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:0000922 | spindle pole | 2 | 11 |
GO:0000923 | equatorial microtubule organizing center | 3 | 2 |
GO:0000930 | gamma-tubulin complex | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 11 |
GO:0005813 | centrosome | 3 | 2 |
GO:0005815 | microtubule organizing center | 2 | 11 |
GO:0005874 | microtubule | 6 | 11 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0036064 | ciliary basal body | 3 | 2 |
GO:0099080 | supramolecular complex | 2 | 11 |
GO:0099081 | supramolecular polymer | 3 | 11 |
GO:0099512 | supramolecular fiber | 4 | 11 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4Q7K9
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 11 |
GO:0000278 | mitotic cell cycle | 3 | 2 |
GO:0006996 | organelle organization | 4 | 11 |
GO:0007010 | cytoskeleton organization | 5 | 11 |
GO:0007017 | microtubule-based process | 2 | 11 |
GO:0007020 | microtubule nucleation | 4 | 11 |
GO:0007049 | cell cycle | 2 | 2 |
GO:0007051 | spindle organization | 3 | 2 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0022414 | reproductive process | 1 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0031122 | cytoplasmic microtubule organization | 4 | 2 |
GO:0051225 | spindle assembly | 4 | 2 |
GO:0051321 | meiotic cell cycle | 2 | 2 |
GO:0070925 | organelle assembly | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0097435 | supramolecular fiber organization | 4 | 2 |
GO:0140694 | non-membrane-bounded organelle assembly | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 11 |
GO:0008092 | cytoskeletal protein binding | 3 | 11 |
GO:0015631 | tubulin binding | 4 | 11 |
GO:0043015 | gamma-tubulin binding | 5 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 25 | 29 | PF00656 | 0.608 |
CLV_MEL_PAP_1 | 539 | 545 | PF00089 | 0.249 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 750 | 752 | PF00675 | 0.791 |
CLV_NRD_NRD_1 | 778 | 780 | PF00675 | 0.702 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.250 |
CLV_PCSK_KEX2_1 | 750 | 752 | PF00082 | 0.791 |
CLV_PCSK_KEX2_1 | 778 | 780 | PF00082 | 0.708 |
CLV_PCSK_PC1ET2_1 | 618 | 620 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.184 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.236 |
DEG_APCC_DBOX_1 | 459 | 467 | PF00400 | 0.389 |
DEG_APCC_DBOX_1 | 499 | 507 | PF00400 | 0.449 |
DEG_APCC_DBOX_1 | 532 | 540 | PF00400 | 0.461 |
DEG_APCC_DBOX_1 | 541 | 549 | PF00400 | 0.418 |
DEG_APCC_DBOX_1 | 679 | 687 | PF00400 | 0.531 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.370 |
DOC_CYCLIN_RxL_1 | 102 | 112 | PF00134 | 0.348 |
DOC_CYCLIN_RxL_1 | 165 | 174 | PF00134 | 0.450 |
DOC_CYCLIN_RxL_1 | 497 | 507 | PF00134 | 0.517 |
DOC_CYCLIN_RxL_1 | 549 | 557 | PF00134 | 0.539 |
DOC_CYCLIN_RxL_1 | 65 | 75 | PF00134 | 0.476 |
DOC_CYCLIN_yCln2_LP_2 | 727 | 733 | PF00134 | 0.456 |
DOC_MAPK_DCC_7 | 327 | 336 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 50 | 58 | PF00069 | 0.457 |
DOC_MAPK_HePTP_8 | 324 | 336 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 146 | 153 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 327 | 336 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 729 | 736 | PF00069 | 0.567 |
DOC_PP1_RVXF_1 | 102 | 109 | PF00149 | 0.345 |
DOC_PP1_RVXF_1 | 714 | 720 | PF00149 | 0.436 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.482 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 735 | 739 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 760 | 764 | PF00917 | 0.718 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 672 | 677 | PF00397 | 0.531 |
LIG_14-3-3_CanoR_1 | 17 | 21 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 433 | 441 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 542 | 546 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 552 | 560 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 570 | 576 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 643 | 649 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 680 | 690 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 737 | 746 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 74 | 80 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 753 | 760 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 762 | 767 | PF00244 | 0.738 |
LIG_14-3-3_CanoR_1 | 81 | 88 | PF00244 | 0.350 |
LIG_Actin_WH2_2 | 1 | 19 | PF00022 | 0.301 |
LIG_Actin_WH2_2 | 321 | 337 | PF00022 | 0.297 |
LIG_Actin_WH2_2 | 436 | 451 | PF00022 | 0.517 |
LIG_AP2alpha_1 | 620 | 624 | PF02296 | 0.482 |
LIG_BRCT_BRCA1_1 | 220 | 224 | PF00533 | 0.585 |
LIG_BRCT_BRCA1_1 | 435 | 439 | PF00533 | 0.469 |
LIG_Clathr_ClatBox_1 | 503 | 507 | PF01394 | 0.451 |
LIG_deltaCOP1_diTrp_1 | 351 | 356 | PF00928 | 0.436 |
LIG_DLG_GKlike_1 | 571 | 578 | PF00625 | 0.435 |
LIG_eIF4E_1 | 531 | 537 | PF01652 | 0.435 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.356 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.635 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.429 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.389 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.443 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.495 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.546 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.531 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.464 |
LIG_FHA_1 | 697 | 703 | PF00498 | 0.422 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.499 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.397 |
LIG_FHA_2 | 610 | 616 | PF00498 | 0.482 |
LIG_FHA_2 | 673 | 679 | PF00498 | 0.507 |
LIG_Integrin_RGD_1 | 349 | 351 | PF01839 | 0.236 |
LIG_LIR_Gen_1 | 133 | 141 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 173 | 184 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 198 | 205 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 351 | 362 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 451 | 461 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 574 | 582 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 75 | 82 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 507 | 513 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 574 | 579 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 699 | 704 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 718 | 722 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.461 |
LIG_NRBOX | 574 | 580 | PF00104 | 0.441 |
LIG_PCNA_yPIPBox_3 | 591 | 601 | PF02747 | 0.451 |
LIG_PCNA_yPIPBox_3 | 689 | 698 | PF02747 | 0.531 |
LIG_Pex14_2 | 290 | 294 | PF04695 | 0.462 |
LIG_Pex14_2 | 620 | 624 | PF04695 | 0.482 |
LIG_Pex14_2 | 719 | 723 | PF04695 | 0.531 |
LIG_SH2_CRK | 531 | 535 | PF00017 | 0.436 |
LIG_SH2_CRK | 662 | 666 | PF00017 | 0.475 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.465 |
LIG_SH2_PTP2 | 513 | 516 | PF00017 | 0.436 |
LIG_SH2_SRC | 110 | 113 | PF00017 | 0.335 |
LIG_SH2_SRC | 513 | 516 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 656 | 660 | PF00017 | 0.404 |
LIG_SH2_STAT3 | 273 | 276 | PF00017 | 0.442 |
LIG_SH2_STAT3 | 588 | 591 | PF00017 | 0.436 |
LIG_SH2_STAT3 | 722 | 725 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 701 | 704 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 722 | 725 | PF00017 | 0.597 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.476 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.586 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.525 |
LIG_SH3_3 | 727 | 733 | PF00018 | 0.691 |
LIG_SUMO_SIM_par_1 | 501 | 507 | PF11976 | 0.588 |
LIG_SUMO_SIM_par_1 | 518 | 524 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 593 | 599 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 693 | 699 | PF11976 | 0.454 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.524 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.410 |
LIG_TYR_ITIM | 352 | 357 | PF00017 | 0.531 |
LIG_TYR_ITIM | 664 | 669 | PF00017 | 0.531 |
LIG_UBA3_1 | 249 | 256 | PF00899 | 0.312 |
LIG_UBA3_1 | 519 | 526 | PF00899 | 0.482 |
LIG_WRC_WIRS_1 | 154 | 159 | PF05994 | 0.347 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.368 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.506 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.480 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.463 |
MOD_CK1_1 | 553 | 559 | PF00069 | 0.520 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.531 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.412 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.487 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.411 |
MOD_CK1_1 | 742 | 748 | PF00069 | 0.716 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.437 |
MOD_CK1_1 | 761 | 767 | PF00069 | 0.488 |
MOD_CK1_1 | 777 | 783 | PF00069 | 0.621 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.498 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.551 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.586 |
MOD_CK2_1 | 672 | 678 | PF00069 | 0.507 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.471 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.474 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.440 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.751 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.607 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.309 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.363 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.313 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.267 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.235 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.235 |
MOD_GlcNHglycan | 739 | 742 | PF01048 | 0.613 |
MOD_GlcNHglycan | 780 | 783 | PF01048 | 0.659 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.490 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.659 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.298 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.403 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.482 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.484 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.596 |
MOD_GSK3_1 | 749 | 756 | PF00069 | 0.637 |
MOD_GSK3_1 | 758 | 765 | PF00069 | 0.684 |
MOD_GSK3_1 | 773 | 780 | PF00069 | 0.729 |
MOD_N-GLC_1 | 672 | 677 | PF02516 | 0.297 |
MOD_N-GLC_2 | 649 | 651 | PF02516 | 0.331 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.464 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.383 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.226 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.276 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.496 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.395 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.434 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.419 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.467 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.563 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.452 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.417 |
MOD_NEK2_2 | 340 | 345 | PF00069 | 0.435 |
MOD_NEK2_2 | 651 | 656 | PF00069 | 0.468 |
MOD_OFUCOSY | 645 | 651 | PF10250 | 0.317 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.530 |
MOD_PIKK_1 | 721 | 727 | PF00454 | 0.620 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.411 |
MOD_PK_1 | 762 | 768 | PF00069 | 0.591 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.491 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.417 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.568 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.443 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.482 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.455 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.516 |
MOD_PKA_2 | 679 | 685 | PF00069 | 0.556 |
MOD_PKA_2 | 749 | 755 | PF00069 | 0.711 |
MOD_PKA_2 | 761 | 767 | PF00069 | 0.640 |
MOD_PKA_2 | 777 | 783 | PF00069 | 0.712 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.411 |
MOD_PKB_1 | 751 | 759 | PF00069 | 0.580 |
MOD_Plk_1 | 582 | 588 | PF00069 | 0.482 |
MOD_Plk_1 | 629 | 635 | PF00069 | 0.531 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.450 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.321 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.413 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.391 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.364 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.436 |
MOD_Plk_4 | 651 | 657 | PF00069 | 0.470 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.401 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.407 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.535 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.564 |
MOD_ProDKin_1 | 672 | 678 | PF00069 | 0.531 |
MOD_SUMO_for_1 | 600 | 603 | PF00179 | 0.517 |
MOD_SUMO_rev_2 | 2 | 7 | PF00179 | 0.404 |
TRG_DiLeu_BaEn_1 | 246 | 251 | PF01217 | 0.347 |
TRG_DiLeu_BaEn_1 | 257 | 262 | PF01217 | 0.279 |
TRG_DiLeu_BaLyEn_6 | 149 | 154 | PF01217 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 166 | 171 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 383 | 388 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 637 | 642 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 531 | 534 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 666 | 669 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 701 | 704 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 258 | 260 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 569 | 571 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 749 | 751 | PF00400 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 168 | 173 | PF00026 | 0.356 |
TRG_Pf-PMV_PEXEL_1 | 259 | 264 | PF00026 | 0.407 |
TRG_Pf-PMV_PEXEL_1 | 552 | 557 | PF00026 | 0.292 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IC04 | Leptomonas seymouri | 65% | 98% |
A0A1X0P204 | Trypanosomatidae | 44% | 100% |
A0A3Q8IEU3 | Leishmania donovani | 89% | 100% |
A0A422P4W6 | Trypanosoma rangeli | 44% | 100% |
A4HI49 | Leishmania braziliensis | 82% | 100% |
A4I5C5 | Leishmania infantum | 90% | 100% |
C9ZQQ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B0M3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5B937 | Trypanosoma cruzi | 44% | 100% |