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:0005930 | axoneme | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8IFU8
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0022607 | cellular component assembly | 4 | 10 |
GO:0036158 | outer dynein arm assembly | 7 | 10 |
GO:0036159 | inner dynein arm assembly | 7 | 10 |
GO:0043933 | protein-containing complex organization | 4 | 10 |
GO:0065003 | protein-containing complex assembly | 5 | 10 |
GO:0070286 | axonemal dynein complex assembly | 6 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0044877 | protein-containing complex binding | 2 | 10 |
GO:0070840 | dynein complex binding | 3 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.705 |
CLV_C14_Caspase3-7 | 525 | 529 | PF00656 | 0.734 |
CLV_C14_Caspase3-7 | 552 | 556 | PF00656 | 0.788 |
CLV_C14_Caspase3-7 | 593 | 597 | PF00656 | 0.712 |
CLV_C14_Caspase3-7 | 600 | 604 | PF00656 | 0.729 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.515 |
CLV_PCSK_FUR_1 | 437 | 441 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 439 | 441 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.355 |
DEG_COP1_1 | 655 | 667 | PF00400 | 0.607 |
DEG_ODPH_VHL_1 | 72 | 85 | PF01847 | 0.486 |
DEG_SIAH_1 | 106 | 114 | PF03145 | 0.594 |
DEG_SPOP_SBC_1 | 624 | 628 | PF00917 | 0.675 |
DOC_CDC14_PxL_1 | 407 | 415 | PF14671 | 0.441 |
DOC_CYCLIN_RxL_1 | 433 | 446 | PF00134 | 0.532 |
DOC_MAPK_gen_1 | 201 | 210 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 296 | 303 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 338 | 345 | PF00069 | 0.751 |
DOC_MAPK_gen_1 | 409 | 418 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 437 | 444 | PF00069 | 0.493 |
DOC_PP1_RVXF_1 | 82 | 88 | PF00149 | 0.397 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.800 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.616 |
LIG_14-3-3_CanoR_1 | 267 | 275 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 305 | 315 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 338 | 344 | PF00244 | 0.791 |
LIG_14-3-3_CanoR_1 | 356 | 365 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 412 | 417 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 454 | 462 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 623 | 630 | PF00244 | 0.819 |
LIG_14-3-3_CanoR_1 | 635 | 643 | PF00244 | 0.641 |
LIG_Actin_WH2_2 | 403 | 419 | PF00022 | 0.413 |
LIG_AP2alpha_2 | 112 | 114 | PF02296 | 0.693 |
LIG_APCC_ABBA_1 | 77 | 82 | PF00400 | 0.461 |
LIG_APCC_ABBAyCdc20_2 | 439 | 445 | PF00400 | 0.493 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.696 |
LIG_BRCT_BRCA1_1 | 210 | 214 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_2 | 210 | 216 | PF00533 | 0.377 |
LIG_Clathr_ClatBox_1 | 404 | 408 | PF01394 | 0.404 |
LIG_Clathr_ClatBox_1 | 441 | 445 | PF01394 | 0.404 |
LIG_eIF4E_1 | 187 | 193 | PF01652 | 0.546 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.351 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.445 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.446 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.561 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.752 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.655 |
LIG_FHA_2 | 557 | 563 | PF00498 | 0.691 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.542 |
LIG_LIR_Gen_1 | 174 | 183 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 200 | 210 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 310 | 321 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 488 | 493 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.419 |
LIG_LYPXL_S_1 | 179 | 183 | PF13949 | 0.400 |
LIG_LYPXL_yS_3 | 180 | 183 | PF13949 | 0.401 |
LIG_PDZ_Class_1 | 663 | 668 | PF00595 | 0.558 |
LIG_PTB_Apo_2 | 187 | 194 | PF02174 | 0.522 |
LIG_PTB_Apo_2 | 63 | 70 | PF02174 | 0.497 |
LIG_PTB_Phospho_1 | 63 | 69 | PF10480 | 0.567 |
LIG_REV1ctd_RIR_1 | 212 | 219 | PF16727 | 0.386 |
LIG_SH2_CRK | 102 | 106 | PF00017 | 0.605 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.445 |
LIG_SH2_CRK | 53 | 57 | PF00017 | 0.441 |
LIG_SH2_CRK | 69 | 73 | PF00017 | 0.418 |
LIG_SH2_GRB2like | 510 | 513 | PF00017 | 0.607 |
LIG_SH2_NCK_1 | 69 | 73 | PF00017 | 0.562 |
LIG_SH2_SRC | 510 | 513 | PF00017 | 0.685 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.577 |
LIG_SH2_STAP1 | 69 | 73 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.410 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.586 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.737 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.658 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.744 |
LIG_SH3_5 | 506 | 510 | PF00018 | 0.677 |
LIG_SUMO_SIM_anti_2 | 283 | 290 | PF11976 | 0.698 |
LIG_SUMO_SIM_anti_2 | 386 | 391 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 401 | 408 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 287 | 294 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 388 | 393 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 401 | 408 | PF11976 | 0.386 |
LIG_TRAF2_1 | 474 | 477 | PF00917 | 0.615 |
LIG_TYR_ITIM | 382 | 387 | PF00017 | 0.439 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.737 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.670 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.673 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.596 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.376 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.771 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.733 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.779 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.501 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.596 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.580 |
MOD_CK2_1 | 535 | 541 | PF00069 | 0.710 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.716 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.798 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.457 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.470 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.390 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.652 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.739 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.660 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.708 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.401 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.807 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.776 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.629 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.732 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.686 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.472 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.624 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.319 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.749 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.717 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.724 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.537 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.436 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.413 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.430 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.619 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.745 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.704 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.694 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.537 |
MOD_LATS_1 | 336 | 342 | PF00433 | 0.612 |
MOD_LATS_1 | 546 | 552 | PF00433 | 0.699 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.727 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.395 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.629 |
MOD_N-GLC_1 | 590 | 595 | PF02516 | 0.797 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.545 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.674 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.657 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.362 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.407 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.441 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.567 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.573 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.802 |
MOD_NEK2_2 | 175 | 180 | PF00069 | 0.475 |
MOD_NEK2_2 | 358 | 363 | PF00069 | 0.469 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.541 |
MOD_PIKK_1 | 609 | 615 | PF00454 | 0.801 |
MOD_PIKK_1 | 625 | 631 | PF00454 | 0.815 |
MOD_PKA_1 | 338 | 344 | PF00069 | 0.717 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.486 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.795 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.793 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.671 |
MOD_PKB_1 | 305 | 313 | PF00069 | 0.279 |
MOD_PKB_1 | 431 | 439 | PF00069 | 0.521 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.677 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.501 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.750 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.640 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.552 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.398 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.589 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.758 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.571 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.737 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.664 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.621 |
MOD_SUMO_rev_2 | 612 | 619 | PF00179 | 0.721 |
MOD_SUMO_rev_2 | 78 | 86 | PF00179 | 0.410 |
TRG_DiLeu_BaEn_1 | 401 | 406 | PF01217 | 0.402 |
TRG_DiLeu_BaLyEn_6 | 437 | 442 | PF01217 | 0.570 |
TRG_DiLeu_BaLyEn_6 | 489 | 494 | PF01217 | 0.600 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.342 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.761 |
TRG_ER_diArg_1 | 430 | 433 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 490 | 492 | PF00400 | 0.519 |
TRG_NLS_MonoExtN_4 | 428 | 435 | PF00514 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 440 | 445 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 617 | 621 | PF00026 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4C5 | Leptomonas seymouri | 53% | 100% |
A0A0S4JQS0 | Bodo saltans | 37% | 100% |
A0A422N6Q2 | Trypanosoma rangeli | 41% | 100% |
A4HEX7 | Leishmania braziliensis | 71% | 98% |
A4I251 | Leishmania infantum | 99% | 100% |
C9ZRV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AYA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q972 | Leishmania major | 90% | 100% |
V5DQX0 | Trypanosoma cruzi | 39% | 90% |