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: 93 |
NetGPI | no | yes: 0, no: 95 |
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: Q4QCS9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 96 |
GO:0006807 | nitrogen compound metabolic process | 2 | 96 |
GO:0008152 | metabolic process | 1 | 96 |
GO:0019538 | protein metabolic process | 3 | 96 |
GO:0043170 | macromolecule metabolic process | 3 | 96 |
GO:0044238 | primary metabolic process | 2 | 96 |
GO:0071704 | organic substance metabolic process | 2 | 96 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 96 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 96 |
GO:0004175 | endopeptidase activity | 4 | 96 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 96 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 96 |
GO:0008233 | peptidase activity | 3 | 96 |
GO:0008234 | cysteine-type peptidase activity | 4 | 96 |
GO:0016787 | hydrolase activity | 2 | 96 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 96 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.789 |
CLV_C14_Caspase3-7 | 297 | 301 | PF00656 | 0.458 |
CLV_C14_Caspase3-7 | 459 | 463 | PF00656 | 0.574 |
CLV_C14_Caspase3-7 | 534 | 538 | PF00656 | 0.487 |
CLV_C14_Caspase3-7 | 773 | 777 | PF00656 | 0.576 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 777 | 779 | PF00675 | 0.225 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 830 | 832 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 930 | 932 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 960 | 962 | PF00082 | 0.329 |
CLV_PCSK_PC1ET2_1 | 830 | 832 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 930 | 932 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 960 | 962 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 587 | 591 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 872 | 876 | PF00082 | 0.495 |
DEG_SIAH_1 | 273 | 281 | PF03145 | 0.429 |
DOC_CKS1_1 | 23 | 28 | PF01111 | 0.545 |
DOC_PP1_RVXF_1 | 575 | 581 | PF00149 | 0.506 |
DOC_PP1_RVXF_1 | 733 | 740 | PF00149 | 0.565 |
DOC_PP4_FxxP_1 | 345 | 348 | PF00568 | 0.335 |
DOC_PP4_FxxP_1 | 478 | 481 | PF00568 | 0.559 |
DOC_PP4_FxxP_1 | 558 | 561 | PF00568 | 0.512 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.502 |
DOC_USP7_MATH_2 | 511 | 517 | PF00917 | 0.563 |
DOC_USP7_UBL2_3 | 621 | 625 | PF12436 | 0.512 |
DOC_USP7_UBL2_3 | 775 | 779 | PF12436 | 0.534 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.820 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 681 | 686 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 814 | 819 | PF00397 | 0.439 |
LIG_14-3-3_CanoR_1 | 283 | 289 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 440 | 448 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 577 | 581 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 867 | 876 | PF00244 | 0.567 |
LIG_Actin_WH2_2 | 588 | 605 | PF00022 | 0.592 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.551 |
LIG_BIR_III_2 | 751 | 755 | PF00653 | 0.420 |
LIG_BRCT_BRCA1_1 | 494 | 498 | PF00533 | 0.541 |
LIG_BRCT_BRCA1_1 | 925 | 929 | PF00533 | 0.580 |
LIG_Clathr_ClatBox_1 | 949 | 953 | PF01394 | 0.343 |
LIG_CtBP_PxDLS_1 | 511 | 515 | PF00389 | 0.422 |
LIG_deltaCOP1_diTrp_1 | 738 | 743 | PF00928 | 0.502 |
LIG_deltaCOP1_diTrp_1 | 871 | 875 | PF00928 | 0.456 |
LIG_eIF4E_1 | 700 | 706 | PF01652 | 0.524 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.622 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.370 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.505 |
LIG_FHA_1 | 801 | 807 | PF00498 | 0.457 |
LIG_FHA_1 | 820 | 826 | PF00498 | 0.458 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.807 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.440 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.614 |
LIG_FHA_2 | 710 | 716 | PF00498 | 0.518 |
LIG_LIR_Apic_2 | 343 | 348 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 620 | 631 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 646 | 653 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 664 | 675 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 698 | 706 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 819 | 825 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 870 | 881 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 9 | 20 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 361 | 365 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 495 | 501 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 592 | 597 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 613 | 618 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 620 | 626 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 629 | 633 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 664 | 670 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 698 | 703 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 819 | 824 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 838 | 842 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 852 | 858 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 870 | 876 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 926 | 932 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 940 | 945 | PF02991 | 0.604 |
LIG_PDZ_Class_3 | 971 | 976 | PF00595 | 0.336 |
LIG_Pex14_2 | 770 | 774 | PF04695 | 0.512 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.583 |
LIG_SH2_CRK | 623 | 627 | PF00017 | 0.505 |
LIG_SH2_CRK | 630 | 634 | PF00017 | 0.503 |
LIG_SH2_CRK | 678 | 682 | PF00017 | 0.515 |
LIG_SH2_CRK | 700 | 704 | PF00017 | 0.517 |
LIG_SH2_CRK | 839 | 843 | PF00017 | 0.428 |
LIG_SH2_CRK | 855 | 859 | PF00017 | 0.469 |
LIG_SH2_GRB2like | 436 | 439 | PF00017 | 0.596 |
LIG_SH2_GRB2like | 780 | 783 | PF00017 | 0.475 |
LIG_SH2_NCK_1 | 240 | 244 | PF00017 | 0.569 |
LIG_SH2_NCK_1 | 247 | 251 | PF00017 | 0.817 |
LIG_SH2_NCK_1 | 700 | 704 | PF00017 | 0.512 |
LIG_SH2_PTP2 | 892 | 895 | PF00017 | 0.426 |
LIG_SH2_SRC | 594 | 597 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 224 | 228 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.561 |
LIG_SH2_STAP1 | 371 | 375 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 604 | 608 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 794 | 798 | PF00017 | 0.380 |
LIG_SH2_STAT3 | 199 | 202 | PF00017 | 0.860 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.860 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 678 | 681 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 780 | 783 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 892 | 895 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 910 | 913 | PF00017 | 0.384 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.800 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.820 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.545 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.734 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.747 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.363 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.574 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.608 |
LIG_SH3_3 | 812 | 818 | PF00018 | 0.416 |
LIG_SH3_3 | 901 | 907 | PF00018 | 0.629 |
LIG_SH3_3 | 949 | 955 | PF00018 | 0.367 |
LIG_SH3_5 | 792 | 796 | PF00018 | 0.477 |
LIG_SUMO_SIM_anti_2 | 880 | 885 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 808 | 814 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 840 | 845 | PF11976 | 0.397 |
LIG_TRAF2_1 | 118 | 121 | PF00917 | 0.339 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.781 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.831 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.208 |
LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.200 |
LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.197 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.203 |
LIG_TRAF2_2 | 143 | 148 | PF00917 | 0.546 |
LIG_TRAF2_2 | 29 | 34 | PF00917 | 0.542 |
LIG_TYR_ITIM | 350 | 355 | PF00017 | 0.365 |
LIG_TYR_ITIM | 837 | 842 | PF00017 | 0.499 |
LIG_UBA3_1 | 350 | 358 | PF00899 | 0.381 |
LIG_UBA3_1 | 769 | 775 | PF00899 | 0.420 |
LIG_UBA3_1 | 883 | 891 | PF00899 | 0.478 |
LIG_WRPW_2 | 498 | 501 | PF00400 | 0.420 |
MOD_CDK_SPxK_1 | 681 | 687 | PF00069 | 0.518 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.732 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.574 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.749 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.507 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.471 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.518 |
MOD_CK2_1 | 709 | 715 | PF00069 | 0.565 |
MOD_CK2_1 | 842 | 848 | PF00069 | 0.435 |
MOD_CMANNOS | 771 | 774 | PF00535 | 0.305 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.636 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.616 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.341 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.385 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.308 |
MOD_GlcNHglycan | 738 | 742 | PF01048 | 0.372 |
MOD_GlcNHglycan | 807 | 810 | PF01048 | 0.545 |
MOD_GlcNHglycan | 861 | 864 | PF01048 | 0.455 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.504 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.573 |
MOD_GSK3_1 | 819 | 826 | PF00069 | 0.460 |
MOD_N-GLC_1 | 365 | 370 | PF02516 | 0.359 |
MOD_N-GLC_1 | 389 | 394 | PF02516 | 0.379 |
MOD_N-GLC_1 | 859 | 864 | PF02516 | 0.444 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.463 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.314 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.469 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.539 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.549 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.521 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.576 |
MOD_NEK2_1 | 770 | 775 | PF00069 | 0.508 |
MOD_NEK2_1 | 859 | 864 | PF00069 | 0.493 |
MOD_NEK2_2 | 647 | 652 | PF00069 | 0.594 |
MOD_NEK2_2 | 923 | 928 | PF00069 | 0.534 |
MOD_OFUCOSY | 337 | 344 | PF10250 | 0.229 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.768 |
MOD_PIKK_1 | 177 | 183 | PF00454 | 0.643 |
MOD_PIKK_1 | 513 | 519 | PF00454 | 0.578 |
MOD_PIKK_1 | 823 | 829 | PF00454 | 0.391 |
MOD_PIKK_1 | 967 | 973 | PF00454 | 0.354 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.549 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.491 |
MOD_PKA_2 | 866 | 872 | PF00069 | 0.561 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.621 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.377 |
MOD_Plk_1 | 388 | 394 | PF00069 | 0.345 |
MOD_Plk_1 | 653 | 659 | PF00069 | 0.550 |
MOD_Plk_1 | 879 | 885 | PF00069 | 0.404 |
MOD_Plk_1 | 923 | 929 | PF00069 | 0.545 |
MOD_Plk_2-3 | 655 | 661 | PF00069 | 0.604 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.613 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.519 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.544 |
MOD_Plk_4 | 676 | 682 | PF00069 | 0.619 |
MOD_Plk_4 | 709 | 715 | PF00069 | 0.526 |
MOD_Plk_4 | 879 | 885 | PF00069 | 0.459 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.819 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.552 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.546 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.659 |
MOD_ProDKin_1 | 681 | 687 | PF00069 | 0.520 |
MOD_ProDKin_1 | 814 | 820 | PF00069 | 0.443 |
MOD_SUMO_for_1 | 943 | 946 | PF00179 | 0.334 |
MOD_SUMO_rev_2 | 654 | 663 | PF00179 | 0.571 |
MOD_SUMO_rev_2 | 715 | 724 | PF00179 | 0.553 |
TRG_DiLeu_BaEn_2 | 410 | 416 | PF01217 | 0.298 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.826 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 623 | 626 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 630 | 633 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 678 | 681 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 700 | 703 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 711 | 714 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 839 | 842 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 855 | 858 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 892 | 895 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 280 | 283 | PF00400 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 441 | 445 | PF00026 | 0.614 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 34% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 29% | 99% |
A0A0N1IGQ2 | Leptomonas seymouri | 32% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 40% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 34% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 39% | 100% |
A0A0N1PCA9 | Leptomonas seymouri | 35% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 27% | 100% |
A0A0S4JLK6 | Bodo saltans | 27% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 28% | 80% |
A0A1X0NJK2 | Trypanosomatidae | 31% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 36% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 32% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 32% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 42% | 100% |
A0A1X0NW84 | Trypanosomatidae | 38% | 100% |
A0A1X0NW89 | Trypanosomatidae | 54% | 100% |
A0A1X0NWA6 | Trypanosomatidae | 30% | 100% |
A0A1X0NWW1 | Trypanosomatidae | 40% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 92% | 100% |
A0A3Q8IDD4 | Leishmania donovani | 33% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 26% | 100% |
A0A3S5H5A5 | Leishmania donovani | 41% | 100% |
A0A3S5ISG2 | Trypanosoma rangeli | 31% | 100% |
A0A3S7WW13 | Leishmania donovani | 27% | 88% |
A0A3S7WW18 | Leishmania donovani | 95% | 100% |
A0A3S7WW41 | Leishmania donovani | 35% | 100% |
A0A3S7WW71 | Leishmania donovani | 39% | 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 | 39% | 100% |
A4H3W4 | Leishmania braziliensis | 41% | 100% |
A4HE81 | Leishmania braziliensis | 33% | 100% |
A4HJ14 | Leishmania braziliensis | 34% | 100% |
A4HJ22 | Leishmania braziliensis | 32% | 100% |
A4HJ24 | Leishmania braziliensis | 34% | 100% |
A4HS39 | Leishmania infantum | 41% | 100% |
A4HYN0 | Leishmania infantum | 95% | 100% |
A4HYW1 | Leishmania infantum | 90% | 96% |
A4HYW2 | Leishmania infantum | 39% | 100% |
A4HYW3 | Leishmania infantum | 35% | 100% |
A4HYW4 | Leishmania infantum | 28% | 98% |
A4I1J4 | Leishmania infantum | 33% | 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) | 44% | 91% |
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% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 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 | 84% | 100% |
E9AIH3 | Leishmania braziliensis | 39% | 100% |
E9AIH4 | Leishmania braziliensis | 35% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 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) | 35% | 100% |
Q4Q6L7 | Leishmania major | 35% | 100% |
Q4Q6L9 | Leishmania major | 35% | 100% |
Q4Q6M0 | Leishmania major | 31% | 100% |
Q4Q6M2 | Leishmania major | 25% | 100% |
Q4Q6M3 | Leishmania major | 27% | 100% |
Q4Q6M4 | Leishmania major | 33% | 100% |
Q4Q9U3 | Leishmania major | 34% | 100% |
Q4QCS6 | Leishmania major | 35% | 100% |
Q4QCS7 | Leishmania major | 39% | 100% |
Q4QCS8 | Leishmania major | 100% | 100% |
Q9U0T9 | Leishmania major | 40% | 100% |
V5AYJ1 | Trypanosoma cruzi | 31% | 100% |
V5B5I4 | Trypanosoma cruzi | 50% | 100% |
V5BA05 | Trypanosoma cruzi | 41% | 100% |
V5BEL3 | Trypanosoma cruzi | 36% | 100% |
V5BII7 | Trypanosoma cruzi | 28% | 79% |
V5BN20 | Trypanosoma cruzi | 35% | 100% |
V5D9Y2 | Trypanosoma cruzi | 40% | 100% |
V5DES7 | Trypanosoma cruzi | 31% | 100% |