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: A4H862
| 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 | 240 | 244 | PF00656 | 0.596 |
| CLV_C14_Caspase3-7 | 35 | 39 | PF00656 | 0.711 |
| CLV_C14_Caspase3-7 | 46 | 50 | PF00656 | 0.709 |
| CLV_C14_Caspase3-7 | 607 | 611 | PF00656 | 0.473 |
| CLV_C14_Caspase3-7 | 76 | 80 | PF00656 | 0.581 |
| CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.325 |
| CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.399 |
| CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.391 |
| CLV_PCSK_FUR_1 | 143 | 147 | PF00082 | 0.346 |
| CLV_PCSK_FUR_1 | 652 | 656 | PF00082 | 0.464 |
| CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.352 |
| CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.357 |
| CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.305 |
| CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.330 |
| CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.363 |
| CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.343 |
| CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.349 |
| CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.305 |
| CLV_PCSK_PC1ET2_1 | 388 | 390 | PF00082 | 0.312 |
| CLV_PCSK_PC1ET2_1 | 653 | 655 | PF00082 | 0.314 |
| CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.564 |
| CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.325 |
| CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.365 |
| DEG_APCC_DBOX_1 | 654 | 662 | PF00400 | 0.664 |
| DEG_MDM2_SWIB_1 | 387 | 395 | PF02201 | 0.600 |
| DEG_MDM2_SWIB_1 | 512 | 520 | PF02201 | 0.369 |
| DEG_SCF_FBW7_1 | 29 | 36 | PF00400 | 0.626 |
| DEG_SCF_FBW7_1 | 601 | 607 | PF00400 | 0.493 |
| DOC_CKS1_1 | 30 | 35 | PF01111 | 0.632 |
| DOC_CKS1_1 | 601 | 606 | PF01111 | 0.448 |
| DOC_CKS1_1 | 694 | 699 | PF01111 | 0.706 |
| DOC_CKS1_1 | 730 | 735 | PF01111 | 0.749 |
| DOC_CYCLIN_RxL_1 | 185 | 196 | PF00134 | 0.553 |
| DOC_CYCLIN_RxL_1 | 82 | 92 | PF00134 | 0.555 |
| DOC_CYCLIN_yCln2_LP_2 | 730 | 736 | PF00134 | 0.749 |
| DOC_MAPK_gen_1 | 388 | 395 | PF00069 | 0.561 |
| DOC_MAPK_gen_1 | 652 | 660 | PF00069 | 0.557 |
| DOC_PP1_RVXF_1 | 58 | 65 | PF00149 | 0.617 |
| DOC_PP1_RVXF_1 | 655 | 661 | PF00149 | 0.588 |
| DOC_PP1_RVXF_1 | 83 | 90 | PF00149 | 0.653 |
| DOC_PP1_SILK_1 | 206 | 211 | PF00149 | 0.529 |
| DOC_PP2B_LxvP_1 | 16 | 19 | PF13499 | 0.750 |
| DOC_PP2B_LxvP_1 | 203 | 206 | PF13499 | 0.479 |
| DOC_PP2B_LxvP_1 | 325 | 328 | PF13499 | 0.527 |
| DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.599 |
| DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.628 |
| DOC_USP7_MATH_1 | 673 | 677 | PF00917 | 0.605 |
| DOC_USP7_MATH_1 | 695 | 699 | PF00917 | 0.696 |
| DOC_USP7_MATH_1 | 703 | 707 | PF00917 | 0.745 |
| DOC_USP7_MATH_1 | 713 | 717 | PF00917 | 0.582 |
| DOC_USP7_UBL2_3 | 653 | 657 | PF12436 | 0.624 |
| DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.810 |
| DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.503 |
| DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.479 |
| DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.777 |
| DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.600 |
| DOC_WW_Pin1_4 | 597 | 602 | PF00397 | 0.424 |
| DOC_WW_Pin1_4 | 667 | 672 | PF00397 | 0.567 |
| DOC_WW_Pin1_4 | 693 | 698 | PF00397 | 0.698 |
| DOC_WW_Pin1_4 | 725 | 730 | PF00397 | 0.729 |
| DOC_WW_Pin1_4 | 736 | 741 | PF00397 | 0.762 |
| LIG_14-3-3_CanoR_1 | 146 | 151 | PF00244 | 0.547 |
| LIG_14-3-3_CanoR_1 | 183 | 190 | PF00244 | 0.518 |
| LIG_14-3-3_CanoR_1 | 192 | 196 | PF00244 | 0.522 |
| LIG_14-3-3_CanoR_1 | 404 | 410 | PF00244 | 0.359 |
| LIG_14-3-3_CanoR_1 | 594 | 598 | PF00244 | 0.451 |
| LIG_14-3-3_CanoR_1 | 624 | 630 | PF00244 | 0.238 |
| LIG_14-3-3_CanoR_1 | 672 | 682 | PF00244 | 0.636 |
| LIG_Actin_WH2_2 | 625 | 642 | PF00022 | 0.398 |
| LIG_APCC_ABBA_1 | 277 | 282 | PF00400 | 0.486 |
| LIG_BRCT_BRCA1_1 | 273 | 277 | PF00533 | 0.494 |
| LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.586 |
| LIG_BRCT_BRCA1_1 | 645 | 649 | PF00533 | 0.212 |
| LIG_BRCT_MDC1_1 | 746 | 750 | PF00533 | 0.614 |
| LIG_deltaCOP1_diTrp_1 | 484 | 491 | PF00928 | 0.479 |
| LIG_EH_1 | 228 | 232 | PF12763 | 0.594 |
| LIG_FHA_1 | 117 | 123 | PF00498 | 0.528 |
| LIG_FHA_1 | 15 | 21 | PF00498 | 0.802 |
| LIG_FHA_1 | 184 | 190 | PF00498 | 0.535 |
| LIG_FHA_1 | 222 | 228 | PF00498 | 0.512 |
| LIG_FHA_1 | 237 | 243 | PF00498 | 0.565 |
| LIG_FHA_1 | 35 | 41 | PF00498 | 0.807 |
| LIG_FHA_1 | 356 | 362 | PF00498 | 0.624 |
| LIG_FHA_1 | 473 | 479 | PF00498 | 0.508 |
| LIG_FHA_1 | 562 | 568 | PF00498 | 0.333 |
| LIG_FHA_1 | 68 | 74 | PF00498 | 0.566 |
| LIG_FHA_2 | 160 | 166 | PF00498 | 0.524 |
| LIG_FHA_2 | 238 | 244 | PF00498 | 0.552 |
| LIG_FHA_2 | 30 | 36 | PF00498 | 0.816 |
| LIG_FHA_2 | 360 | 366 | PF00498 | 0.577 |
| LIG_FHA_2 | 491 | 497 | PF00498 | 0.348 |
| LIG_FHA_2 | 605 | 611 | PF00498 | 0.399 |
| LIG_FHA_2 | 733 | 739 | PF00498 | 0.802 |
| LIG_LIR_Apic_2 | 306 | 312 | PF02991 | 0.509 |
| LIG_LIR_Apic_2 | 70 | 74 | PF02991 | 0.593 |
| LIG_LIR_Gen_1 | 228 | 238 | PF02991 | 0.504 |
| LIG_LIR_Gen_1 | 274 | 285 | PF02991 | 0.517 |
| LIG_LIR_Gen_1 | 302 | 312 | PF02991 | 0.543 |
| LIG_LIR_Gen_1 | 318 | 328 | PF02991 | 0.439 |
| LIG_LIR_Gen_1 | 408 | 419 | PF02991 | 0.331 |
| LIG_LIR_Gen_1 | 484 | 495 | PF02991 | 0.392 |
| LIG_LIR_Gen_1 | 589 | 598 | PF02991 | 0.387 |
| LIG_LIR_Gen_1 | 628 | 637 | PF02991 | 0.415 |
| LIG_LIR_Gen_1 | 65 | 74 | PF02991 | 0.557 |
| LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.504 |
| LIG_LIR_Nem_3 | 274 | 280 | PF02991 | 0.517 |
| LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.543 |
| LIG_LIR_Nem_3 | 318 | 324 | PF02991 | 0.439 |
| LIG_LIR_Nem_3 | 390 | 394 | PF02991 | 0.501 |
| LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.253 |
| LIG_LIR_Nem_3 | 469 | 474 | PF02991 | 0.495 |
| LIG_LIR_Nem_3 | 484 | 490 | PF02991 | 0.367 |
| LIG_LIR_Nem_3 | 493 | 498 | PF02991 | 0.345 |
| LIG_LIR_Nem_3 | 589 | 595 | PF02991 | 0.289 |
| LIG_LIR_Nem_3 | 628 | 632 | PF02991 | 0.401 |
| LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.548 |
| LIG_LIR_Nem_3 | 83 | 87 | PF02991 | 0.594 |
| LIG_MLH1_MIPbox_1 | 645 | 649 | PF16413 | 0.212 |
| LIG_MYND_1 | 352 | 356 | PF01753 | 0.642 |
| LIG_PCNA_PIPBox_1 | 438 | 447 | PF02747 | 0.461 |
| LIG_Pex14_1 | 487 | 491 | PF04695 | 0.455 |
| LIG_Pex14_2 | 379 | 383 | PF04695 | 0.550 |
| LIG_Pex14_2 | 387 | 391 | PF04695 | 0.497 |
| LIG_Pex14_2 | 410 | 414 | PF04695 | 0.374 |
| LIG_Pex14_2 | 491 | 495 | PF04695 | 0.342 |
| LIG_Pex14_2 | 501 | 505 | PF04695 | 0.292 |
| LIG_Pex14_2 | 512 | 516 | PF04695 | 0.374 |
| LIG_Pex14_2 | 529 | 533 | PF04695 | 0.383 |
| LIG_Pex14_2 | 588 | 592 | PF04695 | 0.299 |
| LIG_PTB_Apo_2 | 134 | 141 | PF02174 | 0.504 |
| LIG_PTB_Apo_2 | 439 | 446 | PF02174 | 0.354 |
| LIG_PTB_Apo_2 | 521 | 528 | PF02174 | 0.412 |
| LIG_PTB_Apo_2 | 619 | 626 | PF02174 | 0.379 |
| LIG_PTB_Phospho_1 | 134 | 140 | PF10480 | 0.529 |
| LIG_PTB_Phospho_1 | 521 | 527 | PF10480 | 0.412 |
| LIG_PTB_Phospho_1 | 619 | 625 | PF10480 | 0.378 |
| LIG_Rb_pABgroove_1 | 274 | 282 | PF01858 | 0.594 |
| LIG_REV1ctd_RIR_1 | 166 | 176 | PF16727 | 0.403 |
| LIG_REV1ctd_RIR_1 | 534 | 542 | PF16727 | 0.567 |
| LIG_REV1ctd_RIR_1 | 646 | 657 | PF16727 | 0.578 |
| LIG_SH2_CRK | 144 | 148 | PF00017 | 0.482 |
| LIG_SH2_CRK | 293 | 297 | PF00017 | 0.479 |
| LIG_SH2_CRK | 309 | 313 | PF00017 | 0.528 |
| LIG_SH2_CRK | 437 | 441 | PF00017 | 0.388 |
| LIG_SH2_CRK | 71 | 75 | PF00017 | 0.618 |
| LIG_SH2_CRK | 84 | 88 | PF00017 | 0.587 |
| LIG_SH2_NCK_1 | 309 | 313 | PF00017 | 0.594 |
| LIG_SH2_SRC | 635 | 638 | PF00017 | 0.453 |
| LIG_SH2_SRC | 9 | 12 | PF00017 | 0.617 |
| LIG_SH2_STAP1 | 474 | 478 | PF00017 | 0.551 |
| LIG_SH2_STAT3 | 150 | 153 | PF00017 | 0.513 |
| LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.529 |
| LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.505 |
| LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.505 |
| LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.573 |
| LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.595 |
| LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.569 |
| LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.495 |
| LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.296 |
| LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.304 |
| LIG_SH2_STAT5 | 584 | 587 | PF00017 | 0.321 |
| LIG_SH3_3 | 266 | 272 | PF00018 | 0.561 |
| LIG_SH3_3 | 5 | 11 | PF00018 | 0.740 |
| LIG_SH3_3 | 598 | 604 | PF00018 | 0.431 |
| LIG_SH3_3 | 665 | 671 | PF00018 | 0.610 |
| LIG_SUMO_SIM_anti_2 | 281 | 287 | PF11976 | 0.505 |
| LIG_SUMO_SIM_anti_2 | 593 | 600 | PF11976 | 0.334 |
| LIG_SUMO_SIM_anti_2 | 628 | 634 | PF11976 | 0.389 |
| LIG_SUMO_SIM_par_1 | 737 | 745 | PF11976 | 0.789 |
| LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.594 |
| LIG_TRAF2_1 | 735 | 738 | PF00917 | 0.616 |
| LIG_TYR_ITIM | 498 | 503 | PF00017 | 0.387 |
| LIG_TYR_ITIM | 82 | 87 | PF00017 | 0.619 |
| LIG_UBA3_1 | 114 | 121 | PF00899 | 0.506 |
| LIG_UBA3_1 | 202 | 210 | PF00899 | 0.546 |
| LIG_UBA3_1 | 253 | 259 | PF00899 | 0.521 |
| LIG_UBA3_1 | 279 | 288 | PF00899 | 0.489 |
| LIG_UBA3_1 | 87 | 96 | PF00899 | 0.594 |
| LIG_WRC_WIRS_1 | 533 | 538 | PF05994 | 0.512 |
| LIG_WW_3 | 311 | 315 | PF00397 | 0.486 |
| MOD_CDK_SPK_2 | 159 | 164 | PF00069 | 0.506 |
| MOD_CDK_SPK_2 | 667 | 672 | PF00069 | 0.567 |
| MOD_CDK_SPxxK_3 | 14 | 21 | PF00069 | 0.631 |
| MOD_CK1_1 | 12 | 18 | PF00069 | 0.770 |
| MOD_CK1_1 | 271 | 277 | PF00069 | 0.479 |
| MOD_CK1_1 | 405 | 411 | PF00069 | 0.463 |
| MOD_CK1_1 | 600 | 606 | PF00069 | 0.371 |
| MOD_CK1_1 | 676 | 682 | PF00069 | 0.619 |
| MOD_CK1_1 | 693 | 699 | PF00069 | 0.627 |
| MOD_CK1_1 | 739 | 745 | PF00069 | 0.748 |
| MOD_CK2_1 | 159 | 165 | PF00069 | 0.489 |
| MOD_CK2_1 | 210 | 216 | PF00069 | 0.502 |
| MOD_CK2_1 | 610 | 616 | PF00069 | 0.326 |
| MOD_CK2_1 | 732 | 738 | PF00069 | 0.826 |
| MOD_CK2_1 | 739 | 745 | PF00069 | 0.803 |
| MOD_CMANNOS | 336 | 339 | PF00535 | 0.305 |
| MOD_CMANNOS | 623 | 626 | PF00535 | 0.534 |
| MOD_Cter_Amidation | 650 | 653 | PF01082 | 0.384 |
| MOD_DYRK1A_RPxSP_1 | 667 | 671 | PF00069 | 0.594 |
| MOD_GlcNHglycan | 10 | 14 | PF01048 | 0.540 |
| MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.318 |
| MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.382 |
| MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.301 |
| MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.504 |
| MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.406 |
| MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.295 |
| MOD_GSK3_1 | 110 | 117 | PF00069 | 0.475 |
| MOD_GSK3_1 | 217 | 224 | PF00069 | 0.504 |
| MOD_GSK3_1 | 237 | 244 | PF00069 | 0.576 |
| MOD_GSK3_1 | 261 | 268 | PF00069 | 0.547 |
| MOD_GSK3_1 | 29 | 36 | PF00069 | 0.766 |
| MOD_GSK3_1 | 355 | 362 | PF00069 | 0.639 |
| MOD_GSK3_1 | 50 | 57 | PF00069 | 0.664 |
| MOD_GSK3_1 | 593 | 600 | PF00069 | 0.423 |
| MOD_GSK3_1 | 681 | 688 | PF00069 | 0.714 |
| MOD_GSK3_1 | 725 | 732 | PF00069 | 0.749 |
| MOD_N-GLC_1 | 123 | 128 | PF02516 | 0.351 |
| MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.327 |
| MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.306 |
| MOD_N-GLC_1 | 89 | 94 | PF02516 | 0.318 |
| MOD_NEK2_1 | 114 | 119 | PF00069 | 0.546 |
| MOD_NEK2_1 | 177 | 182 | PF00069 | 0.527 |
| MOD_NEK2_1 | 193 | 198 | PF00069 | 0.516 |
| MOD_NEK2_1 | 387 | 392 | PF00069 | 0.533 |
| MOD_NEK2_1 | 436 | 441 | PF00069 | 0.384 |
| MOD_NEK2_1 | 532 | 537 | PF00069 | 0.389 |
| MOD_NEK2_1 | 690 | 695 | PF00069 | 0.755 |
| MOD_NEK2_1 | 89 | 94 | PF00069 | 0.569 |
| MOD_NEK2_2 | 643 | 648 | PF00069 | 0.353 |
| MOD_NEK2_2 | 703 | 708 | PF00069 | 0.754 |
| MOD_PIKK_1 | 330 | 336 | PF00454 | 0.566 |
| MOD_PIKK_1 | 537 | 543 | PF00454 | 0.595 |
| MOD_PKA_1 | 191 | 197 | PF00069 | 0.577 |
| MOD_PKA_1 | 217 | 223 | PF00069 | 0.513 |
| MOD_PKA_2 | 191 | 197 | PF00069 | 0.518 |
| MOD_PKA_2 | 20 | 26 | PF00069 | 0.746 |
| MOD_PKA_2 | 593 | 599 | PF00069 | 0.449 |
| MOD_Plk_1 | 62 | 68 | PF00069 | 0.515 |
| MOD_Plk_1 | 703 | 709 | PF00069 | 0.731 |
| MOD_Plk_1 | 80 | 86 | PF00069 | 0.520 |
| MOD_Plk_2-3 | 610 | 616 | PF00069 | 0.364 |
| MOD_Plk_4 | 110 | 116 | PF00069 | 0.509 |
| MOD_Plk_4 | 146 | 152 | PF00069 | 0.519 |
| MOD_Plk_4 | 198 | 204 | PF00069 | 0.470 |
| MOD_Plk_4 | 405 | 411 | PF00069 | 0.346 |
| MOD_Plk_4 | 436 | 442 | PF00069 | 0.434 |
| MOD_Plk_4 | 472 | 478 | PF00069 | 0.520 |
| MOD_Plk_4 | 490 | 496 | PF00069 | 0.228 |
| MOD_Plk_4 | 532 | 538 | PF00069 | 0.380 |
| MOD_Plk_4 | 593 | 599 | PF00069 | 0.446 |
| MOD_Plk_4 | 610 | 616 | PF00069 | 0.373 |
| MOD_Plk_4 | 625 | 631 | PF00069 | 0.339 |
| MOD_Plk_4 | 643 | 649 | PF00069 | 0.243 |
| MOD_Plk_4 | 686 | 692 | PF00069 | 0.769 |
| MOD_Plk_4 | 713 | 719 | PF00069 | 0.824 |
| MOD_Plk_4 | 83 | 89 | PF00069 | 0.546 |
| MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.811 |
| MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.503 |
| MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.479 |
| MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.776 |
| MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.610 |
| MOD_ProDKin_1 | 597 | 603 | PF00069 | 0.426 |
| MOD_ProDKin_1 | 667 | 673 | PF00069 | 0.566 |
| MOD_ProDKin_1 | 693 | 699 | PF00069 | 0.700 |
| MOD_ProDKin_1 | 725 | 731 | PF00069 | 0.730 |
| MOD_ProDKin_1 | 736 | 742 | PF00069 | 0.761 |
| MOD_SUMO_rev_2 | 213 | 220 | PF00179 | 0.488 |
| MOD_SUMO_rev_2 | 369 | 377 | PF00179 | 0.641 |
| MOD_SUMO_rev_2 | 46 | 56 | PF00179 | 0.754 |
| TRG_DiLeu_BaEn_2 | 129 | 135 | PF01217 | 0.529 |
| TRG_DiLeu_BaEn_2 | 457 | 463 | PF01217 | 0.486 |
| TRG_DiLeu_BaEn_4 | 369 | 375 | PF01217 | 0.643 |
| TRG_DiLeu_BaLyEn_6 | 545 | 550 | PF01217 | 0.449 |
| TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.469 |
| TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.348 |
| TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.530 |
| TRG_ENDOCYTIC_2 | 500 | 503 | PF00928 | 0.321 |
| TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.305 |
| TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.325 |
| TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.613 |
| TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.509 |
| TRG_ER_diArg_1 | 652 | 655 | PF00400 | 0.626 |
| TRG_ER_diArg_1 | 664 | 667 | PF00400 | 0.623 |
| TRG_NES_CRM1_1 | 326 | 341 | PF08389 | 0.637 |
| TRG_NLS_MonoCore_2 | 651 | 656 | PF00514 | 0.588 |
| TRG_NLS_MonoExtC_3 | 652 | 657 | PF00514 | 0.558 |
| TRG_NLS_MonoExtN_4 | 652 | 657 | PF00514 | 0.639 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HSP2 | Leptomonas seymouri | 84% | 100% |
| A0A0N1HZC7 | Leptomonas seymouri | 28% | 100% |
| A0A0S4IJ55 | Bodo saltans | 57% | 98% |
| A0A0S4IQG2 | Bodo saltans | 54% | 100% |
| A0A0S4IUG8 | Bodo saltans | 37% | 100% |
| A0A0S4IUY5 | Bodo saltans | 30% | 100% |
| A0A0S4J7U2 | Bodo saltans | 54% | 100% |
| A0A0S4JAS9 | Bodo saltans | 24% | 92% |
| A0A0S4JBG7 | Bodo saltans | 22% | 100% |
| A0A0S4JPA7 | Bodo saltans | 52% | 100% |
| A0A0S4KMF6 | Bodo saltans | 22% | 93% |
| A0A1X0NKI4 | Trypanosomatidae | 30% | 100% |
| A0A1X0NM50 | Trypanosomatidae | 36% | 100% |
| A0A1X0NTW9 | Trypanosomatidae | 74% | 100% |
| A0A1X0P4K0 | Trypanosomatidae | 20% | 100% |
| A0A3Q8IA65 | Leishmania donovani | 86% | 100% |
| A0A3Q8IHD8 | Leishmania donovani | 26% | 100% |
| A0A3R7KEQ6 | Trypanosoma rangeli | 30% | 100% |
| A0A3R7MNM8 | Trypanosoma rangeli | 34% | 100% |
| A0A3S5H5N0 | Leishmania donovani | 36% | 100% |
| A0A3S7WPB9 | Leishmania donovani | 34% | 100% |
| A0A422N4V5 | Trypanosoma rangeli | 72% | 100% |
| A4H4G9 | Leishmania braziliensis | 35% | 100% |
| A4H4H6 | Leishmania braziliensis | 36% | 100% |
| A4HPF5 | Leishmania braziliensis | 28% | 100% |
| A4HSQ0 | Leishmania infantum | 34% | 100% |
| A4HSQ1 | Leishmania infantum | 36% | 100% |
| A4HWI7 | Leishmania infantum | 86% | 100% |
| A4ID77 | Leishmania infantum | 26% | 100% |
| B8ALI0 | Oryza sativa subsp. indica | 27% | 95% |
| C9ZXW1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 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 | 27% | 100% |
| E9AKN6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
| E9AKN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
| E9AQ88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
| E9AT67 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
| H9BZ66 | Petunia hybrida | 31% | 100% |
| O80946 | Arabidopsis thaliana | 28% | 100% |
| P10090 | Drosophila melanogaster | 33% | 100% |
| P12428 | Drosophila melanogaster | 23% | 100% |
| P45843 | Drosophila melanogaster | 28% | 100% |
| P45844 | Homo sapiens | 30% | 100% |
| P58428 | Rattus norvegicus | 26% | 100% |
| Q05360 | Lucilia cuprina | 30% | 100% |
| Q09466 | Caenorhabditis elegans | 27% | 100% |
| Q11180 | Caenorhabditis elegans | 31% | 100% |
| Q16928 | Anopheles albimanus | 33% | 100% |
| Q17320 | Ceratitis capitata | 32% | 100% |
| Q24739 | Drosophila virilis | 21% | 100% |
| Q27256 | Anopheles gambiae | 32% | 100% |
| Q3E9B8 | Arabidopsis thaliana | 26% | 100% |
| Q4GZT4 | Bos taurus | 29% | 100% |
| Q4Q1D0 | Leishmania major | 27% | 100% |
| Q4QF95 | Leishmania major | 85% | 99% |
| Q4QJ70 | Leishmania major | 35% | 100% |
| Q4QJ71 | Leishmania major | 35% | 100% |
| Q55DA0 | Dictyostelium discoideum | 28% | 100% |
| Q5MB13 | Macaca mulatta | 30% | 100% |
| Q64343 | Mus musculus | 30% | 100% |
| Q7TMS5 | Mus musculus | 29% | 100% |
| Q7XA72 | Arabidopsis thaliana | 28% | 100% |
| Q80W57 | Rattus norvegicus | 28% | 100% |
| Q84TH5 | Arabidopsis thaliana | 28% | 100% |
| Q86HQ2 | Dictyostelium discoideum | 29% | 100% |
| Q8H8V7 | Oryza sativa subsp. japonica | 27% | 95% |
| Q8MIB3 | Sus scrofa | 28% | 100% |
| Q8RWI9 | Arabidopsis thaliana | 30% | 100% |
| Q8RXN0 | Arabidopsis thaliana | 30% | 100% |
| Q8T685 | Dictyostelium discoideum | 28% | 100% |
| Q8T686 | Dictyostelium discoideum | 27% | 92% |
| Q8T689 | Dictyostelium discoideum | 26% | 94% |
| Q91WA9 | Mus musculus | 28% | 100% |
| Q93YS4 | Arabidopsis thaliana | 30% | 100% |
| Q99P81 | Mus musculus | 27% | 100% |
| Q99PE7 | Rattus norvegicus | 28% | 100% |
| Q99PE8 | Mus musculus | 28% | 100% |
| Q9C6W5 | Arabidopsis thaliana | 28% | 100% |
| Q9C8J8 | Arabidopsis thaliana | 28% | 100% |
| Q9C8K2 | Arabidopsis thaliana | 29% | 100% |
| Q9DBM0 | Mus musculus | 27% | 100% |
| Q9FLX5 | Arabidopsis thaliana | 29% | 100% |
| Q9FNB5 | Arabidopsis thaliana | 28% | 100% |
| Q9FT51 | Arabidopsis thaliana | 29% | 100% |
| Q9H172 | Homo sapiens | 28% | 100% |
| Q9H221 | Homo sapiens | 27% | 100% |
| Q9H222 | Homo sapiens | 27% | 100% |
| Q9LFG8 | Arabidopsis thaliana | 28% | 100% |
| Q9LK50 | Arabidopsis thaliana | 30% | 100% |
| Q9M2V5 | Arabidopsis thaliana | 26% | 100% |
| Q9M2V6 | Arabidopsis thaliana | 28% | 100% |
| Q9M2V7 | Arabidopsis thaliana | 27% | 100% |
| Q9M3D6 | Arabidopsis thaliana | 27% | 100% |
| Q9MAH4 | Arabidopsis thaliana | 25% | 100% |
| Q9SIT6 | Arabidopsis thaliana | 27% | 100% |
| Q9SJK6 | Arabidopsis thaliana | 28% | 69% |
| Q9SW08 | Arabidopsis thaliana | 30% | 100% |
| Q9SZR9 | Arabidopsis thaliana | 30% | 100% |
| Q9UNQ0 | Homo sapiens | 30% | 100% |
| Q9ZU35 | Arabidopsis thaliana | 29% | 100% |
| Q9ZUT0 | Arabidopsis thaliana | 27% | 99% |
| Q9ZUU9 | Arabidopsis thaliana | 23% | 100% |
| V5BCE1 | Trypanosoma cruzi | 29% | 74% |
| V5BPQ0 | Trypanosoma cruzi | 72% | 100% |
| V5D8T8 | Trypanosoma cruzi | 36% | 100% |
| V5DGN9 | Trypanosoma cruzi | 28% | 100% |