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. | yes | 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. | no | 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: E9AUQ7
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 | 416 | 420 | PF00656 | 0.579 |
CLV_C14_Caspase3-7 | 491 | 495 | PF00656 | 0.498 |
CLV_C14_Caspase3-7 | 730 | 734 | PF00656 | 0.598 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 734 | 736 | PF00675 | 0.441 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 787 | 789 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 887 | 889 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 917 | 919 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 787 | 789 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 887 | 889 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 917 | 919 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 682 | 686 | PF00082 | 0.320 |
DEG_SIAH_1 | 230 | 238 | PF03145 | 0.450 |
DOC_MAPK_gen_1 | 383 | 391 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 383 | 391 | PF00069 | 0.468 |
DOC_PIKK_1 | 62 | 70 | PF02985 | 0.553 |
DOC_PIKK_1 | 75 | 83 | PF02985 | 0.544 |
DOC_PP1_RVXF_1 | 532 | 538 | PF00149 | 0.533 |
DOC_PP4_FxxP_1 | 302 | 305 | PF00568 | 0.354 |
DOC_PP4_FxxP_1 | 435 | 438 | PF00568 | 0.576 |
DOC_PP4_FxxP_1 | 515 | 518 | PF00568 | 0.536 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.535 |
DOC_USP7_MATH_2 | 468 | 474 | PF00917 | 0.588 |
DOC_USP7_UBL2_3 | 578 | 582 | PF12436 | 0.531 |
DOC_USP7_UBL2_3 | 732 | 736 | PF12436 | 0.551 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 638 | 643 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 771 | 776 | PF00397 | 0.452 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 397 | 405 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 479 | 483 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 534 | 538 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 824 | 833 | PF00244 | 0.578 |
LIG_Actin_WH2_2 | 545 | 562 | PF00022 | 0.615 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.567 |
LIG_BIR_III_2 | 708 | 712 | PF00653 | 0.435 |
LIG_BRCT_BRCA1_1 | 451 | 455 | PF00533 | 0.568 |
LIG_BRCT_BRCA1_1 | 882 | 886 | PF00533 | 0.529 |
LIG_Clathr_ClatBox_1 | 906 | 910 | PF01394 | 0.624 |
LIG_CtBP_PxDLS_1 | 468 | 472 | PF00389 | 0.437 |
LIG_deltaCOP1_diTrp_1 | 695 | 700 | PF00928 | 0.527 |
LIG_deltaCOP1_diTrp_1 | 828 | 832 | PF00928 | 0.492 |
LIG_eIF4E_1 | 657 | 663 | PF01652 | 0.552 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.702 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.702 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.387 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.542 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.530 |
LIG_FHA_1 | 758 | 764 | PF00498 | 0.472 |
LIG_FHA_1 | 777 | 783 | PF00498 | 0.500 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.828 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.475 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.571 |
LIG_FHA_2 | 667 | 673 | PF00498 | 0.545 |
LIG_FHA_2 | 703 | 709 | PF00498 | 0.597 |
LIG_LIR_Apic_2 | 198 | 204 | PF02991 | 0.866 |
LIG_LIR_Apic_2 | 300 | 305 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 164 | 171 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 577 | 587 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 603 | 610 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 621 | 632 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 655 | 663 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 776 | 782 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 827 | 838 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 9 | 20 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 549 | 554 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 570 | 575 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 577 | 583 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 586 | 590 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 621 | 627 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 655 | 660 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 776 | 781 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 794 | 799 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 810 | 815 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 827 | 833 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 883 | 889 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 897 | 902 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.581 |
LIG_Pex14_2 | 161 | 165 | PF04695 | 0.619 |
LIG_Pex14_2 | 727 | 731 | PF04695 | 0.529 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.837 |
LIG_SH2_CRK | 580 | 584 | PF00017 | 0.532 |
LIG_SH2_CRK | 587 | 591 | PF00017 | 0.528 |
LIG_SH2_CRK | 635 | 639 | PF00017 | 0.549 |
LIG_SH2_CRK | 657 | 661 | PF00017 | 0.532 |
LIG_SH2_CRK | 796 | 800 | PF00017 | 0.457 |
LIG_SH2_CRK | 812 | 816 | PF00017 | 0.549 |
LIG_SH2_GRB2like | 393 | 396 | PF00017 | 0.570 |
LIG_SH2_GRB2like | 737 | 740 | PF00017 | 0.504 |
LIG_SH2_NCK_1 | 201 | 205 | PF00017 | 0.589 |
LIG_SH2_NCK_1 | 657 | 661 | PF00017 | 0.548 |
LIG_SH2_PTP2 | 849 | 852 | PF00017 | 0.453 |
LIG_SH2_SRC | 551 | 554 | PF00017 | 0.546 |
LIG_SH2_SRC | 675 | 678 | PF00017 | 0.566 |
LIG_SH2_STAP1 | 328 | 332 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 561 | 565 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 751 | 755 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 668 | 671 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 675 | 678 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 737 | 740 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 849 | 852 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 867 | 870 | PF00017 | 0.411 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.556 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.790 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.743 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.375 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.566 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.597 |
LIG_SH3_3 | 769 | 775 | PF00018 | 0.436 |
LIG_SH3_3 | 858 | 864 | PF00018 | 0.649 |
LIG_SH3_3 | 906 | 912 | PF00018 | 0.509 |
LIG_SUMO_SIM_anti_2 | 837 | 843 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 130 | 137 | PF11976 | 0.765 |
LIG_SUMO_SIM_par_1 | 387 | 392 | PF11976 | 0.326 |
LIG_SUMO_SIM_par_1 | 765 | 771 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 797 | 802 | PF11976 | 0.432 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.830 |
LIG_TRAF2_1 | 148 | 151 | PF00917 | 0.672 |
LIG_TRAF2_1 | 184 | 187 | PF00917 | 0.599 |
LIG_TRAF2_1 | 189 | 192 | PF00917 | 0.898 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.800 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.569 |
LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.813 |
LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.659 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.548 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.551 |
LIG_TRAF2_2 | 104 | 109 | PF00917 | 0.562 |
LIG_TRAF2_2 | 29 | 34 | PF00917 | 0.567 |
LIG_TYR_ITIM | 307 | 312 | PF00017 | 0.389 |
LIG_UBA3_1 | 307 | 315 | PF00899 | 0.406 |
LIG_UBA3_1 | 726 | 732 | PF00899 | 0.435 |
LIG_UBA3_1 | 840 | 848 | PF00899 | 0.504 |
LIG_WRPW_2 | 455 | 458 | PF00400 | 0.435 |
MOD_CDK_SPxK_1 | 638 | 644 | PF00069 | 0.545 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.666 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.331 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.552 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.826 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.538 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.535 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.649 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.521 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.589 |
MOD_CK2_1 | 799 | 805 | PF00069 | 0.438 |
MOD_CMANNOS | 728 | 731 | PF00535 | 0.325 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.647 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.777 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.692 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.566 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.370 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.370 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.328 |
MOD_GlcNHglycan | 695 | 699 | PF01048 | 0.382 |
MOD_GlcNHglycan | 764 | 767 | PF01048 | 0.548 |
MOD_GlcNHglycan | 818 | 821 | PF01048 | 0.485 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.330 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.528 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.537 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.527 |
MOD_GSK3_1 | 776 | 783 | PF00069 | 0.484 |
MOD_GSK3_1 | 824 | 831 | PF00069 | 0.465 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.381 |
MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.399 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.600 |
MOD_N-GLC_1 | 791 | 796 | PF02516 | 0.619 |
MOD_N-GLC_1 | 816 | 821 | PF02516 | 0.463 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.569 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.333 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.503 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.552 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.537 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.586 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.541 |
MOD_NEK2_1 | 816 | 821 | PF00069 | 0.513 |
MOD_NEK2_2 | 604 | 609 | PF00069 | 0.617 |
MOD_NEK2_2 | 880 | 885 | PF00069 | 0.614 |
MOD_PIKK_1 | 120 | 126 | PF00454 | 0.819 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.823 |
MOD_PIKK_1 | 370 | 376 | PF00454 | 0.503 |
MOD_PIKK_1 | 470 | 476 | PF00454 | 0.595 |
MOD_PIKK_1 | 780 | 786 | PF00454 | 0.415 |
MOD_PIKK_1 | 924 | 930 | PF00454 | 0.603 |
MOD_PKA_1 | 398 | 404 | PF00069 | 0.415 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.488 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.431 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.512 |
MOD_PKA_2 | 823 | 829 | PF00069 | 0.586 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.647 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.384 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.349 |
MOD_Plk_1 | 610 | 616 | PF00069 | 0.568 |
MOD_Plk_1 | 836 | 842 | PF00069 | 0.427 |
MOD_Plk_1 | 880 | 886 | PF00069 | 0.500 |
MOD_Plk_2-3 | 127 | 133 | PF00069 | 0.547 |
MOD_Plk_2-3 | 612 | 618 | PF00069 | 0.579 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.649 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.536 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.562 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.569 |
MOD_Plk_4 | 666 | 672 | PF00069 | 0.547 |
MOD_Plk_4 | 836 | 842 | PF00069 | 0.481 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.716 |
MOD_ProDKin_1 | 638 | 644 | PF00069 | 0.537 |
MOD_ProDKin_1 | 771 | 777 | PF00069 | 0.448 |
MOD_SUMO_for_1 | 294 | 297 | PF00179 | 0.354 |
MOD_SUMO_for_1 | 900 | 903 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 109 | 116 | PF00179 | 0.763 |
MOD_SUMO_rev_2 | 611 | 620 | PF00179 | 0.536 |
MOD_SUMO_rev_2 | 672 | 681 | PF00179 | 0.579 |
MOD_SUMO_rev_2 | 794 | 799 | PF00179 | 0.528 |
TRG_DiLeu_BaEn_4 | 113 | 119 | PF01217 | 0.557 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 580 | 583 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 587 | 590 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 657 | 660 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 668 | 671 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 796 | 799 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 812 | 815 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 849 | 852 | PF00928 | 0.387 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.675 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 398 | 402 | PF00026 | 0.622 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 33% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 29% | 95% |
A0A0N1IGQ2 | Leptomonas seymouri | 32% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 42% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 34% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 40% | 100% |
A0A0N1PCA9 | Leptomonas seymouri | 35% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 27% | 100% |
A0A0N1PFI4 | Leptomonas seymouri | 36% | 100% |
A0A0S4JLK6 | Bodo saltans | 28% | 100% |
A0A0S4KGT2 | Bodo saltans | 40% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 28% | 76% |
A0A1X0NJK2 | Trypanosomatidae | 31% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 34% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 32% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 31% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 40% | 100% |
A0A1X0NW84 | Trypanosomatidae | 40% | 100% |
A0A1X0NW85 | Trypanosomatidae | 39% | 100% |
A0A1X0NW89 | Trypanosomatidae | 54% | 100% |
A0A1X0NWA6 | Trypanosomatidae | 31% | 100% |
A0A1X0NWW1 | Trypanosomatidae | 40% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 88% | 100% |
A0A3Q8IDD4 | Leishmania donovani | 34% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 25% | 100% |
A0A3S5H5A5 | Leishmania donovani | 41% | 100% |
A0A3S5ISG2 | Trypanosoma rangeli | 31% | 100% |
A0A3S7WW13 | Leishmania donovani | 27% | 85% |
A0A3S7WW18 | Leishmania donovani | 92% | 100% |
A0A3S7WW41 | Leishmania donovani | 35% | 100% |
A0A3S7WW71 | Leishmania donovani | 40% | 100% |
A0A3S7X430 | Leishmania donovani | 34% | 100% |
A0A3S7X438 | Leishmania donovani | 30% | 99% |
A0A3S7X460 | Leishmania donovani | 35% | 100% |
A0A3S7X463 | Leishmania donovani | 27% | 100% |
A0A3S7X470 | Leishmania donovani | 35% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 52% | 100% |
A0A422MYX0 | Trypanosoma rangeli | 38% | 100% |
A4H3W4 | Leishmania braziliensis | 40% | 100% |
A4HE81 | Leishmania braziliensis | 34% | 100% |
A4HJ14 | Leishmania braziliensis | 35% | 100% |
A4HJ22 | Leishmania braziliensis | 31% | 100% |
A4HJ24 | Leishmania braziliensis | 34% | 100% |
A4HS39 | Leishmania infantum | 41% | 100% |
A4HYN0 | Leishmania infantum | 93% | 100% |
A4HYW1 | Leishmania infantum | 90% | 92% |
A4HYW2 | Leishmania infantum | 40% | 100% |
A4HYW3 | Leishmania infantum | 36% | 100% |
A4HYW4 | Leishmania infantum | 28% | 93% |
A4I1J4 | Leishmania infantum | 34% | 100% |
A4I6E4 | Leishmania infantum | 35% | 100% |
A4I6E6 | Leishmania infantum | 35% | 100% |
A4I6F0 | Leishmania infantum | 30% | 99% |
A4I6K4 | Leishmania infantum | 34% | 100% |
A4I6K5 | Leishmania infantum | 27% | 100% |
A4I6K6 | Leishmania infantum | 25% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 87% |
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) | 34% | 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) | 38% | 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 | 84% | 100% |
E9AIH3 | Leishmania braziliensis | 40% | 100% |
E9AIH4 | Leishmania braziliensis | 36% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 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 | 25% | 100% |
Q4Q6M3 | Leishmania major | 26% | 100% |
Q4Q6M4 | Leishmania major | 34% | 100% |
Q4Q9U3 | Leishmania major | 34% | 100% |
Q4QCS6 | Leishmania major | 36% | 100% |
Q4QCS7 | Leishmania major | 40% | 100% |
Q4QCS8 | Leishmania major | 91% | 100% |
Q4QCS9 | Leishmania major | 85% | 100% |
Q9U0T9 | Leishmania major | 41% | 100% |
V5AYJ1 | Trypanosoma cruzi | 30% | 100% |
V5B5I4 | Trypanosoma cruzi | 53% | 100% |
V5BA05 | Trypanosoma cruzi | 42% | 100% |
V5BEL3 | Trypanosoma cruzi | 36% | 100% |
V5BII7 | Trypanosoma cruzi | 29% | 76% |
V5BN20 | Trypanosoma cruzi | 35% | 100% |
V5D9Y2 | Trypanosoma cruzi | 41% | 100% |
V5DES7 | Trypanosoma cruzi | 32% | 100% |