Proteases, calpain-like cysteine peptidase
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | yes | yes: 3 |
Forrest at al. (procyclic) | yes | 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: 85 |
NetGPI | no | yes: 0, no: 87 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005930 | axoneme | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
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 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HYW1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 88 |
GO:0006807 | nitrogen compound metabolic process | 2 | 88 |
GO:0008152 | metabolic process | 1 | 88 |
GO:0019538 | protein metabolic process | 3 | 88 |
GO:0043170 | macromolecule metabolic process | 3 | 88 |
GO:0044238 | primary metabolic process | 2 | 88 |
GO:0071704 | organic substance metabolic process | 2 | 88 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 88 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 88 |
GO:0004175 | endopeptidase activity | 4 | 88 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 88 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 88 |
GO:0008233 | peptidase activity | 3 | 88 |
GO:0008234 | cysteine-type peptidase activity | 4 | 88 |
GO:0016787 | hydrolase activity | 2 | 88 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 88 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 334 | 338 | PF00656 | 0.731 |
CLV_C14_Caspase3-7 | 496 | 500 | PF00656 | 0.585 |
CLV_C14_Caspase3-7 | 571 | 575 | PF00656 | 0.552 |
CLV_C14_Caspase3-7 | 810 | 814 | PF00656 | 0.657 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 814 | 816 | PF00675 | 0.458 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 867 | 869 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 967 | 969 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 997 | 999 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 867 | 869 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 967 | 969 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 997 | 999 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 640 | 644 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 762 | 766 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 909 | 913 | PF00082 | 0.512 |
DEG_SCF_FBW7_2 | 349 | 354 | PF00400 | 0.591 |
DEG_SIAH_1 | 310 | 318 | PF03145 | 0.476 |
DOC_CKS1_1 | 26 | 31 | PF01111 | 0.594 |
DOC_PP1_RVXF_1 | 612 | 618 | PF00149 | 0.549 |
DOC_PP1_RVXF_1 | 770 | 777 | PF00149 | 0.624 |
DOC_PP4_FxxP_1 | 382 | 385 | PF00568 | 0.383 |
DOC_PP4_FxxP_1 | 515 | 518 | PF00568 | 0.636 |
DOC_PP4_FxxP_1 | 595 | 598 | PF00568 | 0.566 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.569 |
DOC_USP7_MATH_2 | 548 | 554 | PF00917 | 0.599 |
DOC_USP7_UBL2_3 | 658 | 662 | PF12436 | 0.567 |
DOC_USP7_UBL2_3 | 812 | 816 | PF12436 | 0.563 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.834 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.853 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.831 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.827 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 718 | 723 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 851 | 856 | PF00397 | 0.475 |
LIG_14-3-3_CanoR_1 | 320 | 326 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 477 | 485 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 614 | 618 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 904 | 913 | PF00244 | 0.560 |
LIG_Actin_WH2_2 | 450 | 467 | PF00022 | 0.385 |
LIG_Actin_WH2_2 | 625 | 642 | PF00022 | 0.631 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.608 |
LIG_BIR_III_2 | 788 | 792 | PF00653 | 0.469 |
LIG_BRCT_BRCA1_1 | 962 | 966 | PF00533 | 0.540 |
LIG_Clathr_ClatBox_1 | 986 | 990 | PF01394 | 0.391 |
LIG_CtBP_PxDLS_1 | 548 | 552 | PF00389 | 0.472 |
LIG_deltaCOP1_diTrp_1 | 775 | 780 | PF00928 | 0.554 |
LIG_deltaCOP1_diTrp_1 | 908 | 912 | PF00928 | 0.483 |
LIG_eIF4E_1 | 737 | 743 | PF01652 | 0.571 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.669 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.426 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.591 |
LIG_FHA_1 | 838 | 844 | PF00498 | 0.536 |
LIG_FHA_1 | 857 | 863 | PF00498 | 0.513 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.558 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.479 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.565 |
LIG_FHA_2 | 747 | 753 | PF00498 | 0.540 |
LIG_FHA_2 | 783 | 789 | PF00498 | 0.620 |
LIG_LIR_Apic_2 | 380 | 385 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 657 | 668 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 683 | 690 | PF02991 | 0.603 |
LIG_LIR_Gen_1 | 701 | 712 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 735 | 743 | PF02991 | 0.616 |
LIG_LIR_Gen_1 | 856 | 862 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 9 | 20 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 907 | 918 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 398 | 402 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 629 | 634 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 650 | 655 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 657 | 663 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 666 | 670 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 701 | 707 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 735 | 740 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 856 | 861 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 874 | 879 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 890 | 895 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 907 | 913 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 963 | 969 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 977 | 982 | PF02991 | 0.559 |
LIG_Pex14_2 | 807 | 811 | PF04695 | 0.576 |
LIG_SH2_CRK | 279 | 283 | PF00017 | 0.800 |
LIG_SH2_CRK | 660 | 664 | PF00017 | 0.566 |
LIG_SH2_CRK | 667 | 671 | PF00017 | 0.556 |
LIG_SH2_CRK | 715 | 719 | PF00017 | 0.569 |
LIG_SH2_CRK | 737 | 741 | PF00017 | 0.548 |
LIG_SH2_CRK | 876 | 880 | PF00017 | 0.482 |
LIG_SH2_CRK | 892 | 896 | PF00017 | 0.534 |
LIG_SH2_GRB2like | 473 | 476 | PF00017 | 0.630 |
LIG_SH2_GRB2like | 817 | 820 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 279 | 283 | PF00017 | 0.598 |
LIG_SH2_NCK_1 | 286 | 290 | PF00017 | 0.594 |
LIG_SH2_NCK_1 | 737 | 741 | PF00017 | 0.606 |
LIG_SH2_PTP2 | 929 | 932 | PF00017 | 0.491 |
LIG_SH2_SRC | 631 | 634 | PF00017 | 0.579 |
LIG_SH2_STAP1 | 286 | 290 | PF00017 | 0.812 |
LIG_SH2_STAP1 | 408 | 412 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 641 | 645 | PF00017 | 0.610 |
LIG_SH2_STAP1 | 831 | 835 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 715 | 718 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 748 | 751 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 817 | 820 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 929 | 932 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 947 | 950 | PF00017 | 0.453 |
LIG_SH3_1 | 23 | 29 | PF00018 | 0.593 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.765 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.820 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.819 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.420 |
LIG_SH3_3 | 515 | 521 | PF00018 | 0.609 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.644 |
LIG_SH3_3 | 849 | 855 | PF00018 | 0.461 |
LIG_SH3_3 | 938 | 944 | PF00018 | 0.680 |
LIG_SH3_3 | 986 | 992 | PF00018 | 0.548 |
LIG_SH3_5 | 829 | 833 | PF00018 | 0.533 |
LIG_SUMO_SIM_anti_2 | 917 | 922 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 845 | 851 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 877 | 882 | PF11976 | 0.469 |
LIG_TRAF2_1 | 105 | 108 | PF00917 | 0.248 |
LIG_TRAF2_1 | 118 | 121 | PF00917 | 0.248 |
LIG_TRAF2_1 | 131 | 134 | PF00917 | 0.245 |
LIG_TRAF2_1 | 144 | 147 | PF00917 | 0.341 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.391 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.329 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.807 |
LIG_TRAF2_1 | 197 | 200 | PF00917 | 0.796 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.868 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.825 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.597 |
LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.586 |
LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.584 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.594 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.247 |
LIG_TRAF2_2 | 182 | 187 | PF00917 | 0.603 |
LIG_TRAF2_2 | 29 | 34 | PF00917 | 0.602 |
LIG_TYR_ITIM | 387 | 392 | PF00017 | 0.413 |
LIG_UBA3_1 | 387 | 395 | PF00899 | 0.433 |
LIG_UBA3_1 | 806 | 812 | PF00899 | 0.469 |
LIG_UBA3_1 | 920 | 928 | PF00899 | 0.554 |
LIG_WRPW_2 | 535 | 538 | PF00400 | 0.469 |
MOD_CDK_SPxK_1 | 718 | 724 | PF00069 | 0.566 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.619 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.784 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.551 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.544 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.569 |
MOD_CK2_1 | 746 | 752 | PF00069 | 0.631 |
MOD_CK2_1 | 879 | 885 | PF00069 | 0.510 |
MOD_CMANNOS | 808 | 811 | PF00535 | 0.358 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.678 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.556 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.390 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.403 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.351 |
MOD_GlcNHglycan | 775 | 779 | PF01048 | 0.412 |
MOD_GlcNHglycan | 844 | 847 | PF01048 | 0.600 |
MOD_GlcNHglycan | 898 | 901 | PF01048 | 0.505 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.540 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.569 |
MOD_GSK3_1 | 713 | 720 | PF00069 | 0.594 |
MOD_GSK3_1 | 856 | 863 | PF00069 | 0.504 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.653 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.419 |
MOD_N-GLC_1 | 426 | 431 | PF02516 | 0.441 |
MOD_N-GLC_1 | 871 | 876 | PF02516 | 0.400 |
MOD_N-GLC_1 | 896 | 901 | PF02516 | 0.519 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.810 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.603 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.370 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.508 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.611 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.594 |
MOD_NEK2_1 | 663 | 668 | PF00069 | 0.566 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.651 |
MOD_NEK2_1 | 807 | 812 | PF00069 | 0.566 |
MOD_NEK2_1 | 896 | 901 | PF00069 | 0.514 |
MOD_NEK2_2 | 684 | 689 | PF00069 | 0.635 |
MOD_NEK2_2 | 960 | 965 | PF00069 | 0.358 |
MOD_OFUCOSY | 374 | 381 | PF10250 | 0.279 |
MOD_PIKK_1 | 1004 | 1010 | PF00454 | 0.619 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.607 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.586 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.619 |
MOD_PIKK_1 | 860 | 866 | PF00454 | 0.464 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.544 |
MOD_PKA_2 | 903 | 909 | PF00069 | 0.608 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.654 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.429 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.428 |
MOD_Plk_1 | 690 | 696 | PF00069 | 0.619 |
MOD_Plk_1 | 916 | 922 | PF00069 | 0.450 |
MOD_Plk_1 | 960 | 966 | PF00069 | 0.520 |
MOD_Plk_2-3 | 187 | 193 | PF00069 | 0.862 |
MOD_Plk_2-3 | 692 | 698 | PF00069 | 0.645 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.687 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.580 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.595 |
MOD_Plk_4 | 713 | 719 | PF00069 | 0.612 |
MOD_Plk_4 | 746 | 752 | PF00069 | 0.580 |
MOD_Plk_4 | 916 | 922 | PF00069 | 0.514 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.833 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.854 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.830 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.817 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.557 |
MOD_ProDKin_1 | 718 | 724 | PF00069 | 0.570 |
MOD_ProDKin_1 | 851 | 857 | PF00069 | 0.479 |
MOD_SUMO_for_1 | 980 | 983 | PF00179 | 0.527 |
MOD_SUMO_rev_2 | 187 | 194 | PF00179 | 0.699 |
MOD_SUMO_rev_2 | 691 | 700 | PF00179 | 0.640 |
MOD_SUMO_rev_2 | 752 | 761 | PF00179 | 0.591 |
MOD_SUMO_rev_2 | 874 | 879 | PF00179 | 0.649 |
TRG_DiLeu_BaEn_2 | 447 | 453 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.830 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 631 | 634 | PF00928 | 0.584 |
TRG_ENDOCYTIC_2 | 660 | 663 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 667 | 670 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 715 | 718 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 737 | 740 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 748 | 751 | PF00928 | 0.601 |
TRG_ENDOCYTIC_2 | 876 | 879 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 892 | 895 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 929 | 932 | PF00928 | 0.412 |
TRG_ER_diArg_1 | 317 | 320 | PF00400 | 0.673 |
TRG_Pf-PMV_PEXEL_1 | 478 | 482 | PF00026 | 0.648 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1W0 | Leptomonas seymouri | 26% | 68% |
A0A0N1I8N2 | Leptomonas seymouri | 29% | 100% |
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% |
A0A0S4JLK6 | Bodo saltans | 28% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 28% | 83% |
A0A1X0NJK2 | Trypanosomatidae | 31% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 36% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 32% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 41% | 100% |
A0A1X0NW89 | Trypanosomatidae | 55% | 100% |
A0A1X0NWA6 | Trypanosomatidae | 30% | 100% |
A0A1X0NWW1 | Trypanosomatidae | 40% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 97% | 100% |
A0A3Q8IDD4 | Leishmania donovani | 34% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 26% | 100% |
A0A3S5H5A5 | Leishmania donovani | 41% | 100% |
A0A3S7WW13 | Leishmania donovani | 27% | 92% |
A0A3S7WW18 | Leishmania donovani | 99% | 100% |
A0A3S7WW41 | Leishmania donovani | 35% | 100% |
A0A3S7WW71 | Leishmania donovani | 40% | 100% |
A0A3S7X430 | Leishmania donovani | 34% | 100% |
A0A3S7X438 | Leishmania donovani | 30% | 100% |
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 | 41% | 100% |
A4HE81 | Leishmania braziliensis | 33% | 100% |
A4HJ14 | Leishmania braziliensis | 34% | 100% |
A4HJ15 | Leishmania braziliensis | 26% | 68% |
A4HJ22 | Leishmania braziliensis | 32% | 100% |
A4HJ24 | Leishmania braziliensis | 34% | 100% |
A4HS39 | Leishmania infantum | 41% | 100% |
A4HYN0 | Leishmania infantum | 99% | 100% |
A4HYW2 | Leishmania infantum | 40% | 100% |
A4HYW3 | Leishmania infantum | 36% | 100% |
A4HYW4 | Leishmania infantum | 27% | 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 | 27% | 100% |
A4I6K6 | Leishmania infantum | 26% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 94% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 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) | 90% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 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) | 35% | 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 | 90% | 96% |
Q9U0T9 | Leishmania major | 41% | 100% |
V5B5I4 | Trypanosoma cruzi | 54% | 100% |
V5BII7 | Trypanosoma cruzi | 29% | 82% |
V5D9Y2 | Trypanosoma cruzi | 41% | 100% |