| 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:0000151 | ubiquitin ligase complex | 3 | 1 |
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
| GO:0032991 | protein-containing complex | 1 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
| GO:0140535 | intracellular protein-containing complex | 2 | 1 |
| GO:1902494 | catalytic complex | 2 | 1 |
| GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8IF31
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006508 | proteolysis | 4 | 12 |
| GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 12 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
| GO:0008152 | metabolic process | 1 | 12 |
| GO:0009056 | catabolic process | 2 | 12 |
| GO:0009057 | macromolecule catabolic process | 4 | 12 |
| GO:0009987 | cellular process | 1 | 12 |
| GO:0019538 | protein metabolic process | 3 | 12 |
| GO:0019941 | modification-dependent protein catabolic process | 6 | 12 |
| GO:0043170 | macromolecule metabolic process | 3 | 12 |
| GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 12 |
| GO:0044237 | cellular metabolic process | 2 | 12 |
| GO:0044238 | primary metabolic process | 2 | 12 |
| GO:0044248 | cellular catabolic process | 3 | 12 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
| GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 12 |
| GO:0051603 | proteolysis involved in protein catabolic process | 5 | 12 |
| GO:0071704 | organic substance metabolic process | 2 | 12 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
| GO:1901575 | organic substance catabolic process | 3 | 12 |
| GO:0016567 | protein ubiquitination | 7 | 1 |
| GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
| GO:0036211 | protein modification process | 4 | 1 |
| GO:0043412 | macromolecule modification | 4 | 1 |
| GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005488 | binding | 1 | 12 |
| GO:0005515 | protein binding | 2 | 12 |
| GO:0019899 | enzyme binding | 3 | 12 |
| GO:0031625 | ubiquitin protein ligase binding | 5 | 12 |
| GO:0044389 | ubiquitin-like protein ligase binding | 4 | 12 |
| GO:0030674 | protein-macromolecule adaptor activity | 2 | 1 |
| GO:0060090 | molecular adaptor activity | 1 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.529 |
| CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.330 |
| CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.367 |
| CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.271 |
| CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.451 |
| CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.341 |
| CLV_NRD_NRD_1 | 648 | 650 | PF00675 | 0.480 |
| CLV_NRD_NRD_1 | 674 | 676 | PF00675 | 0.275 |
| CLV_NRD_NRD_1 | 690 | 692 | PF00675 | 0.250 |
| CLV_NRD_NRD_1 | 726 | 728 | PF00675 | 0.257 |
| CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.437 |
| CLV_PCSK_FUR_1 | 646 | 650 | PF00082 | 0.580 |
| CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.360 |
| CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.324 |
| CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.324 |
| CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.271 |
| CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.431 |
| CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.541 |
| CLV_PCSK_KEX2_1 | 690 | 692 | PF00082 | 0.273 |
| CLV_PCSK_KEX2_1 | 726 | 728 | PF00082 | 0.316 |
| CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.360 |
| CLV_PCSK_PC7_1 | 237 | 243 | PF00082 | 0.360 |
| CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.340 |
| CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.286 |
| CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.256 |
| CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.269 |
| CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.265 |
| CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.466 |
| CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.316 |
| CLV_PCSK_SKI1_1 | 628 | 632 | PF00082 | 0.351 |
| CLV_PCSK_SKI1_1 | 685 | 689 | PF00082 | 0.255 |
| CLV_PCSK_SKI1_1 | 715 | 719 | PF00082 | 0.255 |
| CLV_Separin_Metazoa | 537 | 541 | PF03568 | 0.560 |
| DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.545 |
| DEG_MDM2_SWIB_1 | 212 | 219 | PF02201 | 0.505 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.477 |
| DEG_SPOP_SBC_1 | 379 | 383 | PF00917 | 0.557 |
| DOC_CKS1_1 | 592 | 597 | PF01111 | 0.560 |
| DOC_CYCLIN_RxL_1 | 153 | 161 | PF00134 | 0.541 |
| DOC_MAPK_gen_1 | 298 | 305 | PF00069 | 0.487 |
| DOC_MAPK_gen_1 | 568 | 575 | PF00069 | 0.533 |
| DOC_MAPK_MEF2A_6 | 519 | 528 | PF00069 | 0.524 |
| DOC_MAPK_MEF2A_6 | 709 | 716 | PF00069 | 0.541 |
| DOC_PP1_RVXF_1 | 548 | 555 | PF00149 | 0.455 |
| DOC_PP4_FxxP_1 | 197 | 200 | PF00568 | 0.458 |
| DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.517 |
| DOC_USP7_MATH_1 | 657 | 661 | PF00917 | 0.604 |
| DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.466 |
| DOC_USP7_UBL2_3 | 156 | 160 | PF12436 | 0.541 |
| DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.512 |
| DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.480 |
| DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.505 |
| LIG_14-3-3_CanoR_1 | 165 | 174 | PF00244 | 0.494 |
| LIG_14-3-3_CanoR_1 | 242 | 252 | PF00244 | 0.479 |
| LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.516 |
| LIG_14-3-3_CanoR_1 | 432 | 441 | PF00244 | 0.514 |
| LIG_14-3-3_CanoR_1 | 49 | 57 | PF00244 | 0.505 |
| LIG_14-3-3_CanoR_1 | 519 | 527 | PF00244 | 0.480 |
| LIG_14-3-3_CanoR_1 | 550 | 555 | PF00244 | 0.466 |
| LIG_14-3-3_CanoR_1 | 601 | 607 | PF00244 | 0.528 |
| LIG_14-3-3_CanoR_1 | 658 | 662 | PF00244 | 0.598 |
| LIG_14-3-3_CanoR_1 | 690 | 694 | PF00244 | 0.480 |
| LIG_APCC_ABBA_1 | 135 | 140 | PF00400 | 0.455 |
| LIG_APCC_ABBA_1 | 198 | 203 | PF00400 | 0.516 |
| LIG_APCC_ABBA_1 | 391 | 396 | PF00400 | 0.516 |
| LIG_APCC_Cbox_2 | 431 | 437 | PF00515 | 0.541 |
| LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.496 |
| LIG_BRCT_BRCA1_1 | 485 | 489 | PF00533 | 0.512 |
| LIG_BRCT_BRCA1_1 | 706 | 710 | PF00533 | 0.480 |
| LIG_Clathr_ClatBox_1 | 630 | 634 | PF01394 | 0.560 |
| LIG_Clathr_ClatBox_1 | 65 | 69 | PF01394 | 0.496 |
| LIG_CtBP_PxDLS_1 | 653 | 657 | PF00389 | 0.569 |
| LIG_deltaCOP1_diTrp_1 | 482 | 489 | PF00928 | 0.563 |
| LIG_EH1_1 | 503 | 511 | PF00400 | 0.541 |
| LIG_eIF4E_1 | 60 | 66 | PF01652 | 0.480 |
| LIG_eIF4E_2 | 612 | 618 | PF01652 | 0.505 |
| LIG_FHA_1 | 152 | 158 | PF00498 | 0.445 |
| LIG_FHA_1 | 187 | 193 | PF00498 | 0.541 |
| LIG_FHA_1 | 314 | 320 | PF00498 | 0.510 |
| LIG_FHA_1 | 471 | 477 | PF00498 | 0.466 |
| LIG_FHA_1 | 501 | 507 | PF00498 | 0.536 |
| LIG_FHA_1 | 73 | 79 | PF00498 | 0.460 |
| LIG_FHA_2 | 16 | 22 | PF00498 | 0.363 |
| LIG_FHA_2 | 203 | 209 | PF00498 | 0.541 |
| LIG_FHA_2 | 244 | 250 | PF00498 | 0.499 |
| LIG_FHA_2 | 252 | 258 | PF00498 | 0.464 |
| LIG_FHA_2 | 426 | 432 | PF00498 | 0.466 |
| LIG_FHA_2 | 434 | 440 | PF00498 | 0.460 |
| LIG_FHA_2 | 636 | 642 | PF00498 | 0.560 |
| LIG_GBD_Chelix_1 | 149 | 157 | PF00786 | 0.341 |
| LIG_LIR_Apic_2 | 195 | 200 | PF02991 | 0.471 |
| LIG_LIR_Gen_1 | 15 | 23 | PF02991 | 0.435 |
| LIG_LIR_Gen_1 | 208 | 213 | PF02991 | 0.493 |
| LIG_LIR_Gen_1 | 215 | 224 | PF02991 | 0.476 |
| LIG_LIR_Gen_1 | 605 | 614 | PF02991 | 0.560 |
| LIG_LIR_Gen_1 | 69 | 78 | PF02991 | 0.469 |
| LIG_LIR_Gen_1 | 91 | 99 | PF02991 | 0.533 |
| LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.405 |
| LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.324 |
| LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.424 |
| LIG_LIR_Nem_3 | 208 | 212 | PF02991 | 0.477 |
| LIG_LIR_Nem_3 | 215 | 219 | PF02991 | 0.464 |
| LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.489 |
| LIG_LIR_Nem_3 | 346 | 351 | PF02991 | 0.459 |
| LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.466 |
| LIG_LIR_Nem_3 | 605 | 609 | PF02991 | 0.560 |
| LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.445 |
| LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.498 |
| LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.466 |
| LIG_LYPXL_S_1 | 347 | 351 | PF13949 | 0.341 |
| LIG_LYPXL_yS_3 | 348 | 351 | PF13949 | 0.541 |
| LIG_PCNA_yPIPBox_3 | 71 | 82 | PF02747 | 0.455 |
| LIG_PDZ_Class_2 | 739 | 744 | PF00595 | 0.402 |
| LIG_Pex14_1 | 397 | 401 | PF04695 | 0.541 |
| LIG_Pex14_2 | 212 | 216 | PF04695 | 0.560 |
| LIG_Pex14_2 | 356 | 360 | PF04695 | 0.541 |
| LIG_PTB_Apo_2 | 21 | 28 | PF02174 | 0.473 |
| LIG_PTB_Apo_2 | 290 | 297 | PF02174 | 0.560 |
| LIG_PTB_Apo_2 | 400 | 407 | PF02174 | 0.560 |
| LIG_REV1ctd_RIR_1 | 293 | 303 | PF16727 | 0.541 |
| LIG_SH2_CRK | 103 | 107 | PF00017 | 0.466 |
| LIG_SH2_CRK | 40 | 44 | PF00017 | 0.455 |
| LIG_SH2_CRK | 740 | 744 | PF00017 | 0.492 |
| LIG_SH2_GRB2like | 401 | 404 | PF00017 | 0.541 |
| LIG_SH2_NCK_1 | 40 | 44 | PF00017 | 0.455 |
| LIG_SH2_SRC | 401 | 404 | PF00017 | 0.459 |
| LIG_SH2_SRC | 612 | 615 | PF00017 | 0.505 |
| LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.516 |
| LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.455 |
| LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.455 |
| LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.464 |
| LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.443 |
| LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.475 |
| LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.523 |
| LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.484 |
| LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.455 |
| LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.478 |
| LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.460 |
| LIG_SH2_STAT5 | 612 | 615 | PF00017 | 0.560 |
| LIG_SH2_STAT5 | 729 | 732 | PF00017 | 0.480 |
| LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.511 |
| LIG_SH3_3 | 258 | 264 | PF00018 | 0.541 |
| LIG_SH3_3 | 268 | 274 | PF00018 | 0.541 |
| LIG_SH3_3 | 524 | 530 | PF00018 | 0.537 |
| LIG_SH3_3 | 532 | 538 | PF00018 | 0.553 |
| LIG_SH3_3 | 589 | 595 | PF00018 | 0.560 |
| LIG_SH3_4 | 127 | 134 | PF00018 | 0.480 |
| LIG_SUMO_SIM_anti_2 | 301 | 307 | PF11976 | 0.542 |
| LIG_SUMO_SIM_anti_2 | 331 | 336 | PF11976 | 0.546 |
| LIG_SUMO_SIM_anti_2 | 505 | 510 | PF11976 | 0.506 |
| LIG_SUMO_SIM_par_1 | 95 | 101 | PF11976 | 0.534 |
| LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.533 |
| LIG_TRAF2_2 | 595 | 600 | PF00917 | 0.560 |
| LIG_UBA3_1 | 305 | 312 | PF00899 | 0.538 |
| LIG_WRC_WIRS_1 | 111 | 116 | PF05994 | 0.516 |
| LIG_WRC_WIRS_1 | 30 | 35 | PF05994 | 0.567 |
| MOD_CDK_SPxxK_3 | 260 | 267 | PF00069 | 0.538 |
| MOD_CK1_1 | 126 | 132 | PF00069 | 0.496 |
| MOD_CK1_1 | 151 | 157 | PF00069 | 0.447 |
| MOD_CK1_1 | 263 | 269 | PF00069 | 0.480 |
| MOD_CK1_1 | 294 | 300 | PF00069 | 0.487 |
| MOD_CK1_1 | 518 | 524 | PF00069 | 0.560 |
| MOD_CK1_1 | 545 | 551 | PF00069 | 0.499 |
| MOD_CK1_1 | 85 | 91 | PF00069 | 0.549 |
| MOD_CK2_1 | 243 | 249 | PF00069 | 0.474 |
| MOD_CK2_1 | 251 | 257 | PF00069 | 0.455 |
| MOD_CK2_1 | 280 | 286 | PF00069 | 0.533 |
| MOD_CK2_1 | 433 | 439 | PF00069 | 0.541 |
| MOD_CK2_1 | 556 | 562 | PF00069 | 0.529 |
| MOD_CK2_1 | 657 | 663 | PF00069 | 0.619 |
| MOD_CK2_1 | 85 | 91 | PF00069 | 0.503 |
| MOD_Cter_Amidation | 688 | 691 | PF01082 | 0.341 |
| MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.303 |
| MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.307 |
| MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.301 |
| MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.187 |
| MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.341 |
| MOD_GlcNHglycan | 83 | 87 | PF01048 | 0.343 |
| MOD_GSK3_1 | 188 | 195 | PF00069 | 0.541 |
| MOD_GSK3_1 | 231 | 238 | PF00069 | 0.537 |
| MOD_GSK3_1 | 256 | 263 | PF00069 | 0.515 |
| MOD_GSK3_1 | 294 | 301 | PF00069 | 0.538 |
| MOD_GSK3_1 | 45 | 52 | PF00069 | 0.492 |
| MOD_GSK3_1 | 552 | 559 | PF00069 | 0.459 |
| MOD_GSK3_1 | 587 | 594 | PF00069 | 0.499 |
| MOD_GSK3_1 | 616 | 623 | PF00069 | 0.500 |
| MOD_GSK3_1 | 657 | 664 | PF00069 | 0.585 |
| MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.329 |
| MOD_N-GLC_1 | 587 | 592 | PF02516 | 0.333 |
| MOD_NEK2_1 | 180 | 185 | PF00069 | 0.461 |
| MOD_NEK2_1 | 202 | 207 | PF00069 | 0.496 |
| MOD_NEK2_1 | 225 | 230 | PF00069 | 0.532 |
| MOD_NEK2_1 | 291 | 296 | PF00069 | 0.561 |
| MOD_NEK2_1 | 358 | 363 | PF00069 | 0.496 |
| MOD_NEK2_1 | 433 | 438 | PF00069 | 0.532 |
| MOD_NEK2_1 | 563 | 568 | PF00069 | 0.517 |
| MOD_NEK2_1 | 616 | 621 | PF00069 | 0.479 |
| MOD_NEK2_1 | 73 | 78 | PF00069 | 0.503 |
| MOD_PIKK_1 | 151 | 157 | PF00454 | 0.459 |
| MOD_PIKK_1 | 186 | 192 | PF00454 | 0.541 |
| MOD_PIKK_1 | 243 | 249 | PF00454 | 0.505 |
| MOD_PIKK_1 | 568 | 574 | PF00454 | 0.541 |
| MOD_PKA_1 | 298 | 304 | PF00069 | 0.541 |
| MOD_PKA_1 | 450 | 456 | PF00069 | 0.533 |
| MOD_PKA_1 | 568 | 574 | PF00069 | 0.541 |
| MOD_PKA_2 | 298 | 304 | PF00069 | 0.503 |
| MOD_PKA_2 | 48 | 54 | PF00069 | 0.466 |
| MOD_PKA_2 | 518 | 524 | PF00069 | 0.541 |
| MOD_PKA_2 | 623 | 629 | PF00069 | 0.516 |
| MOD_PKA_2 | 657 | 663 | PF00069 | 0.591 |
| MOD_PKA_2 | 689 | 695 | PF00069 | 0.541 |
| MOD_PKB_1 | 618 | 626 | PF00069 | 0.560 |
| MOD_PKB_1 | 80 | 88 | PF00069 | 0.560 |
| MOD_Plk_1 | 235 | 241 | PF00069 | 0.491 |
| MOD_Plk_1 | 256 | 262 | PF00069 | 0.534 |
| MOD_Plk_1 | 328 | 334 | PF00069 | 0.543 |
| MOD_Plk_1 | 358 | 364 | PF00069 | 0.507 |
| MOD_Plk_1 | 635 | 641 | PF00069 | 0.555 |
| MOD_Plk_2-3 | 15 | 21 | PF00069 | 0.346 |
| MOD_Plk_2-3 | 328 | 334 | PF00069 | 0.525 |
| MOD_Plk_2-3 | 635 | 641 | PF00069 | 0.541 |
| MOD_Plk_4 | 133 | 139 | PF00069 | 0.490 |
| MOD_Plk_4 | 188 | 194 | PF00069 | 0.497 |
| MOD_Plk_4 | 256 | 262 | PF00069 | 0.493 |
| MOD_Plk_4 | 291 | 297 | PF00069 | 0.498 |
| MOD_Plk_4 | 39 | 45 | PF00069 | 0.466 |
| MOD_Plk_4 | 475 | 481 | PF00069 | 0.484 |
| MOD_Plk_4 | 73 | 79 | PF00069 | 0.529 |
| MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.512 |
| MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.480 |
| MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.505 |
| MOD_SUMO_for_1 | 310 | 313 | PF00179 | 0.563 |
| MOD_SUMO_for_1 | 325 | 328 | PF00179 | 0.509 |
| MOD_SUMO_rev_2 | 164 | 174 | PF00179 | 0.558 |
| MOD_SUMO_rev_2 | 668 | 678 | PF00179 | 0.470 |
| MOD_SUMO_rev_2 | 707 | 717 | PF00179 | 0.459 |
| TRG_DiLeu_BaEn_1 | 505 | 510 | PF01217 | 0.560 |
| TRG_DiLeu_BaEn_2 | 428 | 434 | PF01217 | 0.541 |
| TRG_DiLeu_BaLyEn_6 | 612 | 617 | PF01217 | 0.480 |
| TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.455 |
| TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.455 |
| TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.470 |
| TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.491 |
| TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.514 |
| TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.418 |
| TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.463 |
| TRG_ENDOCYTIC_2 | 740 | 743 | PF00928 | 0.475 |
| TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.475 |
| TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.556 |
| TRG_ER_diArg_1 | 281 | 284 | PF00400 | 0.496 |
| TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.451 |
| TRG_ER_diArg_1 | 464 | 467 | PF00400 | 0.540 |
| TRG_ER_diArg_1 | 617 | 620 | PF00400 | 0.541 |
| TRG_ER_diArg_1 | 646 | 649 | PF00400 | 0.592 |
| TRG_ER_diArg_1 | 725 | 727 | PF00400 | 0.516 |
| TRG_NLS_MonoExtC_3 | 9 | 15 | PF00514 | 0.565 |
| TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.325 |
| TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.305 |
| TRG_Pf-PMV_PEXEL_1 | 458 | 462 | PF00026 | 0.333 |
| TRG_Pf-PMV_PEXEL_1 | 709 | 713 | PF00026 | 0.207 |
| TRG_Pf-PMV_PEXEL_1 | 82 | 87 | PF00026 | 0.316 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I048 | Leptomonas seymouri | 81% | 100% |
| A0A0S4J5R6 | Bodo saltans | 23% | 90% |
| A0A0S4KHD2 | Bodo saltans | 22% | 100% |
| A0A0S4KHS5 | Bodo saltans | 33% | 100% |
| A0A1X0NXD6 | Trypanosomatidae | 45% | 100% |
| A0A3R7K785 | Trypanosoma rangeli | 46% | 100% |
| A2A432 | Mus musculus | 24% | 77% |
| A4HDU0 | Leishmania braziliensis | 92% | 100% |
| A4I137 | Leishmania infantum | 99% | 100% |
| A4IHP4 | Xenopus tropicalis | 26% | 97% |
| B5DF89 | Rattus norvegicus | 26% | 97% |
| C9ZW70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
| E9AX75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
| O13790 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 97% |
| O14122 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
| O60999 | Dictyostelium discoideum | 24% | 97% |
| P0CH31 | Arabidopsis thaliana | 24% | 100% |
| Q09760 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 95% |
| Q12018 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 91% |
| Q13616 | Homo sapiens | 25% | 96% |
| Q13617 | Homo sapiens | 23% | 100% |
| Q13618 | Homo sapiens | 26% | 97% |
| Q13619 | Homo sapiens | 25% | 98% |
| Q13620 | Homo sapiens | 24% | 81% |
| Q17389 | Caenorhabditis elegans | 24% | 95% |
| Q17390 | Caenorhabditis elegans | 22% | 94% |
| Q17391 | Caenorhabditis elegans | 26% | 96% |
| Q21346 | Caenorhabditis elegans | 25% | 100% |
| Q23639 | Caenorhabditis elegans | 24% | 97% |
| Q24311 | Drosophila melanogaster | 23% | 96% |
| Q29425 | Oryctolagus cuniculus | 21% | 95% |
| Q3TCH7 | Mus musculus | 24% | 98% |
| Q4QAA1 | Leishmania major | 97% | 100% |
| Q54CS2 | Dictyostelium discoideum | 22% | 93% |
| Q54NZ5 | Dictyostelium discoideum | 23% | 97% |
| Q54XF7 | Dictyostelium discoideum | 22% | 99% |
| Q5R4G6 | Pongo abelii | 25% | 96% |
| Q5RB36 | Pongo abelii | 21% | 95% |
| Q5RCF3 | Pongo abelii | 23% | 100% |
| Q5ZC88 | Oryza sativa subsp. japonica | 27% | 100% |
| Q6DE95 | Xenopus laevis | 26% | 97% |
| Q6GPF3 | Xenopus laevis | 26% | 97% |
| Q8LGH4 | Arabidopsis thaliana | 24% | 94% |
| Q93034 | Homo sapiens | 21% | 95% |
| Q94AH6 | Arabidopsis thaliana | 27% | 100% |
| Q9C9L0 | Arabidopsis thaliana | 25% | 100% |
| Q9D4H8 | Mus musculus | 23% | 100% |
| Q9D5V5 | Mus musculus | 22% | 95% |
| Q9JJ31 | Rattus norvegicus | 22% | 95% |
| Q9JLV5 | Mus musculus | 26% | 97% |
| Q9SRZ0 | Arabidopsis thaliana | 26% | 100% |
| Q9WTX6 | Mus musculus | 25% | 96% |
| Q9XZJ3 | Dictyostelium discoideum | 22% | 96% |
| Q9ZVH4 | Arabidopsis thaliana | 25% | 100% |
| V5APS6 | Trypanosoma cruzi | 45% | 100% |