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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 11 |
GO:0042995 | cell projection | 2 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 11 |
Related structures:
AlphaFold database: A4HMI6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 11 |
GO:0007017 | microtubule-based process | 2 | 11 |
GO:0007018 | microtubule-based movement | 3 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0010970 | transport along microtubule | 4 | 11 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 11 |
GO:0031503 | protein-containing complex localization | 2 | 11 |
GO:0035735 | intraciliary transport involved in cilium assembly | 4 | 11 |
GO:0042073 | intraciliary transport | 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:0099111 | microtubule-based transport | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 11 | 15 | PF00656 | 0.601 |
CLV_C14_Caspase3-7 | 535 | 539 | PF00656 | 0.571 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.595 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 110 | 112 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.641 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 532 | 534 | PF00082 | 0.563 |
CLV_PCSK_PC7_1 | 332 | 338 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.640 |
CLV_Separin_Metazoa | 362 | 366 | PF03568 | 0.638 |
DEG_APCC_KENBOX_2 | 605 | 609 | PF00400 | 0.617 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.616 |
DEG_SPOP_SBC_1 | 40 | 44 | PF00917 | 0.670 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 395 | 403 | PF00134 | 0.485 |
DOC_MAPK_DCC_7 | 76 | 85 | PF00069 | 0.748 |
DOC_MAPK_gen_1 | 109 | 117 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 358 | 366 | PF00069 | 0.647 |
DOC_MAPK_gen_1 | 400 | 407 | PF00069 | 0.623 |
DOC_MAPK_gen_1 | 475 | 484 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 400 | 407 | PF00069 | 0.650 |
DOC_MAPK_MEF2A_6 | 475 | 484 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 76 | 85 | PF00069 | 0.755 |
DOC_MAPK_NFAT4_5 | 400 | 408 | PF00069 | 0.649 |
DOC_PP2B_LxvP_1 | 70 | 73 | PF13499 | 0.713 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.671 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.735 |
LIG_14-3-3_CanoR_1 | 562 | 570 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 572 | 579 | PF00244 | 0.601 |
LIG_Actin_WH2_2 | 144 | 161 | PF00022 | 0.637 |
LIG_deltaCOP1_diTrp_1 | 538 | 548 | PF00928 | 0.439 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.473 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.498 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.505 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.761 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.611 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.550 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.667 |
LIG_FHA_2 | 491 | 497 | PF00498 | 0.578 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.579 |
LIG_LIR_Gen_1 | 468 | 476 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 104 | 108 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 468 | 473 | PF02991 | 0.637 |
LIG_PDZ_Class_2 | 634 | 639 | PF00595 | 0.595 |
LIG_RPA_C_Fungi | 255 | 267 | PF08784 | 0.477 |
LIG_RPA_C_Fungi | 494 | 506 | PF08784 | 0.626 |
LIG_SH2_GRB2like | 272 | 275 | PF00017 | 0.575 |
LIG_SH2_PTP2 | 470 | 473 | PF00017 | 0.659 |
LIG_SH2_SRC | 12 | 15 | PF00017 | 0.578 |
LIG_SH2_STAP1 | 272 | 276 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 530 | 534 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.609 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.700 |
LIG_SUMO_SIM_anti_2 | 253 | 259 | PF11976 | 0.480 |
LIG_SUMO_SIM_anti_2 | 483 | 489 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 599 | 604 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 614 | 622 | PF11976 | 0.432 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.599 |
LIG_TRAF2_1 | 224 | 227 | PF00917 | 0.557 |
LIG_TRAF2_1 | 289 | 292 | PF00917 | 0.476 |
LIG_TRAF2_1 | 414 | 417 | PF00917 | 0.596 |
LIG_TRAF2_1 | 566 | 569 | PF00917 | 0.602 |
LIG_TRAF2_1 | 619 | 622 | PF00917 | 0.587 |
MOD_CDK_SPxK_1 | 63 | 69 | PF00069 | 0.536 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.586 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.707 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.637 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.610 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.662 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.557 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.618 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.504 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.646 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.533 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.549 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.287 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.553 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.521 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.587 |
MOD_DYRK1A_RPxSP_1 | 76 | 80 | PF00069 | 0.763 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.655 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.593 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.505 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.542 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.763 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.616 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.560 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.654 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.523 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.501 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.711 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.627 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.690 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.742 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.575 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.735 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.609 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.634 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.615 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.597 |
MOD_N-GLC_1 | 512 | 517 | PF02516 | 0.563 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.710 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.507 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.582 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.553 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.712 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.597 |
MOD_NEK2_2 | 215 | 220 | PF00069 | 0.570 |
MOD_PIKK_1 | 547 | 553 | PF00454 | 0.555 |
MOD_PIKK_1 | 590 | 596 | PF00454 | 0.573 |
MOD_PK_1 | 286 | 292 | PF00069 | 0.550 |
MOD_PK_1 | 532 | 538 | PF00069 | 0.601 |
MOD_PKA_1 | 532 | 538 | PF00069 | 0.601 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.545 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.564 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.764 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.714 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.654 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.601 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.463 |
MOD_PKB_1 | 315 | 323 | PF00069 | 0.627 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.479 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.504 |
MOD_Plk_1 | 590 | 596 | PF00069 | 0.481 |
MOD_Plk_1 | 606 | 612 | PF00069 | 0.490 |
MOD_Plk_2-3 | 373 | 379 | PF00069 | 0.646 |
MOD_Plk_2-3 | 580 | 586 | PF00069 | 0.518 |
MOD_Plk_2-3 | 622 | 628 | PF00069 | 0.582 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.635 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.601 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.537 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.677 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.692 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.677 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.735 |
MOD_SUMO_for_1 | 169 | 172 | PF00179 | 0.587 |
MOD_SUMO_for_1 | 179 | 182 | PF00179 | 0.582 |
MOD_SUMO_for_1 | 573 | 576 | PF00179 | 0.455 |
MOD_SUMO_rev_2 | 161 | 169 | PF00179 | 0.629 |
MOD_SUMO_rev_2 | 232 | 242 | PF00179 | 0.426 |
MOD_SUMO_rev_2 | 287 | 295 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 342 | 351 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 520 | 526 | PF00179 | 0.613 |
MOD_SUMO_rev_2 | 575 | 584 | PF00179 | 0.584 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.614 |
TRG_DiLeu_BaEn_4 | 328 | 334 | PF01217 | 0.572 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.587 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 129 | 132 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 192 | 195 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 276 | 279 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.624 |
TRG_NES_CRM1_1 | 394 | 406 | PF08389 | 0.662 |
TRG_NES_CRM1_1 | 615 | 630 | PF08389 | 0.544 |
TRG_NLS_MonoExtC_3 | 166 | 172 | PF00514 | 0.619 |
TRG_NLS_MonoExtN_4 | 164 | 171 | PF00514 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 331 | 335 | PF00026 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 543 | 547 | PF00026 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5Z0 | Leptomonas seymouri | 72% | 95% |
A0A0S4J233 | Bodo saltans | 30% | 78% |
A0A1X0P6M5 | Trypanosomatidae | 48% | 100% |
A0A3Q8IHW5 | Leishmania donovani | 89% | 100% |
A4IB66 | Leishmania infantum | 89% | 100% |
C9ZZH6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 97% |
E9AEY7 | Leishmania major | 89% | 100% |
E9B643 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BTK9 | Trypanosoma cruzi | 47% | 96% |