Proteins belonging to the subfamily G of Eukaryotic ABC transporters. Probably functional as dimers, with broad substrate specificity.. Expanded in Kinetoplastids (also in free-living forms)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 45 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 14 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 21 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 29 |
NetGPI | no | yes: 0, no: 29 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 30 |
GO:0110165 | cellular anatomical entity | 1 | 30 |
GO:0005635 | nuclear envelope | 4 | 1 |
GO:0031967 | organelle envelope | 3 | 1 |
GO:0031975 | envelope | 2 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0030139 | endocytic vesicle | 7 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
Related structures:
AlphaFold database: E9AQ88
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0055085 | transmembrane transport | 2 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 29 |
GO:0005215 | transporter activity | 1 | 30 |
GO:0005488 | binding | 1 | 29 |
GO:0005524 | ATP binding | 5 | 29 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 30 |
GO:0017076 | purine nucleotide binding | 4 | 29 |
GO:0022804 | active transmembrane transporter activity | 3 | 30 |
GO:0022857 | transmembrane transporter activity | 2 | 30 |
GO:0030554 | adenyl nucleotide binding | 5 | 29 |
GO:0032553 | ribonucleotide binding | 3 | 29 |
GO:0032555 | purine ribonucleotide binding | 4 | 29 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 29 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 29 |
GO:0036094 | small molecule binding | 2 | 29 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 30 |
GO:0043167 | ion binding | 2 | 29 |
GO:0043168 | anion binding | 3 | 29 |
GO:0097159 | organic cyclic compound binding | 2 | 29 |
GO:0097367 | carbohydrate derivative binding | 2 | 29 |
GO:0140359 | ABC-type transporter activity | 3 | 30 |
GO:0140657 | ATP-dependent activity | 1 | 30 |
GO:1901265 | nucleoside phosphate binding | 3 | 29 |
GO:1901363 | heterocyclic compound binding | 2 | 29 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0005319 | lipid transporter activity | 2 | 1 |
GO:0005548 | phospholipid transporter activity | 3 | 1 |
GO:0090556 | phosphatidylserine floppase activity | 4 | 1 |
GO:0140303 | intramembrane lipid transporter activity | 3 | 1 |
GO:0140326 | ATPase-coupled intramembrane lipid transporter activity | 2 | 1 |
GO:0140328 | floppase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 229 | 233 | PF00656 | 0.594 |
CLV_C14_Caspase3-7 | 596 | 600 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.579 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 653 | 655 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 738 | 740 | PF00675 | 0.453 |
CLV_PCSK_FUR_1 | 132 | 136 | PF00082 | 0.346 |
CLV_PCSK_FUR_1 | 641 | 645 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 643 | 645 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 655 | 657 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 737 | 739 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.349 |
CLV_PCSK_PC1ET2_1 | 207 | 209 | PF00082 | 0.301 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.312 |
CLV_PCSK_PC1ET2_1 | 655 | 657 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.369 |
DEG_APCC_DBOX_1 | 643 | 651 | PF00400 | 0.674 |
DEG_APCC_DBOX_1 | 713 | 721 | PF00400 | 0.689 |
DEG_MDM2_SWIB_1 | 376 | 384 | PF02201 | 0.600 |
DEG_MDM2_SWIB_1 | 501 | 509 | PF02201 | 0.370 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.624 |
DEG_SCF_FBW7_1 | 590 | 596 | PF00400 | 0.498 |
DOC_CDC14_PxL_1 | 538 | 546 | PF14671 | 0.196 |
DOC_CKS1_1 | 13 | 18 | PF01111 | 0.798 |
DOC_CKS1_1 | 590 | 595 | PF01111 | 0.453 |
DOC_CKS1_1 | 683 | 688 | PF01111 | 0.725 |
DOC_CKS1_1 | 720 | 725 | PF01111 | 0.757 |
DOC_CYCLIN_RxL_1 | 174 | 185 | PF00134 | 0.553 |
DOC_CYCLIN_RxL_1 | 71 | 81 | PF00134 | 0.560 |
DOC_CYCLIN_yCln2_LP_2 | 720 | 726 | PF00134 | 0.757 |
DOC_MAPK_gen_1 | 377 | 384 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 641 | 649 | PF00069 | 0.567 |
DOC_MAPK_MEF2A_6 | 421 | 429 | PF00069 | 0.315 |
DOC_PP1_RVXF_1 | 47 | 54 | PF00149 | 0.610 |
DOC_PP1_RVXF_1 | 644 | 650 | PF00149 | 0.595 |
DOC_PP1_RVXF_1 | 72 | 79 | PF00149 | 0.651 |
DOC_PP1_SILK_1 | 195 | 200 | PF00149 | 0.529 |
DOC_PP2B_LxvP_1 | 192 | 195 | PF13499 | 0.479 |
DOC_PP2B_LxvP_1 | 314 | 317 | PF13499 | 0.530 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.629 |
DOC_USP7_MATH_2 | 16 | 22 | PF00917 | 0.654 |
DOC_USP7_MATH_2 | 317 | 323 | PF00917 | 0.604 |
DOC_USP7_UBL2_3 | 651 | 655 | PF12436 | 0.640 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.810 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 656 | 661 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 682 | 687 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 693 | 698 | PF00397 | 0.799 |
DOC_WW_Pin1_4 | 719 | 724 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 726 | 731 | PF00397 | 0.761 |
LIG_14-3-3_CanoR_1 | 135 | 140 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 393 | 399 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 583 | 587 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 613 | 619 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 714 | 718 | PF00244 | 0.784 |
LIG_Actin_WH2_2 | 614 | 631 | PF00022 | 0.398 |
LIG_APCC_ABBA_1 | 266 | 271 | PF00400 | 0.486 |
LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_1 | 372 | 376 | PF00533 | 0.586 |
LIG_deltaCOP1_diTrp_1 | 473 | 480 | PF00928 | 0.479 |
LIG_EH_1 | 217 | 221 | PF12763 | 0.594 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.522 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.515 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.562 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.633 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.508 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.333 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.569 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.802 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.818 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.524 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.545 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.580 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.348 |
LIG_FHA_2 | 594 | 600 | PF00498 | 0.402 |
LIG_FHA_2 | 723 | 729 | PF00498 | 0.807 |
LIG_GBD_Chelix_1 | 622 | 630 | PF00786 | 0.323 |
LIG_LIR_Apic_2 | 295 | 301 | PF02991 | 0.509 |
LIG_LIR_Apic_2 | 59 | 63 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 263 | 274 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 291 | 301 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 307 | 317 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 397 | 408 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 473 | 484 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 54 | 63 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 578 | 587 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 617 | 626 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 379 | 383 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 458 | 463 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 473 | 479 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 488 | 492 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 54 | 58 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 578 | 584 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 605 | 609 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 617 | 621 | PF02991 | 0.402 |
LIG_MYND_1 | 341 | 345 | PF01753 | 0.656 |
LIG_PCNA_PIPBox_1 | 419 | 428 | PF02747 | 0.405 |
LIG_Pex14_1 | 476 | 480 | PF04695 | 0.455 |
LIG_Pex14_2 | 368 | 372 | PF04695 | 0.552 |
LIG_Pex14_2 | 376 | 380 | PF04695 | 0.497 |
LIG_Pex14_2 | 480 | 484 | PF04695 | 0.342 |
LIG_Pex14_2 | 501 | 505 | PF04695 | 0.374 |
LIG_Pex14_2 | 518 | 522 | PF04695 | 0.384 |
LIG_PTB_Apo_2 | 123 | 130 | PF02174 | 0.504 |
LIG_PTB_Apo_2 | 428 | 435 | PF02174 | 0.354 |
LIG_PTB_Apo_2 | 510 | 517 | PF02174 | 0.412 |
LIG_PTB_Phospho_1 | 123 | 129 | PF10480 | 0.529 |
LIG_PTB_Phospho_1 | 510 | 516 | PF10480 | 0.412 |
LIG_Rb_pABgroove_1 | 263 | 271 | PF01858 | 0.594 |
LIG_REV1ctd_RIR_1 | 523 | 531 | PF16727 | 0.567 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.484 |
LIG_SH2_CRK | 282 | 286 | PF00017 | 0.479 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.528 |
LIG_SH2_CRK | 60 | 64 | PF00017 | 0.619 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.584 |
LIG_SH2_NCK_1 | 298 | 302 | PF00017 | 0.594 |
LIG_SH2_PTP2 | 426 | 429 | PF00017 | 0.390 |
LIG_SH2_SRC | 624 | 627 | PF00017 | 0.454 |
LIG_SH2_SRC | 726 | 729 | PF00017 | 0.670 |
LIG_SH2_STAP1 | 463 | 467 | PF00017 | 0.551 |
LIG_SH2_STAT3 | 139 | 142 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 726 | 729 | PF00017 | 0.670 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.754 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.513 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.561 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.767 |
LIG_SH3_3 | 587 | 593 | PF00018 | 0.438 |
LIG_SH3_3 | 654 | 660 | PF00018 | 0.616 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.784 |
LIG_SUMO_SIM_anti_2 | 270 | 276 | PF11976 | 0.505 |
LIG_SUMO_SIM_anti_2 | 582 | 588 | PF11976 | 0.340 |
LIG_SUMO_SIM_anti_2 | 617 | 623 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 728 | 735 | PF11976 | 0.772 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.594 |
LIG_TYR_ITIM | 487 | 492 | PF00017 | 0.387 |
LIG_TYR_ITIM | 71 | 76 | PF00017 | 0.615 |
LIG_UBA3_1 | 103 | 110 | PF00899 | 0.508 |
LIG_UBA3_1 | 191 | 199 | PF00899 | 0.546 |
LIG_UBA3_1 | 242 | 248 | PF00899 | 0.519 |
LIG_UBA3_1 | 268 | 277 | PF00899 | 0.489 |
LIG_UBA3_1 | 76 | 85 | PF00899 | 0.594 |
LIG_WRC_WIRS_1 | 522 | 527 | PF05994 | 0.512 |
LIG_WW_3 | 300 | 304 | PF00397 | 0.486 |
LIG_WW_3 | 31 | 35 | PF00397 | 0.622 |
MOD_CDK_SPK_2 | 148 | 153 | PF00069 | 0.506 |
MOD_CDK_SPK_2 | 656 | 661 | PF00069 | 0.573 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.775 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.473 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.463 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.646 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.647 |
MOD_CK1_1 | 719 | 725 | PF00069 | 0.689 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.767 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.489 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.505 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.811 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.654 |
MOD_CK2_1 | 722 | 728 | PF00069 | 0.832 |
MOD_CMANNOS | 325 | 328 | PF00535 | 0.314 |
MOD_CMANNOS | 612 | 615 | PF00535 | 0.540 |
MOD_DYRK1A_RPxSP_1 | 656 | 660 | PF00069 | 0.598 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.363 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.304 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.504 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.438 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.290 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.322 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.771 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.518 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.577 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.544 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.561 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.642 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.465 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.731 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.627 |
MOD_GSK3_1 | 722 | 729 | PF00069 | 0.781 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.470 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.379 |
MOD_N-GLC_1 | 51 | 56 | PF02516 | 0.327 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.308 |
MOD_N-GLC_2 | 367 | 369 | PF02516 | 0.325 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.547 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.517 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.533 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.348 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.384 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.323 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.354 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.389 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.516 |
MOD_NEK2_2 | 632 | 637 | PF00069 | 0.353 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.568 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.191 |
MOD_PIKK_1 | 526 | 532 | PF00454 | 0.595 |
MOD_PKA_1 | 180 | 186 | PF00069 | 0.582 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.527 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.460 |
MOD_PKA_2 | 713 | 719 | PF00069 | 0.822 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.807 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.517 |
MOD_Plk_1 | 675 | 681 | PF00069 | 0.682 |
MOD_Plk_2-3 | 670 | 676 | PF00069 | 0.657 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.491 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.468 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.347 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.520 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.229 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.381 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.457 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.339 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.243 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.788 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.545 |
MOD_Plk_4 | 722 | 728 | PF00069 | 0.797 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.509 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.811 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.500 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.479 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.624 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.449 |
MOD_ProDKin_1 | 656 | 662 | PF00069 | 0.575 |
MOD_ProDKin_1 | 682 | 688 | PF00069 | 0.720 |
MOD_ProDKin_1 | 693 | 699 | PF00069 | 0.799 |
MOD_ProDKin_1 | 719 | 725 | PF00069 | 0.754 |
MOD_ProDKin_1 | 726 | 732 | PF00069 | 0.759 |
MOD_SUMO_rev_2 | 202 | 209 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 358 | 366 | PF00179 | 0.646 |
MOD_SUMO_rev_2 | 37 | 45 | PF00179 | 0.777 |
TRG_DiLeu_BaEn_2 | 118 | 124 | PF01217 | 0.529 |
TRG_DiLeu_BaEn_2 | 446 | 452 | PF01217 | 0.486 |
TRG_DiLeu_BaEn_4 | 358 | 364 | PF01217 | 0.648 |
TRG_DiLeu_BaLyEn_6 | 534 | 539 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 626 | 631 | PF01217 | 0.213 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 463 | 466 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 565 | 568 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.609 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 172 | 174 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 641 | 644 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 653 | 656 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 736 | 739 | PF00400 | 0.585 |
TRG_NES_CRM1_1 | 315 | 330 | PF08389 | 0.642 |
TRG_NLS_Bipartite_1 | 643 | 658 | PF00514 | 0.509 |
TRG_NLS_MonoExtN_4 | 651 | 658 | PF00514 | 0.687 |
TRG_NLS_MonoExtN_4 | 737 | 743 | PF00514 | 0.653 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSP2 | Leptomonas seymouri | 82% | 100% |
A0A0N1HZC7 | Leptomonas seymouri | 28% | 100% |
A0A0S4IJ55 | Bodo saltans | 56% | 97% |
A0A0S4IQG2 | Bodo saltans | 54% | 100% |
A0A0S4IUG8 | Bodo saltans | 36% | 100% |
A0A0S4IUY5 | Bodo saltans | 32% | 100% |
A0A0S4J7U2 | Bodo saltans | 54% | 100% |
A0A0S4JAS9 | Bodo saltans | 24% | 91% |
A0A0S4JBG7 | Bodo saltans | 22% | 100% |
A0A0S4JPA7 | Bodo saltans | 51% | 99% |
A0A0S4KMF6 | Bodo saltans | 22% | 92% |
A0A1X0NKI4 | Trypanosomatidae | 31% | 100% |
A0A1X0NM50 | Trypanosomatidae | 36% | 100% |
A0A1X0NTW9 | Trypanosomatidae | 72% | 100% |
A0A1X0P4K0 | Trypanosomatidae | 21% | 100% |
A0A3Q8IA65 | Leishmania donovani | 93% | 100% |
A0A3Q8IHD8 | Leishmania donovani | 28% | 100% |
A0A3R7KEQ6 | Trypanosoma rangeli | 31% | 100% |
A0A3R7MNM8 | Trypanosoma rangeli | 35% | 100% |
A0A3S5H5N0 | Leishmania donovani | 36% | 100% |
A0A3S7WPB9 | Leishmania donovani | 34% | 100% |
A0A422N4V5 | Trypanosoma rangeli | 72% | 100% |
A4H4G9 | Leishmania braziliensis | 35% | 100% |
A4H4H6 | Leishmania braziliensis | 35% | 100% |
A4H862 | Leishmania braziliensis | 84% | 100% |
A4HPF5 | Leishmania braziliensis | 29% | 100% |
A4HSQ0 | Leishmania infantum | 35% | 100% |
A4HSQ1 | Leishmania infantum | 36% | 100% |
A4HWI7 | Leishmania infantum | 93% | 100% |
A4ID77 | Leishmania infantum | 28% | 100% |
B8ALI0 | Oryza sativa subsp. indica | 28% | 94% |
B9G5Y5 | Oryza sativa subsp. japonica | 28% | 74% |
C9ZXW1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
D0A3G8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A3K9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D3ZCM3 | Rattus norvegicus | 29% | 100% |
E9AKN6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AKN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AT67 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
H9BZ66 | Petunia hybrida | 31% | 100% |
O80946 | Arabidopsis thaliana | 29% | 100% |
P10090 | Drosophila melanogaster | 34% | 100% |
P12428 | Drosophila melanogaster | 23% | 100% |
P45843 | Drosophila melanogaster | 28% | 100% |
P45844 | Homo sapiens | 31% | 100% |
P58428 | Rattus norvegicus | 26% | 100% |
Q05360 | Lucilia cuprina | 33% | 100% |
Q09466 | Caenorhabditis elegans | 28% | 100% |
Q11180 | Caenorhabditis elegans | 30% | 100% |
Q16928 | Anopheles albimanus | 32% | 100% |
Q17320 | Ceratitis capitata | 32% | 100% |
Q24739 | Drosophila virilis | 21% | 100% |
Q27256 | Anopheles gambiae | 33% | 100% |
Q3E9B8 | Arabidopsis thaliana | 26% | 100% |
Q4GZT4 | Bos taurus | 30% | 100% |
Q4Q1D0 | Leishmania major | 28% | 100% |
Q4QF95 | Leishmania major | 92% | 100% |
Q4QJ70 | Leishmania major | 36% | 100% |
Q4QJ71 | Leishmania major | 36% | 100% |
Q55DA0 | Dictyostelium discoideum | 28% | 100% |
Q5MB13 | Macaca mulatta | 30% | 100% |
Q64343 | Mus musculus | 31% | 100% |
Q7TMS5 | Mus musculus | 30% | 100% |
Q7XA72 | Arabidopsis thaliana | 29% | 100% |
Q80W57 | Rattus norvegicus | 30% | 100% |
Q84TH5 | Arabidopsis thaliana | 29% | 100% |
Q86HQ2 | Dictyostelium discoideum | 30% | 100% |
Q8H8V7 | Oryza sativa subsp. japonica | 28% | 94% |
Q8MIB3 | Sus scrofa | 30% | 100% |
Q8RWI9 | Arabidopsis thaliana | 30% | 100% |
Q8RXN0 | Arabidopsis thaliana | 31% | 100% |
Q8T685 | Dictyostelium discoideum | 30% | 100% |
Q8T686 | Dictyostelium discoideum | 28% | 91% |
Q8T689 | Dictyostelium discoideum | 28% | 93% |
Q91WA9 | Mus musculus | 29% | 100% |
Q93YS4 | Arabidopsis thaliana | 29% | 99% |
Q99P81 | Mus musculus | 28% | 100% |
Q99PE7 | Rattus norvegicus | 28% | 100% |
Q99PE8 | Mus musculus | 28% | 100% |
Q9C6W5 | Arabidopsis thaliana | 29% | 100% |
Q9C8J8 | Arabidopsis thaliana | 28% | 100% |
Q9C8K2 | Arabidopsis thaliana | 31% | 100% |
Q9DBM0 | Mus musculus | 28% | 100% |
Q9FF46 | Arabidopsis thaliana | 28% | 67% |
Q9FLX5 | Arabidopsis thaliana | 29% | 100% |
Q9FNB5 | Arabidopsis thaliana | 29% | 100% |
Q9FT51 | Arabidopsis thaliana | 28% | 100% |
Q9H172 | Homo sapiens | 29% | 100% |
Q9H221 | Homo sapiens | 27% | 100% |
Q9H222 | Homo sapiens | 27% | 100% |
Q9LFG8 | Arabidopsis thaliana | 29% | 100% |
Q9LK50 | Arabidopsis thaliana | 31% | 100% |
Q9M2V5 | Arabidopsis thaliana | 28% | 100% |
Q9M2V6 | Arabidopsis thaliana | 28% | 100% |
Q9M2V7 | Arabidopsis thaliana | 29% | 100% |
Q9M3D6 | Arabidopsis thaliana | 28% | 100% |
Q9MAH4 | Arabidopsis thaliana | 24% | 100% |
Q9SIT6 | Arabidopsis thaliana | 28% | 100% |
Q9SJK6 | Arabidopsis thaliana | 28% | 69% |
Q9SW08 | Arabidopsis thaliana | 29% | 100% |
Q9SZR9 | Arabidopsis thaliana | 30% | 100% |
Q9UNQ0 | Homo sapiens | 29% | 100% |
Q9ZU35 | Arabidopsis thaliana | 30% | 100% |
Q9ZUT0 | Arabidopsis thaliana | 29% | 98% |
Q9ZUU9 | Arabidopsis thaliana | 25% | 100% |
V5BCE1 | Trypanosoma cruzi | 29% | 73% |
V5BPQ0 | Trypanosoma cruzi | 72% | 100% |
V5D8T8 | Trypanosoma cruzi | 37% | 100% |
V5DGN9 | Trypanosoma cruzi | 29% | 100% |