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:0005819 | spindle | 5 | 2 |
GO:0005930 | axoneme | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0072686 | mitotic spindle | 6 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AD64
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0000281 | mitotic cytokinesis | 4 | 2 |
GO:0000910 | cytokinesis | 3 | 2 |
GO:0001539 | cilium or flagellum-dependent cell motility | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0007051 | spindle organization | 3 | 2 |
GO:0007052 | mitotic spindle organization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0048870 | cell motility | 2 | 2 |
GO:0060285 | cilium-dependent cell motility | 4 | 2 |
GO:0061640 | cytoskeleton-dependent cytokinesis | 4 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 2 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005509 | calcium ion binding | 5 | 7 |
GO:0005515 | protein binding | 2 | 2 |
GO:0008092 | cytoskeletal protein binding | 3 | 2 |
GO:0015631 | tubulin binding | 4 | 2 |
GO:0043014 | alpha-tubulin binding | 5 | 2 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 723 | 729 | PF00089 | 0.499 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 646 | 648 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 669 | 671 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 699 | 701 | PF00675 | 0.458 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 669 | 671 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 699 | 701 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.255 |
CLV_PCSK_PC7_1 | 30 | 36 | PF00082 | 0.655 |
CLV_PCSK_PC7_1 | 474 | 480 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.152 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 670 | 674 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 717 | 721 | PF00082 | 0.476 |
CLV_Separin_Metazoa | 26 | 30 | PF03568 | 0.553 |
DEG_APCC_KENBOX_2 | 329 | 333 | PF00400 | 0.509 |
DEG_SIAH_1 | 198 | 206 | PF03145 | 0.598 |
DOC_ANK_TNKS_1 | 604 | 611 | PF00023 | 0.487 |
DOC_CDC14_PxL_1 | 15 | 23 | PF14671 | 0.664 |
DOC_CYCLIN_RxL_1 | 185 | 193 | PF00134 | 0.637 |
DOC_CYCLIN_RxL_1 | 568 | 579 | PF00134 | 0.380 |
DOC_CYCLIN_RxL_1 | 664 | 676 | PF00134 | 0.410 |
DOC_CYCLIN_RxL_1 | 695 | 708 | PF00134 | 0.520 |
DOC_MAPK_FxFP_2 | 141 | 144 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 114 | 122 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 242 | 250 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 34 | 42 | PF00069 | 0.671 |
DOC_MAPK_gen_1 | 439 | 449 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 114 | 122 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 441 | 449 | PF00069 | 0.525 |
DOC_PP4_FxxP_1 | 13 | 16 | PF00568 | 0.535 |
DOC_PP4_FxxP_1 | 141 | 144 | PF00568 | 0.452 |
DOC_PP4_FxxP_1 | 389 | 392 | PF00568 | 0.595 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 631 | 635 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 684 | 688 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 725 | 729 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 748 | 752 | PF00917 | 0.542 |
DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.544 |
DOC_USP7_UBL2_3 | 530 | 534 | PF12436 | 0.544 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.584 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 726 | 730 | PF00244 | 0.432 |
LIG_AP2alpha_2 | 184 | 186 | PF02296 | 0.558 |
LIG_AP2alpha_2 | 298 | 300 | PF02296 | 0.455 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.565 |
LIG_BIR_III_2 | 182 | 186 | PF00653 | 0.558 |
LIG_BRCT_BRCA1_1 | 169 | 173 | PF00533 | 0.475 |
LIG_BRCT_BRCA1_1 | 283 | 287 | PF00533 | 0.563 |
LIG_BRCT_BRCA1_1 | 315 | 319 | PF00533 | 0.528 |
LIG_BRCT_BRCA1_1 | 325 | 329 | PF00533 | 0.468 |
LIG_BRCT_BRCA1_1 | 499 | 503 | PF00533 | 0.534 |
LIG_BRCT_BRCA1_1 | 690 | 694 | PF00533 | 0.486 |
LIG_eIF4E_1 | 683 | 689 | PF01652 | 0.536 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.504 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.453 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.455 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.523 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.463 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.432 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.356 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.534 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.462 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.441 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.603 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.509 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.419 |
LIG_LIR_Apic_2 | 12 | 16 | PF02991 | 0.541 |
LIG_LIR_Apic_2 | 139 | 144 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 206 | 217 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 270 | 280 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 500 | 510 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 564 | 573 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 598 | 607 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 661 | 666 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 676 | 684 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 728 | 736 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 177 | 181 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 360 | 364 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 455 | 460 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 500 | 506 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 564 | 569 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 594 | 599 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 661 | 665 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 676 | 680 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 728 | 732 | PF02991 | 0.496 |
LIG_Pex14_1 | 620 | 624 | PF04695 | 0.540 |
LIG_Pex14_2 | 673 | 677 | PF04695 | 0.447 |
LIG_SH2_NCK_1 | 599 | 603 | PF00017 | 0.419 |
LIG_SH2_SRC | 599 | 602 | PF00017 | 0.419 |
LIG_SH2_SRC | 624 | 627 | PF00017 | 0.601 |
LIG_SH2_STAP1 | 599 | 603 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 729 | 733 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 742 | 746 | PF00017 | 0.532 |
LIG_SH2_STAT3 | 352 | 355 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.308 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.534 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.533 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.507 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.492 |
LIG_SUMO_SIM_anti_2 | 581 | 587 | PF11976 | 0.327 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.455 |
LIG_TRAF2_1 | 578 | 581 | PF00917 | 0.308 |
LIG_TRAF2_1 | 598 | 601 | PF00917 | 0.122 |
LIG_TRAF2_1 | 708 | 711 | PF00917 | 0.508 |
LIG_TRAF2_1 | 728 | 731 | PF00917 | 0.295 |
LIG_TYR_ITIM | 597 | 602 | PF00017 | 0.406 |
LIG_UBA3_1 | 582 | 591 | PF00899 | 0.319 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.503 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.525 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.587 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.414 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.308 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.491 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.457 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.450 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.530 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.485 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.590 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.490 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.485 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.308 |
MOD_CK2_1 | 595 | 601 | PF00069 | 0.122 |
MOD_CK2_1 | 705 | 711 | PF00069 | 0.435 |
MOD_CK2_1 | 725 | 731 | PF00069 | 0.344 |
MOD_GlcNHglycan | 137 | 141 | PF01048 | 0.250 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.245 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.122 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.255 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.363 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.531 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.475 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.511 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.605 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.514 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.500 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.468 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.444 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.667 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.461 |
MOD_GSK3_1 | 738 | 745 | PF00069 | 0.532 |
MOD_GSK3_1 | 748 | 755 | PF00069 | 0.571 |
MOD_N-GLC_1 | 555 | 560 | PF02516 | 0.400 |
MOD_N-GLC_1 | 592 | 597 | PF02516 | 0.316 |
MOD_N-GLC_1 | 736 | 741 | PF02516 | 0.411 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.501 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.527 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.492 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.517 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.402 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.485 |
MOD_NEK2_1 | 736 | 741 | PF00069 | 0.429 |
MOD_NEK2_2 | 208 | 213 | PF00069 | 0.549 |
MOD_NEK2_2 | 325 | 330 | PF00069 | 0.485 |
MOD_NEK2_2 | 65 | 70 | PF00069 | 0.737 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.553 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.468 |
MOD_PKA_2 | 646 | 652 | PF00069 | 0.622 |
MOD_PKA_2 | 725 | 731 | PF00069 | 0.433 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.534 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.534 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.587 |
MOD_Plk_1 | 450 | 456 | PF00069 | 0.446 |
MOD_Plk_1 | 509 | 515 | PF00069 | 0.530 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.662 |
MOD_Plk_1 | 592 | 598 | PF00069 | 0.297 |
MOD_Plk_1 | 702 | 708 | PF00069 | 0.509 |
MOD_Plk_2-3 | 703 | 709 | PF00069 | 0.486 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.478 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.534 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.620 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.515 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.409 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.468 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.534 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.537 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.352 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.209 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.308 |
MOD_Plk_4 | 631 | 637 | PF00069 | 0.650 |
MOD_Plk_4 | 684 | 690 | PF00069 | 0.428 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.451 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.539 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.497 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.592 |
MOD_SUMO_rev_2 | 249 | 255 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 432 | 440 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 634 | 642 | PF00179 | 0.580 |
MOD_SUMO_rev_2 | 643 | 649 | PF00179 | 0.505 |
MOD_SUMO_rev_2 | 687 | 696 | PF00179 | 0.437 |
TRG_DiLeu_BaEn_1 | 731 | 736 | PF01217 | 0.482 |
TRG_DiLeu_BaEn_4 | 710 | 716 | PF01217 | 0.487 |
TRG_DiLeu_LyEn_5 | 731 | 736 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 729 | 732 | PF00928 | 0.453 |
TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 415 | 417 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 477 | 479 | PF00400 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 188 | 193 | PF00026 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 397 | 401 | PF00026 | 0.658 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H4 | Leptomonas seymouri | 23% | 90% |
A0A0N1HZ98 | Leptomonas seymouri | 25% | 98% |
A0A0N1I3M2 | Leptomonas seymouri | 76% | 99% |
A0A0N1PBW1 | Leptomonas seymouri | 28% | 100% |
A0A0S4IJW8 | Bodo saltans | 26% | 92% |
A0A0S4IQM0 | Bodo saltans | 25% | 100% |
A0A0S4J8J7 | Bodo saltans | 27% | 82% |
A0A1X0NEV8 | Trypanosomatidae | 25% | 95% |
A0A1X0NLI2 | Trypanosomatidae | 27% | 100% |
A0A1X0NMQ3 | Trypanosomatidae | 25% | 97% |
A0A1X0P419 | Trypanosomatidae | 62% | 99% |
A0A3Q1N1R0 | Bos taurus | 30% | 100% |
A0A3Q8IDH4 | Leishmania donovani | 25% | 98% |
A0A3Q8IPU3 | Leishmania donovani | 97% | 100% |
A0A3R7KM50 | Trypanosoma rangeli | 27% | 95% |
A0A3R7L048 | Trypanosoma rangeli | 59% | 100% |
A0A3S5H688 | Leishmania donovani | 22% | 87% |
A0A3S7XC76 | Leishmania donovani | 27% | 100% |
A0A422N0Z6 | Trypanosoma rangeli | 24% | 97% |
A0A422NK00 | Trypanosoma rangeli | 29% | 100% |
A4HE78 | Leishmania braziliensis | 26% | 98% |
A4HFK9 | Leishmania braziliensis | 88% | 100% |
A4HQF8 | Leishmania braziliensis | 26% | 100% |
A4I1J2 | Leishmania infantum | 25% | 98% |
A4IC94 | Leishmania infantum | 27% | 100% |
C9ZJX4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 94% |
C9ZPE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 97% |
D0A3K7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A5T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E1BKH1 | Bos taurus | 29% | 100% |
E9AHF6 | Leishmania infantum | 98% | 100% |
E9AI34 | Leishmania braziliensis | 23% | 88% |
E9AMI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 88% |
E9AU74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AXM7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 98% |
E9AYY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q32TF8 | Danio rerio | 31% | 100% |
Q32TG3 | Gallus gallus | 28% | 100% |
Q4Q0C0 | Leishmania major | 27% | 100% |
Q4Q9U5 | Leishmania major | 25% | 98% |
Q4QI57 | Leishmania major | 23% | 87% |
Q5JST6 | Homo sapiens | 28% | 100% |
Q5JVL4 | Homo sapiens | 30% | 100% |
Q9D485 | Mus musculus | 29% | 100% |
Q9D9T8 | Mus musculus | 30% | 100% |
V5ASV2 | Trypanosoma cruzi | 26% | 100% |
V5D3X9 | Trypanosoma cruzi | 24% | 97% |
V5DA42 | Trypanosoma cruzi | 59% | 100% |