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:0000922 | spindle pole | 2 | 12 |
GO:0005737 | cytoplasm | 2 | 12 |
GO:0005815 | microtubule organizing center | 2 | 12 |
GO:0005874 | microtubule | 6 | 12 |
GO:0099080 | supramolecular complex | 2 | 12 |
GO:0099081 | supramolecular polymer | 3 | 12 |
GO:0099512 | supramolecular fiber | 4 | 12 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0000923 | equatorial microtubule organizing center | 3 | 1 |
GO:0000930 | gamma-tubulin complex | 2 | 1 |
GO:0005813 | centrosome | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8IEU3
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0007010 | cytoskeleton organization | 5 | 12 |
GO:0007017 | microtubule-based process | 2 | 12 |
GO:0007020 | microtubule nucleation | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0000278 | mitotic cell cycle | 3 | 1 |
GO:0007049 | cell cycle | 2 | 1 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0031122 | cytoplasmic microtubule organization | 4 | 1 |
GO:0051225 | spindle assembly | 4 | 1 |
GO:0051321 | meiotic cell cycle | 2 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0097435 | supramolecular fiber organization | 4 | 1 |
GO:0140694 | non-membrane-bounded organelle assembly | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0008092 | cytoskeletal protein binding | 3 | 12 |
GO:0015631 | tubulin binding | 4 | 12 |
GO:0043015 | gamma-tubulin binding | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 25 | 29 | PF00656 | 0.693 |
CLV_C14_Caspase3-7 | 34 | 38 | PF00656 | 0.699 |
CLV_MEL_PAP_1 | 517 | 523 | PF00089 | 0.301 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 704 | 706 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 756 | 758 | PF00675 | 0.765 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 596 | 598 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 703 | 705 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 756 | 758 | PF00082 | 0.768 |
CLV_PCSK_PC1ET2_1 | 596 | 598 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.210 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.317 |
CLV_Separin_Metazoa | 45 | 49 | PF03568 | 0.339 |
DEG_APCC_DBOX_1 | 256 | 264 | PF00400 | 0.486 |
DEG_APCC_DBOX_1 | 477 | 485 | PF00400 | 0.501 |
DEG_APCC_DBOX_1 | 510 | 518 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 519 | 527 | PF00400 | 0.454 |
DEG_APCC_DBOX_1 | 657 | 665 | PF00400 | 0.562 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.452 |
DOC_CYCLIN_RxL_1 | 100 | 110 | PF00134 | 0.446 |
DOC_CYCLIN_RxL_1 | 163 | 172 | PF00134 | 0.499 |
DOC_CYCLIN_RxL_1 | 475 | 485 | PF00134 | 0.553 |
DOC_CYCLIN_RxL_1 | 527 | 535 | PF00134 | 0.566 |
DOC_CYCLIN_RxL_1 | 63 | 73 | PF00134 | 0.532 |
DOC_MAPK_DCC_7 | 325 | 334 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 48 | 56 | PF00069 | 0.616 |
DOC_MAPK_gen_1 | 703 | 714 | PF00069 | 0.583 |
DOC_MAPK_HePTP_8 | 322 | 334 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 144 | 151 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 325 | 334 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 703 | 712 | PF00069 | 0.654 |
DOC_PP1_RVXF_1 | 100 | 107 | PF00149 | 0.446 |
DOC_PP1_RVXF_1 | 692 | 698 | PF00149 | 0.476 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.587 |
DOC_PP4_FxxP_1 | 724 | 727 | PF00568 | 0.731 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 713 | 717 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 738 | 742 | PF00917 | 0.788 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 650 | 655 | PF00397 | 0.562 |
LIG_14-3-3_CanoR_1 | 411 | 419 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 520 | 524 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 530 | 538 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 548 | 554 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 621 | 627 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 658 | 662 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 715 | 724 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 72 | 78 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 731 | 738 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 740 | 745 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 79 | 86 | PF00244 | 0.428 |
LIG_Actin_WH2_2 | 414 | 429 | PF00022 | 0.548 |
LIG_AP2alpha_1 | 598 | 602 | PF02296 | 0.581 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.700 |
LIG_BRCT_BRCA1_1 | 413 | 417 | PF00533 | 0.525 |
LIG_Clathr_ClatBox_1 | 481 | 485 | PF01394 | 0.525 |
LIG_Clathr_ClatBox_1 | 661 | 665 | PF01394 | 0.428 |
LIG_deltaCOP1_diTrp_1 | 349 | 354 | PF00928 | 0.476 |
LIG_eIF4E_1 | 509 | 515 | PF01652 | 0.498 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.454 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.687 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.495 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.524 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.547 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.552 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.512 |
LIG_FHA_1 | 630 | 636 | PF00498 | 0.493 |
LIG_FHA_1 | 675 | 681 | PF00498 | 0.470 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.521 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.581 |
LIG_FHA_2 | 651 | 657 | PF00498 | 0.554 |
LIG_Integrin_RGD_1 | 347 | 349 | PF01839 | 0.276 |
LIG_LIR_Apic_2 | 723 | 727 | PF02991 | 0.740 |
LIG_LIR_Gen_1 | 131 | 139 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 171 | 182 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 196 | 203 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 349 | 360 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 429 | 439 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 552 | 560 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 73 | 80 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 131 | 135 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 429 | 435 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 552 | 557 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 696 | 700 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 73 | 77 | PF02991 | 0.476 |
LIG_MYND_1 | 367 | 371 | PF01753 | 0.511 |
LIG_PCNA_yPIPBox_3 | 569 | 579 | PF02747 | 0.525 |
LIG_PCNA_yPIPBox_3 | 667 | 676 | PF02747 | 0.562 |
LIG_Pex14_2 | 288 | 292 | PF04695 | 0.508 |
LIG_Pex14_2 | 598 | 602 | PF04695 | 0.581 |
LIG_Pex14_2 | 697 | 701 | PF04695 | 0.562 |
LIG_SH2_CRK | 509 | 513 | PF00017 | 0.476 |
LIG_SH2_CRK | 640 | 644 | PF00017 | 0.524 |
LIG_SH2_CRK | 74 | 78 | PF00017 | 0.518 |
LIG_SH2_PTP2 | 491 | 494 | PF00017 | 0.487 |
LIG_SH2_SRC | 108 | 111 | PF00017 | 0.394 |
LIG_SH2_SRC | 491 | 494 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 108 | 112 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.562 |
LIG_SH2_STAT3 | 271 | 274 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 566 | 569 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 700 | 703 | PF00017 | 0.710 |
LIG_SH3_1 | 705 | 711 | PF00018 | 0.599 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.494 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.534 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.588 |
LIG_SH3_3 | 705 | 711 | PF00018 | 0.727 |
LIG_SUMO_SIM_par_1 | 479 | 485 | PF11976 | 0.569 |
LIG_SUMO_SIM_par_1 | 496 | 502 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 571 | 577 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 660 | 665 | PF11976 | 0.519 |
LIG_SUMO_SIM_par_1 | 671 | 677 | PF11976 | 0.505 |
LIG_TRAF2_1 | 226 | 229 | PF00917 | 0.586 |
LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.555 |
LIG_TYR_ITIM | 350 | 355 | PF00017 | 0.562 |
LIG_TYR_ITIM | 642 | 647 | PF00017 | 0.562 |
LIG_UBA3_1 | 134 | 140 | PF00899 | 0.370 |
LIG_UBA3_1 | 247 | 254 | PF00899 | 0.377 |
LIG_UBA3_1 | 497 | 504 | PF00899 | 0.581 |
LIG_WRC_WIRS_1 | 152 | 157 | PF05994 | 0.425 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.489 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.581 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.645 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.554 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.562 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.553 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.472 |
MOD_CK1_1 | 720 | 726 | PF00069 | 0.752 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.498 |
MOD_CK1_1 | 739 | 745 | PF00069 | 0.692 |
MOD_CK1_1 | 755 | 761 | PF00069 | 0.771 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.500 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.538 |
MOD_CK2_1 | 650 | 656 | PF00069 | 0.562 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.509 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.536 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.667 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.612 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.562 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.364 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.346 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.313 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.298 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.676 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.675 |
MOD_GlcNHglycan | 758 | 761 | PF01048 | 0.741 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.486 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.511 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.651 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.630 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.581 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.510 |
MOD_GSK3_1 | 713 | 720 | PF00069 | 0.665 |
MOD_GSK3_1 | 727 | 734 | PF00069 | 0.663 |
MOD_GSK3_1 | 736 | 743 | PF00069 | 0.693 |
MOD_GSK3_1 | 751 | 758 | PF00069 | 0.760 |
MOD_LATS_1 | 729 | 735 | PF00433 | 0.626 |
MOD_N-GLC_1 | 650 | 655 | PF02516 | 0.345 |
MOD_N-GLC_2 | 627 | 629 | PF02516 | 0.362 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.475 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.453 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.276 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.344 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.474 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.452 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.517 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.550 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.490 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.428 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.452 |
MOD_NEK2_2 | 338 | 343 | PF00069 | 0.498 |
MOD_NEK2_2 | 629 | 634 | PF00069 | 0.518 |
MOD_OFUCOSY | 623 | 629 | PF10250 | 0.353 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.651 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.538 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.557 |
MOD_PK_1 | 440 | 446 | PF00069 | 0.400 |
MOD_PK_1 | 740 | 746 | PF00069 | 0.801 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.581 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.493 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.581 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.501 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.525 |
MOD_PKA_2 | 657 | 663 | PF00069 | 0.581 |
MOD_PKA_2 | 739 | 745 | PF00069 | 0.686 |
MOD_PKA_2 | 755 | 761 | PF00069 | 0.735 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.557 |
MOD_Plk_1 | 560 | 566 | PF00069 | 0.581 |
MOD_Plk_1 | 607 | 613 | PF00069 | 0.562 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.458 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.281 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.445 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.442 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.444 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.487 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.518 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.566 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.496 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.489 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.458 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.586 |
MOD_ProDKin_1 | 650 | 656 | PF00069 | 0.562 |
MOD_SUMO_for_1 | 578 | 581 | PF00179 | 0.553 |
MOD_SUMO_rev_2 | 2 | 7 | PF00179 | 0.553 |
TRG_DiLeu_BaEn_1 | 244 | 249 | PF01217 | 0.415 |
TRG_DiLeu_BaEn_1 | 255 | 260 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 147 | 152 | PF01217 | 0.516 |
TRG_DiLeu_BaLyEn_6 | 164 | 169 | PF01217 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 615 | 620 | PF01217 | 0.531 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 567 | 570 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 165 | 167 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 547 | 549 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 703 | 705 | PF00400 | 0.655 |
TRG_Pf-PMV_PEXEL_1 | 166 | 171 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 257 | 262 | PF00026 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 530 | 535 | PF00026 | 0.318 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IC04 | Leptomonas seymouri | 65% | 95% |
A0A0S4JBA6 | Bodo saltans | 26% | 82% |
A0A1X0P204 | Trypanosomatidae | 45% | 100% |
A0A422P4W6 | Trypanosoma rangeli | 44% | 100% |
A4HI49 | Leishmania braziliensis | 79% | 100% |
A4I5C5 | Leishmania infantum | 99% | 100% |
C9ZQQ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B0M3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q7K9 | Leishmania major | 89% | 100% |
V5B937 | Trypanosoma cruzi | 45% | 100% |