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: 9 |
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:0005858 | axonemal dynein complex | 4 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0030286 | dynein complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0036157 | outer dynein arm | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
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 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: E9AWL7
Term | Name | Level | Count |
---|---|---|---|
GO:0003341 | cilium movement | 4 | 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:0022607 | cellular component assembly | 4 | 1 |
GO:0033058 | directional locomotion | 2 | 1 |
GO:0036158 | outer dynein arm assembly | 7 | 1 |
GO:0040011 | locomotion | 1 | 1 |
GO:0043056 | forward locomotion | 3 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0060294 | cilium movement involved in cell motility | 5 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0070286 | axonemal dynein complex assembly | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003774 | cytoskeletal motor activity | 1 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0045503 | dynein light chain binding | 3 | 1 |
GO:0045504 | dynein heavy chain binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.509 |
CLV_C14_Caspase3-7 | 564 | 568 | PF00656 | 0.360 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.473 |
CLV_PCSK_FUR_1 | 116 | 120 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 454 | 456 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.437 |
DEG_APCC_DBOX_1 | 251 | 259 | PF00400 | 0.407 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.559 |
DEG_SPOP_SBC_1 | 576 | 580 | PF00917 | 0.295 |
DOC_MAPK_DCC_7 | 554 | 562 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 116 | 125 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 302 | 311 | PF00069 | 0.325 |
DOC_MAPK_gen_1 | 330 | 338 | PF00069 | 0.206 |
DOC_MAPK_gen_1 | 611 | 620 | PF00069 | 0.314 |
DOC_MAPK_gen_1 | 679 | 686 | PF00069 | 0.447 |
DOC_MAPK_HePTP_8 | 551 | 563 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 554 | 563 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 633 | 641 | PF00069 | 0.296 |
DOC_MAPK_MEF2A_6 | 669 | 678 | PF00069 | 0.330 |
DOC_PP4_FxxP_1 | 328 | 331 | PF00568 | 0.514 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.696 |
DOC_USP7_UBL2_3 | 300 | 304 | PF12436 | 0.489 |
DOC_USP7_UBL2_3 | 550 | 554 | PF12436 | 0.423 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 553 | 558 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.309 |
LIG_14-3-3_CanoR_1 | 154 | 160 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 166 | 172 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 27 | 37 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 89 | 95 | PF00244 | 0.486 |
LIG_Actin_WH2_2 | 632 | 648 | PF00022 | 0.410 |
LIG_APCC_ABBA_1 | 69 | 74 | PF00400 | 0.442 |
LIG_BIR_III_2 | 622 | 626 | PF00653 | 0.217 |
LIG_BIR_III_4 | 400 | 404 | PF00653 | 0.450 |
LIG_BIR_III_4 | 567 | 571 | PF00653 | 0.366 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.508 |
LIG_BRCT_BRCA1_1 | 324 | 328 | PF00533 | 0.322 |
LIG_BRCT_BRCA1_1 | 578 | 582 | PF00533 | 0.275 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.566 |
LIG_BRCT_BRCA1_2 | 324 | 330 | PF00533 | 0.429 |
LIG_Clathr_ClatBox_1 | 560 | 564 | PF01394 | 0.314 |
LIG_Clathr_ClatBox_1 | 94 | 98 | PF01394 | 0.496 |
LIG_deltaCOP1_diTrp_1 | 422 | 429 | PF00928 | 0.302 |
LIG_deltaCOP1_diTrp_1 | 546 | 552 | PF00928 | 0.412 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.437 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.660 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.403 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.420 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.429 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.338 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.436 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.377 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.547 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.605 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.486 |
LIG_FHA_2 | 675 | 681 | PF00498 | 0.360 |
LIG_LIR_Apic_2 | 325 | 331 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 325 | 331 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 422 | 430 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 579 | 587 | PF02991 | 0.428 |
LIG_LIR_LC3C_4 | 558 | 562 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 529 | 535 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 571 | 577 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 579 | 585 | PF02991 | 0.303 |
LIG_LYPXL_yS_3 | 315 | 318 | PF13949 | 0.207 |
LIG_PDZ_Class_2 | 681 | 686 | PF00595 | 0.533 |
LIG_REV1ctd_RIR_1 | 294 | 304 | PF16727 | 0.362 |
LIG_REV1ctd_RIR_1 | 336 | 345 | PF16727 | 0.210 |
LIG_SH2_CRK | 326 | 330 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 528 | 532 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 577 | 581 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.419 |
LIG_SH3_1 | 531 | 537 | PF00018 | 0.421 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.403 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.437 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.435 |
LIG_SUMO_SIM_anti_2 | 624 | 632 | PF11976 | 0.234 |
LIG_SUMO_SIM_par_1 | 431 | 437 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 558 | 564 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 624 | 632 | PF11976 | 0.234 |
LIG_SUMO_SIM_par_1 | 663 | 668 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 672 | 677 | PF11976 | 0.352 |
MOD_CDK_SPK_2 | 3 | 8 | PF00069 | 0.685 |
MOD_CDK_SPxxK_3 | 245 | 252 | PF00069 | 0.402 |
MOD_CDK_SPxxK_3 | 639 | 646 | PF00069 | 0.314 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.607 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.350 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.289 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.552 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.413 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.534 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.513 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.563 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.221 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.550 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.225 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.531 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.576 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.665 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.467 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.507 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.415 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.482 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.363 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.387 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.407 |
MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.490 |
MOD_N-GLC_1 | 598 | 603 | PF02516 | 0.496 |
MOD_N-GLC_2 | 265 | 267 | PF02516 | 0.374 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.527 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.262 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.344 |
MOD_NEK2_2 | 227 | 232 | PF00069 | 0.542 |
MOD_NEK2_2 | 357 | 362 | PF00069 | 0.309 |
MOD_NEK2_2 | 545 | 550 | PF00069 | 0.430 |
MOD_NEK2_2 | 577 | 582 | PF00069 | 0.282 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.494 |
MOD_PIKK_1 | 497 | 503 | PF00454 | 0.317 |
MOD_PKA_1 | 27 | 33 | PF00069 | 0.606 |
MOD_PKA_1 | 646 | 652 | PF00069 | 0.462 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.520 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.583 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.562 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.615 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.309 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.663 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.569 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.617 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.265 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.463 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.423 |
MOD_Plk_1 | 674 | 680 | PF00069 | 0.339 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.467 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.456 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.307 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.352 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.307 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.534 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.569 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.494 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.695 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.503 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.516 |
MOD_ProDKin_1 | 553 | 559 | PF00069 | 0.499 |
MOD_ProDKin_1 | 639 | 645 | PF00069 | 0.309 |
TRG_DiLeu_BaEn_1 | 218 | 223 | PF01217 | 0.344 |
TRG_DiLeu_BaEn_1 | 286 | 291 | PF01217 | 0.376 |
TRG_DiLeu_BaEn_1 | 502 | 507 | PF01217 | 0.448 |
TRG_DiLeu_BaEn_4 | 218 | 224 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.429 |
TRG_LysEnd_GGAAcLL_1 | 680 | 686 | PF00790 | 0.493 |
TRG_NES_CRM1_1 | 668 | 680 | PF08389 | 0.480 |
TRG_NLS_MonoExtN_4 | 300 | 306 | PF00514 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.569 |
TRG_Pf-PMV_PEXEL_1 | 143 | 148 | PF00026 | 0.583 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I862 | Leptomonas seymouri | 81% | 100% |
A0A0S4INJ7 | Bodo saltans | 57% | 100% |
A0A1X0NJ43 | Trypanosomatidae | 60% | 100% |
A0A3Q8ICR4 | Leishmania donovani | 95% | 100% |
A0A422P471 | Trypanosoma rangeli | 61% | 100% |
A4HD84 | Leishmania braziliensis | 88% | 100% |
A4HK88 | Leishmania braziliensis | 27% | 100% |
C9ZJC3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 79% |
D0A6Z5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9AH39 | Leishmania infantum | 94% | 100% |
F1QHZ6 | Danio rerio | 28% | 88% |
Q16959 | Heliocidaris crassispina | 41% | 98% |
Q32KS2 | Bos taurus | 37% | 98% |
Q39578 | Chlamydomonas reinhardtii | 38% | 100% |
Q4QAV3 | Leishmania major | 94% | 100% |
Q4V8G4 | Rattus norvegicus | 25% | 85% |
Q5VTH9 | Homo sapiens | 25% | 81% |
Q5XIL8 | Rattus norvegicus | 37% | 97% |
Q6GPB9 | Xenopus laevis | 27% | 92% |
Q8C0M8 | Mus musculus | 37% | 98% |
Q9UI46 | Homo sapiens | 38% | 98% |
V5BJK6 | Trypanosoma cruzi | 29% | 83% |
V5DSN6 | Trypanosoma cruzi | 60% | 100% |