Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 12 |
GO:0031514 | motile cilium | 5 | 12 |
GO:0042995 | cell projection | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 12 |
GO:0005814 | centriole | 5 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0030990 | intraciliary transport particle | 2 | 1 |
GO:0030992 | intraciliary transport particle B | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0035869 | ciliary transition zone | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4H9Z0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007018 | microtubule-based movement | 3 | 1 |
GO:0009987 | cellular process | 1 | 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:0035735 | intraciliary transport involved in cilium assembly | 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.537 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 663 | 667 | PF00082 | 0.530 |
CLV_Separin_Metazoa | 379 | 383 | PF03568 | 0.501 |
DEG_APCC_DBOX_1 | 340 | 348 | PF00400 | 0.398 |
DEG_APCC_DBOX_1 | 460 | 468 | PF00400 | 0.515 |
DEG_APCC_DBOX_1 | 501 | 509 | PF00400 | 0.439 |
DEG_APCC_DBOX_1 | 662 | 670 | PF00400 | 0.538 |
DEG_SCF_FBW7_2 | 91 | 97 | PF00400 | 0.510 |
DOC_ANK_TNKS_1 | 103 | 110 | PF00023 | 0.478 |
DOC_CKS1_1 | 424 | 429 | PF01111 | 0.576 |
DOC_CKS1_1 | 91 | 96 | PF01111 | 0.503 |
DOC_CYCLIN_RxL_1 | 302 | 313 | PF00134 | 0.299 |
DOC_CYCLIN_yCln2_LP_2 | 283 | 289 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 419 | 422 | PF00134 | 0.527 |
DOC_MAPK_DCC_7 | 409 | 419 | PF00069 | 0.630 |
DOC_MAPK_FxFP_2 | 256 | 259 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 302 | 311 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 9 | 17 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 441 | 450 | PF00069 | 0.543 |
DOC_MAPK_RevD_3 | 503 | 517 | PF00069 | 0.463 |
DOC_PP1_RVXF_1 | 36 | 42 | PF00149 | 0.448 |
DOC_PP2B_LxvP_1 | 419 | 422 | PF13499 | 0.527 |
DOC_PP4_FxxP_1 | 256 | 259 | PF00568 | 0.348 |
DOC_PP4_FxxP_1 | 424 | 427 | PF00568 | 0.544 |
DOC_PP4_FxxP_1 | 88 | 91 | PF00568 | 0.444 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.292 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.738 |
DOC_USP7_UBL2_3 | 172 | 176 | PF12436 | 0.475 |
DOC_USP7_UBL2_3 | 409 | 413 | PF12436 | 0.466 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 563 | 568 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.566 |
LIG_14-3-3_CanoR_1 | 573 | 577 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 79 | 87 | PF00244 | 0.587 |
LIG_Actin_WH2_2 | 633 | 651 | PF00022 | 0.424 |
LIG_APCC_ABBAyCdc20_2 | 573 | 579 | PF00400 | 0.440 |
LIG_BIR_III_2 | 564 | 568 | PF00653 | 0.542 |
LIG_BRCT_BRCA1_1 | 252 | 256 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 274 | 278 | PF00533 | 0.377 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_1 | 596 | 600 | PF00533 | 0.485 |
LIG_Clathr_ClatBox_1 | 387 | 391 | PF01394 | 0.558 |
LIG_Clathr_ClatBox_1 | 450 | 454 | PF01394 | 0.534 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.505 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.799 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.427 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.382 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.329 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.525 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.487 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.492 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.403 |
LIG_FHA_2 | 531 | 537 | PF00498 | 0.560 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.510 |
LIG_FHA_2 | 666 | 672 | PF00498 | 0.596 |
LIG_GBD_Chelix_1 | 330 | 338 | PF00786 | 0.509 |
LIG_LIR_Apic_2 | 14 | 19 | PF02991 | 0.708 |
LIG_LIR_Apic_2 | 253 | 259 | PF02991 | 0.373 |
LIG_LIR_Apic_2 | 423 | 427 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 332 | 342 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 355 | 364 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 383 | 390 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 405 | 414 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 383 | 387 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 514 | 518 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 622 | 626 | PF02991 | 0.429 |
LIG_PCNA_yPIPBox_3 | 324 | 334 | PF02747 | 0.294 |
LIG_PDZ_Class_3 | 667 | 672 | PF00595 | 0.469 |
LIG_Pex14_2 | 317 | 321 | PF04695 | 0.531 |
LIG_Pex14_2 | 384 | 388 | PF04695 | 0.480 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.419 |
LIG_SH2_CRK | 407 | 411 | PF00017 | 0.495 |
LIG_SH2_CRK | 515 | 519 | PF00017 | 0.541 |
LIG_SH2_GRB2like | 127 | 130 | PF00017 | 0.421 |
LIG_SH2_GRB2like | 337 | 340 | PF00017 | 0.312 |
LIG_SH2_PTP2 | 637 | 640 | PF00017 | 0.519 |
LIG_SH2_SRC | 106 | 109 | PF00017 | 0.448 |
LIG_SH2_SRC | 153 | 156 | PF00017 | 0.457 |
LIG_SH2_SRC | 337 | 340 | PF00017 | 0.509 |
LIG_SH2_SRC | 577 | 580 | PF00017 | 0.544 |
LIG_SH2_STAT3 | 479 | 482 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 577 | 580 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 667 | 670 | PF00017 | 0.525 |
LIG_SH3_2 | 427 | 432 | PF14604 | 0.559 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.425 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.552 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.640 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.525 |
LIG_SUMO_SIM_anti_2 | 112 | 117 | PF11976 | 0.396 |
LIG_SUMO_SIM_anti_2 | 415 | 421 | PF11976 | 0.514 |
LIG_SUMO_SIM_par_1 | 112 | 119 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 307 | 313 | PF11976 | 0.369 |
LIG_TRAF2_1 | 243 | 246 | PF00917 | 0.702 |
LIG_TRAF2_1 | 524 | 527 | PF00917 | 0.765 |
LIG_TRAF2_1 | 668 | 671 | PF00917 | 0.552 |
LIG_TYR_ITIM | 476 | 481 | PF00017 | 0.578 |
LIG_TYR_ITIM | 513 | 518 | PF00017 | 0.515 |
LIG_TYR_ITIM | 635 | 640 | PF00017 | 0.526 |
LIG_UBA3_1 | 334 | 343 | PF00899 | 0.386 |
LIG_UBA3_1 | 387 | 394 | PF00899 | 0.532 |
LIG_WRC_WIRS_1 | 390 | 395 | PF05994 | 0.505 |
MOD_CDK_SPK_2 | 492 | 497 | PF00069 | 0.541 |
MOD_CDK_SPxxK_3 | 492 | 499 | PF00069 | 0.534 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.688 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.548 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.460 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.399 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.512 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.699 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.601 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.745 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.766 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.391 |
MOD_GlcNHglycan | 325 | 330 | PF01048 | 0.448 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.586 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.469 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.502 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.662 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.524 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.530 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.630 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.630 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.635 |
MOD_N-GLC_2 | 42 | 44 | PF02516 | 0.439 |
MOD_N-GLC_2 | 469 | 471 | PF02516 | 0.452 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.639 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.655 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.593 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.488 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.322 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.487 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.699 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.530 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.336 |
MOD_NEK2_2 | 572 | 577 | PF00069 | 0.608 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.693 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.628 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.457 |
MOD_PIKK_1 | 522 | 528 | PF00454 | 0.738 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.326 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.447 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.529 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.494 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.478 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.596 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.658 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.672 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.585 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.481 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.592 |
MOD_Plk_1 | 595 | 601 | PF00069 | 0.588 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.469 |
MOD_Plk_2-3 | 362 | 368 | PF00069 | 0.492 |
MOD_Plk_2-3 | 73 | 79 | PF00069 | 0.469 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.349 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.496 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.805 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.429 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.400 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.526 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.577 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.537 |
MOD_ProDKin_1 | 563 | 569 | PF00069 | 0.489 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.569 |
MOD_SUMO_for_1 | 412 | 415 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 604 | 614 | PF00179 | 0.624 |
MOD_SUMO_rev_2 | 96 | 103 | PF00179 | 0.470 |
TRG_DiLeu_BaEn_1 | 250 | 255 | PF01217 | 0.564 |
TRG_DiLeu_BaEn_1 | 415 | 420 | PF01217 | 0.512 |
TRG_DiLeu_BaEn_4 | 325 | 331 | PF01217 | 0.394 |
TRG_DiLeu_BaLyEn_6 | 269 | 274 | PF01217 | 0.516 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 515 | 518 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 637 | 640 | PF00928 | 0.519 |
TRG_ER_diArg_1 | 369 | 372 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 461 | 464 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 496 | 499 | PF00400 | 0.591 |
TRG_NES_CRM1_1 | 378 | 391 | PF08389 | 0.630 |
TRG_Pf-PMV_PEXEL_1 | 502 | 506 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 60 | 64 | PF00026 | 0.479 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDM4 | Leptomonas seymouri | 79% | 99% |
A0A0S4KG78 | Bodo saltans | 55% | 100% |
A0A1X0P7F0 | Trypanosomatidae | 66% | 100% |
A0A3R7NUY6 | Trypanosoma rangeli | 65% | 100% |
A0A3S5H752 | Leishmania donovani | 86% | 100% |
A4HY54 | Leishmania infantum | 87% | 100% |
D0A0G1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
E9ARY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QDI9 | Leishmania major | 89% | 100% |
V5DTK4 | Trypanosoma cruzi | 65% | 100% |