| 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: 15 |
| 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: 10 |
| NetGPI | no | yes: 0, no: 10 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000139 | Golgi membrane | 5 | 11 |
| GO:0012506 | vesicle membrane | 4 | 10 |
| GO:0016020 | membrane | 2 | 11 |
| GO:0030117 | membrane coat | 3 | 11 |
| GO:0030659 | cytoplasmic vesicle membrane | 5 | 10 |
| GO:0030660 | Golgi-associated vesicle membrane | 5 | 10 |
| GO:0030662 | coated vesicle membrane | 5 | 10 |
| GO:0030663 | COPI-coated vesicle membrane | 6 | 10 |
| GO:0031090 | organelle membrane | 3 | 11 |
| GO:0032991 | protein-containing complex | 1 | 11 |
| GO:0098588 | bounding membrane of organelle | 4 | 11 |
| GO:0098796 | membrane protein complex | 2 | 11 |
| GO:0110165 | cellular anatomical entity | 1 | 11 |
| GO:0030120 | vesicle coat | 4 | 1 |
| GO:0030126 | COPI vesicle coat | 5 | 1 |
Related structures:
AlphaFold database: E9B4G0
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 11 |
| GO:0006886 | intracellular protein transport | 4 | 11 |
| GO:0008104 | protein localization | 4 | 11 |
| GO:0009987 | cellular process | 1 | 11 |
| GO:0015031 | protein transport | 4 | 11 |
| GO:0016192 | vesicle-mediated transport | 4 | 11 |
| GO:0033036 | macromolecule localization | 2 | 11 |
| GO:0045184 | establishment of protein localization | 3 | 11 |
| GO:0046907 | intracellular transport | 3 | 11 |
| GO:0051179 | localization | 1 | 11 |
| GO:0051234 | establishment of localization | 2 | 11 |
| GO:0051641 | cellular localization | 2 | 11 |
| GO:0051649 | establishment of localization in cell | 3 | 11 |
| GO:0070727 | cellular macromolecule localization | 3 | 11 |
| GO:0071702 | organic substance transport | 4 | 11 |
| GO:0071705 | nitrogen compound transport | 4 | 11 |
| GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 1 |
| GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 1 |
| GO:0006891 | intra-Golgi vesicle-mediated transport | 6 | 1 |
| GO:0048193 | Golgi vesicle transport | 5 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005198 | structural molecule activity | 1 | 11 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.468 |
| CLV_C14_Caspase3-7 | 335 | 339 | PF00656 | 0.484 |
| CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.404 |
| CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.417 |
| CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.373 |
| CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.477 |
| CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.445 |
| CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.223 |
| CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.274 |
| CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.273 |
| CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.276 |
| CLV_PCSK_SKI1_1 | 629 | 633 | PF00082 | 0.358 |
| DEG_APCC_KENBOX_2 | 569 | 573 | PF00400 | 0.494 |
| DEG_SCF_FBW7_2 | 334 | 340 | PF00400 | 0.478 |
| DEG_SPOP_SBC_1 | 481 | 485 | PF00917 | 0.478 |
| DOC_CKS1_1 | 175 | 180 | PF01111 | 0.444 |
| DOC_CKS1_1 | 334 | 339 | PF01111 | 0.478 |
| DOC_CYCLIN_RxL_1 | 650 | 660 | PF00134 | 0.534 |
| DOC_CYCLIN_yCln2_LP_2 | 788 | 794 | PF00134 | 0.545 |
| DOC_MAPK_gen_1 | 282 | 289 | PF00069 | 0.366 |
| DOC_MAPK_gen_1 | 417 | 427 | PF00069 | 0.461 |
| DOC_MAPK_gen_1 | 644 | 652 | PF00069 | 0.577 |
| DOC_MAPK_HePTP_8 | 430 | 442 | PF00069 | 0.539 |
| DOC_MAPK_HePTP_8 | 626 | 638 | PF00069 | 0.476 |
| DOC_MAPK_MEF2A_6 | 433 | 442 | PF00069 | 0.458 |
| DOC_MAPK_MEF2A_6 | 629 | 638 | PF00069 | 0.473 |
| DOC_MAPK_MEF2A_6 | 644 | 652 | PF00069 | 0.440 |
| DOC_PP1_RVXF_1 | 524 | 531 | PF00149 | 0.463 |
| DOC_PP1_RVXF_1 | 60 | 67 | PF00149 | 0.338 |
| DOC_PP2B_LxvP_1 | 425 | 428 | PF13499 | 0.558 |
| DOC_PP2B_PxIxI_1 | 611 | 617 | PF00149 | 0.509 |
| DOC_PP4_FxxP_1 | 435 | 438 | PF00568 | 0.463 |
| DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.482 |
| DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.444 |
| DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.509 |
| DOC_USP7_MATH_1 | 782 | 786 | PF00917 | 0.483 |
| DOC_USP7_MATH_1 | 825 | 829 | PF00917 | 0.746 |
| DOC_USP7_MATH_1 | 851 | 855 | PF00917 | 0.638 |
| DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.417 |
| DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.613 |
| DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.519 |
| DOC_WW_Pin1_4 | 787 | 792 | PF00397 | 0.453 |
| DOC_WW_Pin1_4 | 804 | 809 | PF00397 | 0.431 |
| LIG_14-3-3_CanoR_1 | 263 | 273 | PF00244 | 0.390 |
| LIG_14-3-3_CanoR_1 | 275 | 280 | PF00244 | 0.338 |
| LIG_14-3-3_CanoR_1 | 385 | 390 | PF00244 | 0.476 |
| LIG_14-3-3_CanoR_1 | 422 | 428 | PF00244 | 0.476 |
| LIG_14-3-3_CanoR_1 | 69 | 74 | PF00244 | 0.340 |
| LIG_14-3-3_CanoR_1 | 783 | 791 | PF00244 | 0.453 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.544 |
| LIG_BIR_III_4 | 311 | 315 | PF00653 | 0.553 |
| LIG_BIR_III_4 | 879 | 883 | PF00653 | 0.535 |
| LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.530 |
| LIG_BRCT_BRCA1_1 | 234 | 238 | PF00533 | 0.391 |
| LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.463 |
| LIG_BRCT_BRCA1_1 | 483 | 487 | PF00533 | 0.558 |
| LIG_Clathr_ClatBox_1 | 574 | 578 | PF01394 | 0.544 |
| LIG_deltaCOP1_diTrp_1 | 128 | 133 | PF00928 | 0.362 |
| LIG_eIF4E_1 | 44 | 50 | PF01652 | 0.517 |
| LIG_FHA_1 | 165 | 171 | PF00498 | 0.459 |
| LIG_FHA_1 | 209 | 215 | PF00498 | 0.463 |
| LIG_FHA_1 | 259 | 265 | PF00498 | 0.389 |
| LIG_FHA_1 | 4 | 10 | PF00498 | 0.382 |
| LIG_FHA_1 | 410 | 416 | PF00498 | 0.476 |
| LIG_FHA_1 | 44 | 50 | PF00498 | 0.427 |
| LIG_FHA_1 | 453 | 459 | PF00498 | 0.519 |
| LIG_FHA_1 | 472 | 478 | PF00498 | 0.519 |
| LIG_FHA_1 | 582 | 588 | PF00498 | 0.460 |
| LIG_FHA_1 | 611 | 617 | PF00498 | 0.509 |
| LIG_FHA_2 | 115 | 121 | PF00498 | 0.463 |
| LIG_FHA_2 | 318 | 324 | PF00498 | 0.417 |
| LIG_FHA_2 | 465 | 471 | PF00498 | 0.490 |
| LIG_FHA_2 | 503 | 509 | PF00498 | 0.466 |
| LIG_FHA_2 | 638 | 644 | PF00498 | 0.442 |
| LIG_FHA_2 | 837 | 843 | PF00498 | 0.788 |
| LIG_Integrin_isoDGR_2 | 313 | 315 | PF01839 | 0.521 |
| LIG_Integrin_RGD_1 | 197 | 199 | PF01839 | 0.358 |
| LIG_LIR_Gen_1 | 373 | 384 | PF02991 | 0.482 |
| LIG_LIR_Gen_1 | 401 | 408 | PF02991 | 0.468 |
| LIG_LIR_Gen_1 | 512 | 521 | PF02991 | 0.463 |
| LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.522 |
| LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.482 |
| LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.481 |
| LIG_LIR_Nem_3 | 452 | 456 | PF02991 | 0.463 |
| LIG_LIR_Nem_3 | 512 | 518 | PF02991 | 0.463 |
| LIG_LIR_Nem_3 | 669 | 674 | PF02991 | 0.558 |
| LIG_LIR_Nem_3 | 696 | 700 | PF02991 | 0.560 |
| LIG_LIR_Nem_3 | 761 | 766 | PF02991 | 0.496 |
| LIG_LYPXL_yS_3 | 763 | 766 | PF13949 | 0.335 |
| LIG_LYPXL_yS_3 | 794 | 797 | PF13949 | 0.445 |
| LIG_MYND_1 | 795 | 799 | PF01753 | 0.440 |
| LIG_Pex14_2 | 487 | 491 | PF04695 | 0.463 |
| LIG_PTB_Apo_2 | 429 | 436 | PF02174 | 0.439 |
| LIG_SH2_CRK | 376 | 380 | PF00017 | 0.476 |
| LIG_SH2_CRK | 704 | 708 | PF00017 | 0.519 |
| LIG_SH2_GRB2like | 537 | 540 | PF00017 | 0.558 |
| LIG_SH2_NCK_1 | 376 | 380 | PF00017 | 0.558 |
| LIG_SH2_STAP1 | 758 | 762 | PF00017 | 0.548 |
| LIG_SH2_STAT3 | 42 | 45 | PF00017 | 0.482 |
| LIG_SH2_STAT3 | 499 | 502 | PF00017 | 0.558 |
| LIG_SH2_STAT3 | 537 | 540 | PF00017 | 0.558 |
| LIG_SH2_STAT3 | 586 | 589 | PF00017 | 0.544 |
| LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.463 |
| LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.463 |
| LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.483 |
| LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.494 |
| LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.484 |
| LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.445 |
| LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.463 |
| LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.376 |
| LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.463 |
| LIG_SH2_STAT5 | 704 | 707 | PF00017 | 0.544 |
| LIG_SH3_3 | 22 | 28 | PF00018 | 0.393 |
| LIG_SH3_3 | 237 | 243 | PF00018 | 0.351 |
| LIG_SH3_3 | 300 | 306 | PF00018 | 0.493 |
| LIG_SH3_3 | 331 | 337 | PF00018 | 0.478 |
| LIG_SH3_3 | 393 | 399 | PF00018 | 0.476 |
| LIG_SH3_3 | 606 | 612 | PF00018 | 0.392 |
| LIG_SH3_3 | 811 | 817 | PF00018 | 0.643 |
| LIG_SH3_3 | 819 | 825 | PF00018 | 0.746 |
| LIG_SUMO_SIM_anti_2 | 455 | 460 | PF11976 | 0.558 |
| LIG_SUMO_SIM_anti_2 | 476 | 485 | PF11976 | 0.460 |
| LIG_SUMO_SIM_anti_2 | 698 | 706 | PF11976 | 0.524 |
| LIG_SUMO_SIM_anti_2 | 741 | 747 | PF11976 | 0.464 |
| LIG_SUMO_SIM_par_1 | 112 | 117 | PF11976 | 0.464 |
| LIG_SUMO_SIM_par_1 | 438 | 445 | PF11976 | 0.546 |
| LIG_SUMO_SIM_par_1 | 476 | 485 | PF11976 | 0.478 |
| LIG_SUMO_SIM_par_1 | 612 | 617 | PF11976 | 0.509 |
| LIG_SUMO_SIM_par_1 | 698 | 706 | PF11976 | 0.473 |
| LIG_TRAF2_1 | 875 | 878 | PF00917 | 0.653 |
| LIG_TYR_ITIM | 702 | 707 | PF00017 | 0.376 |
| LIG_UBA3_1 | 378 | 387 | PF00899 | 0.316 |
| LIG_UBA3_1 | 564 | 570 | PF00899 | 0.316 |
| LIG_UBA3_1 | 574 | 581 | PF00899 | 0.273 |
| LIG_WRC_WIRS_1 | 225 | 230 | PF05994 | 0.429 |
| LIG_WRC_WIRS_1 | 50 | 55 | PF05994 | 0.370 |
| LIG_WRC_WIRS_1 | 70 | 75 | PF05994 | 0.207 |
| MOD_CDC14_SPxK_1 | 807 | 810 | PF00782 | 0.450 |
| MOD_CDK_SPxK_1 | 804 | 810 | PF00069 | 0.419 |
| MOD_CK1_1 | 2 | 8 | PF00069 | 0.565 |
| MOD_CK1_1 | 258 | 264 | PF00069 | 0.516 |
| MOD_CK1_1 | 278 | 284 | PF00069 | 0.252 |
| MOD_CK1_1 | 33 | 39 | PF00069 | 0.243 |
| MOD_CK1_1 | 380 | 386 | PF00069 | 0.308 |
| MOD_CK1_1 | 52 | 58 | PF00069 | 0.487 |
| MOD_CK1_1 | 777 | 783 | PF00069 | 0.557 |
| MOD_CK1_1 | 866 | 872 | PF00069 | 0.639 |
| MOD_CK2_1 | 224 | 230 | PF00069 | 0.454 |
| MOD_CK2_1 | 244 | 250 | PF00069 | 0.297 |
| MOD_CK2_1 | 317 | 323 | PF00069 | 0.517 |
| MOD_CK2_1 | 423 | 429 | PF00069 | 0.346 |
| MOD_CK2_1 | 464 | 470 | PF00069 | 0.399 |
| MOD_CK2_1 | 637 | 643 | PF00069 | 0.332 |
| MOD_CK2_1 | 762 | 768 | PF00069 | 0.429 |
| MOD_CK2_1 | 866 | 872 | PF00069 | 0.629 |
| MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.618 |
| MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.426 |
| MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.298 |
| MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.344 |
| MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.431 |
| MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.357 |
| MOD_GlcNHglycan | 696 | 700 | PF01048 | 0.376 |
| MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.471 |
| MOD_GlcNHglycan | 827 | 830 | PF01048 | 0.684 |
| MOD_GlcNHglycan | 865 | 868 | PF01048 | 0.693 |
| MOD_GSK3_1 | 154 | 161 | PF00069 | 0.298 |
| MOD_GSK3_1 | 204 | 211 | PF00069 | 0.457 |
| MOD_GSK3_1 | 244 | 251 | PF00069 | 0.432 |
| MOD_GSK3_1 | 264 | 271 | PF00069 | 0.256 |
| MOD_GSK3_1 | 278 | 285 | PF00069 | 0.390 |
| MOD_GSK3_1 | 29 | 36 | PF00069 | 0.230 |
| MOD_GSK3_1 | 348 | 355 | PF00069 | 0.319 |
| MOD_GSK3_1 | 374 | 381 | PF00069 | 0.277 |
| MOD_GSK3_1 | 5 | 12 | PF00069 | 0.442 |
| MOD_GSK3_1 | 610 | 617 | PF00069 | 0.334 |
| MOD_GSK3_1 | 758 | 765 | PF00069 | 0.352 |
| MOD_GSK3_1 | 827 | 834 | PF00069 | 0.716 |
| MOD_GSK3_1 | 86 | 93 | PF00069 | 0.378 |
| MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.484 |
| MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.308 |
| MOD_N-GLC_1 | 471 | 476 | PF02516 | 0.362 |
| MOD_N-GLC_1 | 502 | 507 | PF02516 | 0.362 |
| MOD_N-GLC_1 | 581 | 586 | PF02516 | 0.281 |
| MOD_NEK2_1 | 11 | 16 | PF00069 | 0.490 |
| MOD_NEK2_1 | 114 | 119 | PF00069 | 0.431 |
| MOD_NEK2_1 | 164 | 169 | PF00069 | 0.298 |
| MOD_NEK2_1 | 264 | 269 | PF00069 | 0.515 |
| MOD_NEK2_1 | 30 | 35 | PF00069 | 0.211 |
| MOD_NEK2_1 | 317 | 322 | PF00069 | 0.471 |
| MOD_NEK2_1 | 407 | 412 | PF00069 | 0.341 |
| MOD_NEK2_1 | 480 | 485 | PF00069 | 0.471 |
| MOD_NEK2_1 | 625 | 630 | PF00069 | 0.376 |
| MOD_NEK2_1 | 702 | 707 | PF00069 | 0.277 |
| MOD_NEK2_1 | 728 | 733 | PF00069 | 0.342 |
| MOD_NEK2_1 | 746 | 751 | PF00069 | 0.229 |
| MOD_NEK2_1 | 831 | 836 | PF00069 | 0.630 |
| MOD_NEK2_1 | 90 | 95 | PF00069 | 0.386 |
| MOD_NEK2_2 | 409 | 414 | PF00069 | 0.411 |
| MOD_NEK2_2 | 827 | 832 | PF00069 | 0.644 |
| MOD_NEK2_2 | 851 | 856 | PF00069 | 0.518 |
| MOD_PIKK_1 | 12 | 18 | PF00454 | 0.519 |
| MOD_PIKK_1 | 43 | 49 | PF00454 | 0.377 |
| MOD_PIKK_1 | 733 | 739 | PF00454 | 0.362 |
| MOD_PKA_1 | 282 | 288 | PF00069 | 0.414 |
| MOD_PKA_2 | 282 | 288 | PF00069 | 0.433 |
| MOD_PKA_2 | 442 | 448 | PF00069 | 0.411 |
| MOD_PKA_2 | 782 | 788 | PF00069 | 0.468 |
| MOD_Plk_1 | 120 | 126 | PF00069 | 0.298 |
| MOD_Plk_1 | 154 | 160 | PF00069 | 0.341 |
| MOD_Plk_1 | 164 | 170 | PF00069 | 0.256 |
| MOD_Plk_1 | 208 | 214 | PF00069 | 0.306 |
| MOD_Plk_1 | 322 | 328 | PF00069 | 0.316 |
| MOD_Plk_1 | 374 | 380 | PF00069 | 0.295 |
| MOD_Plk_1 | 511 | 517 | PF00069 | 0.400 |
| MOD_Plk_1 | 526 | 532 | PF00069 | 0.316 |
| MOD_Plk_1 | 581 | 587 | PF00069 | 0.296 |
| MOD_Plk_1 | 614 | 620 | PF00069 | 0.362 |
| MOD_Plk_2-3 | 348 | 354 | PF00069 | 0.411 |
| MOD_Plk_2-3 | 637 | 643 | PF00069 | 0.266 |
| MOD_Plk_2-3 | 680 | 686 | PF00069 | 0.198 |
| MOD_Plk_4 | 232 | 238 | PF00069 | 0.391 |
| MOD_Plk_4 | 30 | 36 | PF00069 | 0.229 |
| MOD_Plk_4 | 374 | 380 | PF00069 | 0.313 |
| MOD_Plk_4 | 391 | 397 | PF00069 | 0.246 |
| MOD_Plk_4 | 444 | 450 | PF00069 | 0.344 |
| MOD_Plk_4 | 482 | 488 | PF00069 | 0.352 |
| MOD_Plk_4 | 526 | 532 | PF00069 | 0.305 |
| MOD_Plk_4 | 582 | 588 | PF00069 | 0.294 |
| MOD_Plk_4 | 69 | 75 | PF00069 | 0.353 |
| MOD_Plk_4 | 762 | 768 | PF00069 | 0.396 |
| MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.411 |
| MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.508 |
| MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.376 |
| MOD_ProDKin_1 | 787 | 793 | PF00069 | 0.458 |
| MOD_ProDKin_1 | 804 | 810 | PF00069 | 0.443 |
| MOD_SUMO_rev_2 | 323 | 332 | PF00179 | 0.298 |
| MOD_SUMO_rev_2 | 516 | 525 | PF00179 | 0.431 |
| TRG_DiLeu_BaEn_1 | 260 | 265 | PF01217 | 0.476 |
| TRG_DiLeu_BaEn_1 | 476 | 481 | PF01217 | 0.411 |
| TRG_DiLeu_BaEn_1 | 627 | 632 | PF01217 | 0.431 |
| TRG_DiLeu_BaEn_1 | 741 | 746 | PF01217 | 0.431 |
| TRG_DiLeu_BaLyEn_6 | 435 | 440 | PF01217 | 0.316 |
| TRG_DiLeu_BaLyEn_6 | 856 | 861 | PF01217 | 0.513 |
| TRG_DiLeu_LyEn_5 | 260 | 265 | PF01217 | 0.476 |
| TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.326 |
| TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.308 |
| TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.278 |
| TRG_ENDOCYTIC_2 | 704 | 707 | PF00928 | 0.341 |
| TRG_ENDOCYTIC_2 | 763 | 766 | PF00928 | 0.335 |
| TRG_ENDOCYTIC_2 | 794 | 797 | PF00928 | 0.445 |
| TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.375 |
| TRG_ER_diArg_1 | 644 | 646 | PF00400 | 0.319 |
| TRG_NES_CRM1_1 | 647 | 660 | PF08389 | 0.281 |
| TRG_Pf-PMV_PEXEL_1 | 460 | 464 | PF00026 | 0.298 |
| TRG_Pf-PMV_PEXEL_1 | 629 | 633 | PF00026 | 0.431 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P2R6 | Leptomonas seymouri | 23% | 74% |
| A0A0N1HWQ8 | Leptomonas seymouri | 79% | 98% |
| A0A0S4IPS1 | Bodo saltans | 25% | 73% |
| A0A0S4J4T7 | Bodo saltans | 42% | 89% |
| A0A1X0NT50 | Trypanosomatidae | 61% | 92% |
| A0A3Q8IGV8 | Leishmania donovani | 94% | 100% |
| A0A3S7X8J8 | Leishmania donovani | 23% | 74% |
| A0A422N6J5 | Trypanosoma rangeli | 62% | 96% |
| A4HBF3 | Leishmania braziliensis | 23% | 74% |
| A4HM28 | Leishmania braziliensis | 84% | 100% |
| A4I9G2 | Leishmania infantum | 94% | 100% |
| A4IAK2 | Leishmania infantum | 23% | 74% |
| C9ZJT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
| E9B5M6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 74% |
| O35142 | Rattus norvegicus | 41% | 98% |
| O42937 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 100% |
| O55029 | Mus musculus | 41% | 98% |
| O62621 | Drosophila melanogaster | 40% | 97% |
| P35605 | Bos taurus | 41% | 98% |
| P35606 | Homo sapiens | 41% | 98% |
| P41811 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 36% | 99% |
| P53621 | Homo sapiens | 24% | 72% |
| P53622 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 74% |
| Q0J3D9 | Oryza sativa subsp. japonica | 25% | 73% |
| Q20168 | Caenorhabditis elegans | 38% | 88% |
| Q27954 | Bos taurus | 24% | 72% |
| Q4Q2B0 | Leishmania major | 22% | 74% |
| Q4Q3L5 | Leishmania major | 94% | 100% |
| Q4R4I8 | Macaca fascicularis | 41% | 98% |
| Q54YD8 | Dictyostelium discoideum | 42% | 88% |
| Q5R664 | Pongo abelii | 41% | 98% |
| Q5VQ78 | Oryza sativa subsp. japonica | 42% | 97% |
| Q6H8D5 | Oryza sativa subsp. japonica | 43% | 97% |
| Q6H8D6 | Oryza sativa subsp. japonica | 44% | 97% |
| Q8CIE6 | Mus musculus | 24% | 72% |
| Q8L828 | Arabidopsis thaliana | 43% | 97% |
| Q94A40 | Arabidopsis thaliana | 25% | 73% |
| Q96WV5 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 73% |
| Q9AUR7 | Oryza sativa subsp. japonica | 25% | 73% |
| Q9AUR8 | Oryza sativa subsp. japonica | 25% | 73% |
| Q9C827 | Arabidopsis thaliana | 42% | 95% |
| Q9CAA0 | Arabidopsis thaliana | 43% | 96% |
| Q9SJT9 | Arabidopsis thaliana | 26% | 73% |
| V5AUU0 | Trypanosoma cruzi | 59% | 97% |