ABC transporters probably involved in multidrug resistance. A member of this family confers vinblastine resistance to Leishmania enriettii.
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 17 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0005215 | transporter activity | 1 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 17 |
GO:0016787 | hydrolase activity | 2 | 5 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0022804 | active transmembrane transporter activity | 3 | 17 |
GO:0022857 | transmembrane transporter activity | 2 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:0140359 | ABC-type transporter activity | 3 | 17 |
GO:0140657 | ATP-dependent activity | 1 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1264 | 1268 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 699 | 703 | PF00656 | 0.498 |
CLV_MEL_PAP_1 | 1118 | 1124 | PF00089 | 0.209 |
CLV_NRD_NRD_1 | 1099 | 1101 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 1151 | 1153 | PF00675 | 0.209 |
CLV_NRD_NRD_1 | 1172 | 1174 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 1252 | 1254 | PF00675 | 0.209 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 622 | 624 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 761 | 763 | PF00675 | 0.305 |
CLV_PCSK_KEX2_1 | 1069 | 1071 | PF00082 | 0.225 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 1151 | 1153 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 1172 | 1174 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 1252 | 1254 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 761 | 763 | PF00082 | 0.370 |
CLV_PCSK_PC1ET2_1 | 1069 | 1071 | PF00082 | 0.244 |
CLV_PCSK_PC1ET2_1 | 108 | 110 | PF00082 | 0.375 |
CLV_PCSK_PC1ET2_1 | 607 | 609 | PF00082 | 0.303 |
CLV_PCSK_PC7_1 | 1147 | 1153 | PF00082 | 0.209 |
CLV_PCSK_PC7_1 | 1248 | 1254 | PF00082 | 0.262 |
CLV_PCSK_PC7_1 | 603 | 609 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 1069 | 1073 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 1248 | 1252 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 1255 | 1259 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 854 | 858 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 921 | 925 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 968 | 972 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 993 | 997 | PF00082 | 0.220 |
CLV_Separin_Metazoa | 990 | 994 | PF03568 | 0.395 |
DEG_APCC_DBOX_1 | 1151 | 1159 | PF00400 | 0.409 |
DEG_APCC_DBOX_1 | 1252 | 1260 | PF00400 | 0.503 |
DEG_MDM2_SWIB_1 | 269 | 277 | PF02201 | 0.257 |
DEG_MDM2_SWIB_1 | 916 | 924 | PF02201 | 0.209 |
DOC_CKS1_1 | 580 | 585 | PF01111 | 0.503 |
DOC_CYCLIN_RxL_1 | 1252 | 1263 | PF00134 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 820 | 826 | PF00134 | 0.303 |
DOC_MAPK_DCC_7 | 428 | 438 | PF00069 | 0.483 |
DOC_MAPK_FxFP_2 | 459 | 462 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 1151 | 1158 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 1172 | 1179 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 1252 | 1259 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 607 | 614 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 623 | 629 | PF00069 | 0.609 |
DOC_MAPK_gen_1 | 737 | 745 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 768 | 776 | PF00069 | 0.520 |
DOC_MAPK_JIP1_4 | 1253 | 1259 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 1172 | 1179 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 174 | 182 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 203 | 212 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 607 | 614 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 639 | 646 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 714 | 723 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 770 | 778 | PF00069 | 0.541 |
DOC_PP1_RVXF_1 | 207 | 213 | PF00149 | 0.462 |
DOC_PP1_RVXF_1 | 453 | 460 | PF00149 | 0.479 |
DOC_PP1_RVXF_1 | 480 | 486 | PF00149 | 0.438 |
DOC_PP1_RVXF_1 | 852 | 859 | PF00149 | 0.508 |
DOC_PP2B_LxvP_1 | 820 | 823 | PF13499 | 0.303 |
DOC_PP2B_PxIxI_1 | 283 | 289 | PF00149 | 0.345 |
DOC_PP4_FxxP_1 | 408 | 411 | PF00568 | 0.314 |
DOC_PP4_FxxP_1 | 459 | 462 | PF00568 | 0.466 |
DOC_PP4_FxxP_1 | 503 | 506 | PF00568 | 0.446 |
DOC_PP4_FxxP_1 | 869 | 872 | PF00568 | 0.436 |
DOC_USP7_MATH_1 | 1040 | 1044 | PF00917 | 0.239 |
DOC_USP7_MATH_1 | 1064 | 1068 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 1265 | 1269 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.230 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 963 | 967 | PF00917 | 0.568 |
DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.456 |
DOC_USP7_UBL2_3 | 1089 | 1093 | PF12436 | 0.578 |
DOC_USP7_UBL2_3 | 306 | 310 | PF12436 | 0.409 |
DOC_USP7_UBL2_3 | 478 | 482 | PF12436 | 0.475 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 1070 | 1075 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 1172 | 1178 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 156 | 165 | PF00244 | 0.220 |
LIG_14-3-3_CanoR_1 | 458 | 462 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 49 | 59 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 623 | 629 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 639 | 645 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 788 | 797 | PF00244 | 0.253 |
LIG_14-3-3_CanoR_1 | 968 | 974 | PF00244 | 0.436 |
LIG_APCC_ABBA_1 | 467 | 472 | PF00400 | 0.524 |
LIG_BIR_III_4 | 439 | 443 | PF00653 | 0.510 |
LIG_BRCT_BRCA1_1 | 1042 | 1046 | PF00533 | 0.199 |
LIG_BRCT_BRCA1_1 | 150 | 154 | PF00533 | 0.262 |
LIG_BRCT_BRCA1_1 | 450 | 454 | PF00533 | 0.445 |
LIG_BRCT_BRCA1_1 | 675 | 679 | PF00533 | 0.541 |
LIG_BRCT_BRCA1_1 | 756 | 760 | PF00533 | 0.401 |
LIG_CaM_IQ_9 | 322 | 338 | PF13499 | 0.409 |
LIG_Clathr_ClatBox_1 | 1256 | 1260 | PF01394 | 0.446 |
LIG_deltaCOP1_diTrp_1 | 18 | 26 | PF00928 | 0.554 |
LIG_FHA_1 | 1006 | 1012 | PF00498 | 0.223 |
LIG_FHA_1 | 1261 | 1267 | PF00498 | 0.441 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.319 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.446 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.441 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.444 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.589 |
LIG_FHA_1 | 641 | 647 | PF00498 | 0.451 |
LIG_FHA_1 | 788 | 794 | PF00498 | 0.384 |
LIG_FHA_1 | 848 | 854 | PF00498 | 0.436 |
LIG_FHA_1 | 902 | 908 | PF00498 | 0.289 |
LIG_FHA_1 | 959 | 965 | PF00498 | 0.462 |
LIG_FHA_1 | 984 | 990 | PF00498 | 0.543 |
LIG_FHA_2 | 1186 | 1192 | PF00498 | 0.420 |
LIG_FHA_2 | 1199 | 1205 | PF00498 | 0.422 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.501 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.437 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.436 |
LIG_FHA_2 | 676 | 682 | PF00498 | 0.546 |
LIG_GBD_Chelix_1 | 830 | 838 | PF00786 | 0.307 |
LIG_Integrin_RGD_1 | 39 | 41 | PF01839 | 0.348 |
LIG_KLC1_Yacidic_2 | 67 | 71 | PF13176 | 0.481 |
LIG_LIR_Apic_2 | 578 | 583 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 1031 | 1042 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 147 | 158 | PF02991 | 0.256 |
LIG_LIR_Gen_1 | 394 | 404 | PF02991 | 0.247 |
LIG_LIR_Gen_1 | 676 | 685 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 688 | 695 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 717 | 726 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 1008 | 1013 | PF02991 | 0.216 |
LIG_LIR_Nem_3 | 1031 | 1037 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 425 | 430 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 676 | 682 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 717 | 721 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 757 | 763 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 818 | 824 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 865 | 871 | PF02991 | 0.459 |
LIG_PCNA_yPIPBox_3 | 623 | 637 | PF02747 | 0.515 |
LIG_Pex14_1 | 1221 | 1225 | PF04695 | 0.503 |
LIG_Pex14_2 | 150 | 154 | PF04695 | 0.286 |
LIG_Pex14_2 | 269 | 273 | PF04695 | 0.265 |
LIG_Pex14_2 | 404 | 408 | PF04695 | 0.331 |
LIG_Pex14_2 | 916 | 920 | PF04695 | 0.220 |
LIG_PTB_Apo_2 | 453 | 460 | PF02174 | 0.509 |
LIG_PTB_Apo_2 | 95 | 102 | PF02174 | 0.517 |
LIG_REV1ctd_RIR_1 | 210 | 218 | PF16727 | 0.409 |
LIG_RPA_C_Fungi | 1168 | 1180 | PF08784 | 0.239 |
LIG_SH2_CRK | 504 | 508 | PF00017 | 0.199 |
LIG_SH2_CRK | 580 | 584 | PF00017 | 0.316 |
LIG_SH2_CRK | 821 | 825 | PF00017 | 0.391 |
LIG_SH2_NCK_1 | 1336 | 1340 | PF00017 | 0.363 |
LIG_SH2_NCK_1 | 371 | 375 | PF00017 | 0.255 |
LIG_SH2_NCK_1 | 504 | 508 | PF00017 | 0.255 |
LIG_SH2_PTP2 | 181 | 184 | PF00017 | 0.314 |
LIG_SH2_SRC | 504 | 507 | PF00017 | 0.268 |
LIG_SH2_STAP1 | 1013 | 1017 | PF00017 | 0.223 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 371 | 375 | PF00017 | 0.255 |
LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.343 |
LIG_SH2_STAT3 | 333 | 336 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 1336 | 1339 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 662 | 665 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 947 | 950 | PF00017 | 0.371 |
LIG_SH3_1 | 22 | 28 | PF00018 | 0.404 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.452 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.395 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.371 |
LIG_SH3_3 | 603 | 609 | PF00018 | 0.314 |
LIG_SH3_3 | 986 | 992 | PF00018 | 0.239 |
LIG_SUMO_SIM_anti_2 | 1303 | 1310 | PF11976 | 0.351 |
LIG_SUMO_SIM_anti_2 | 274 | 279 | PF11976 | 0.290 |
LIG_SUMO_SIM_anti_2 | 394 | 401 | PF11976 | 0.393 |
LIG_SUMO_SIM_anti_2 | 643 | 648 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 1255 | 1261 | PF11976 | 0.279 |
LIG_SUMO_SIM_par_1 | 1303 | 1310 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 434 | 439 | PF11976 | 0.281 |
LIG_SUMO_SIM_par_1 | 609 | 616 | PF11976 | 0.278 |
LIG_TRAF2_1 | 103 | 106 | PF00917 | 0.361 |
LIG_TRAF2_1 | 1201 | 1204 | PF00917 | 0.289 |
LIG_TRAF2_1 | 1318 | 1321 | PF00917 | 0.470 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.239 |
LIG_TRAF2_1 | 555 | 558 | PF00917 | 0.308 |
LIG_TRAF2_1 | 744 | 747 | PF00917 | 0.488 |
LIG_UBA3_1 | 292 | 299 | PF00899 | 0.371 |
LIG_UBA3_1 | 469 | 478 | PF00899 | 0.331 |
LIG_UBA3_1 | 763 | 770 | PF00899 | 0.450 |
LIG_WRC_WIRS_1 | 149 | 154 | PF05994 | 0.406 |
LIG_WRC_WIRS_1 | 393 | 398 | PF05994 | 0.268 |
LIG_WRC_WIRS_1 | 401 | 406 | PF05994 | 0.240 |
LIG_WRC_WIRS_1 | 913 | 918 | PF05994 | 0.379 |
LIG_WRC_WIRS_1 | 970 | 975 | PF05994 | 0.290 |
MOD_CK1_1 | 1234 | 1240 | PF00069 | 0.239 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.328 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.222 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.288 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.264 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.281 |
MOD_CK1_1 | 671 | 677 | PF00069 | 0.388 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.575 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.539 |
MOD_CK1_1 | 966 | 972 | PF00069 | 0.368 |
MOD_CK2_1 | 1185 | 1191 | PF00069 | 0.288 |
MOD_CK2_1 | 1198 | 1204 | PF00069 | 0.303 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.453 |
MOD_CK2_1 | 1265 | 1271 | PF00069 | 0.400 |
MOD_CK2_1 | 1315 | 1321 | PF00069 | 0.375 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.239 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.239 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.272 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.283 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.444 |
MOD_CK2_1 | 675 | 681 | PF00069 | 0.419 |
MOD_CK2_1 | 934 | 940 | PF00069 | 0.386 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.369 |
MOD_Cter_Amidation | 384 | 387 | PF01082 | 0.371 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.430 |
MOD_GlcNHglycan | 1013 | 1016 | PF01048 | 0.380 |
MOD_GlcNHglycan | 1065 | 1069 | PF01048 | 0.304 |
MOD_GlcNHglycan | 1084 | 1088 | PF01048 | 0.342 |
MOD_GlcNHglycan | 1106 | 1109 | PF01048 | 0.410 |
MOD_GlcNHglycan | 1152 | 1155 | PF01048 | 0.337 |
MOD_GlcNHglycan | 1185 | 1188 | PF01048 | 0.277 |
MOD_GlcNHglycan | 1233 | 1236 | PF01048 | 0.283 |
MOD_GlcNHglycan | 1263 | 1266 | PF01048 | 0.365 |
MOD_GlcNHglycan | 1309 | 1312 | PF01048 | 0.447 |
MOD_GlcNHglycan | 1337 | 1340 | PF01048 | 0.310 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.412 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.248 |
MOD_GlcNHglycan | 169 | 173 | PF01048 | 0.292 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.325 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.300 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.258 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.277 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.423 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.402 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.490 |
MOD_GlcNHglycan | 780 | 783 | PF01048 | 0.247 |
MOD_GlcNHglycan | 815 | 818 | PF01048 | 0.371 |
MOD_GlcNHglycan | 883 | 886 | PF01048 | 0.290 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.481 |
MOD_GlcNHglycan | 909 | 912 | PF01048 | 0.223 |
MOD_GSK3_1 | 1261 | 1268 | PF00069 | 0.381 |
MOD_GSK3_1 | 1334 | 1341 | PF00069 | 0.441 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.428 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.300 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.251 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.443 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.255 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.330 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.389 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.501 |
MOD_GSK3_1 | 958 | 965 | PF00069 | 0.276 |
MOD_N-GLC_1 | 1173 | 1178 | PF02516 | 0.231 |
MOD_N-GLC_1 | 356 | 361 | PF02516 | 0.264 |
MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.328 |
MOD_N-GLC_1 | 553 | 558 | PF02516 | 0.239 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.304 |
MOD_NEK2_1 | 1038 | 1043 | PF00069 | 0.323 |
MOD_NEK2_1 | 1104 | 1109 | PF00069 | 0.417 |
MOD_NEK2_1 | 1131 | 1136 | PF00069 | 0.285 |
MOD_NEK2_1 | 1185 | 1190 | PF00069 | 0.290 |
MOD_NEK2_1 | 1307 | 1312 | PF00069 | 0.437 |
MOD_NEK2_1 | 1335 | 1340 | PF00069 | 0.364 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.383 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.428 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.275 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.319 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.239 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.211 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.333 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.344 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.305 |
MOD_NEK2_1 | 983 | 988 | PF00069 | 0.406 |
MOD_NEK2_2 | 963 | 968 | PF00069 | 0.424 |
MOD_PIKK_1 | 1005 | 1011 | PF00454 | 0.226 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.371 |
MOD_PIKK_1 | 51 | 57 | PF00454 | 0.340 |
MOD_PIKK_1 | 531 | 537 | PF00454 | 0.277 |
MOD_PIKK_1 | 586 | 592 | PF00454 | 0.290 |
MOD_PK_1 | 1070 | 1076 | PF00069 | 0.343 |
MOD_PK_1 | 1173 | 1179 | PF00069 | 0.278 |
MOD_PK_1 | 12 | 18 | PF00069 | 0.469 |
MOD_PKA_2 | 1150 | 1156 | PF00069 | 0.416 |
MOD_PKA_2 | 1294 | 1300 | PF00069 | 0.329 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.321 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.266 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.444 |
MOD_PKA_2 | 787 | 793 | PF00069 | 0.469 |
MOD_Plk_1 | 1161 | 1167 | PF00069 | 0.366 |
MOD_Plk_1 | 1173 | 1179 | PF00069 | 0.214 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.304 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.257 |
MOD_Plk_1 | 768 | 774 | PF00069 | 0.405 |
MOD_Plk_1 | 803 | 809 | PF00069 | 0.446 |
MOD_Plk_1 | 983 | 989 | PF00069 | 0.338 |
MOD_Plk_2-3 | 1162 | 1168 | PF00069 | 0.315 |
MOD_Plk_2-3 | 1198 | 1204 | PF00069 | 0.278 |
MOD_Plk_2-3 | 622 | 628 | PF00069 | 0.444 |
MOD_Plk_2-3 | 675 | 681 | PF00069 | 0.415 |
MOD_Plk_4 | 1000 | 1006 | PF00069 | 0.380 |
MOD_Plk_4 | 1040 | 1046 | PF00069 | 0.428 |
MOD_Plk_4 | 1137 | 1143 | PF00069 | 0.326 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.469 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.463 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.323 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.322 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.351 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.260 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.290 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.287 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.278 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.366 |
MOD_Plk_4 | 789 | 795 | PF00069 | 0.328 |
MOD_Plk_4 | 912 | 918 | PF00069 | 0.350 |
MOD_Plk_4 | 955 | 961 | PF00069 | 0.308 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.435 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.354 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.371 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.468 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.371 |
MOD_SUMO_for_1 | 103 | 106 | PF00179 | 0.445 |
MOD_SUMO_for_1 | 749 | 752 | PF00179 | 0.294 |
MOD_SUMO_rev_2 | 102 | 110 | PF00179 | 0.572 |
MOD_SUMO_rev_2 | 1267 | 1274 | PF00179 | 0.367 |
MOD_SUMO_rev_2 | 616 | 625 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 67 | 75 | PF00179 | 0.359 |
TRG_DiLeu_BaEn_4 | 1206 | 1212 | PF01217 | 0.239 |
TRG_DiLeu_BaEn_4 | 1320 | 1326 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 928 | 933 | PF01217 | 0.371 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 821 | 824 | PF00928 | 0.382 |
TRG_ER_diArg_1 | 1171 | 1173 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 1251 | 1253 | PF00400 | 0.314 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.239 |
TRG_ER_diArg_1 | 760 | 762 | PF00400 | 0.299 |
TRG_NES_CRM1_1 | 317 | 331 | PF08389 | 0.371 |
TRG_NES_CRM1_1 | 860 | 875 | PF08389 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 631 | 635 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 800 | 804 | PF00026 | 0.257 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A059JJ46 | Trichophyton interdigitale (strain MR816) | 35% | 100% |
A0A059JK44 | Trichophyton interdigitale (strain MR816) | 29% | 97% |
A0A095C325 | Cryptococcus gattii serotype B (strain R265) | 34% | 95% |
A0A0D1BUH6 | Ustilago maydis (strain 521 / FGSC 9021) | 31% | 97% |
A0A0D1CZ63 | Ustilago maydis (strain 521 / FGSC 9021) | 23% | 100% |
A0A0N0P6R0 | Leptomonas seymouri | 57% | 98% |
A0A0N1IM38 | Leptomonas seymouri | 48% | 100% |
A0A0S4IRS2 | Bodo saltans | 56% | 100% |
A0A0S4JDP8 | Bodo saltans | 56% | 100% |
A0A0S4JGM3 | Bodo saltans | 57% | 100% |
A0A0U1LQE1 | Talaromyces islandicus | 25% | 86% |
A0A1U8QG99 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 32% | 100% |
A0A1U9YI12 | Clonostachys rogersoniana | 30% | 100% |
A0A1X0P748 | Trypanosomatidae | 45% | 100% |
A0A1X0P9E7 | Trypanosomatidae | 65% | 100% |
A0A348AXX9 | Curvularia clavata | 31% | 100% |
A0A3Q8ICF5 | Leishmania donovani | 47% | 100% |
A0A3S7WXE4 | Leishmania donovani | 24% | 86% |
A4HCN5 | Leishmania braziliensis | 24% | 85% |
A4HFB1 | Leishmania braziliensis | 47% | 100% |
A4I059 | Leishmania infantum | 24% | 85% |
A4I2J3 | Leishmania infantum | 47% | 100% |
A4I9R3 | Leishmania infantum | 100% | 100% |
B2KWH4 | Ajellomyces capsulatus | 30% | 100% |
B5X0E4 | Mus musculus | 35% | 100% |
B8K1W2 | Canis lupus familiaris | 35% | 100% |
E9AW22 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 86% |
E9AW28 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 85% |
E9AYP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9B4S1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
F2PRR1 | Trichophyton equinum (strain ATCC MYA-4606 / CBS 127.97) | 35% | 100% |
F2Q5G0 | Trichophyton equinum (strain ATCC MYA-4606 / CBS 127.97) | 29% | 97% |
F2RP52 | Trichophyton tonsurans (strain CBS 112818) | 35% | 100% |
F2RPA4 | Trichophyton tonsurans (strain CBS 112818) | 28% | 98% |
F2SQT8 | Trichophyton rubrum (strain ATCC MYA-4607 / CBS 118892) | 33% | 100% |
F2T1C4 | Trichophyton rubrum (strain ATCC MYA-4607 / CBS 118892) | 35% | 100% |
G4N2B5 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 23% | 80% |
G5EE72 | Caenorhabditis elegans | 24% | 94% |
H6TB12 | Starmerella bombicola | 33% | 100% |
J9VF33 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 35% | 95% |
K3VYH8 | Fusarium pseudograminearum (strain CS3096) | 30% | 100% |
O15440 | Homo sapiens | 25% | 93% |
O70127 | Rattus norvegicus | 33% | 100% |
O80725 | Arabidopsis thaliana | 33% | 100% |
O95342 | Homo sapiens | 35% | 100% |
P06795 | Mus musculus | 36% | 100% |
P08183 | Homo sapiens | 38% | 100% |
P0CU83 | Trichophyton rubrum (strain ATCC MYA-4607 / CBS 118892) | 29% | 98% |
P12866 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P13568 | Plasmodium falciparum (isolate FC27 / Papua New Guinea) | 27% | 95% |
P21439 | Homo sapiens | 36% | 100% |
P21440 | Mus musculus | 37% | 100% |
P21447 | Mus musculus | 37% | 100% |
P21448 | Cricetulus griseus | 38% | 100% |
P21449 | Cricetulus griseus | 36% | 100% |
P23174 | Cricetulus griseus | 37% | 100% |
P34712 | Caenorhabditis elegans | 33% | 100% |
P34713 | Caenorhabditis elegans | 33% | 100% |
P36619 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 98% |
P43245 | Rattus norvegicus | 36% | 100% |
P53706 | Candida albicans (strain WO-1) | 23% | 100% |
P78966 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
P91660 | Drosophila melanogaster | 25% | 98% |
Q00748 | Drosophila melanogaster | 34% | 100% |
Q06034 | Leishmania enriettii | 83% | 100% |
Q08201 | Rattus norvegicus | 37% | 100% |
Q2M3G0 | Homo sapiens | 35% | 100% |
Q42093 | Arabidopsis thaliana | 24% | 83% |
Q4Q3A6 | Leishmania major | 94% | 100% |
Q4Q8S4 | Leishmania major | 47% | 100% |
Q4QBF4 | Leishmania major | 24% | 85% |
Q4WA92 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 32% | 100% |
Q4WD46 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 33% | 100% |
Q4WSI1 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 31% | 100% |
Q4WTT9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 34% | 99% |
Q54BT3 | Dictyostelium discoideum | 35% | 96% |
Q5AV01 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 24% | 86% |
Q5BAY0 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 35% | 100% |
Q5F364 | Gallus gallus | 23% | 88% |
Q6Q876 | Leptosphaeria maculans | 31% | 100% |
Q6YUU5 | Oryza sativa subsp. japonica | 35% | 100% |
Q8LPK2 | Arabidopsis thaliana | 35% | 100% |
Q8T9W4 | Dictyostelium discoideum | 35% | 94% |
Q8VZZ4 | Arabidopsis thaliana | 25% | 91% |
Q96J66 | Homo sapiens | 25% | 97% |
Q9C7F2 | Arabidopsis thaliana | 35% | 100% |
Q9C7F8 | Arabidopsis thaliana | 35% | 100% |
Q9FHF1 | Arabidopsis thaliana | 33% | 100% |
Q9FWX7 | Arabidopsis thaliana | 35% | 100% |
Q9FWX8 | Arabidopsis thaliana | 34% | 100% |
Q9LHD1 | Arabidopsis thaliana | 34% | 100% |
Q9LHK4 | Arabidopsis thaliana | 31% | 100% |
Q9LJX0 | Arabidopsis thaliana | 34% | 100% |
Q9LK62 | Arabidopsis thaliana | 24% | 90% |
Q9LK64 | Arabidopsis thaliana | 24% | 89% |
Q9LSJ2 | Arabidopsis thaliana | 34% | 100% |
Q9LSJ5 | Arabidopsis thaliana | 35% | 100% |
Q9LSJ6 | Arabidopsis thaliana | 34% | 100% |
Q9LSJ8 | Arabidopsis thaliana | 35% | 100% |
Q9M0M2 | Arabidopsis thaliana | 33% | 100% |
Q9M1Q9 | Arabidopsis thaliana | 34% | 100% |
Q9N0V3 | Oryctolagus cuniculus | 34% | 100% |
Q9P5N0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 92% |
Q9QY30 | Mus musculus | 34% | 100% |
Q9SGY1 | Arabidopsis thaliana | 35% | 100% |
Q9SYI2 | Arabidopsis thaliana | 35% | 100% |
Q9SYI3 | Arabidopsis thaliana | 34% | 100% |
Q9Y8G1 | Emericella nidulans | 35% | 99% |
Q9Y8G2 | Emericella nidulans | 32% | 100% |
Q9ZR72 | Arabidopsis thaliana | 35% | 100% |
S0EGU4 | Gibberella fujikuroi (strain CBS 195.34 / IMI 58289 / NRRL A-6831) | 30% | 100% |