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: A4HD84
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 | 564 | 568 | PF00656 | 0.358 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.471 |
CLV_PCSK_FUR_1 | 116 | 120 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.436 |
DEG_SPOP_SBC_1 | 576 | 580 | PF00917 | 0.289 |
DOC_CYCLIN_yCln2_LP_2 | 531 | 537 | PF00134 | 0.353 |
DOC_MAPK_DCC_7 | 554 | 562 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 116 | 125 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 302 | 311 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 611 | 620 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 633 | 641 | PF00069 | 0.295 |
DOC_MAPK_MEF2A_6 | 669 | 678 | PF00069 | 0.332 |
DOC_PP4_FxxP_1 | 328 | 331 | PF00568 | 0.503 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.289 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.289 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.326 |
DOC_USP7_UBL2_3 | 300 | 304 | PF12436 | 0.487 |
DOC_USP7_UBL2_3 | 550 | 554 | PF12436 | 0.422 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 553 | 558 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.306 |
LIG_14-3-3_CanoR_1 | 154 | 160 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 166 | 172 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 179 | 188 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 395 | 401 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 8 | 12 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 89 | 95 | PF00244 | 0.490 |
LIG_Actin_WH2_2 | 632 | 648 | PF00022 | 0.409 |
LIG_APCC_ABBA_1 | 69 | 74 | PF00400 | 0.443 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.571 |
LIG_BIR_III_4 | 567 | 571 | PF00653 | 0.369 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.410 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 324 | 328 | PF00533 | 0.312 |
LIG_BRCT_BRCA1_1 | 578 | 582 | PF00533 | 0.272 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.569 |
LIG_BRCT_BRCA1_2 | 324 | 330 | PF00533 | 0.418 |
LIG_Clathr_ClatBox_1 | 94 | 98 | PF01394 | 0.493 |
LIG_CSL_BTD_1 | 531 | 534 | PF09270 | 0.353 |
LIG_deltaCOP1_diTrp_1 | 422 | 429 | PF00928 | 0.300 |
LIG_deltaCOP1_diTrp_1 | 546 | 552 | PF00928 | 0.411 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.422 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.398 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.418 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.427 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.336 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.434 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.557 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.592 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.481 |
LIG_FHA_2 | 675 | 681 | PF00498 | 0.367 |
LIG_Integrin_isoDGR_2 | 312 | 314 | PF01839 | 0.379 |
LIG_LIR_Apic_2 | 325 | 331 | PF02991 | 0.482 |
LIG_LIR_Apic_2 | 404 | 409 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 325 | 331 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 422 | 430 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 579 | 587 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 529 | 535 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 571 | 577 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 579 | 585 | PF02991 | 0.300 |
LIG_REV1ctd_RIR_1 | 294 | 304 | PF16727 | 0.359 |
LIG_SH2_CRK | 326 | 330 | PF00017 | 0.420 |
LIG_SH2_CRK | 406 | 410 | PF00017 | 0.319 |
LIG_SH2_STAP1 | 315 | 319 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 528 | 532 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 577 | 581 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.417 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.370 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.396 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.436 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.434 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.361 |
LIG_SUMO_SIM_anti_2 | 624 | 632 | PF11976 | 0.233 |
LIG_SUMO_SIM_par_1 | 431 | 437 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 558 | 564 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 624 | 632 | PF11976 | 0.233 |
LIG_SUMO_SIM_par_1 | 672 | 677 | PF11976 | 0.358 |
LIG_TRAF2_1 | 190 | 193 | PF00917 | 0.280 |
LIG_TYR_ITAM | 312 | 329 | PF00017 | 0.353 |
LIG_WRPW_2 | 82 | 85 | PF00400 | 0.314 |
MOD_CDK_SPK_2 | 3 | 8 | PF00069 | 0.683 |
MOD_CDK_SPxxK_3 | 639 | 646 | PF00069 | 0.311 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.413 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.283 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.693 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.407 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.480 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.557 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.468 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.511 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.671 |
MOD_GlcNHglycan | 217 | 222 | PF01048 | 0.615 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.590 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.511 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.541 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.532 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.224 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.530 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.536 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.661 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.460 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.502 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.411 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.480 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.362 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.386 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.417 |
MOD_LATS_1 | 373 | 379 | PF00433 | 0.508 |
MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.489 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.552 |
MOD_N-GLC_1 | 598 | 603 | PF02516 | 0.494 |
MOD_N-GLC_2 | 265 | 267 | PF02516 | 0.369 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.524 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.255 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.317 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.337 |
MOD_NEK2_2 | 227 | 232 | PF00069 | 0.568 |
MOD_NEK2_2 | 332 | 337 | PF00069 | 0.423 |
MOD_NEK2_2 | 357 | 362 | PF00069 | 0.308 |
MOD_NEK2_2 | 545 | 550 | PF00069 | 0.429 |
MOD_NEK2_2 | 577 | 582 | PF00069 | 0.279 |
MOD_NEK2_2 | 7 | 12 | PF00069 | 0.457 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.489 |
MOD_PIKK_1 | 497 | 503 | PF00454 | 0.315 |
MOD_PKA_1 | 27 | 33 | PF00069 | 0.601 |
MOD_PKA_1 | 646 | 652 | PF00069 | 0.462 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.515 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.546 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.596 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.309 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.655 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.582 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.264 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.430 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.456 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.422 |
MOD_Plk_1 | 674 | 680 | PF00069 | 0.347 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.464 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.471 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.449 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.353 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.304 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.347 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.307 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.537 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.561 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.497 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.691 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.495 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.514 |
MOD_ProDKin_1 | 553 | 559 | PF00069 | 0.497 |
MOD_ProDKin_1 | 639 | 645 | PF00069 | 0.307 |
TRG_DiLeu_BaEn_1 | 286 | 291 | PF01217 | 0.372 |
TRG_DiLeu_BaEn_1 | 502 | 507 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.403 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.418 |
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 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.564 |
TRG_Pf-PMV_PEXEL_1 | 143 | 148 | PF00026 | 0.570 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I862 | Leptomonas seymouri | 81% | 100% |
A0A0S4INJ7 | Bodo saltans | 58% | 100% |
A0A1X0NJ43 | Trypanosomatidae | 61% | 100% |
A0A3Q8ICR4 | Leishmania donovani | 90% | 100% |
A0A422P471 | Trypanosoma rangeli | 61% | 100% |
A4HK88 | Leishmania braziliensis | 26% | 100% |
C9ZJC3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 79% |
D0A6Z5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9AH39 | Leishmania infantum | 89% | 100% |
E9AWL7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
F1QHZ6 | Danio rerio | 28% | 88% |
Q16959 | Heliocidaris crassispina | 41% | 98% |
Q32KS2 | Bos taurus | 36% | 98% |
Q39578 | Chlamydomonas reinhardtii | 38% | 100% |
Q4QAV3 | Leishmania major | 89% | 100% |
Q4V8G4 | Rattus norvegicus | 26% | 85% |
Q5U4F6 | Mus musculus | 27% | 100% |
Q5VTH9 | Homo sapiens | 26% | 81% |
Q5XIL8 | Rattus norvegicus | 36% | 97% |
Q6GPB9 | Xenopus laevis | 27% | 92% |
Q8C0M8 | Mus musculus | 38% | 98% |
Q9UI46 | Homo sapiens | 37% | 98% |
V5BJK6 | Trypanosoma cruzi | 29% | 83% |
V5DSN6 | Trypanosoma cruzi | 61% | 100% |