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. | no | 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 |
Related structures:
AlphaFold database: E9AYP8
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: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: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 |
GO:0003824 | catalytic activity | 1 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1117 | 1121 | PF00656 | 0.463 |
CLV_C14_Caspase3-7 | 1125 | 1129 | PF00656 | 0.443 |
CLV_C14_Caspase3-7 | 1193 | 1197 | PF00656 | 0.543 |
CLV_NRD_NRD_1 | 1212 | 1214 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 802 | 804 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 924 | 926 | PF00675 | 0.281 |
CLV_PCSK_KEX2_1 | 1212 | 1214 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 802 | 804 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 912 | 914 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 924 | 926 | PF00082 | 0.244 |
CLV_PCSK_PC1ET2_1 | 438 | 440 | PF00082 | 0.204 |
CLV_PCSK_PC1ET2_1 | 912 | 914 | PF00082 | 0.286 |
CLV_PCSK_PC7_1 | 434 | 440 | PF00082 | 0.204 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 1184 | 1188 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 1224 | 1228 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.226 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 691 | 695 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 745 | 749 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 783 | 787 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 850 | 854 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 896 | 900 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 906 | 910 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 925 | 929 | PF00082 | 0.202 |
DEG_APCC_DBOX_1 | 1100 | 1108 | PF00400 | 0.475 |
DEG_APCC_DBOX_1 | 151 | 159 | PF00400 | 0.514 |
DEG_APCC_DBOX_1 | 924 | 932 | PF00400 | 0.514 |
DEG_MDM2_SWIB_1 | 180 | 188 | PF02201 | 0.253 |
DOC_CYCLIN_RxL_1 | 1181 | 1192 | PF00134 | 0.447 |
DOC_MAPK_FxFP_2 | 1033 | 1036 | PF00069 | 0.449 |
DOC_MAPK_FxFP_2 | 369 | 372 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 23 | 30 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 388 | 395 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 434 | 442 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 533 | 539 | PF00069 | 0.601 |
DOC_MAPK_gen_1 | 697 | 705 | PF00069 | 0.555 |
DOC_MAPK_gen_1 | 81 | 91 | PF00069 | 0.211 |
DOC_MAPK_gen_1 | 909 | 917 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 924 | 931 | PF00069 | 0.374 |
DOC_MAPK_HePTP_8 | 921 | 933 | PF00069 | 0.345 |
DOC_MAPK_JIP1_4 | 374 | 380 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 1042 | 1051 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 1101 | 1108 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 699 | 707 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 745 | 753 | PF00069 | 0.203 |
DOC_MAPK_MEF2A_6 | 84 | 93 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 924 | 933 | PF00069 | 0.433 |
DOC_PP1_RVXF_1 | 363 | 370 | PF00149 | 0.484 |
DOC_PP1_RVXF_1 | 390 | 396 | PF00149 | 0.434 |
DOC_PP1_RVXF_1 | 781 | 788 | PF00149 | 0.497 |
DOC_PP2B_LxvP_1 | 484 | 487 | PF13499 | 0.426 |
DOC_PP2B_PxIxI_1 | 194 | 200 | PF00149 | 0.332 |
DOC_PP4_FxxP_1 | 1033 | 1036 | PF00568 | 0.449 |
DOC_PP4_FxxP_1 | 369 | 372 | PF00568 | 0.488 |
DOC_PP4_FxxP_1 | 413 | 416 | PF00568 | 0.442 |
DOC_PP4_FxxP_1 | 798 | 801 | PF00568 | 0.432 |
DOC_SPAK_OSR1_1 | 1213 | 1217 | PF12202 | 0.577 |
DOC_USP7_MATH_1 | 1009 | 1013 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 1053 | 1057 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 718 | 722 | PF00917 | 0.301 |
DOC_USP7_MATH_1 | 891 | 895 | PF00917 | 0.567 |
DOC_USP7_MATH_2 | 140 | 146 | PF00917 | 0.450 |
DOC_USP7_UBL2_3 | 258 | 262 | PF12436 | 0.483 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.351 |
LIG_14-3-3_CanoR_1 | 1213 | 1221 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 161 | 166 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 248 | 254 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 462 | 468 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 533 | 539 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 598 | 603 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 662 | 669 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 683 | 688 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 735 | 743 | PF00244 | 0.233 |
LIG_14-3-3_CanoR_1 | 745 | 750 | PF00244 | 0.180 |
LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 830 | 835 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 896 | 902 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 994 | 1001 | PF00244 | 0.517 |
LIG_Actin_WH2_2 | 767 | 785 | PF00022 | 0.366 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.650 |
LIG_BRCT_BRCA1_1 | 1047 | 1051 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 303 | 307 | PF00533 | 0.266 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.404 |
LIG_BRCT_BRCA1_1 | 463 | 467 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 783 | 787 | PF00533 | 0.490 |
LIG_Clathr_ClatBox_1 | 1185 | 1189 | PF01394 | 0.442 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.291 |
LIG_FHA_1 | 1080 | 1086 | PF00498 | 0.553 |
LIG_FHA_1 | 1190 | 1196 | PF00498 | 0.437 |
LIG_FHA_1 | 1216 | 1222 | PF00498 | 0.514 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.451 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.157 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.207 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.445 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.711 |
LIG_FHA_1 | 711 | 717 | PF00498 | 0.383 |
LIG_FHA_1 | 723 | 729 | PF00498 | 0.309 |
LIG_FHA_1 | 731 | 737 | PF00498 | 0.313 |
LIG_FHA_1 | 746 | 752 | PF00498 | 0.274 |
LIG_FHA_1 | 777 | 783 | PF00498 | 0.432 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.599 |
LIG_FHA_1 | 840 | 846 | PF00498 | 0.271 |
LIG_FHA_1 | 856 | 862 | PF00498 | 0.323 |
LIG_FHA_1 | 912 | 918 | PF00498 | 0.541 |
LIG_FHA_2 | 1097 | 1103 | PF00498 | 0.498 |
LIG_FHA_2 | 1115 | 1121 | PF00498 | 0.416 |
LIG_FHA_2 | 1128 | 1134 | PF00498 | 0.419 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.496 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.577 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.432 |
LIG_FHA_2 | 586 | 592 | PF00498 | 0.513 |
LIG_FHA_2 | 676 | 682 | PF00498 | 0.563 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.160 |
LIG_FHA_2 | 794 | 800 | PF00498 | 0.514 |
LIG_FHA_2 | 951 | 957 | PF00498 | 0.262 |
LIG_GBD_Chelix_1 | 284 | 292 | PF00786 | 0.263 |
LIG_Integrin_isoDGR_2 | 596 | 598 | PF01839 | 0.368 |
LIG_LIR_Apic_2 | 366 | 372 | PF02991 | 0.552 |
LIG_LIR_Apic_2 | 620 | 626 | PF02991 | 0.610 |
LIG_LIR_Apic_2 | 796 | 801 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 1027 | 1036 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 304 | 315 | PF02991 | 0.243 |
LIG_LIR_Gen_1 | 40 | 51 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 464 | 473 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 588 | 595 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 59 | 69 | PF02991 | 0.251 |
LIG_LIR_Gen_1 | 664 | 674 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 698 | 708 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 748 | 757 | PF02991 | 0.245 |
LIG_LIR_Gen_1 | 784 | 791 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 83 | 93 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 959 | 970 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 1027 | 1031 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.246 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 588 | 592 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 619 | 625 | PF02991 | 0.698 |
LIG_LIR_Nem_3 | 660 | 666 | PF02991 | 0.718 |
LIG_LIR_Nem_3 | 698 | 704 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 748 | 753 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 768 | 774 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 784 | 790 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 959 | 965 | PF02991 | 0.238 |
LIG_NRBOX | 807 | 813 | PF00104 | 0.450 |
LIG_PCNA_yPIPBox_3 | 23 | 34 | PF02747 | 0.563 |
LIG_Pex14_2 | 1210 | 1214 | PF04695 | 0.593 |
LIG_Pex14_2 | 180 | 184 | PF04695 | 0.261 |
LIG_Pex14_2 | 62 | 66 | PF04695 | 0.283 |
LIG_PTB_Apo_2 | 1027 | 1034 | PF02174 | 0.410 |
LIG_PTB_Apo_2 | 68 | 75 | PF02174 | 0.334 |
LIG_PTB_Phospho_1 | 68 | 74 | PF10480 | 0.314 |
LIG_REV1ctd_RIR_1 | 63 | 72 | PF16727 | 0.300 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.441 |
LIG_SH2_CRK | 771 | 775 | PF00017 | 0.386 |
LIG_SH2_NCK_1 | 1124 | 1128 | PF00017 | 0.475 |
LIG_SH2_NCK_1 | 219 | 223 | PF00017 | 0.475 |
LIG_SH2_NCK_1 | 666 | 670 | PF00017 | 0.550 |
LIG_SH2_PTP2 | 750 | 753 | PF00017 | 0.300 |
LIG_SH2_SRC | 1013 | 1016 | PF00017 | 0.550 |
LIG_SH2_SRC | 623 | 626 | PF00017 | 0.612 |
LIG_SH2_STAP1 | 490 | 494 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 589 | 593 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.226 |
LIG_SH2_STAT3 | 1160 | 1163 | PF00017 | 0.472 |
LIG_SH2_STAT3 | 74 | 77 | PF00017 | 0.145 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 571 | 574 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.704 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 750 | 753 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 761 | 764 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 773 | 776 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 777 | 780 | PF00017 | 0.514 |
LIG_SH3_1 | 623 | 629 | PF00018 | 0.530 |
LIG_SH3_2 | 626 | 631 | PF14604 | 0.530 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.562 |
LIG_SH3_3 | 623 | 629 | PF00018 | 0.530 |
LIG_Sin3_3 | 512 | 519 | PF02671 | 0.505 |
LIG_SUMO_SIM_anti_2 | 1093 | 1099 | PF11976 | 0.461 |
LIG_SUMO_SIM_anti_2 | 1102 | 1108 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 185 | 190 | PF11976 | 0.242 |
LIG_SUMO_SIM_anti_2 | 404 | 411 | PF11976 | 0.475 |
LIG_SUMO_SIM_anti_2 | 520 | 526 | PF11976 | 0.432 |
LIG_SUMO_SIM_anti_2 | 936 | 943 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 1184 | 1190 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 1233 | 1239 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 520 | 526 | PF11976 | 0.433 |
LIG_TRAF2_1 | 1129 | 1132 | PF00917 | 0.443 |
LIG_TRAF2_1 | 466 | 469 | PF00917 | 0.475 |
LIG_TRFH_1 | 622 | 626 | PF08558 | 0.522 |
LIG_UBA3_1 | 1147 | 1152 | PF00899 | 0.366 |
LIG_UBA3_1 | 692 | 697 | PF00899 | 0.493 |
LIG_WRC_WIRS_1 | 236 | 241 | PF05994 | 0.248 |
LIG_WRC_WIRS_1 | 324 | 329 | PF05994 | 0.360 |
LIG_WRC_WIRS_1 | 898 | 903 | PF05994 | 0.285 |
MOD_CK1_1 | 1112 | 1118 | PF00069 | 0.338 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.389 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.359 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.264 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.297 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.356 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.426 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.712 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.561 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.559 |
MOD_CK1_1 | 710 | 716 | PF00069 | 0.239 |
MOD_CK1_1 | 737 | 743 | PF00069 | 0.327 |
MOD_CK1_1 | 765 | 771 | PF00069 | 0.233 |
MOD_CK1_1 | 894 | 900 | PF00069 | 0.363 |
MOD_CK1_1 | 985 | 991 | PF00069 | 0.588 |
MOD_CK2_1 | 1127 | 1133 | PF00069 | 0.297 |
MOD_CK2_1 | 1257 | 1263 | PF00069 | 0.403 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.475 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.347 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.357 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.266 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.278 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.426 |
MOD_CK2_1 | 585 | 591 | PF00069 | 0.371 |
MOD_CK2_1 | 675 | 681 | PF00069 | 0.468 |
MOD_CK2_1 | 950 | 956 | PF00069 | 0.305 |
MOD_Cter_Amidation | 136 | 139 | PF01082 | 0.179 |
MOD_Cter_Amidation | 460 | 463 | PF01082 | 0.263 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.583 |
MOD_GlcNHglycan | 1114 | 1117 | PF01048 | 0.272 |
MOD_GlcNHglycan | 1165 | 1168 | PF01048 | 0.266 |
MOD_GlcNHglycan | 1192 | 1195 | PF01048 | 0.390 |
MOD_GlcNHglycan | 1238 | 1241 | PF01048 | 0.482 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.331 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.380 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.305 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.415 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.249 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.271 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.243 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.272 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.395 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.426 |
MOD_GlcNHglycan | 812 | 815 | PF01048 | 0.310 |
MOD_GlcNHglycan | 881 | 884 | PF01048 | 0.380 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.448 |
MOD_GSK3_1 | 1224 | 1231 | PF00069 | 0.423 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.325 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.336 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.335 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.315 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.331 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.366 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.435 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.733 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.643 |
MOD_GSK3_1 | 718 | 725 | PF00069 | 0.212 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.233 |
MOD_GSK3_1 | 826 | 833 | PF00069 | 0.331 |
MOD_GSK3_1 | 879 | 886 | PF00069 | 0.270 |
MOD_GSK3_1 | 936 | 943 | PF00069 | 0.376 |
MOD_GSK3_1 | 970 | 977 | PF00069 | 0.434 |
MOD_GSK3_1 | 978 | 985 | PF00069 | 0.334 |
MOD_N-GLC_1 | 1196 | 1201 | PF02516 | 0.413 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.350 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.285 |
MOD_N-GLC_1 | 645 | 650 | PF02516 | 0.512 |
MOD_N-GLC_2 | 612 | 614 | PF02516 | 0.452 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.372 |
MOD_NEK2_1 | 1060 | 1065 | PF00069 | 0.279 |
MOD_NEK2_1 | 1114 | 1119 | PF00069 | 0.284 |
MOD_NEK2_1 | 1214 | 1219 | PF00069 | 0.406 |
MOD_NEK2_1 | 1236 | 1241 | PF00069 | 0.457 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.285 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.466 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.341 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.299 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.275 |
MOD_NEK2_1 | 693 | 698 | PF00069 | 0.412 |
MOD_NEK2_1 | 707 | 712 | PF00069 | 0.248 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.247 |
MOD_NEK2_1 | 762 | 767 | PF00069 | 0.362 |
MOD_NEK2_1 | 862 | 867 | PF00069 | 0.266 |
MOD_NEK2_1 | 873 | 878 | PF00069 | 0.234 |
MOD_NEK2_1 | 940 | 945 | PF00069 | 0.302 |
MOD_NEK2_1 | 970 | 975 | PF00069 | 0.323 |
MOD_NEK2_2 | 891 | 896 | PF00069 | 0.421 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.272 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.285 |
MOD_PIKK_1 | 661 | 667 | PF00454 | 0.647 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.590 |
MOD_PIKK_1 | 722 | 728 | PF00454 | 0.386 |
MOD_PIKK_1 | 873 | 879 | PF00454 | 0.370 |
MOD_PK_1 | 683 | 689 | PF00069 | 0.425 |
MOD_PK_1 | 830 | 836 | PF00069 | 0.263 |
MOD_PK_1 | 999 | 1005 | PF00069 | 0.345 |
MOD_PKA_1 | 683 | 689 | PF00069 | 0.384 |
MOD_PKA_2 | 1228 | 1234 | PF00069 | 0.376 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.346 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.319 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.386 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.417 |
MOD_PKA_2 | 661 | 667 | PF00069 | 0.507 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.397 |
MOD_PKA_2 | 682 | 688 | PF00069 | 0.376 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.462 |
MOD_PKA_2 | 734 | 740 | PF00069 | 0.391 |
MOD_PKA_2 | 879 | 885 | PF00069 | 0.391 |
MOD_PKA_2 | 993 | 999 | PF00069 | 0.459 |
MOD_PKB_1 | 35 | 43 | PF00069 | 0.305 |
MOD_Plk_1 | 1045 | 1051 | PF00069 | 0.307 |
MOD_Plk_1 | 1090 | 1096 | PF00069 | 0.361 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.298 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.526 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.389 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.279 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.273 |
MOD_Plk_1 | 618 | 624 | PF00069 | 0.698 |
MOD_Plk_1 | 639 | 645 | PF00069 | 0.672 |
MOD_Plk_1 | 793 | 799 | PF00069 | 0.228 |
MOD_Plk_1 | 936 | 942 | PF00069 | 0.386 |
MOD_Plk_2-3 | 1091 | 1097 | PF00069 | 0.309 |
MOD_Plk_2-3 | 532 | 538 | PF00069 | 0.417 |
MOD_Plk_2-3 | 585 | 591 | PF00069 | 0.377 |
MOD_Plk_4 | 1066 | 1072 | PF00069 | 0.320 |
MOD_Plk_4 | 1102 | 1108 | PF00069 | 0.265 |
MOD_Plk_4 | 1109 | 1115 | PF00069 | 0.232 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.386 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.316 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.274 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.369 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.263 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.272 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.282 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.273 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.388 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.451 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.545 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.451 |
MOD_Plk_4 | 707 | 713 | PF00069 | 0.262 |
MOD_Plk_4 | 718 | 724 | PF00069 | 0.322 |
MOD_Plk_4 | 762 | 768 | PF00069 | 0.316 |
MOD_Plk_4 | 793 | 799 | PF00069 | 0.250 |
MOD_Plk_4 | 807 | 813 | PF00069 | 0.323 |
MOD_Plk_4 | 862 | 868 | PF00069 | 0.297 |
MOD_Plk_4 | 883 | 889 | PF00069 | 0.300 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.325 |
MOD_Plk_4 | 944 | 950 | PF00069 | 0.262 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.351 |
MOD_SUMO_for_1 | 261 | 264 | PF00179 | 0.249 |
MOD_SUMO_rev_2 | 1255 | 1260 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 526 | 535 | PF00179 | 0.401 |
MOD_SUMO_rev_2 | 679 | 686 | PF00179 | 0.510 |
TRG_DiLeu_BaEn_1 | 185 | 190 | PF01217 | 0.296 |
TRG_DiLeu_BaLyEn_6 | 192 | 197 | PF01217 | 0.271 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 666 | 669 | PF00928 | 0.604 |
TRG_ENDOCYTIC_2 | 750 | 753 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 771 | 774 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 1212 | 1214 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 436 | 439 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 801 | 803 | PF00400 | 0.383 |
TRG_NLS_MonoExtN_4 | 434 | 441 | PF00514 | 0.233 |
TRG_Pf-PMV_PEXEL_1 | 1205 | 1209 | PF00026 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 906 | 910 | PF00026 | 0.362 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A059JJ46 | Trichophyton interdigitale (strain MR816) | 33% | 95% |
A0A059JK44 | Trichophyton interdigitale (strain MR816) | 28% | 92% |
A0A095C325 | Cryptococcus gattii serotype B (strain R265) | 33% | 90% |
A0A0D1BUH6 | Ustilago maydis (strain 521 / FGSC 9021) | 29% | 92% |
A0A0D1CZ63 | Ustilago maydis (strain 521 / FGSC 9021) | 23% | 95% |
A0A0N0P6R0 | Leptomonas seymouri | 46% | 92% |
A0A0N1IM38 | Leptomonas seymouri | 72% | 99% |
A0A0S4IJN7 | Bodo saltans | 24% | 100% |
A0A0S4IRS2 | Bodo saltans | 46% | 100% |
A0A0S4JDP8 | Bodo saltans | 46% | 100% |
A0A0S4JGM3 | Bodo saltans | 48% | 100% |
A0A1U8QG99 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 30% | 99% |
A0A1U9YI12 | Clonostachys rogersoniana | 30% | 100% |
A0A1X0P748 | Trypanosomatidae | 45% | 100% |
A0A1X0P9E7 | Trypanosomatidae | 46% | 99% |
A0A348AXX9 | Curvularia clavata | 29% | 95% |
A0A3Q8ICF5 | Leishmania donovani | 95% | 100% |
A0A3S7X7M2 | Leishmania donovani | 47% | 94% |
A2XCD4 | Oryza sativa subsp. indica | 25% | 84% |
A4HCN5 | Leishmania braziliensis | 22% | 80% |
A4HFB1 | Leishmania braziliensis | 84% | 100% |
A4I2J3 | Leishmania infantum | 95% | 100% |
A4I9R3 | Leishmania infantum | 47% | 94% |
A7KVC2 | Zea mays | 24% | 84% |
B2KWH4 | Ajellomyces capsulatus | 28% | 95% |
B5X0E4 | Mus musculus | 33% | 100% |
B8K1W2 | Canis lupus familiaris | 34% | 96% |
E9B4S1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 94% |
E9Q236 | Mus musculus | 25% | 96% |
F1M3J4 | Rattus norvegicus | 25% | 96% |
F2PRR1 | Trichophyton equinum (strain ATCC MYA-4606 / CBS 127.97) | 33% | 95% |
F2Q5G0 | Trichophyton equinum (strain ATCC MYA-4606 / CBS 127.97) | 28% | 92% |
F2RP52 | Trichophyton tonsurans (strain CBS 112818) | 33% | 95% |
F2RPA4 | Trichophyton tonsurans (strain CBS 112818) | 27% | 93% |
F2SQT8 | Trichophyton rubrum (strain ATCC MYA-4607 / CBS 118892) | 31% | 98% |
F2T1C4 | Trichophyton rubrum (strain ATCC MYA-4607 / CBS 118892) | 33% | 95% |
G5EE72 | Caenorhabditis elegans | 24% | 89% |
H6TB12 | Starmerella bombicola | 31% | 98% |
J9VF33 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 33% | 90% |
O15439 | Homo sapiens | 25% | 96% |
O35379 | Mus musculus | 24% | 83% |
O70127 | Rattus norvegicus | 34% | 96% |
O80725 | Arabidopsis thaliana | 32% | 99% |
O95255 | Homo sapiens | 24% | 84% |
O95342 | Homo sapiens | 34% | 96% |
P06795 | Mus musculus | 35% | 99% |
P08183 | Homo sapiens | 35% | 99% |
P0CU83 | Trichophyton rubrum (strain ATCC MYA-4607 / CBS 118892) | 28% | 93% |
P12866 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 98% |
P13568 | Plasmodium falciparum (isolate FC27 / Papua New Guinea) | 27% | 89% |
P21439 | Homo sapiens | 35% | 99% |
P21440 | Mus musculus | 35% | 99% |
P21447 | Mus musculus | 35% | 99% |
P21448 | Cricetulus griseus | 35% | 99% |
P21449 | Cricetulus griseus | 35% | 99% |
P23174 | Cricetulus griseus | 35% | 99% |
P32386 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 76% |
P33527 | Homo sapiens | 24% | 83% |
P34712 | Caenorhabditis elegans | 31% | 96% |
P34713 | Caenorhabditis elegans | 32% | 100% |
P36619 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 93% |
P43245 | Rattus norvegicus | 35% | 99% |
P53049 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 86% |
P53706 | Candida albicans (strain WO-1) | 22% | 96% |
P78966 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 95% |
Q00449 | Drosophila melanogaster | 32% | 97% |
Q00748 | Drosophila melanogaster | 31% | 97% |
Q06034 | Leishmania enriettii | 45% | 99% |
Q08201 | Rattus norvegicus | 35% | 99% |
Q10RX7 | Oryza sativa subsp. japonica | 25% | 84% |
Q28689 | Oryctolagus cuniculus | 23% | 81% |
Q2M3G0 | Homo sapiens | 33% | 100% |
Q42093 | Arabidopsis thaliana | 25% | 78% |
Q4Q3A6 | Leishmania major | 47% | 100% |
Q4Q8S4 | Leishmania major | 94% | 100% |
Q4WA92 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 31% | 99% |
Q4WD46 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 32% | 99% |
Q4WSI1 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 29% | 95% |
Q4WTT9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 31% | 94% |
Q54BT3 | Dictyostelium discoideum | 34% | 91% |
Q5A762 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 22% | 79% |
Q5BAY0 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 32% | 94% |
Q5F364 | Gallus gallus | 23% | 83% |
Q6Q876 | Leptosphaeria maculans | 30% | 100% |
Q6UR05 | Canis lupus familiaris | 24% | 83% |
Q6YUU5 | Oryza sativa subsp. japonica | 32% | 100% |
Q7DM58 | Arabidopsis thaliana | 25% | 84% |
Q864R9 | Macaca fascicularis | 24% | 83% |
Q8CG09 | Rattus norvegicus | 24% | 83% |
Q8HXQ5 | Bos taurus | 25% | 83% |
Q8LPK2 | Arabidopsis thaliana | 32% | 100% |
Q8T9W4 | Dictyostelium discoideum | 32% | 88% |
Q8VZZ4 | Arabidopsis thaliana | 26% | 86% |
Q96J66 | Homo sapiens | 24% | 92% |
Q9C7F2 | Arabidopsis thaliana | 33% | 100% |
Q9C8G9 | Arabidopsis thaliana | 25% | 78% |
Q9C8H1 | Arabidopsis thaliana | 25% | 85% |
Q9FHF1 | Arabidopsis thaliana | 31% | 100% |
Q9FWX7 | Arabidopsis thaliana | 34% | 99% |
Q9FWX8 | Arabidopsis thaliana | 32% | 100% |
Q9LHD1 | Arabidopsis thaliana | 32% | 100% |
Q9LHK4 | Arabidopsis thaliana | 31% | 100% |
Q9LJX0 | Arabidopsis thaliana | 34% | 100% |
Q9LK62 | Arabidopsis thaliana | 25% | 85% |
Q9LK64 | Arabidopsis thaliana | 24% | 84% |
Q9LSJ2 | Arabidopsis thaliana | 32% | 100% |
Q9LSJ5 | Arabidopsis thaliana | 32% | 100% |
Q9LSJ6 | Arabidopsis thaliana | 32% | 100% |
Q9LSJ8 | Arabidopsis thaliana | 32% | 100% |
Q9LZJ5 | Arabidopsis thaliana | 22% | 82% |
Q9M0M2 | Arabidopsis thaliana | 33% | 100% |
Q9M1C7 | Arabidopsis thaliana | 25% | 84% |
Q9M1Q9 | Arabidopsis thaliana | 33% | 98% |
Q9N0V3 | Oryctolagus cuniculus | 33% | 96% |
Q9P5N0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 86% |
Q9QY30 | Mus musculus | 34% | 96% |
Q9R1S7 | Mus musculus | 24% | 85% |
Q9SGY1 | Arabidopsis thaliana | 33% | 100% |
Q9SYI2 | Arabidopsis thaliana | 33% | 100% |
Q9SYI3 | Arabidopsis thaliana | 33% | 100% |
Q9Y8G1 | Emericella nidulans | 32% | 94% |
Q9Y8G2 | Emericella nidulans | 29% | 99% |
Q9ZR72 | Arabidopsis thaliana | 32% | 99% |
S0EGU4 | Gibberella fujikuroi (strain CBS 195.34 / IMI 58289 / NRRL A-6831) | 29% | 97% |