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: 3 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005840 | ribosome | 5 | 13 |
GO:0005875 | microtubule associated complex | 2 | 16 |
GO:0030286 | dynein complex | 3 | 16 |
GO:0032991 | protein-containing complex | 1 | 17 |
GO:0043226 | organelle | 2 | 13 |
GO:0043228 | non-membrane-bounded organelle | 3 | 13 |
GO:0043229 | intracellular organelle | 3 | 13 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:1902494 | catalytic complex | 2 | 16 |
GO:1990904 | ribonucleoprotein complex | 2 | 13 |
Related structures:
AlphaFold database: Q4Q6U8
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 16 |
GO:0007018 | microtubule-based movement | 3 | 16 |
GO:0009987 | cellular process | 1 | 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003774 | cytoskeletal motor activity | 1 | 16 |
GO:0003777 | microtubule motor activity | 2 | 16 |
GO:0008569 | minus-end-directed microtubule motor activity | 3 | 16 |
GO:0140657 | ATP-dependent activity | 1 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.418 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.420 |
DEG_APCC_DBOX_1 | 367 | 375 | PF00400 | 0.537 |
DOC_CYCLIN_RxL_1 | 214 | 226 | PF00134 | 0.524 |
DOC_CYCLIN_RxL_1 | 589 | 601 | PF00134 | 0.454 |
DOC_CYCLIN_yClb3_PxF_3 | 100 | 106 | PF00134 | 0.529 |
DOC_MAPK_DCC_7 | 368 | 376 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 150 | 158 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 24 | 34 | PF00069 | 0.331 |
DOC_MAPK_gen_1 | 288 | 295 | PF00069 | 0.584 |
DOC_MAPK_gen_1 | 575 | 583 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 368 | 376 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 66 | 73 | PF00069 | 0.563 |
DOC_PP2B_LxvP_1 | 73 | 76 | PF13499 | 0.540 |
DOC_PP2B_LxvP_1 | 93 | 96 | PF13499 | 0.497 |
DOC_SPAK_OSR1_1 | 353 | 357 | PF12202 | 0.363 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.682 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.379 |
DOC_USP7_UBL2_3 | 179 | 183 | PF12436 | 0.457 |
DOC_USP7_UBL2_3 | 288 | 292 | PF12436 | 0.721 |
LIG_14-3-3_CanoR_1 | 167 | 171 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 200 | 209 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 458 | 464 | PF00244 | 0.375 |
LIG_APCC_ABBA_1 | 185 | 190 | PF00400 | 0.446 |
LIG_APCC_ABBAyCdc20_2 | 267 | 273 | PF00400 | 0.692 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.573 |
LIG_BRCT_BRCA1_1 | 388 | 392 | PF00533 | 0.439 |
LIG_EVH1_1 | 99 | 103 | PF00568 | 0.721 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.480 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.360 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.448 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.357 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.402 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.288 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.311 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.496 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.579 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.543 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.343 |
LIG_FHA_2 | 489 | 495 | PF00498 | 0.318 |
LIG_KLC1_Yacidic_2 | 154 | 159 | PF13176 | 0.546 |
LIG_LIR_Apic_2 | 431 | 435 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 3 | 13 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 307 | 316 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 360 | 366 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 523 | 532 | PF02991 | 0.323 |
LIG_LIR_LC3C_4 | 67 | 72 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 3 | 8 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 360 | 365 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 523 | 529 | PF02991 | 0.445 |
LIG_MYND_1 | 100 | 104 | PF01753 | 0.718 |
LIG_Pex14_1 | 384 | 388 | PF04695 | 0.326 |
LIG_Pex14_2 | 388 | 392 | PF04695 | 0.456 |
LIG_PTB_Apo_2 | 422 | 429 | PF02174 | 0.432 |
LIG_SH2_CRK | 432 | 436 | PF00017 | 0.525 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.569 |
LIG_SH2_GRB2like | 432 | 435 | PF00017 | 0.386 |
LIG_SH2_NCK_1 | 408 | 412 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 432 | 436 | PF00017 | 0.401 |
LIG_SH2_NCK_1 | 5 | 9 | PF00017 | 0.407 |
LIG_SH2_PTP2 | 362 | 365 | PF00017 | 0.356 |
LIG_SH2_SRC | 432 | 435 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 119 | 123 | PF00017 | 0.512 |
LIG_SH2_STAT3 | 188 | 191 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 560 | 563 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.343 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.446 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.278 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.745 |
LIG_SUMO_SIM_anti_2 | 195 | 200 | PF11976 | 0.457 |
LIG_SUMO_SIM_anti_2 | 219 | 226 | PF11976 | 0.514 |
LIG_SUMO_SIM_anti_2 | 67 | 73 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 341 | 347 | PF11976 | 0.275 |
LIG_SUMO_SIM_par_1 | 362 | 367 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 416 | 422 | PF11976 | 0.498 |
LIG_TRAF2_1 | 411 | 414 | PF00917 | 0.563 |
LIG_TYR_ITSM | 1 | 8 | PF00017 | 0.424 |
LIG_WRC_WIRS_1 | 420 | 425 | PF05994 | 0.439 |
LIG_WW_2 | 100 | 103 | PF00397 | 0.735 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.761 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.698 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.547 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.492 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.416 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.414 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.644 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.517 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.573 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.349 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.554 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.674 |
MOD_GlcNHglycan | 311 | 315 | PF01048 | 0.543 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.575 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.490 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.445 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.344 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.304 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.362 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.340 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.454 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.347 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.347 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.508 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.598 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.445 |
MOD_N-GLC_1 | 459 | 464 | PF02516 | 0.460 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.620 |
MOD_N-GLC_2 | 496 | 498 | PF02516 | 0.524 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.687 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.561 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.454 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.597 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.538 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.504 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.281 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.383 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.362 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.382 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.207 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.383 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.486 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.366 |
MOD_NEK2_2 | 119 | 124 | PF00069 | 0.487 |
MOD_NEK2_2 | 238 | 243 | PF00069 | 0.457 |
MOD_PIKK_1 | 387 | 393 | PF00454 | 0.477 |
MOD_PIKK_1 | 473 | 479 | PF00454 | 0.430 |
MOD_PIKK_1 | 540 | 546 | PF00454 | 0.375 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.573 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.495 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.465 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.619 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.357 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.609 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.454 |
MOD_Plk_1 | 304 | 310 | PF00069 | 0.559 |
MOD_Plk_1 | 384 | 390 | PF00069 | 0.381 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.467 |
MOD_Plk_1 | 459 | 465 | PF00069 | 0.488 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.518 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.654 |
MOD_Plk_2-3 | 305 | 311 | PF00069 | 0.573 |
MOD_Plk_2-3 | 82 | 88 | PF00069 | 0.670 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.620 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.461 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.365 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.414 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.314 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.404 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.395 |
MOD_SUMO_for_1 | 151 | 154 | PF00179 | 0.526 |
MOD_SUMO_for_1 | 282 | 285 | PF00179 | 0.739 |
MOD_SUMO_for_1 | 77 | 80 | PF00179 | 0.690 |
TRG_DiLeu_BaEn_2 | 304 | 310 | PF01217 | 0.558 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.346 |
TRG_DiLeu_BaLyEn_6 | 369 | 374 | PF01217 | 0.416 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.576 |
TRG_ER_diArg_1 | 242 | 245 | PF00400 | 0.529 |
TRG_NES_CRM1_1 | 175 | 190 | PF08389 | 0.504 |
TRG_NES_CRM1_1 | 546 | 558 | PF08389 | 0.445 |
TRG_NLS_MonoExtC_3 | 289 | 294 | PF00514 | 0.584 |
TRG_NLS_MonoExtN_4 | 288 | 295 | PF00514 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 200 | 204 | PF00026 | 0.246 |
TRG_Pf-PMV_PEXEL_1 | 545 | 549 | PF00026 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 593 | 598 | PF00026 | 0.364 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3S6 | Leptomonas seymouri | 83% | 100% |
A0A0N1PCL0 | Leptomonas seymouri | 27% | 70% |
A0A0S4J7X8 | Bodo saltans | 28% | 83% |
A0A0S4JKZ2 | Bodo saltans | 49% | 93% |
A0A1X0P1Y1 | Trypanosomatidae | 51% | 99% |
A0A1X0P3P9 | Trypanosomatidae | 28% | 80% |
A0A3R7KEX8 | Trypanosoma rangeli | 27% | 82% |
A0A3S7X3V5 | Leishmania donovani | 98% | 100% |
A0A3S7X707 | Leishmania donovani | 27% | 71% |
A0A422NMN1 | Trypanosoma rangeli | 51% | 100% |
A4HIS9 | Leishmania braziliensis | 88% | 100% |
A4HLS7 | Leishmania braziliensis | 27% | 71% |
A4I631 | Leishmania infantum | 98% | 100% |
A4I986 | Leishmania infantum | 27% | 71% |
C9ZRE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 99% |
D0A6A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 80% |
E9B1B6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9B453 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 71% |
Q9GRN2 | Leishmania major | 28% | 71% |
V5DNT3 | Trypanosoma cruzi | 52% | 100% |
V5DQD1 | Trypanosoma cruzi | 28% | 82% |