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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0001534 | radial spoke | 2 | 12 |
GO:0005929 | cilium | 4 | 12 |
GO:0031514 | motile cilium | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 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:0005930 | axoneme | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IE67
Term | Name | Level | Count |
---|---|---|---|
GO:0003341 | cilium movement | 4 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0007017 | microtubule-based process | 2 | 12 |
GO:0007018 | microtubule-based movement | 3 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0022607 | cellular component assembly | 4 | 12 |
GO:0030030 | cell projection organization | 4 | 11 |
GO:0030031 | cell projection assembly | 5 | 11 |
GO:0044782 | cilium organization | 5 | 11 |
GO:0060271 | cilium assembly | 6 | 11 |
GO:0060294 | cilium movement involved in cell motility | 5 | 12 |
GO:0070925 | organelle assembly | 5 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 11 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 11 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0001578 | microtubule bundle formation | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0035082 | axoneme assembly | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 158 | 162 | PF00656 | 0.436 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 607 | 609 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.480 |
CLV_PCSK_FUR_1 | 221 | 225 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.690 |
DEG_APCC_DBOX_1 | 35 | 43 | PF00400 | 0.638 |
DEG_COP1_1 | 458 | 468 | PF00400 | 0.554 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.387 |
DEG_SCF_FBW7_1 | 42 | 48 | PF00400 | 0.463 |
DOC_ANK_TNKS_1 | 701 | 708 | PF00023 | 0.661 |
DOC_CDC14_PxL_1 | 487 | 495 | PF14671 | 0.462 |
DOC_CKS1_1 | 32 | 37 | PF01111 | 0.458 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.462 |
DOC_CYCLIN_yCln2_LP_2 | 2 | 8 | PF00134 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 588 | 594 | PF00134 | 0.554 |
DOC_MAPK_gen_1 | 13 | 21 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 13 | 21 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 95 | 104 | PF00069 | 0.413 |
DOC_PP1_RVXF_1 | 622 | 629 | PF00149 | 0.537 |
DOC_PP2B_LxvP_1 | 2 | 5 | PF13499 | 0.378 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 272 | 275 | PF13499 | 0.537 |
DOC_PP2B_LxvP_1 | 422 | 425 | PF13499 | 0.500 |
DOC_PP2B_LxvP_1 | 588 | 591 | PF13499 | 0.554 |
DOC_PP2B_LxvP_1 | 667 | 670 | PF13499 | 0.537 |
DOC_PP2B_LxvP_1 | 69 | 72 | PF13499 | 0.414 |
DOC_SPAK_OSR1_1 | 95 | 99 | PF12202 | 0.423 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.511 |
DOC_USP7_UBL2_3 | 515 | 519 | PF12436 | 0.492 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.584 |
LIG_14-3-3_CanoR_1 | 136 | 144 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 20 | 30 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 41 | 45 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 446 | 455 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 540 | 545 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 57 | 62 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 641 | 647 | PF00244 | 0.499 |
LIG_APCC_ABBAyCdc20_2 | 180 | 186 | PF00400 | 0.532 |
LIG_BIR_III_4 | 161 | 165 | PF00653 | 0.492 |
LIG_eIF4E_1 | 517 | 523 | PF01652 | 0.450 |
LIG_EVH1_2 | 668 | 672 | PF00568 | 0.414 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.497 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.442 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.403 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.550 |
LIG_FHA_1 | 631 | 637 | PF00498 | 0.460 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.516 |
LIG_FHA_2 | 516 | 522 | PF00498 | 0.492 |
LIG_FHA_2 | 687 | 693 | PF00498 | 0.461 |
LIG_LIR_Apic_2 | 693 | 699 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 395 | 405 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 645 | 651 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.588 |
LIG_MYND_1 | 491 | 495 | PF01753 | 0.462 |
LIG_MYND_1 | 665 | 669 | PF01753 | 0.431 |
LIG_NRBOX | 7 | 13 | PF00104 | 0.388 |
LIG_PDZ_Class_3 | 710 | 715 | PF00595 | 0.726 |
LIG_Pex14_1 | 513 | 517 | PF04695 | 0.450 |
LIG_PTAP_UEV_1 | 369 | 374 | PF05743 | 0.492 |
LIG_RPA_C_Fungi | 441 | 453 | PF08784 | 0.423 |
LIG_SH2_CRK | 280 | 284 | PF00017 | 0.423 |
LIG_SH2_CRK | 487 | 491 | PF00017 | 0.318 |
LIG_SH2_CRK | 663 | 667 | PF00017 | 0.423 |
LIG_SH2_CRK | 696 | 700 | PF00017 | 0.554 |
LIG_SH2_GRB2like | 266 | 269 | PF00017 | 0.448 |
LIG_SH2_NCK_1 | 63 | 67 | PF00017 | 0.452 |
LIG_SH2_NCK_1 | 696 | 700 | PF00017 | 0.554 |
LIG_SH2_PTP2 | 97 | 100 | PF00017 | 0.413 |
LIG_SH2_SRC | 184 | 187 | PF00017 | 0.337 |
LIG_SH2_SRC | 663 | 666 | PF00017 | 0.423 |
LIG_SH2_SRC | 675 | 678 | PF00017 | 0.448 |
LIG_SH2_SRC | 696 | 699 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 621 | 624 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 675 | 678 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.413 |
LIG_SH3_1 | 662 | 668 | PF00018 | 0.423 |
LIG_SH3_1 | 695 | 701 | PF00018 | 0.663 |
LIG_SH3_2 | 215 | 220 | PF14604 | 0.303 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.301 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.439 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.448 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.311 |
LIG_SH3_3 | 570 | 576 | PF00018 | 0.404 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.305 |
LIG_SH3_3 | 673 | 679 | PF00018 | 0.350 |
LIG_SH3_3 | 695 | 701 | PF00018 | 0.544 |
LIG_TRAF2_1 | 373 | 376 | PF00917 | 0.423 |
LIG_TRAF2_1 | 499 | 502 | PF00917 | 0.317 |
LIG_TRAF2_1 | 545 | 548 | PF00917 | 0.390 |
LIG_WRC_WIRS_1 | 197 | 202 | PF05994 | 0.448 |
LIG_WRC_WIRS_1 | 456 | 461 | PF05994 | 0.448 |
LIG_WW_2 | 665 | 668 | PF00397 | 0.423 |
LIG_WW_3 | 214 | 218 | PF00397 | 0.393 |
LIG_WW_3 | 699 | 703 | PF00397 | 0.691 |
MOD_CDC14_SPxK_1 | 92 | 95 | PF00782 | 0.413 |
MOD_CDK_SPK_2 | 31 | 36 | PF00069 | 0.450 |
MOD_CDK_SPxK_1 | 31 | 37 | PF00069 | 0.454 |
MOD_CDK_SPxK_1 | 89 | 95 | PF00069 | 0.422 |
MOD_CDK_SPxxK_3 | 31 | 38 | PF00069 | 0.457 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.459 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.267 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.457 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.620 |
MOD_CK2_1 | 515 | 521 | PF00069 | 0.448 |
MOD_CK2_1 | 686 | 692 | PF00069 | 0.422 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.415 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.448 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.399 |
MOD_GlcNHglycan | 233 | 239 | PF01048 | 0.399 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.317 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.362 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.286 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.423 |
MOD_GlcNHglycan | 472 | 478 | PF01048 | 0.360 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.581 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.343 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.388 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.385 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.458 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.284 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.466 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.440 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.382 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.454 |
MOD_LATS_1 | 55 | 61 | PF00433 | 0.470 |
MOD_N-GLC_1 | 565 | 570 | PF02516 | 0.360 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.417 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.396 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.448 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.444 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.455 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.437 |
MOD_NEK2_2 | 294 | 299 | PF00069 | 0.388 |
MOD_NEK2_2 | 603 | 608 | PF00069 | 0.283 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.422 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.410 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.409 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.448 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.412 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.423 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.467 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.412 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.306 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.388 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.649 |
MOD_Plk_1 | 584 | 590 | PF00069 | 0.448 |
MOD_Plk_1 | 686 | 692 | PF00069 | 0.388 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.627 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.308 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.451 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.692 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.322 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.654 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.425 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.585 |
TRG_DiLeu_BaLyEn_6 | 14 | 19 | PF01217 | 0.386 |
TRG_DiLeu_BaLyEn_6 | 278 | 283 | PF01217 | 0.380 |
TRG_DiLeu_BaLyEn_6 | 489 | 494 | PF01217 | 0.388 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 646 | 649 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.413 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 222 | 224 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 414 | 417 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.481 |
TRG_NLS_MonoExtN_4 | 35 | 40 | PF00514 | 0.609 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8Q1 | Leptomonas seymouri | 70% | 100% |
A0A0S4JES8 | Bodo saltans | 40% | 100% |
A0A1X0P128 | Trypanosomatidae | 47% | 100% |
A0A3R7KK84 | Trypanosoma rangeli | 47% | 100% |
A4H732 | Leishmania braziliensis | 24% | 100% |
A4HH73 | Leishmania braziliensis | 83% | 100% |
A4I4B9 | Leishmania infantum | 99% | 100% |
C9ZL49 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9ADR8 | Leishmania major | 95% | 100% |
E9AM12 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4QGB1 | Leishmania major | 24% | 100% |
Q8BYM7 | Mus musculus | 25% | 100% |
V5B4W9 | Trypanosoma cruzi | 46% | 100% |