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. | yes | yes: 25 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 11 |
GO:0042995 | cell projection | 2 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 11 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005874 | microtubule | 6 | 1 |
GO:0005879 | axonemal microtubule | 8 | 1 |
GO:0005881 | cytoplasmic microtubule | 7 | 1 |
GO:0030990 | intraciliary transport particle | 2 | 1 |
GO:0030992 | intraciliary transport particle B | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0099081 | supramolecular polymer | 3 | 1 |
GO:0099512 | supramolecular fiber | 4 | 1 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 1 |
GO:0031514 | motile cilium | 5 | 2 |
Related structures:
AlphaFold database: A4HH23
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0030030 | cell projection organization | 4 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
GO:0006810 | transport | 3 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007018 | microtubule-based movement | 3 | 1 |
GO:0010970 | transport along microtubule | 4 | 1 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0031503 | protein-containing complex localization | 2 | 1 |
GO:0035720 | intraciliary anterograde transport | 4 | 1 |
GO:0035735 | intraciliary transport involved in cilium assembly | 4 | 1 |
GO:0042073 | intraciliary transport | 3 | 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:0099111 | microtubule-based transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0120170 | intraciliary transport particle B binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.406 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 553 | 555 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.431 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 618 | 620 | PF00082 | 0.396 |
CLV_PCSK_PC7_1 | 422 | 428 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 619 | 623 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.411 |
CLV_Separin_Metazoa | 550 | 554 | PF03568 | 0.451 |
DEG_APCC_DBOX_1 | 510 | 518 | PF00400 | 0.338 |
DOC_CYCLIN_RxL_1 | 681 | 692 | PF00134 | 0.439 |
DOC_CYCLIN_yClb1_LxF_4 | 352 | 358 | PF00134 | 0.379 |
DOC_MAPK_DCC_7 | 308 | 318 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 618 | 624 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 681 | 690 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 82 | 89 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 569 | 576 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 618 | 626 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 681 | 690 | PF00069 | 0.410 |
DOC_MAPK_NFAT4_5 | 619 | 627 | PF00069 | 0.410 |
DOC_PP4_FxxP_1 | 660 | 663 | PF00568 | 0.533 |
DOC_PP4_MxPP_1 | 9 | 12 | PF00568 | 0.720 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.570 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 668 | 673 | PF00397 | 0.646 |
LIG_14-3-3_CanoR_1 | 139 | 144 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 30 | 36 | PF00244 | 0.766 |
LIG_14-3-3_CanoR_1 | 561 | 565 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 597 | 603 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 607 | 616 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 673 | 677 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 84 | 90 | PF00244 | 0.495 |
LIG_Actin_WH2_2 | 621 | 638 | PF00022 | 0.420 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.603 |
LIG_BRCT_BRCA1_1 | 480 | 484 | PF00533 | 0.421 |
LIG_Clathr_ClatBox_1 | 323 | 327 | PF01394 | 0.582 |
LIG_Clathr_ClatBox_1 | 644 | 648 | PF01394 | 0.471 |
LIG_deltaCOP1_diTrp_1 | 612 | 621 | PF00928 | 0.396 |
LIG_EH1_1 | 592 | 600 | PF00400 | 0.453 |
LIG_EVH1_2 | 347 | 351 | PF00568 | 0.393 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.517 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.670 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.447 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.424 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.446 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.446 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.449 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.604 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.679 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.632 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.532 |
LIG_FHA_2 | 561 | 567 | PF00498 | 0.510 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.557 |
LIG_GBD_Chelix_1 | 624 | 632 | PF00786 | 0.434 |
LIG_HCF-1_HBM_1 | 63 | 66 | PF13415 | 0.352 |
LIG_LIR_Apic_2 | 563 | 567 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 105 | 115 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 349 | 358 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 388 | 397 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 637 | 647 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 655 | 665 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 349 | 354 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 388 | 393 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 469 | 474 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 637 | 643 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 655 | 661 | PF02991 | 0.268 |
LIG_LYPXL_yS_3 | 471 | 474 | PF13949 | 0.396 |
LIG_PCNA_yPIPBox_3 | 578 | 588 | PF02747 | 0.395 |
LIG_PTB_Apo_2 | 340 | 347 | PF02174 | 0.441 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.458 |
LIG_SH2_NCK_1 | 364 | 368 | PF00017 | 0.464 |
LIG_SH2_NCK_1 | 564 | 568 | PF00017 | 0.512 |
LIG_SH2_PTP2 | 454 | 457 | PF00017 | 0.375 |
LIG_SH2_SRC | 134 | 137 | PF00017 | 0.484 |
LIG_SH2_SRC | 454 | 457 | PF00017 | 0.392 |
LIG_SH2_SRC | 513 | 516 | PF00017 | 0.314 |
LIG_SH2_SRC | 564 | 567 | PF00017 | 0.516 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 364 | 368 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 447 | 451 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 605 | 609 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.495 |
LIG_SH2_STAT3 | 123 | 126 | PF00017 | 0.484 |
LIG_SH2_STAT3 | 381 | 384 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 585 | 588 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 687 | 690 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.487 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.415 |
LIG_SUMO_SIM_anti_2 | 67 | 75 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 631 | 639 | PF11976 | 0.438 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.505 |
LIG_TRAF2_1 | 197 | 200 | PF00917 | 0.511 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.540 |
LIG_TRAF2_1 | 450 | 453 | PF00917 | 0.417 |
LIG_TRAF2_1 | 639 | 642 | PF00917 | 0.438 |
LIG_TYR_ITSM | 54 | 61 | PF00017 | 0.476 |
LIG_WW_3 | 305 | 309 | PF00397 | 0.458 |
MOD_CDK_SPK_2 | 668 | 673 | PF00069 | 0.646 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.339 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.744 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.299 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.589 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.509 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.450 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.511 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.538 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.604 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.453 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.527 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.432 |
MOD_CK2_1 | 686 | 692 | PF00069 | 0.553 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.585 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.738 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.472 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.413 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.400 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.457 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.749 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.516 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.553 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.669 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.497 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.430 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.418 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.534 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.540 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.457 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.380 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.508 |
MOD_N-GLC_1 | 385 | 390 | PF02516 | 0.461 |
MOD_N-GLC_2 | 534 | 536 | PF02516 | 0.357 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.703 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.409 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.421 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.449 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.406 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.469 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.362 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.425 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.382 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.353 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.459 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.533 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.459 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.545 |
MOD_NEK2_2 | 672 | 677 | PF00069 | 0.393 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.462 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.460 |
MOD_PIKK_1 | 431 | 437 | PF00454 | 0.583 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.570 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.513 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.683 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.419 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.500 |
MOD_PKA_2 | 560 | 566 | PF00069 | 0.622 |
MOD_PKA_2 | 672 | 678 | PF00069 | 0.512 |
MOD_Plk_1 | 385 | 391 | PF00069 | 0.460 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.527 |
MOD_Plk_1 | 636 | 642 | PF00069 | 0.453 |
MOD_Plk_2-3 | 102 | 108 | PF00069 | 0.589 |
MOD_Plk_2-3 | 483 | 489 | PF00069 | 0.427 |
MOD_Plk_2-3 | 560 | 566 | PF00069 | 0.510 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.589 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.502 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.386 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.480 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.460 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.550 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.446 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.441 |
MOD_Plk_4 | 580 | 586 | PF00069 | 0.387 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.397 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.545 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.610 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.453 |
MOD_ProDKin_1 | 668 | 674 | PF00069 | 0.638 |
MOD_SUMO_rev_2 | 601 | 610 | PF00179 | 0.534 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.545 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 687 | 690 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 552 | 554 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 237 | 241 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 426 | 430 | PF00026 | 0.582 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2B4 | Leptomonas seymouri | 87% | 100% |
A0A0S4J480 | Bodo saltans | 73% | 100% |
A0A1X0NZF0 | Trypanosomatidae | 74% | 100% |
A0A3Q8IE38 | Leishmania donovani | 94% | 100% |
A0A3R7MWT3 | Trypanosoma rangeli | 75% | 100% |
A2AKQ8 | Mus musculus | 55% | 100% |
A2VE45 | Bos taurus | 54% | 100% |
A4I452 | Leishmania infantum | 95% | 100% |
A4IHR1 | Xenopus tropicalis | 56% | 100% |
A6H739 | Bos taurus | 53% | 100% |
A7YE96 | Danio rerio | 55% | 100% |
A8XBR9 | Caenorhabditis briggsae | 42% | 100% |
B2RYD6 | Rattus norvegicus | 55% | 100% |
C9ZKR0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 73% | 100% |
E9ADL7 | Leishmania major | 94% | 100% |
E9AM64 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q16JL4 | Aedes aegypti | 45% | 100% |
Q29L58 | Drosophila pseudoobscura pseudoobscura | 43% | 100% |
Q4QQS2 | Rattus norvegicus | 55% | 100% |
Q6INU8 | Xenopus laevis | 55% | 100% |
Q7PRA4 | Anopheles gambiae | 45% | 100% |
Q86WT1 | Homo sapiens | 55% | 100% |
Q8I7G4 | Caenorhabditis elegans | 43% | 100% |
Q8N4P2 | Homo sapiens | 55% | 100% |
Q99J38 | Mus musculus | 56% | 100% |
Q9CY00 | Mus musculus | 55% | 100% |
Q9VK41 | Drosophila melanogaster | 43% | 100% |
V5BKA3 | Trypanosoma cruzi | 76% | 100% |