| 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: 18 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005856 | cytoskeleton | 5 | 1 |
| GO:0005930 | axoneme | 2 | 1 |
| GO:0015630 | microtubule cytoskeleton | 6 | 1 |
| GO:0043226 | organelle | 2 | 2 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
| GO:0005929 | cilium | 4 | 1 |
| GO:0031514 | motile cilium | 5 | 1 |
| GO:0042995 | cell projection | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: E9AIJ7
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
| GO:0000281 | mitotic cytokinesis | 4 | 1 |
| GO:0000910 | cytokinesis | 3 | 1 |
| GO:0001539 | cilium or flagellum-dependent cell motility | 3 | 1 |
| GO:0001578 | microtubule bundle formation | 4 | 1 |
| GO:0003341 | cilium movement | 4 | 1 |
| GO:0006996 | organelle organization | 4 | 1 |
| GO:0007010 | cytoskeleton organization | 5 | 1 |
| GO:0007017 | microtubule-based process | 2 | 1 |
| GO:0007018 | microtubule-based movement | 3 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0016043 | cellular component organization | 3 | 1 |
| GO:0022402 | cell cycle process | 2 | 1 |
| GO:0022607 | cellular component assembly | 4 | 1 |
| GO:0035082 | axoneme assembly | 5 | 1 |
| GO:0048870 | cell motility | 2 | 1 |
| GO:0060285 | cilium-dependent cell motility | 4 | 1 |
| GO:0060294 | cilium movement involved in cell motility | 5 | 1 |
| GO:0061640 | cytoskeleton-dependent cytokinesis | 4 | 1 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
| GO:1903047 | mitotic cell cycle process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005488 | binding | 1 | 1 |
| GO:0005515 | protein binding | 2 | 1 |
| GO:0008017 | microtubule binding | 5 | 1 |
| GO:0008092 | cytoskeletal protein binding | 3 | 1 |
| GO:0015631 | tubulin binding | 4 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 10 | 14 | PF00656 | 0.470 |
| CLV_C14_Caspase3-7 | 362 | 366 | PF00656 | 0.276 |
| CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.251 |
| CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.328 |
| CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.360 |
| CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.372 |
| CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.251 |
| CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.367 |
| CLV_PCSK_PC1ET2_1 | 544 | 546 | PF00082 | 0.337 |
| CLV_PCSK_PC1ET2_1 | 591 | 593 | PF00082 | 0.372 |
| CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.533 |
| CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.343 |
| CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.311 |
| CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.242 |
| CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.324 |
| DEG_APCC_DBOX_1 | 519 | 527 | PF00400 | 0.241 |
| DOC_CYCLIN_RxL_1 | 187 | 196 | PF00134 | 0.345 |
| DOC_CYCLIN_yCln2_LP_2 | 188 | 194 | PF00134 | 0.338 |
| DOC_MAPK_DCC_7 | 309 | 317 | PF00069 | 0.251 |
| DOC_MAPK_MEF2A_6 | 309 | 317 | PF00069 | 0.251 |
| DOC_MAPK_RevD_3 | 313 | 328 | PF00069 | 0.251 |
| DOC_PP1_RVXF_1 | 158 | 164 | PF00149 | 0.334 |
| DOC_PP1_RVXF_1 | 38 | 44 | PF00149 | 0.412 |
| DOC_PP1_RVXF_1 | 46 | 52 | PF00149 | 0.416 |
| DOC_PP2B_LxvP_1 | 74 | 77 | PF13499 | 0.409 |
| DOC_PP2B_LxvP_1 | 89 | 92 | PF13499 | 0.398 |
| DOC_PP4_FxxP_1 | 4 | 7 | PF00568 | 0.478 |
| DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.427 |
| DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.393 |
| DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.421 |
| DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.333 |
| DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.382 |
| DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.444 |
| DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.476 |
| DOC_USP7_UBL2_3 | 544 | 548 | PF12436 | 0.343 |
| DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.483 |
| DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.521 |
| DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.359 |
| DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.485 |
| DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.421 |
| DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.322 |
| DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.471 |
| DOC_WW_Pin1_4 | 631 | 636 | PF00397 | 0.365 |
| DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.432 |
| LIG_14-3-3_CanoR_1 | 210 | 218 | PF00244 | 0.418 |
| LIG_14-3-3_CanoR_1 | 328 | 337 | PF00244 | 0.266 |
| LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.438 |
| LIG_14-3-3_CanoR_1 | 412 | 421 | PF00244 | 0.453 |
| LIG_Actin_WH2_2 | 312 | 329 | PF00022 | 0.251 |
| LIG_APCC_ABBA_1 | 17 | 22 | PF00400 | 0.477 |
| LIG_BRCT_BRCA1_1 | 244 | 248 | PF00533 | 0.295 |
| LIG_CtBP_PxDLS_1 | 58 | 62 | PF00389 | 0.438 |
| LIG_deltaCOP1_diTrp_1 | 46 | 51 | PF00928 | 0.430 |
| LIG_EVH1_1 | 74 | 78 | PF00568 | 0.405 |
| LIG_EVH1_2 | 67 | 71 | PF00568 | 0.404 |
| LIG_FHA_1 | 227 | 233 | PF00498 | 0.474 |
| LIG_FHA_1 | 423 | 429 | PF00498 | 0.312 |
| LIG_FHA_1 | 467 | 473 | PF00498 | 0.303 |
| LIG_FHA_2 | 115 | 121 | PF00498 | 0.465 |
| LIG_FHA_2 | 150 | 156 | PF00498 | 0.446 |
| LIG_FHA_2 | 164 | 170 | PF00498 | 0.308 |
| LIG_FHA_2 | 281 | 287 | PF00498 | 0.266 |
| LIG_FHA_2 | 331 | 337 | PF00498 | 0.266 |
| LIG_FHA_2 | 360 | 366 | PF00498 | 0.266 |
| LIG_FHA_2 | 638 | 644 | PF00498 | 0.385 |
| LIG_LIR_Apic_2 | 2 | 7 | PF02991 | 0.476 |
| LIG_LIR_Apic_2 | 528 | 533 | PF02991 | 0.372 |
| LIG_LIR_Apic_2 | 62 | 67 | PF02991 | 0.426 |
| LIG_LIR_Apic_2 | 631 | 635 | PF02991 | 0.503 |
| LIG_LIR_LC3C_4 | 388 | 391 | PF02991 | 0.295 |
| LIG_LIR_Nem_3 | 152 | 156 | PF02991 | 0.510 |
| LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.300 |
| LIG_MYND_1 | 558 | 562 | PF01753 | 0.325 |
| LIG_MYND_1 | 59 | 63 | PF01753 | 0.431 |
| LIG_MYND_3 | 557 | 561 | PF01753 | 0.312 |
| LIG_PCNA_yPIPBox_3 | 182 | 190 | PF02747 | 0.262 |
| LIG_Pex14_1 | 290 | 294 | PF04695 | 0.291 |
| LIG_Pex14_1 | 47 | 51 | PF04695 | 0.433 |
| LIG_Pex14_2 | 396 | 400 | PF04695 | 0.294 |
| LIG_Pex14_2 | 43 | 47 | PF04695 | 0.410 |
| LIG_PTB_Apo_2 | 619 | 626 | PF02174 | 0.408 |
| LIG_SH2_CRK | 580 | 584 | PF00017 | 0.451 |
| LIG_SH2_GRB2like | 530 | 533 | PF00017 | 0.297 |
| LIG_SH2_SRC | 530 | 533 | PF00017 | 0.297 |
| LIG_SH2_SRC | 556 | 559 | PF00017 | 0.460 |
| LIG_SH2_STAP1 | 580 | 584 | PF00017 | 0.451 |
| LIG_SH2_STAP1 | 637 | 641 | PF00017 | 0.377 |
| LIG_SH2_STAT3 | 648 | 651 | PF00017 | 0.508 |
| LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.251 |
| LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.333 |
| LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.278 |
| LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.367 |
| LIG_SH2_STAT5 | 556 | 559 | PF00017 | 0.445 |
| LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.185 |
| LIG_SH3_3 | 110 | 116 | PF00018 | 0.468 |
| LIG_SH3_3 | 126 | 132 | PF00018 | 0.417 |
| LIG_SH3_3 | 316 | 322 | PF00018 | 0.251 |
| LIG_SH3_3 | 53 | 59 | PF00018 | 0.431 |
| LIG_SH3_3 | 552 | 558 | PF00018 | 0.327 |
| LIG_SH3_3 | 563 | 569 | PF00018 | 0.319 |
| LIG_SH3_3 | 69 | 75 | PF00018 | 0.382 |
| LIG_SUMO_SIM_anti_2 | 95 | 100 | PF11976 | 0.439 |
| LIG_SUMO_SIM_par_1 | 190 | 196 | PF11976 | 0.346 |
| LIG_SUMO_SIM_par_1 | 95 | 100 | PF11976 | 0.439 |
| LIG_TRAF2_1 | 214 | 217 | PF00917 | 0.440 |
| LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.478 |
| LIG_WRC_WIRS_1 | 150 | 155 | PF05994 | 0.515 |
| MOD_CDK_SPxxK_3 | 112 | 119 | PF00069 | 0.469 |
| MOD_CK1_1 | 196 | 202 | PF00069 | 0.432 |
| MOD_CK1_1 | 332 | 338 | PF00069 | 0.233 |
| MOD_CK1_1 | 464 | 470 | PF00069 | 0.379 |
| MOD_CK2_1 | 149 | 155 | PF00069 | 0.517 |
| MOD_CK2_1 | 211 | 217 | PF00069 | 0.421 |
| MOD_CK2_1 | 280 | 286 | PF00069 | 0.284 |
| MOD_CK2_1 | 610 | 616 | PF00069 | 0.439 |
| MOD_CK2_1 | 637 | 643 | PF00069 | 0.395 |
| MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.315 |
| MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.361 |
| MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.293 |
| MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.224 |
| MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.373 |
| MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.375 |
| MOD_GSK3_1 | 123 | 130 | PF00069 | 0.481 |
| MOD_GSK3_1 | 196 | 203 | PF00069 | 0.335 |
| MOD_GSK3_1 | 280 | 287 | PF00069 | 0.267 |
| MOD_GSK3_1 | 3 | 10 | PF00069 | 0.472 |
| MOD_GSK3_1 | 444 | 451 | PF00069 | 0.436 |
| MOD_GSK3_1 | 610 | 617 | PF00069 | 0.433 |
| MOD_LATS_1 | 21 | 27 | PF00433 | 0.477 |
| MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.410 |
| MOD_N-GLC_2 | 622 | 624 | PF02516 | 0.328 |
| MOD_NEK2_1 | 163 | 168 | PF00069 | 0.328 |
| MOD_NEK2_1 | 193 | 198 | PF00069 | 0.405 |
| MOD_NEK2_1 | 231 | 236 | PF00069 | 0.365 |
| MOD_NEK2_1 | 344 | 349 | PF00069 | 0.490 |
| MOD_NEK2_1 | 466 | 471 | PF00069 | 0.302 |
| MOD_NEK2_1 | 614 | 619 | PF00069 | 0.478 |
| MOD_NEK2_2 | 322 | 327 | PF00069 | 0.263 |
| MOD_PIKK_1 | 102 | 108 | PF00454 | 0.444 |
| MOD_PIKK_1 | 226 | 232 | PF00454 | 0.471 |
| MOD_PIKK_1 | 264 | 270 | PF00454 | 0.252 |
| MOD_PKA_2 | 448 | 454 | PF00069 | 0.305 |
| MOD_PKA_2 | 507 | 513 | PF00069 | 0.336 |
| MOD_Plk_1 | 123 | 129 | PF00069 | 0.467 |
| MOD_Plk_1 | 322 | 328 | PF00069 | 0.251 |
| MOD_Plk_2-3 | 488 | 494 | PF00069 | 0.384 |
| MOD_Plk_4 | 344 | 350 | PF00069 | 0.447 |
| MOD_Plk_4 | 637 | 643 | PF00069 | 0.380 |
| MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.485 |
| MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.518 |
| MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.286 |
| MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.485 |
| MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.416 |
| MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.317 |
| MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.470 |
| MOD_ProDKin_1 | 631 | 637 | PF00069 | 0.362 |
| MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.432 |
| MOD_SUMO_for_1 | 590 | 593 | PF00179 | 0.359 |
| MOD_SUMO_for_1 | 606 | 609 | PF00179 | 0.377 |
| MOD_SUMO_rev_2 | 363 | 368 | PF00179 | 0.317 |
| TRG_DiLeu_BaEn_1 | 34 | 39 | PF01217 | 0.423 |
| TRG_DiLeu_BaEn_1 | 385 | 390 | PF01217 | 0.294 |
| TRG_DiLeu_BaEn_1 | 427 | 432 | PF01217 | 0.312 |
| TRG_DiLeu_BaLyEn_6 | 188 | 193 | PF01217 | 0.330 |
| TRG_DiLeu_BaLyEn_6 | 356 | 361 | PF01217 | 0.305 |
| TRG_DiLeu_BaLyEn_6 | 522 | 527 | PF01217 | 0.359 |
| TRG_DiLeu_BaLyEn_6 | 559 | 564 | PF01217 | 0.318 |
| TRG_ENDOCYTIC_2 | 580 | 583 | PF00928 | 0.456 |
| TRG_ER_diArg_1 | 160 | 163 | PF00400 | 0.427 |
| TRG_ER_diArg_1 | 47 | 50 | PF00400 | 0.429 |
| TRG_NES_CRM1_1 | 34 | 46 | PF08389 | 0.415 |
| TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.390 |
| TRG_Pf-PMV_PEXEL_1 | 190 | 195 | PF00026 | 0.338 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PE96 | Leptomonas seymouri | 94% | 100% |
| A0A0S4J9K3 | Bodo saltans | 81% | 100% |
| A0A1X0NXK0 | Trypanosomatidae | 85% | 100% |
| A0A3Q8IEY0 | Leishmania donovani | 97% | 100% |
| A0A3R7K990 | Trypanosoma rangeli | 85% | 100% |
| A4HYY3 | Leishmania infantum | 97% | 100% |
| C1JZ66 | Bos taurus | 23% | 100% |
| C9ZIJ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 82% | 100% |
| E9AUS9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
| O75602 | Homo sapiens | 62% | 100% |
| Q4QCQ4 | Leishmania major | 96% | 100% |
| Q9JLI7 | Mus musculus | 63% | 100% |
| V5D560 | Trypanosoma cruzi | 86% | 100% |