| 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:0005634 | nucleus | 5 | 11 |
| GO:0005737 | cytoplasm | 2 | 2 |
| GO:0042995 | cell projection | 2 | 11 |
| GO:0043005 | neuron projection | 4 | 11 |
| GO:0043226 | organelle | 2 | 11 |
| GO:0043227 | membrane-bounded organelle | 3 | 11 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
| GO:0043229 | intracellular organelle | 3 | 11 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
| GO:0110165 | cellular anatomical entity | 1 | 11 |
| GO:0120025 | plasma membrane bounded cell projection | 3 | 11 |
| GO:0120293 | dynein axonemal particle | 5 | 11 |
| GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4Q4Z0
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003341 | cilium movement | 4 | 11 |
| GO:0007017 | microtubule-based process | 2 | 11 |
| GO:0007018 | microtubule-based movement | 3 | 11 |
| GO:0007399 | nervous system development | 4 | 11 |
| GO:0009987 | cellular process | 1 | 11 |
| GO:0016043 | cellular component organization | 3 | 2 |
| GO:0022607 | cellular component assembly | 4 | 2 |
| GO:0032502 | developmental process | 1 | 11 |
| GO:0036158 | outer dynein arm assembly | 7 | 2 |
| GO:0036159 | inner dynein arm assembly | 7 | 2 |
| GO:0043933 | protein-containing complex organization | 4 | 2 |
| GO:0048731 | system development | 3 | 11 |
| GO:0048856 | anatomical structure development | 2 | 11 |
| GO:0065003 | protein-containing complex assembly | 5 | 2 |
| GO:0070286 | axonemal dynein complex assembly | 6 | 2 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 422 | 426 | PF00656 | 0.492 |
| CLV_C14_Caspase3-7 | 511 | 515 | PF00656 | 0.643 |
| CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.424 |
| CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.540 |
| CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.313 |
| CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.444 |
| CLV_PCSK_FUR_1 | 549 | 553 | PF00082 | 0.585 |
| CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.424 |
| CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.517 |
| CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.368 |
| CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.376 |
| CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.313 |
| CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.523 |
| CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.481 |
| CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.356 |
| CLV_PCSK_PC1ET2_1 | 336 | 338 | PF00082 | 0.376 |
| CLV_PCSK_PC7_1 | 129 | 135 | PF00082 | 0.473 |
| CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.507 |
| CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.529 |
| CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.470 |
| DEG_SCF_FBW7_2 | 349 | 356 | PF00400 | 0.436 |
| DEG_SPOP_SBC_1 | 229 | 233 | PF00917 | 0.586 |
| DEG_SPOP_SBC_1 | 527 | 531 | PF00917 | 0.520 |
| DOC_CKS1_1 | 173 | 178 | PF01111 | 0.571 |
| DOC_CKS1_1 | 218 | 223 | PF01111 | 0.568 |
| DOC_CKS1_1 | 235 | 240 | PF01111 | 0.524 |
| DOC_CYCLIN_yCln2_LP_2 | 193 | 199 | PF00134 | 0.721 |
| DOC_MAPK_gen_1 | 23 | 32 | PF00069 | 0.448 |
| DOC_MAPK_gen_1 | 272 | 281 | PF00069 | 0.538 |
| DOC_MAPK_gen_1 | 477 | 487 | PF00069 | 0.350 |
| DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.510 |
| DOC_MAPK_MEF2A_6 | 26 | 34 | PF00069 | 0.456 |
| DOC_PP4_FxxP_1 | 258 | 261 | PF00568 | 0.680 |
| DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.570 |
| DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.526 |
| DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.591 |
| DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.662 |
| DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.479 |
| DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.462 |
| DOC_USP7_UBL2_3 | 583 | 587 | PF12436 | 0.413 |
| DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.694 |
| DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.710 |
| DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.719 |
| DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.619 |
| DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.705 |
| DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.449 |
| DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.413 |
| DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.410 |
| DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.387 |
| LIG_14-3-3_CanoR_1 | 419 | 428 | PF00244 | 0.466 |
| LIG_14-3-3_CanoR_1 | 94 | 99 | PF00244 | 0.619 |
| LIG_BRCT_BRCA1_1 | 62 | 66 | PF00533 | 0.491 |
| LIG_Clathr_ClatBox_1 | 48 | 52 | PF01394 | 0.448 |
| LIG_FHA_1 | 244 | 250 | PF00498 | 0.483 |
| LIG_FHA_1 | 27 | 33 | PF00498 | 0.573 |
| LIG_FHA_1 | 480 | 486 | PF00498 | 0.375 |
| LIG_FHA_2 | 10 | 16 | PF00498 | 0.448 |
| LIG_FHA_2 | 125 | 131 | PF00498 | 0.609 |
| LIG_FHA_2 | 398 | 404 | PF00498 | 0.449 |
| LIG_FHA_2 | 420 | 426 | PF00498 | 0.616 |
| LIG_FHA_2 | 555 | 561 | PF00498 | 0.613 |
| LIG_FHA_2 | 597 | 603 | PF00498 | 0.385 |
| LIG_LIR_Apic_2 | 170 | 176 | PF02991 | 0.411 |
| LIG_LIR_Apic_2 | 257 | 261 | PF02991 | 0.677 |
| LIG_LIR_Gen_1 | 326 | 335 | PF02991 | 0.456 |
| LIG_LIR_Gen_1 | 36 | 45 | PF02991 | 0.486 |
| LIG_LIR_Gen_1 | 451 | 462 | PF02991 | 0.350 |
| LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.544 |
| LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.492 |
| LIG_LIR_Nem_3 | 360 | 365 | PF02991 | 0.401 |
| LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.337 |
| LIG_MLH1_MIPbox_1 | 62 | 66 | PF16413 | 0.457 |
| LIG_Pex14_1 | 169 | 173 | PF04695 | 0.384 |
| LIG_RPA_C_Fungi | 102 | 114 | PF08784 | 0.420 |
| LIG_SH2_CRK | 173 | 177 | PF00017 | 0.445 |
| LIG_SH2_CRK | 276 | 280 | PF00017 | 0.518 |
| LIG_SH2_CRK | 362 | 366 | PF00017 | 0.376 |
| LIG_SH2_CRK | 454 | 458 | PF00017 | 0.334 |
| LIG_SH2_CRK | 566 | 570 | PF00017 | 0.360 |
| LIG_SH2_GRB2like | 601 | 604 | PF00017 | 0.479 |
| LIG_SH2_NCK_1 | 173 | 177 | PF00017 | 0.445 |
| LIG_SH2_NCK_1 | 447 | 451 | PF00017 | 0.308 |
| LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.339 |
| LIG_SH2_STAP1 | 454 | 458 | PF00017 | 0.308 |
| LIG_SH2_STAP1 | 601 | 605 | PF00017 | 0.379 |
| LIG_SH2_STAT3 | 118 | 121 | PF00017 | 0.585 |
| LIG_SH2_STAT3 | 270 | 273 | PF00017 | 0.628 |
| LIG_SH2_STAT3 | 296 | 299 | PF00017 | 0.482 |
| LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.525 |
| LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.411 |
| LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.418 |
| LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.305 |
| LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.419 |
| LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.459 |
| LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.289 |
| LIG_SH3_3 | 215 | 221 | PF00018 | 0.564 |
| LIG_SH3_3 | 223 | 229 | PF00018 | 0.655 |
| LIG_SH3_3 | 232 | 238 | PF00018 | 0.619 |
| LIG_SH3_3 | 38 | 44 | PF00018 | 0.368 |
| LIG_SUMO_SIM_anti_2 | 28 | 34 | PF11976 | 0.417 |
| LIG_SUMO_SIM_par_1 | 277 | 284 | PF11976 | 0.517 |
| LIG_SUMO_SIM_par_1 | 47 | 52 | PF11976 | 0.307 |
| LIG_TRAF2_1 | 534 | 537 | PF00917 | 0.643 |
| LIG_UBA3_1 | 17 | 23 | PF00899 | 0.368 |
| LIG_UBA3_1 | 53 | 61 | PF00899 | 0.334 |
| LIG_WW_1 | 44 | 47 | PF00397 | 0.368 |
| MOD_CDK_SPK_2 | 251 | 256 | PF00069 | 0.514 |
| MOD_CK1_1 | 172 | 178 | PF00069 | 0.706 |
| MOD_CK1_1 | 231 | 237 | PF00069 | 0.711 |
| MOD_CK1_1 | 355 | 361 | PF00069 | 0.432 |
| MOD_CK1_1 | 530 | 536 | PF00069 | 0.509 |
| MOD_CK1_1 | 59 | 65 | PF00069 | 0.403 |
| MOD_CK1_1 | 625 | 631 | PF00069 | 0.558 |
| MOD_CK2_1 | 124 | 130 | PF00069 | 0.535 |
| MOD_CK2_1 | 512 | 518 | PF00069 | 0.635 |
| MOD_CK2_1 | 526 | 532 | PF00069 | 0.649 |
| MOD_CK2_1 | 554 | 560 | PF00069 | 0.342 |
| MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.610 |
| MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.493 |
| MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.376 |
| MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.440 |
| MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.364 |
| MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.672 |
| MOD_GlcNHglycan | 560 | 564 | PF01048 | 0.407 |
| MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.289 |
| MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.495 |
| MOD_GSK3_1 | 124 | 131 | PF00069 | 0.531 |
| MOD_GSK3_1 | 177 | 184 | PF00069 | 0.742 |
| MOD_GSK3_1 | 188 | 195 | PF00069 | 0.631 |
| MOD_GSK3_1 | 230 | 237 | PF00069 | 0.745 |
| MOD_GSK3_1 | 243 | 250 | PF00069 | 0.616 |
| MOD_GSK3_1 | 277 | 284 | PF00069 | 0.566 |
| MOD_GSK3_1 | 340 | 347 | PF00069 | 0.359 |
| MOD_GSK3_1 | 5 | 12 | PF00069 | 0.356 |
| MOD_GSK3_1 | 526 | 533 | PF00069 | 0.735 |
| MOD_GSK3_1 | 539 | 546 | PF00069 | 0.660 |
| MOD_GSK3_1 | 56 | 63 | PF00069 | 0.405 |
| MOD_GSK3_1 | 89 | 96 | PF00069 | 0.578 |
| MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.604 |
| MOD_N-GLC_1 | 323 | 328 | PF02516 | 0.383 |
| MOD_NEK2_1 | 18 | 23 | PF00069 | 0.308 |
| MOD_NEK2_1 | 188 | 193 | PF00069 | 0.698 |
| MOD_NEK2_1 | 323 | 328 | PF00069 | 0.448 |
| MOD_NEK2_1 | 344 | 349 | PF00069 | 0.371 |
| MOD_NEK2_1 | 471 | 476 | PF00069 | 0.268 |
| MOD_NEK2_2 | 308 | 313 | PF00069 | 0.348 |
| MOD_PIKK_1 | 124 | 130 | PF00454 | 0.599 |
| MOD_PIKK_1 | 295 | 301 | PF00454 | 0.404 |
| MOD_PIKK_1 | 355 | 361 | PF00454 | 0.432 |
| MOD_PIKK_1 | 479 | 485 | PF00454 | 0.427 |
| MOD_PIKK_1 | 60 | 66 | PF00454 | 0.362 |
| MOD_PIKK_1 | 628 | 634 | PF00454 | 0.592 |
| MOD_PK_1 | 277 | 283 | PF00069 | 0.524 |
| MOD_PK_1 | 94 | 100 | PF00069 | 0.556 |
| MOD_PKA_1 | 26 | 32 | PF00069 | 0.323 |
| MOD_PKA_2 | 124 | 130 | PF00069 | 0.544 |
| MOD_PKA_2 | 271 | 277 | PF00069 | 0.449 |
| MOD_PKA_2 | 93 | 99 | PF00069 | 0.592 |
| MOD_Plk_1 | 169 | 175 | PF00069 | 0.398 |
| MOD_Plk_1 | 247 | 253 | PF00069 | 0.625 |
| MOD_Plk_1 | 340 | 346 | PF00069 | 0.352 |
| MOD_Plk_1 | 450 | 456 | PF00069 | 0.349 |
| MOD_Plk_2-3 | 398 | 404 | PF00069 | 0.565 |
| MOD_Plk_4 | 344 | 350 | PF00069 | 0.379 |
| MOD_Plk_4 | 471 | 477 | PF00069 | 0.329 |
| MOD_Plk_4 | 543 | 549 | PF00069 | 0.415 |
| MOD_Plk_4 | 617 | 623 | PF00069 | 0.418 |
| MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.699 |
| MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.708 |
| MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.711 |
| MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.615 |
| MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.701 |
| MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.452 |
| MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.411 |
| MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.418 |
| MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.384 |
| MOD_SUMO_for_1 | 155 | 158 | PF00179 | 0.463 |
| MOD_SUMO_rev_2 | 381 | 385 | PF00179 | 0.430 |
| TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.525 |
| TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.411 |
| TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.385 |
| TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.274 |
| TRG_ENDOCYTIC_2 | 566 | 569 | PF00928 | 0.343 |
| TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.551 |
| TRG_ER_diArg_1 | 548 | 551 | PF00400 | 0.454 |
| TRG_ER_FFAT_2 | 170 | 179 | PF00635 | 0.432 |
| TRG_Pf-PMV_PEXEL_1 | 135 | 140 | PF00026 | 0.543 |
| TRG_Pf-PMV_PEXEL_1 | 337 | 341 | PF00026 | 0.347 |
| TRG_Pf-PMV_PEXEL_1 | 419 | 423 | PF00026 | 0.460 |
| TRG_Pf-PMV_PEXEL_1 | 556 | 560 | PF00026 | 0.559 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PE30 | Leptomonas seymouri | 70% | 100% |
| A0A0S4IMJ5 | Bodo saltans | 46% | 100% |
| A0A1X0NRQ0 | Trypanosomatidae | 51% | 100% |
| A0A3R7LBE5 | Trypanosoma rangeli | 48% | 100% |
| A0A3S7X5V3 | Leishmania donovani | 93% | 100% |
| A4HKS6 | Leishmania braziliensis | 83% | 100% |
| A4I8A6 | Leishmania infantum | 93% | 100% |
| D0AAH8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 96% |
| E9B364 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
| V5BMH6 | Trypanosoma cruzi | 50% | 100% |