| 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. | no | yes: 0 | 
| 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: 0 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 11 | 
| NetGPI | no | yes: 0, no: 11 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0000145 | exocyst | 3 | 2 | 
| GO:0032991 | protein-containing complex | 1 | 2 | 
| GO:0099023 | vesicle tethering complex | 2 | 2 | 
Related structures:
AlphaFold database: Q4QH64
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006810 | transport | 3 | 12 | 
| GO:0006886 | intracellular protein transport | 4 | 12 | 
| GO:0006887 | exocytosis | 4 | 2 | 
| GO:0006892 | post-Golgi vesicle-mediated transport | 6 | 2 | 
| GO:0006893 | Golgi to plasma membrane transport | 5 | 2 | 
| GO:0008104 | protein localization | 4 | 12 | 
| GO:0009987 | cellular process | 1 | 12 | 
| GO:0015031 | protein transport | 4 | 12 | 
| GO:0016043 | cellular component organization | 3 | 12 | 
| GO:0016192 | vesicle-mediated transport | 4 | 2 | 
| GO:0032940 | secretion by cell | 3 | 2 | 
| GO:0033036 | macromolecule localization | 2 | 12 | 
| GO:0045184 | establishment of protein localization | 3 | 12 | 
| GO:0046903 | secretion | 4 | 2 | 
| GO:0046907 | intracellular transport | 3 | 12 | 
| GO:0048193 | Golgi vesicle transport | 5 | 2 | 
| GO:0051179 | localization | 1 | 12 | 
| GO:0051234 | establishment of localization | 2 | 12 | 
| GO:0051641 | cellular localization | 2 | 12 | 
| GO:0051649 | establishment of localization in cell | 3 | 12 | 
| GO:0051668 | localization within membrane | 3 | 2 | 
| GO:0070727 | cellular macromolecule localization | 3 | 12 | 
| GO:0071702 | organic substance transport | 4 | 12 | 
| GO:0071705 | nitrogen compound transport | 4 | 12 | 
| GO:0071840 | cellular component organization or biogenesis | 2 | 12 | 
| GO:0090522 | vesicle tethering involved in exocytosis | 3 | 12 | 
| GO:0098876 | vesicle-mediated transport to the plasma membrane | 4 | 2 | 
| GO:0099022 | vesicle tethering | 4 | 12 | 
| GO:0140029 | exocytic process | 2 | 12 | 
| GO:0140352 | export from cell | 2 | 2 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.689 | 
| CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.798 | 
| CLV_C14_Caspase3-7 | 175 | 179 | PF00656 | 0.745 | 
| CLV_C14_Caspase3-7 | 225 | 229 | PF00656 | 0.500 | 
| CLV_C14_Caspase3-7 | 286 | 290 | PF00656 | 0.524 | 
| CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.562 | 
| CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.616 | 
| CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.752 | 
| CLV_NRD_NRD_1 | 852 | 854 | PF00675 | 0.522 | 
| CLV_NRD_NRD_1 | 855 | 857 | PF00675 | 0.566 | 
| CLV_NRD_NRD_1 | 943 | 945 | PF00675 | 0.491 | 
| CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.616 | 
| CLV_PCSK_KEX2_1 | 852 | 854 | PF00082 | 0.539 | 
| CLV_PCSK_KEX2_1 | 943 | 945 | PF00082 | 0.469 | 
| CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.622 | 
| CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.574 | 
| CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.520 | 
| CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.495 | 
| CLV_PCSK_SKI1_1 | 735 | 739 | PF00082 | 0.472 | 
| CLV_PCSK_SKI1_1 | 758 | 762 | PF00082 | 0.454 | 
| CLV_PCSK_SKI1_1 | 811 | 815 | PF00082 | 0.524 | 
| DEG_APCC_DBOX_1 | 324 | 332 | PF00400 | 0.545 | 
| DEG_APCC_DBOX_1 | 431 | 439 | PF00400 | 0.308 | 
| DEG_APCC_KENBOX_2 | 257 | 261 | PF00400 | 0.562 | 
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.674 | 
| DOC_CDC14_PxL_1 | 871 | 879 | PF14671 | 0.408 | 
| DOC_CYCLIN_RxL_1 | 20 | 32 | PF00134 | 0.590 | 
| DOC_CYCLIN_RxL_1 | 811 | 822 | PF00134 | 0.538 | 
| DOC_CYCLIN_yCln2_LP_2 | 507 | 513 | PF00134 | 0.518 | 
| DOC_CYCLIN_yCln2_LP_2 | 687 | 693 | PF00134 | 0.516 | 
| DOC_MAPK_gen_1 | 312 | 320 | PF00069 | 0.488 | 
| DOC_MAPK_gen_1 | 551 | 559 | PF00069 | 0.518 | 
| DOC_MAPK_HePTP_8 | 755 | 767 | PF00069 | 0.414 | 
| DOC_MAPK_MEF2A_6 | 20 | 28 | PF00069 | 0.622 | 
| DOC_MAPK_MEF2A_6 | 432 | 439 | PF00069 | 0.307 | 
| DOC_MAPK_MEF2A_6 | 670 | 678 | PF00069 | 0.430 | 
| DOC_MAPK_MEF2A_6 | 758 | 767 | PF00069 | 0.427 | 
| DOC_MAPK_MEF2A_6 | 932 | 940 | PF00069 | 0.462 | 
| DOC_MAPK_NFAT4_5 | 432 | 440 | PF00069 | 0.303 | 
| DOC_MAPK_NFAT4_5 | 758 | 766 | PF00069 | 0.430 | 
| DOC_PP1_RVXF_1 | 23 | 29 | PF00149 | 0.595 | 
| DOC_PP2B_LxvP_1 | 370 | 373 | PF13499 | 0.530 | 
| DOC_PP2B_LxvP_1 | 676 | 679 | PF13499 | 0.407 | 
| DOC_PP2B_LxvP_1 | 687 | 690 | PF13499 | 0.388 | 
| DOC_USP7_MATH_1 | 1011 | 1015 | PF00917 | 0.733 | 
| DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.495 | 
| DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.531 | 
| DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.518 | 
| DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.496 | 
| DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.494 | 
| DOC_USP7_MATH_1 | 838 | 842 | PF00917 | 0.567 | 
| DOC_USP7_MATH_1 | 862 | 866 | PF00917 | 0.491 | 
| DOC_USP7_MATH_2 | 518 | 524 | PF00917 | 0.520 | 
| DOC_USP7_UBL2_3 | 118 | 122 | PF12436 | 0.545 | 
| DOC_USP7_UBL2_3 | 811 | 815 | PF12436 | 0.443 | 
| DOC_USP7_UBL2_3 | 996 | 1000 | PF12436 | 0.628 | 
| DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.673 | 
| DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.537 | 
| DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.543 | 
| DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.746 | 
| LIG_14-3-3_CanoR_1 | 1012 | 1016 | PF00244 | 0.736 | 
| LIG_14-3-3_CanoR_1 | 109 | 114 | PF00244 | 0.402 | 
| LIG_14-3-3_CanoR_1 | 25 | 35 | PF00244 | 0.566 | 
| LIG_14-3-3_CanoR_1 | 432 | 436 | PF00244 | 0.496 | 
| LIG_14-3-3_CanoR_1 | 670 | 675 | PF00244 | 0.479 | 
| LIG_14-3-3_CanoR_1 | 71 | 76 | PF00244 | 0.479 | 
| LIG_14-3-3_CanoR_1 | 823 | 832 | PF00244 | 0.516 | 
| LIG_14-3-3_CanoR_1 | 932 | 937 | PF00244 | 0.531 | 
| LIG_Actin_WH2_2 | 106 | 124 | PF00022 | 0.547 | 
| LIG_APCC_ABBA_1 | 459 | 464 | PF00400 | 0.633 | 
| LIG_APCC_ABBA_1 | 482 | 487 | PF00400 | 0.524 | 
| LIG_BIR_III_2 | 3 | 7 | PF00653 | 0.683 | 
| LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.584 | 
| LIG_BRCT_BRCA1_1 | 644 | 648 | PF00533 | 0.523 | 
| LIG_CaM_IQ_9 | 999 | 1014 | PF13499 | 0.733 | 
| LIG_Clathr_ClatBox_1 | 752 | 756 | PF01394 | 0.553 | 
| LIG_deltaCOP1_diTrp_1 | 444 | 452 | PF00928 | 0.502 | 
| LIG_DLG_GKlike_1 | 670 | 678 | PF00625 | 0.483 | 
| LIG_FHA_1 | 110 | 116 | PF00498 | 0.549 | 
| LIG_FHA_1 | 138 | 144 | PF00498 | 0.543 | 
| LIG_FHA_1 | 222 | 228 | PF00498 | 0.559 | 
| LIG_FHA_1 | 299 | 305 | PF00498 | 0.578 | 
| LIG_FHA_1 | 313 | 319 | PF00498 | 0.571 | 
| LIG_FHA_1 | 52 | 58 | PF00498 | 0.503 | 
| LIG_FHA_1 | 715 | 721 | PF00498 | 0.635 | 
| LIG_FHA_1 | 812 | 818 | PF00498 | 0.433 | 
| LIG_FHA_1 | 933 | 939 | PF00498 | 0.459 | 
| LIG_FHA_2 | 361 | 367 | PF00498 | 0.505 | 
| LIG_FHA_2 | 5 | 11 | PF00498 | 0.648 | 
| LIG_FHA_2 | 620 | 626 | PF00498 | 0.516 | 
| LIG_FHA_2 | 670 | 676 | PF00498 | 0.503 | 
| LIG_FHA_2 | 741 | 747 | PF00498 | 0.421 | 
| LIG_FHA_2 | 83 | 89 | PF00498 | 0.578 | 
| LIG_HCF-1_HBM_1 | 269 | 272 | PF13415 | 0.641 | 
| LIG_LIR_Gen_1 | 218 | 227 | PF02991 | 0.512 | 
| LIG_LIR_Gen_1 | 233 | 242 | PF02991 | 0.488 | 
| LIG_LIR_Gen_1 | 50 | 57 | PF02991 | 0.425 | 
| LIG_LIR_Gen_1 | 520 | 530 | PF02991 | 0.483 | 
| LIG_LIR_Gen_1 | 688 | 698 | PF02991 | 0.403 | 
| LIG_LIR_Gen_1 | 707 | 714 | PF02991 | 0.516 | 
| LIG_LIR_Gen_1 | 868 | 877 | PF02991 | 0.298 | 
| LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.516 | 
| LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.512 | 
| LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.526 | 
| LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.404 | 
| LIG_LIR_Nem_3 | 520 | 525 | PF02991 | 0.504 | 
| LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.408 | 
| LIG_LIR_Nem_3 | 688 | 694 | PF02991 | 0.441 | 
| LIG_LIR_Nem_3 | 707 | 713 | PF02991 | 0.535 | 
| LIG_LIR_Nem_3 | 738 | 744 | PF02991 | 0.396 | 
| LIG_LYPXL_yS_3 | 272 | 275 | PF13949 | 0.617 | 
| LIG_MAD2 | 25 | 33 | PF02301 | 0.577 | 
| LIG_MAD2 | 408 | 416 | PF02301 | 0.514 | 
| LIG_NRBOX | 574 | 580 | PF00104 | 0.523 | 
| LIG_PCNA_yPIPBox_3 | 811 | 825 | PF02747 | 0.435 | 
| LIG_Pex14_1 | 788 | 792 | PF04695 | 0.526 | 
| LIG_REV1ctd_RIR_1 | 810 | 819 | PF16727 | 0.512 | 
| LIG_RPA_C_Fungi | 66 | 78 | PF08784 | 0.565 | 
| LIG_SH2_CRK | 14 | 18 | PF00017 | 0.559 | 
| LIG_SH2_CRK | 234 | 238 | PF00017 | 0.525 | 
| LIG_SH2_CRK | 691 | 695 | PF00017 | 0.462 | 
| LIG_SH2_CRK | 710 | 714 | PF00017 | 0.439 | 
| LIG_SH2_PTP2 | 220 | 223 | PF00017 | 0.581 | 
| LIG_SH2_SRC | 377 | 380 | PF00017 | 0.478 | 
| LIG_SH2_SRC | 913 | 916 | PF00017 | 0.607 | 
| LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.462 | 
| LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.445 | 
| LIG_SH2_STAP1 | 659 | 663 | PF00017 | 0.452 | 
| LIG_SH2_STAP1 | 691 | 695 | PF00017 | 0.346 | 
| LIG_SH2_STAP1 | 710 | 714 | PF00017 | 0.401 | 
| LIG_SH2_STAT3 | 398 | 401 | PF00017 | 0.501 | 
| LIG_SH2_STAT3 | 930 | 933 | PF00017 | 0.550 | 
| LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.553 | 
| LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.702 | 
| LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.487 | 
| LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.497 | 
| LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.400 | 
| LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.454 | 
| LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.423 | 
| LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.367 | 
| LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.354 | 
| LIG_SH2_STAT5 | 682 | 685 | PF00017 | 0.510 | 
| LIG_SH2_STAT5 | 736 | 739 | PF00017 | 0.351 | 
| LIG_SH2_STAT5 | 766 | 769 | PF00017 | 0.379 | 
| LIG_SH2_STAT5 | 869 | 872 | PF00017 | 0.415 | 
| LIG_SH3_3 | 383 | 389 | PF00018 | 0.475 | 
| LIG_Sin3_3 | 300 | 307 | PF02671 | 0.527 | 
| LIG_Sin3_3 | 757 | 764 | PF02671 | 0.507 | 
| LIG_SUMO_SIM_anti_2 | 29 | 38 | PF11976 | 0.582 | 
| LIG_SUMO_SIM_par_1 | 111 | 117 | PF11976 | 0.593 | 
| LIG_SUMO_SIM_par_1 | 773 | 778 | PF11976 | 0.435 | 
| LIG_TRAF2_1 | 926 | 929 | PF00917 | 0.508 | 
| LIG_TRAF2_1 | 965 | 968 | PF00917 | 0.573 | 
| LIG_TYR_ITIM | 689 | 694 | PF00017 | 0.466 | 
| LIG_TYR_ITIM | 734 | 739 | PF00017 | 0.398 | 
| LIG_UBA3_1 | 249 | 258 | PF00899 | 0.577 | 
| LIG_UBA3_1 | 824 | 830 | PF00899 | 0.528 | 
| LIG_UBA3_1 | 870 | 876 | PF00899 | 0.448 | 
| LIG_UBA3_1 | 987 | 996 | PF00899 | 0.666 | 
| MOD_CDC14_SPxK_1 | 216 | 219 | PF00782 | 0.448 | 
| MOD_CDK_SPxK_1 | 213 | 219 | PF00069 | 0.469 | 
| MOD_CDK_SPxxK_3 | 544 | 551 | PF00069 | 0.530 | 
| MOD_CK1_1 | 111 | 117 | PF00069 | 0.540 | 
| MOD_CK1_1 | 168 | 174 | PF00069 | 0.693 | 
| MOD_CK1_1 | 298 | 304 | PF00069 | 0.536 | 
| MOD_CK1_1 | 321 | 327 | PF00069 | 0.548 | 
| MOD_CK1_1 | 583 | 589 | PF00069 | 0.492 | 
| MOD_CK1_1 | 677 | 683 | PF00069 | 0.531 | 
| MOD_CK1_1 | 904 | 910 | PF00069 | 0.506 | 
| MOD_CK2_1 | 169 | 175 | PF00069 | 0.708 | 
| MOD_CK2_1 | 281 | 287 | PF00069 | 0.559 | 
| MOD_CK2_1 | 360 | 366 | PF00069 | 0.498 | 
| MOD_CK2_1 | 514 | 520 | PF00069 | 0.505 | 
| MOD_CK2_1 | 549 | 555 | PF00069 | 0.412 | 
| MOD_CK2_1 | 669 | 675 | PF00069 | 0.503 | 
| MOD_CK2_1 | 740 | 746 | PF00069 | 0.386 | 
| MOD_CK2_1 | 775 | 781 | PF00069 | 0.348 | 
| MOD_CK2_1 | 862 | 868 | PF00069 | 0.496 | 
| MOD_CK2_1 | 95 | 101 | PF00069 | 0.806 | 
| MOD_Cter_Amidation | 202 | 205 | PF01082 | 0.700 | 
| MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.524 | 
| MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.416 | 
| MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.711 | 
| MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.651 | 
| MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.716 | 
| MOD_GlcNHglycan | 295 | 300 | PF01048 | 0.521 | 
| MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.472 | 
| MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.517 | 
| MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.429 | 
| MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.438 | 
| MOD_GlcNHglycan | 691 | 694 | PF01048 | 0.360 | 
| MOD_GlcNHglycan | 825 | 828 | PF01048 | 0.519 | 
| MOD_GlcNHglycan | 952 | 955 | PF01048 | 0.551 | 
| MOD_GSK3_1 | 133 | 140 | PF00069 | 0.555 | 
| MOD_GSK3_1 | 165 | 172 | PF00069 | 0.718 | 
| MOD_GSK3_1 | 180 | 187 | PF00069 | 0.690 | 
| MOD_GSK3_1 | 314 | 321 | PF00069 | 0.564 | 
| MOD_GSK3_1 | 47 | 54 | PF00069 | 0.528 | 
| MOD_GSK3_1 | 670 | 677 | PF00069 | 0.475 | 
| MOD_GSK3_1 | 681 | 688 | PF00069 | 0.405 | 
| MOD_GSK3_1 | 704 | 711 | PF00069 | 0.405 | 
| MOD_GSK3_1 | 712 | 719 | PF00069 | 0.464 | 
| MOD_GSK3_1 | 740 | 747 | PF00069 | 0.425 | 
| MOD_GSK3_1 | 76 | 83 | PF00069 | 0.499 | 
| MOD_GSK3_1 | 876 | 883 | PF00069 | 0.416 | 
| MOD_GSK3_1 | 885 | 892 | PF00069 | 0.362 | 
| MOD_GSK3_1 | 900 | 907 | PF00069 | 0.447 | 
| MOD_GSK3_1 | 95 | 102 | PF00069 | 0.776 | 
| MOD_N-GLC_1 | 514 | 519 | PF02516 | 0.539 | 
| MOD_NEK2_1 | 133 | 138 | PF00069 | 0.535 | 
| MOD_NEK2_1 | 303 | 308 | PF00069 | 0.473 | 
| MOD_NEK2_1 | 318 | 323 | PF00069 | 0.398 | 
| MOD_NEK2_1 | 46 | 51 | PF00069 | 0.477 | 
| MOD_NEK2_1 | 559 | 564 | PF00069 | 0.471 | 
| MOD_NEK2_1 | 56 | 61 | PF00069 | 0.482 | 
| MOD_NEK2_1 | 627 | 632 | PF00069 | 0.464 | 
| MOD_NEK2_1 | 644 | 649 | PF00069 | 0.315 | 
| MOD_NEK2_1 | 674 | 679 | PF00069 | 0.477 | 
| MOD_NEK2_1 | 73 | 78 | PF00069 | 0.310 | 
| MOD_NEK2_1 | 740 | 745 | PF00069 | 0.371 | 
| MOD_NEK2_1 | 813 | 818 | PF00069 | 0.415 | 
| MOD_NEK2_1 | 881 | 886 | PF00069 | 0.420 | 
| MOD_NEK2_1 | 900 | 905 | PF00069 | 0.517 | 
| MOD_NEK2_2 | 1011 | 1016 | PF00069 | 0.657 | 
| MOD_NEK2_2 | 360 | 365 | PF00069 | 0.411 | 
| MOD_NEK2_2 | 431 | 436 | PF00069 | 0.442 | 
| MOD_PIKK_1 | 347 | 353 | PF00454 | 0.546 | 
| MOD_PIKK_1 | 704 | 710 | PF00454 | 0.465 | 
| MOD_PIKK_1 | 980 | 986 | PF00454 | 0.619 | 
| MOD_PK_1 | 71 | 77 | PF00069 | 0.506 | 
| MOD_PK_1 | 876 | 882 | PF00069 | 0.534 | 
| MOD_PKA_1 | 312 | 318 | PF00069 | 0.571 | 
| MOD_PKA_2 | 1011 | 1017 | PF00069 | 0.744 | 
| MOD_PKA_2 | 108 | 114 | PF00069 | 0.411 | 
| MOD_PKA_2 | 203 | 209 | PF00069 | 0.633 | 
| MOD_PKA_2 | 321 | 327 | PF00069 | 0.541 | 
| MOD_PKA_2 | 431 | 437 | PF00069 | 0.489 | 
| MOD_PKA_2 | 669 | 675 | PF00069 | 0.503 | 
| MOD_Plk_1 | 232 | 238 | PF00069 | 0.520 | 
| MOD_Plk_1 | 674 | 680 | PF00069 | 0.484 | 
| MOD_Plk_1 | 715 | 721 | PF00069 | 0.519 | 
| MOD_Plk_4 | 1011 | 1017 | PF00069 | 0.712 | 
| MOD_Plk_4 | 222 | 228 | PF00069 | 0.561 | 
| MOD_Plk_4 | 314 | 320 | PF00069 | 0.502 | 
| MOD_Plk_4 | 51 | 57 | PF00069 | 0.491 | 
| MOD_Plk_4 | 594 | 600 | PF00069 | 0.456 | 
| MOD_Plk_4 | 627 | 633 | PF00069 | 0.444 | 
| MOD_Plk_4 | 709 | 715 | PF00069 | 0.463 | 
| MOD_Plk_4 | 716 | 722 | PF00069 | 0.538 | 
| MOD_Plk_4 | 735 | 741 | PF00069 | 0.376 | 
| MOD_Plk_4 | 768 | 774 | PF00069 | 0.447 | 
| MOD_Plk_4 | 840 | 846 | PF00069 | 0.538 | 
| MOD_Plk_4 | 876 | 882 | PF00069 | 0.400 | 
| MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.668 | 
| MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.536 | 
| MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.535 | 
| MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.746 | 
| MOD_SUMO_rev_2 | 111 | 120 | PF00179 | 0.592 | 
| TRG_DiLeu_BaEn_1 | 245 | 250 | PF01217 | 0.537 | 
| TRG_DiLeu_BaEn_4 | 245 | 251 | PF01217 | 0.560 | 
| TRG_DiLeu_BaLyEn_6 | 820 | 825 | PF01217 | 0.461 | 
| TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.554 | 
| TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.496 | 
| TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.522 | 
| TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.497 | 
| TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.387 | 
| TRG_ENDOCYTIC_2 | 659 | 662 | PF00928 | 0.514 | 
| TRG_ENDOCYTIC_2 | 691 | 694 | PF00928 | 0.369 | 
| TRG_ENDOCYTIC_2 | 710 | 713 | PF00928 | 0.418 | 
| TRG_ENDOCYTIC_2 | 736 | 739 | PF00928 | 0.374 | 
| TRG_ENDOCYTIC_2 | 869 | 872 | PF00928 | 0.294 | 
| TRG_ER_diArg_1 | 11 | 13 | PF00400 | 0.616 | 
| TRG_ER_diArg_1 | 550 | 553 | PF00400 | 0.514 | 
| TRG_ER_diArg_1 | 943 | 945 | PF00400 | 0.473 | 
| TRG_Pf-PMV_PEXEL_1 | 157 | 161 | PF00026 | 0.799 | 
| TRG_Pf-PMV_PEXEL_1 | 408 | 412 | PF00026 | 0.428 | 
| TRG_Pf-PMV_PEXEL_1 | 943 | 947 | PF00026 | 0.563 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1I3J5 | Leptomonas seymouri | 74% | 100% | 
| A0A0S4JSF8 | Bodo saltans | 32% | 91% | 
| A0A1X0NVP2 | Trypanosomatidae | 42% | 98% | 
| A0A3S7WRE4 | Leishmania donovani | 96% | 100% | 
| A0A422NYQ9 | Trypanosoma rangeli | 45% | 98% | 
| A4H9U2 | Leishmania braziliensis | 87% | 98% | 
| A4HUS8 | Leishmania infantum | 96% | 100% | 
| D0A7N6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% | 
| E9ANG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 99% | 
| V5BW65 | Trypanosoma cruzi | 44% | 98% |