Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 3 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 2, no: 98 |
NetGPI | no | yes: 0, no: 100 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005930 | axoneme | 2 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0020038 | subpellicular network | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0036064 | ciliary basal body | 3 | 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 |
Related structures:
AlphaFold database: A0A3Q8IBS3
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 101 |
GO:0006807 | nitrogen compound metabolic process | 2 | 101 |
GO:0008152 | metabolic process | 1 | 101 |
GO:0019538 | protein metabolic process | 3 | 101 |
GO:0043170 | macromolecule metabolic process | 3 | 101 |
GO:0044238 | primary metabolic process | 2 | 101 |
GO:0071704 | organic substance metabolic process | 2 | 101 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 101 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 101 |
GO:0004175 | endopeptidase activity | 4 | 101 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 101 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 101 |
GO:0008233 | peptidase activity | 3 | 101 |
GO:0008234 | cysteine-type peptidase activity | 4 | 101 |
GO:0016787 | hydrolase activity | 2 | 101 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 101 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.410 |
CLV_C14_Caspase3-7 | 392 | 396 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 467 | 471 | PF00656 | 0.444 |
CLV_C14_Caspase3-7 | 706 | 710 | PF00656 | 0.527 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 710 | 712 | PF00675 | 0.395 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 763 | 765 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 863 | 865 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 893 | 895 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 763 | 765 | PF00082 | 0.422 |
CLV_PCSK_PC1ET2_1 | 863 | 865 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 893 | 895 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.198 |
CLV_PCSK_SKI1_1 | 658 | 662 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 805 | 809 | PF00082 | 0.462 |
DEG_SCF_FBW7_2 | 245 | 250 | PF00400 | 0.523 |
DEG_SIAH_1 | 206 | 214 | PF03145 | 0.397 |
DOC_CKS1_1 | 26 | 31 | PF01111 | 0.508 |
DOC_PP1_RVXF_1 | 508 | 514 | PF00149 | 0.478 |
DOC_PP1_RVXF_1 | 666 | 673 | PF00149 | 0.523 |
DOC_PP4_FxxP_1 | 278 | 281 | PF00568 | 0.297 |
DOC_PP4_FxxP_1 | 411 | 414 | PF00568 | 0.522 |
DOC_PP4_FxxP_1 | 491 | 494 | PF00568 | 0.481 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.480 |
DOC_USP7_MATH_2 | 444 | 450 | PF00917 | 0.534 |
DOC_USP7_UBL2_3 | 554 | 558 | PF12436 | 0.476 |
DOC_USP7_UBL2_3 | 708 | 712 | PF12436 | 0.506 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.800 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 614 | 619 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 747 | 752 | PF00397 | 0.392 |
LIG_14-3-3_CanoR_1 | 216 | 222 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 373 | 381 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 510 | 514 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 800 | 809 | PF00244 | 0.515 |
LIG_Actin_WH2_2 | 346 | 363 | PF00022 | 0.321 |
LIG_Actin_WH2_2 | 521 | 538 | PF00022 | 0.562 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.757 |
LIG_BIR_III_2 | 684 | 688 | PF00653 | 0.383 |
LIG_BRCT_BRCA1_1 | 858 | 862 | PF00533 | 0.467 |
LIG_Clathr_ClatBox_1 | 882 | 886 | PF01394 | 0.561 |
LIG_CtBP_PxDLS_1 | 444 | 448 | PF00389 | 0.386 |
LIG_deltaCOP1_diTrp_1 | 671 | 676 | PF00928 | 0.482 |
LIG_deltaCOP1_diTrp_1 | 804 | 808 | PF00928 | 0.430 |
LIG_eIF4E_1 | 633 | 639 | PF01652 | 0.496 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.581 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.334 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.479 |
LIG_FHA_1 | 734 | 740 | PF00498 | 0.427 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.462 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.777 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.413 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.535 |
LIG_FHA_2 | 643 | 649 | PF00498 | 0.501 |
LIG_FHA_2 | 679 | 685 | PF00498 | 0.577 |
LIG_LIR_Apic_2 | 276 | 281 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 553 | 564 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 579 | 586 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 597 | 608 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 631 | 639 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 752 | 758 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 803 | 814 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 9 | 20 | PF02991 | 0.749 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 525 | 530 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 546 | 551 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 553 | 559 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 562 | 566 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 597 | 603 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 631 | 636 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 752 | 757 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 770 | 775 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 786 | 791 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 803 | 809 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 859 | 865 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 873 | 878 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.526 |
LIG_Pex14_2 | 703 | 707 | PF04695 | 0.474 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.807 |
LIG_SH2_CRK | 556 | 560 | PF00017 | 0.469 |
LIG_SH2_CRK | 563 | 567 | PF00017 | 0.469 |
LIG_SH2_CRK | 611 | 615 | PF00017 | 0.487 |
LIG_SH2_CRK | 633 | 637 | PF00017 | 0.481 |
LIG_SH2_CRK | 772 | 776 | PF00017 | 0.417 |
LIG_SH2_CRK | 788 | 792 | PF00017 | 0.485 |
LIG_SH2_GRB2like | 369 | 372 | PF00017 | 0.542 |
LIG_SH2_GRB2like | 713 | 716 | PF00017 | 0.442 |
LIG_SH2_NCK_1 | 175 | 179 | PF00017 | 0.513 |
LIG_SH2_NCK_1 | 182 | 186 | PF00017 | 0.524 |
LIG_SH2_NCK_1 | 633 | 637 | PF00017 | 0.492 |
LIG_SH2_PTP2 | 825 | 828 | PF00017 | 0.393 |
LIG_SH2_SRC | 527 | 530 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 159 | 163 | PF00017 | 0.809 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.835 |
LIG_SH2_STAP1 | 304 | 308 | PF00017 | 0.318 |
LIG_SH2_STAP1 | 537 | 541 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 727 | 731 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.777 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 713 | 716 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 825 | 828 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 843 | 846 | PF00017 | 0.343 |
LIG_SH3_1 | 23 | 29 | PF00018 | 0.503 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.682 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.837 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.319 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.520 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.533 |
LIG_SH3_3 | 745 | 751 | PF00018 | 0.378 |
LIG_SH3_3 | 834 | 840 | PF00018 | 0.573 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.842 |
LIG_SH3_3 | 882 | 888 | PF00018 | 0.453 |
LIG_SH3_5 | 725 | 729 | PF00018 | 0.406 |
LIG_SUMO_SIM_anti_2 | 813 | 818 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 741 | 747 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 773 | 778 | PF11976 | 0.378 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.818 |
LIG_TRAF2_1 | 163 | 166 | PF00917 | 0.738 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.514 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.702 |
LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.505 |
LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.492 |
LIG_TRAF2_1 | 93 | 96 | PF00917 | 0.527 |
LIG_TRAF2_2 | 29 | 34 | PF00917 | 0.517 |
LIG_TRAF2_2 | 78 | 83 | PF00917 | 0.507 |
LIG_TYR_ITIM | 283 | 288 | PF00017 | 0.331 |
LIG_UBA3_1 | 283 | 291 | PF00899 | 0.349 |
LIG_UBA3_1 | 702 | 708 | PF00899 | 0.383 |
LIG_UBA3_1 | 816 | 824 | PF00899 | 0.448 |
LIG_WRPW_2 | 431 | 434 | PF00400 | 0.383 |
MOD_CDK_SPxK_1 | 614 | 620 | PF00069 | 0.490 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.496 |
MOD_CK1_1 | 856 | 862 | PF00069 | 0.404 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.829 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.484 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.469 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.476 |
MOD_CK2_1 | 642 | 648 | PF00069 | 0.524 |
MOD_CK2_1 | 775 | 781 | PF00069 | 0.376 |
MOD_CMANNOS | 704 | 707 | PF00535 | 0.273 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.651 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.510 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.320 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.326 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.281 |
MOD_GlcNHglycan | 671 | 675 | PF01048 | 0.333 |
MOD_GlcNHglycan | 740 | 743 | PF01048 | 0.492 |
MOD_GlcNHglycan | 794 | 797 | PF01048 | 0.426 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.494 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.474 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.487 |
MOD_GSK3_1 | 752 | 759 | PF00069 | 0.424 |
MOD_N-GLC_1 | 298 | 303 | PF02516 | 0.323 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.341 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.505 |
MOD_N-GLC_1 | 767 | 772 | PF02516 | 0.612 |
MOD_N-GLC_1 | 792 | 797 | PF02516 | 0.426 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.506 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.277 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.404 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.487 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.515 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.482 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.538 |
MOD_NEK2_1 | 703 | 708 | PF00069 | 0.493 |
MOD_NEK2_1 | 792 | 797 | PF00069 | 0.443 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.741 |
MOD_NEK2_2 | 580 | 585 | PF00069 | 0.564 |
MOD_OFUCOSY | 270 | 277 | PF10250 | 0.193 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.704 |
MOD_PIKK_1 | 446 | 452 | PF00454 | 0.541 |
MOD_PIKK_1 | 756 | 762 | PF00454 | 0.358 |
MOD_PIKK_1 | 900 | 906 | PF00454 | 0.546 |
MOD_PIKK_1 | 94 | 100 | PF00454 | 0.761 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.457 |
MOD_PKA_2 | 799 | 805 | PF00069 | 0.312 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.631 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.330 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.287 |
MOD_Plk_1 | 586 | 592 | PF00069 | 0.514 |
MOD_Plk_1 | 812 | 818 | PF00069 | 0.385 |
MOD_Plk_1 | 856 | 862 | PF00069 | 0.435 |
MOD_Plk_2-3 | 588 | 594 | PF00069 | 0.524 |
MOD_Plk_2-3 | 83 | 89 | PF00069 | 0.519 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.591 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.482 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.508 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.509 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.498 |
MOD_Plk_4 | 812 | 818 | PF00069 | 0.446 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.773 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.799 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.749 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.675 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.482 |
MOD_ProDKin_1 | 614 | 620 | PF00069 | 0.481 |
MOD_ProDKin_1 | 747 | 753 | PF00069 | 0.393 |
MOD_SUMO_for_1 | 876 | 879 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 587 | 596 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 648 | 657 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 770 | 775 | PF00179 | 0.465 |
MOD_SUMO_rev_2 | 83 | 90 | PF00179 | 0.726 |
TRG_DiLeu_BaEn_2 | 343 | 349 | PF01217 | 0.257 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.722 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 556 | 559 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 611 | 614 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 772 | 775 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 788 | 791 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 825 | 828 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.646 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.573 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 34% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 29% | 92% |
A0A0N1IGQ2 | Leptomonas seymouri | 32% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 40% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 34% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 40% | 100% |
A0A0N1PCA9 | Leptomonas seymouri | 35% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 27% | 100% |
A0A0N1PFI4 | Leptomonas seymouri | 35% | 100% |
A0A0S4JLK6 | Bodo saltans | 28% | 100% |
A0A0S4KGT2 | Bodo saltans | 40% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 29% | 74% |
A0A1X0NJK2 | Trypanosomatidae | 31% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 36% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 32% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 32% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 41% | 100% |
A0A1X0NW84 | Trypanosomatidae | 39% | 100% |
A0A1X0NW85 | Trypanosomatidae | 38% | 100% |
A0A1X0NW89 | Trypanosomatidae | 55% | 100% |
A0A1X0NWA6 | Trypanosomatidae | 30% | 100% |
A0A1X0NWW1 | Trypanosomatidae | 40% | 100% |
A0A3Q8IDD4 | Leishmania donovani | 34% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 26% | 100% |
A0A3S5H5A5 | Leishmania donovani | 41% | 100% |
A0A3S5ISG2 | Trypanosoma rangeli | 32% | 100% |
A0A3S7WW13 | Leishmania donovani | 27% | 82% |
A0A3S7WW18 | Leishmania donovani | 99% | 100% |
A0A3S7WW41 | Leishmania donovani | 35% | 100% |
A0A3S7WW71 | Leishmania donovani | 40% | 100% |
A0A3S7X430 | Leishmania donovani | 34% | 100% |
A0A3S7X438 | Leishmania donovani | 30% | 97% |
A0A3S7X460 | Leishmania donovani | 35% | 100% |
A0A3S7X463 | Leishmania donovani | 28% | 97% |
A0A3S7X470 | Leishmania donovani | 35% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 52% | 99% |
A0A422MYX0 | Trypanosoma rangeli | 38% | 100% |
A4H3W4 | Leishmania braziliensis | 41% | 100% |
A4HE81 | Leishmania braziliensis | 34% | 100% |
A4HJ14 | Leishmania braziliensis | 34% | 100% |
A4HJ22 | Leishmania braziliensis | 32% | 100% |
A4HJ24 | Leishmania braziliensis | 34% | 100% |
A4HS39 | Leishmania infantum | 41% | 100% |
A4HYN0 | Leishmania infantum | 99% | 100% |
A4HYW1 | Leishmania infantum | 97% | 100% |
A4HYW2 | Leishmania infantum | 40% | 100% |
A4HYW3 | Leishmania infantum | 35% | 100% |
A4HYW4 | Leishmania infantum | 28% | 100% |
A4I1J4 | Leishmania infantum | 34% | 100% |
A4I6E4 | Leishmania infantum | 35% | 100% |
A4I6E6 | Leishmania infantum | 35% | 100% |
A4I6F0 | Leishmania infantum | 30% | 100% |
A4I6K4 | Leishmania infantum | 34% | 100% |
A4I6K5 | Leishmania infantum | 28% | 100% |
A4I6K6 | Leishmania infantum | 26% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 84% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AIH1 | Leishmania braziliensis | 85% | 100% |
E9AIH3 | Leishmania braziliensis | 40% | 100% |
E9AIH4 | Leishmania braziliensis | 35% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
Q4Q6L7 | Leishmania major | 35% | 100% |
Q4Q6L9 | Leishmania major | 35% | 100% |
Q4Q6M0 | Leishmania major | 31% | 100% |
Q4Q6M2 | Leishmania major | 26% | 100% |
Q4Q6M3 | Leishmania major | 27% | 100% |
Q4Q6M4 | Leishmania major | 33% | 100% |
Q4Q9U3 | Leishmania major | 34% | 100% |
Q4QCS6 | Leishmania major | 36% | 100% |
Q4QCS7 | Leishmania major | 40% | 100% |
Q4QCS8 | Leishmania major | 95% | 100% |
Q4QCS9 | Leishmania major | 92% | 100% |
Q9U0T9 | Leishmania major | 41% | 100% |
V5AYJ1 | Trypanosoma cruzi | 31% | 100% |
V5B5I4 | Trypanosoma cruzi | 54% | 100% |
V5BA05 | Trypanosoma cruzi | 41% | 100% |
V5BEL3 | Trypanosoma cruzi | 37% | 100% |
V5BII7 | Trypanosoma cruzi | 29% | 74% |
V5BN20 | Trypanosoma cruzi | 35% | 100% |
V5D9Y2 | Trypanosoma cruzi | 41% | 100% |
V5DES7 | Trypanosoma cruzi | 32% | 100% |