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:0005819 | spindle | 5 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0072686 | mitotic spindle | 6 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HQF8
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0000281 | mitotic cytokinesis | 4 | 1 |
GO:0000910 | cytokinesis | 3 | 1 |
GO:0001539 | cilium or flagellum-dependent cell motility | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0007052 | mitotic spindle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0048870 | cell motility | 2 | 1 |
GO:0060285 | cilium-dependent cell motility | 4 | 1 |
GO:0061640 | cytoskeleton-dependent cytokinesis | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005509 | calcium ion binding | 5 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0043014 | alpha-tubulin binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 586 | 590 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 60 | 64 | PF00656 | 0.350 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.212 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.218 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.176 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 728 | 730 | PF00675 | 0.312 |
CLV_PCSK_FUR_1 | 295 | 299 | PF00082 | 0.267 |
CLV_PCSK_FUR_1 | 508 | 512 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.212 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.196 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 728 | 730 | PF00082 | 0.340 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 397 | 399 | PF00082 | 0.641 |
CLV_PCSK_PC1ET2_1 | 510 | 512 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 659 | 663 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 737 | 741 | PF00082 | 0.513 |
DEG_SPOP_SBC_1 | 553 | 557 | PF00917 | 0.508 |
DOC_ANK_TNKS_1 | 141 | 148 | PF00023 | 0.479 |
DOC_CDC14_PxL_1 | 9 | 17 | PF14671 | 0.435 |
DOC_CKS1_1 | 124 | 129 | PF01111 | 0.455 |
DOC_CKS1_1 | 233 | 238 | PF01111 | 0.448 |
DOC_CKS1_1 | 700 | 705 | PF01111 | 0.562 |
DOC_CKS1_1 | 717 | 722 | PF01111 | 0.341 |
DOC_CYCLIN_RxL_1 | 656 | 665 | PF00134 | 0.401 |
DOC_CYCLIN_yClb1_LxF_4 | 250 | 256 | PF00134 | 0.515 |
DOC_CYCLIN_yCln2_LP_2 | 23 | 29 | PF00134 | 0.547 |
DOC_MAPK_gen_1 | 142 | 150 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 261 | 268 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 296 | 308 | PF00069 | 0.504 |
DOC_PP1_RVXF_1 | 263 | 269 | PF00149 | 0.515 |
DOC_PP1_RVXF_1 | 83 | 90 | PF00149 | 0.423 |
DOC_PP4_FxxP_1 | 338 | 341 | PF00568 | 0.515 |
DOC_SPAK_OSR1_1 | 443 | 447 | PF12202 | 0.433 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.466 |
DOC_USP7_UBL2_3 | 413 | 417 | PF12436 | 0.438 |
DOC_USP7_UBL2_3 | 646 | 650 | PF12436 | 0.368 |
DOC_USP7_UBL2_3 | 697 | 701 | PF12436 | 0.525 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 716 | 721 | PF00397 | 0.257 |
LIG_14-3-3_CanoR_1 | 330 | 336 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 398 | 406 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 544 | 552 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 627 | 633 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 659 | 664 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 667 | 671 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 673 | 683 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 728 | 733 | PF00244 | 0.359 |
LIG_Actin_RPEL_3 | 722 | 741 | PF02755 | 0.290 |
LIG_Actin_WH2_2 | 317 | 332 | PF00022 | 0.374 |
LIG_Actin_WH2_2 | 474 | 490 | PF00022 | 0.515 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.615 |
LIG_deltaCOP1_diTrp_1 | 593 | 601 | PF00928 | 0.505 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.459 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.430 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.494 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.423 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.432 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.364 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.563 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.307 |
LIG_FHA_1 | 667 | 673 | PF00498 | 0.445 |
LIG_FHA_1 | 717 | 723 | PF00498 | 0.377 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.479 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.443 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.485 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.630 |
LIG_FHA_2 | 575 | 581 | PF00498 | 0.455 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.442 |
LIG_FHA_2 | 703 | 709 | PF00498 | 0.393 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.515 |
LIG_LIR_Apic_2 | 336 | 341 | PF02991 | 0.515 |
LIG_LIR_Apic_2 | 456 | 461 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 177 | 187 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 19 | 27 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 509 | 520 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 593 | 601 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 7 | 16 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 19 | 23 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 244 | 248 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 288 | 293 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 593 | 598 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 622 | 626 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.443 |
LIG_PDZ_Class_2 | 736 | 741 | PF00595 | 0.369 |
LIG_Pex14_2 | 174 | 178 | PF04695 | 0.533 |
LIG_Pex14_2 | 255 | 259 | PF04695 | 0.412 |
LIG_Pex14_2 | 264 | 268 | PF04695 | 0.412 |
LIG_Pex14_2 | 338 | 342 | PF04695 | 0.423 |
LIG_Pex14_2 | 610 | 614 | PF04695 | 0.507 |
LIG_Rb_pABgroove_1 | 273 | 281 | PF01858 | 0.515 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 421 | 425 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 93 | 97 | PF00017 | 0.515 |
LIG_SH2_STAT3 | 537 | 540 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 718 | 721 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.426 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.414 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.479 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.542 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.414 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.354 |
LIG_SUMO_SIM_anti_2 | 274 | 280 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 452 | 459 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 668 | 674 | PF11976 | 0.506 |
LIG_TRAF2_1 | 369 | 372 | PF00917 | 0.429 |
LIG_TRAF2_1 | 435 | 438 | PF00917 | 0.515 |
LIG_TRAF2_1 | 731 | 734 | PF00917 | 0.471 |
LIG_UBA3_1 | 501 | 510 | PF00899 | 0.458 |
LIG_WRC_WIRS_1 | 611 | 616 | PF05994 | 0.559 |
LIG_WRC_WIRS_1 | 672 | 677 | PF05994 | 0.484 |
MOD_CDK_SPxxK_3 | 232 | 239 | PF00069 | 0.410 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.489 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.465 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.524 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.384 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.417 |
MOD_CK1_1 | 674 | 680 | PF00069 | 0.397 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.547 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.477 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.430 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.354 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.423 |
MOD_CK2_1 | 574 | 580 | PF00069 | 0.500 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.441 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.329 |
MOD_CK2_1 | 702 | 708 | PF00069 | 0.386 |
MOD_CK2_1 | 728 | 734 | PF00069 | 0.361 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.412 |
MOD_Cter_Amidation | 29 | 32 | PF01082 | 0.546 |
MOD_Cter_Amidation | 377 | 380 | PF01082 | 0.627 |
MOD_Cter_Amidation | 395 | 398 | PF01082 | 0.562 |
MOD_Cter_Amidation | 440 | 443 | PF01082 | 0.174 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.212 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.611 |
MOD_GlcNHglycan | 407 | 411 | PF01048 | 0.510 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.193 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.212 |
MOD_GlcNHglycan | 52 | 56 | PF01048 | 0.590 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.497 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.416 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.431 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.522 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.472 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.572 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.444 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.479 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.582 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.459 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.646 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.675 |
MOD_NEK2_2 | 41 | 46 | PF00069 | 0.554 |
MOD_NEK2_2 | 671 | 676 | PF00069 | 0.473 |
MOD_PIKK_1 | 524 | 530 | PF00454 | 0.399 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.574 |
MOD_PIKK_1 | 616 | 622 | PF00454 | 0.678 |
MOD_PIKK_1 | 676 | 682 | PF00454 | 0.276 |
MOD_PK_1 | 728 | 734 | PF00069 | 0.301 |
MOD_PKA_1 | 728 | 734 | PF00069 | 0.361 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.403 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.413 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.383 |
MOD_PKA_2 | 616 | 622 | PF00069 | 0.627 |
MOD_PKA_2 | 666 | 672 | PF00069 | 0.413 |
MOD_PKA_2 | 728 | 734 | PF00069 | 0.361 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.595 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.493 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.412 |
MOD_Plk_2-3 | 453 | 459 | PF00069 | 0.423 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.451 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.437 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.512 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.508 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.423 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.389 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.432 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.573 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.486 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.412 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.414 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.577 |
MOD_ProDKin_1 | 716 | 722 | PF00069 | 0.262 |
MOD_SUMO_rev_2 | 78 | 87 | PF00179 | 0.439 |
TRG_DiLeu_BaEn_1 | 708 | 713 | PF01217 | 0.362 |
TRG_DiLeu_BaEn_2 | 439 | 445 | PF01217 | 0.412 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 442 | 444 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 728 | 730 | PF00400 | 0.315 |
TRG_NLS_MonoExtC_3 | 378 | 383 | PF00514 | 0.568 |
TRG_NLS_MonoExtN_4 | 106 | 112 | PF00514 | 0.423 |
TRG_NLS_MonoExtN_4 | 261 | 266 | PF00514 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 358 | 362 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 70 | 74 | PF00026 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 728 | 733 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.315 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ98 | Leptomonas seymouri | 26% | 96% |
A0A0N1I3M2 | Leptomonas seymouri | 26% | 97% |
A0A0N1PBW1 | Leptomonas seymouri | 74% | 99% |
A0A0S4IJW8 | Bodo saltans | 25% | 90% |
A0A0S4IQM0 | Bodo saltans | 39% | 100% |
A0A0S4J8J7 | Bodo saltans | 26% | 81% |
A0A1X0NEV8 | Trypanosomatidae | 25% | 93% |
A0A1X0NLI2 | Trypanosomatidae | 50% | 100% |
A0A1X0NMQ3 | Trypanosomatidae | 27% | 95% |
A0A1X0P419 | Trypanosomatidae | 25% | 98% |
A0A3Q1N1R0 | Bos taurus | 26% | 100% |
A0A3Q8IDH4 | Leishmania donovani | 28% | 96% |
A0A3Q8IPU3 | Leishmania donovani | 26% | 98% |
A0A3R7KM50 | Trypanosoma rangeli | 25% | 93% |
A0A3R7L048 | Trypanosoma rangeli | 26% | 98% |
A0A3S7XC76 | Leishmania donovani | 87% | 100% |
A0A422N0Z6 | Trypanosoma rangeli | 27% | 95% |
A0A422NK00 | Trypanosoma rangeli | 51% | 100% |
A4HE78 | Leishmania braziliensis | 29% | 100% |
A4HFK9 | Leishmania braziliensis | 25% | 96% |
A4I1J2 | Leishmania infantum | 28% | 96% |
A4IC94 | Leishmania infantum | 87% | 100% |
C9ZJX4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 92% |
C9ZPE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 95% |
D0A3K7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D0A5T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 99% |
E1BKH1 | Bos taurus | 29% | 100% |
E9AD64 | Leishmania major | 26% | 98% |
E9AHF6 | Leishmania infantum | 26% | 98% |
E9AU74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AXM7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 96% |
E9AYY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 98% |
Q32TF8 | Danio rerio | 27% | 99% |
Q32TG3 | Gallus gallus | 27% | 99% |
Q4Q0C0 | Leishmania major | 87% | 100% |
Q4Q9U5 | Leishmania major | 28% | 100% |
Q5JST6 | Homo sapiens | 25% | 99% |
Q9D485 | Mus musculus | 25% | 99% |
V5ASV2 | Trypanosoma cruzi | 51% | 100% |
V5D3X9 | Trypanosoma cruzi | 26% | 95% |
V5DA42 | Trypanosoma cruzi | 28% | 98% |