | 50.54% |
Motif_686 | LFY | Structural basis for LEAFY floral switch function and similarity with helix-turn-helix proteins | | 50.54% |
Motif_289 | LFY | Structural basis for LEAFY floral switch function and similarity with helix-turn-helix proteins | | 50.54% |
Motif_300 | ACGTROOT1; HY5 | Arabidopsis bZIP protein HY5 directly interacts with light-responsive promoters in mediating light control of gene expression. ACGT motif related to root expression; Gene: synthetic; perfect palindromic sequence (PA) containing G-box-related sequence; transacting factor: TAF-1; Binding of SGBF-1 (a Soybean G-box binding bZIP transcription factor) to ABRE is enhanced by SCOF-1 (a zinc finger protein ); Transcription of SCOF-1 is induced by low temperature and ABA | | 50.52% |
Matrix_116 | ANAC55 | Not Available | | 50.43% |
Motif_134 | ANAC092 | NAC Transcription Factor ORE1 and Senescence-Induced BIFUNCTIONAL NUCLEASE1 (BFN1) Constitute a Regulatory Cascade in Arabidopsis | | 50.40% |
Matrix_20 | ANAC030; NST1; NAC066 | Not Available | | 50.40% |
Motif_400 | ABREAZMRAB28 | ABA-responsive element (ABRE A) found at -148 to -139 in maize rab28; Maize rab28 is ABA-inducible in embryos and vegetative tissues | | 50.40% |
Matrix_454 | AT1G77200; ATERF38; AT4G16750; AT5G52020 | Not Available | | 50.39% |
Matrix_69 | AT2G03500 | Not Available | | 50.35% |
Matrix_282 | bZIP60 | Not Available | | 50.28% |
Matrix_195 | GATA2; GATA4 | Not Available | | 50.24% |
Matrix_376 | WRKY45 | Not Available | | 50.16% |
Matrix_167 | ZAT6 | Not Available | | 50.16% |
Matrix_44 | CUC3; anac046; NAC3; ANAC087; ATNAC6; CUC2 | Not Available | | 50.12% |
Motif_631 | MARARS | ARS element; Motif found in SAR (MAR) | | 50.12% |
Matrix_320 | MYC4 | Not Available | | 50.11% |
Matrix_137 | SPL1; SPL12 | Not Available | | 50.04% |
Matrix_384 | ATWRKY17 | Not Available | | 50.03% |