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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005875 | microtubule associated complex | 2 | 10 |
GO:0030286 | dynein complex | 3 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:1902494 | catalytic complex | 2 | 10 |
GO:0005868 | cytoplasmic dynein complex | 4 | 1 |
GO:0005929 | cilium | 4 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0031514 | motile cilium | 5 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A4HJA9
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 10 |
GO:0007018 | microtubule-based movement | 3 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0006810 | transport | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0010970 | transport along microtubule | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0031503 | protein-containing complex localization | 2 | 1 |
GO:0035721 | intraciliary retrograde transport | 4 | 1 |
GO:0042073 | intraciliary transport | 3 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0099111 | microtubule-based transport | 4 | 1 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003774 | cytoskeletal motor activity | 1 | 10 |
GO:0003777 | microtubule motor activity | 2 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005515 | protein binding | 2 | 10 |
GO:0008569 | minus-end-directed microtubule motor activity | 3 | 10 |
GO:0045505 | dynein intermediate chain binding | 3 | 10 |
GO:0051959 | dynein light intermediate chain binding | 3 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.475 |
CLV_C14_Caspase3-7 | 458 | 462 | PF00656 | 0.624 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.756 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.476 |
CLV_PCSK_FUR_1 | 295 | 299 | PF00082 | 0.585 |
CLV_PCSK_FUR_1 | 310 | 314 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.659 |
CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.667 |
CLV_PCSK_PC7_1 | 209 | 215 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.656 |
DEG_APCC_DBOX_1 | 208 | 216 | PF00400 | 0.565 |
DEG_ODPH_VHL_1 | 7 | 19 | PF01847 | 0.550 |
DOC_ANK_TNKS_1 | 297 | 304 | PF00023 | 0.357 |
DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.694 |
DOC_MAPK_gen_1 | 580 | 587 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 74 | 82 | PF00069 | 0.340 |
DOC_PP1_RVXF_1 | 193 | 200 | PF00149 | 0.467 |
DOC_PP1_RVXF_1 | 422 | 429 | PF00149 | 0.398 |
DOC_USP7_UBL2_3 | 105 | 109 | PF12436 | 0.366 |
DOC_USP7_UBL2_3 | 285 | 289 | PF12436 | 0.617 |
DOC_USP7_UBL2_3 | 530 | 534 | PF12436 | 0.744 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.823 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.601 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 240 | 247 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 424 | 429 | PF00244 | 0.617 |
LIG_Actin_WH2_2 | 402 | 420 | PF00022 | 0.616 |
LIG_Actin_WH2_2 | 434 | 451 | PF00022 | 0.383 |
LIG_Clathr_ClatBox_1 | 47 | 51 | PF01394 | 0.496 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.726 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.500 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.514 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.454 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.554 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.524 |
LIG_LIR_Apic_2 | 173 | 177 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 198 | 206 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 25 | 34 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 275 | 283 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 198 | 202 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.562 |
LIG_PDZ_Class_3 | 615 | 620 | PF00595 | 0.576 |
LIG_PTB_Apo_2 | 235 | 242 | PF02174 | 0.464 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.468 |
LIG_SH2_CRK | 399 | 403 | PF00017 | 0.506 |
LIG_SH2_NCK_1 | 399 | 403 | PF00017 | 0.536 |
LIG_SH2_PTP2 | 174 | 177 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 324 | 328 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.513 |
LIG_SH3_1 | 362 | 368 | PF00018 | 0.798 |
LIG_SH3_2 | 13 | 18 | PF14604 | 0.743 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.505 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.798 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.750 |
LIG_SUMO_SIM_par_1 | 188 | 194 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 404 | 410 | PF11976 | 0.628 |
LIG_TRAF2_1 | 117 | 120 | PF00917 | 0.580 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.599 |
LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.470 |
LIG_TRAF2_1 | 89 | 92 | PF00917 | 0.643 |
LIG_UBA3_1 | 577 | 583 | PF00899 | 0.680 |
LIG_WW_3 | 8 | 12 | PF00397 | 0.548 |
MOD_CDC14_SPxK_1 | 15 | 18 | PF00782 | 0.749 |
MOD_CDC14_SPxK_1 | 318 | 321 | PF00782 | 0.542 |
MOD_CDK_SPK_2 | 343 | 348 | PF00069 | 0.800 |
MOD_CDK_SPK_2 | 357 | 362 | PF00069 | 0.573 |
MOD_CDK_SPxK_1 | 12 | 18 | PF00069 | 0.748 |
MOD_CDK_SPxK_1 | 315 | 321 | PF00069 | 0.516 |
MOD_CDK_SPxxK_3 | 357 | 364 | PF00069 | 0.818 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.716 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.389 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.505 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.586 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.522 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.484 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.377 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.658 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.666 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.421 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.520 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.558 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.475 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.464 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.683 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.601 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.543 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.654 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.625 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.599 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.530 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.586 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.604 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.502 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.832 |
MOD_N-GLC_1 | 496 | 501 | PF02516 | 0.643 |
MOD_N-GLC_1 | 535 | 540 | PF02516 | 0.653 |
MOD_N-GLC_2 | 607 | 609 | PF02516 | 0.421 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.531 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.460 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.449 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.539 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.528 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.480 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.545 |
MOD_PIKK_1 | 536 | 542 | PF00454 | 0.551 |
MOD_PIKK_1 | 549 | 555 | PF00454 | 0.507 |
MOD_PK_1 | 33 | 39 | PF00069 | 0.599 |
MOD_PKA_1 | 525 | 531 | PF00069 | 0.578 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.524 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.487 |
MOD_PKA_2 | 602 | 608 | PF00069 | 0.656 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.505 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.473 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.590 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.691 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.669 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.506 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.594 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.668 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.678 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.823 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.570 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.577 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.604 |
MOD_SUMO_for_1 | 581 | 584 | PF00179 | 0.575 |
MOD_SUMO_rev_2 | 155 | 163 | PF00179 | 0.561 |
MOD_SUMO_rev_2 | 267 | 271 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 277 | 287 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 384 | 390 | PF00179 | 0.605 |
MOD_SUMO_rev_2 | 458 | 465 | PF00179 | 0.646 |
MOD_SUMO_rev_2 | 477 | 486 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 538 | 547 | PF00179 | 0.557 |
TRG_DiLeu_BaEn_4 | 119 | 125 | PF01217 | 0.594 |
TRG_DiLeu_BaEn_4 | 306 | 312 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.639 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 361 | 364 | PF00400 | 0.814 |
TRG_NES_CRM1_1 | 119 | 131 | PF08389 | 0.344 |
TRG_NES_CRM1_1 | 179 | 194 | PF08389 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 313 | 317 | PF00026 | 0.684 |
TRG_Pf-PMV_PEXEL_1 | 478 | 482 | PF00026 | 0.597 |
TRG_Pf-PMV_PEXEL_1 | 586 | 591 | PF00026 | 0.622 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDQ0 | Leptomonas seymouri | 52% | 100% |
A0A1X0NQ11 | Trypanosomatidae | 37% | 73% |
A0A3S7X4D8 | Leishmania donovani | 72% | 99% |
A0A422NZ91 | Trypanosoma rangeli | 36% | 76% |
A4I6Q2 | Leishmania infantum | 72% | 99% |
E9B1S4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 99% |
Q4Q6D7 | Leishmania major | 72% | 100% |
V5DGE3 | Trypanosoma cruzi | 36% | 77% |