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. | yes | 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: 103 |
NetGPI | no | yes: 0, no: 105 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
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:0005930 | axoneme | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4QCS8
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 106 |
GO:0006807 | nitrogen compound metabolic process | 2 | 106 |
GO:0008152 | metabolic process | 1 | 106 |
GO:0019538 | protein metabolic process | 3 | 106 |
GO:0043170 | macromolecule metabolic process | 3 | 106 |
GO:0044238 | primary metabolic process | 2 | 106 |
GO:0071704 | organic substance metabolic process | 2 | 106 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 106 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 106 |
GO:0004175 | endopeptidase activity | 4 | 106 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 106 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 106 |
GO:0008233 | peptidase activity | 3 | 106 |
GO:0008234 | cysteine-type peptidase activity | 4 | 106 |
GO:0016787 | hydrolase activity | 2 | 106 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 106 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 143 | 147 | PF00656 | 0.483 |
CLV_C14_Caspase3-7 | 305 | 309 | PF00656 | 0.560 |
CLV_C14_Caspase3-7 | 380 | 384 | PF00656 | 0.521 |
CLV_C14_Caspase3-7 | 619 | 623 | PF00656 | 0.598 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.464 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 676 | 678 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 776 | 778 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 806 | 808 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 676 | 678 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 776 | 778 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 806 | 808 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 718 | 722 | PF00082 | 0.525 |
DEG_SIAH_1 | 119 | 127 | PF03145 | 0.441 |
DOC_PP1_RVXF_1 | 421 | 427 | PF00149 | 0.549 |
DOC_PP1_RVXF_1 | 579 | 586 | PF00149 | 0.608 |
DOC_PP4_FxxP_1 | 191 | 194 | PF00568 | 0.368 |
DOC_PP4_FxxP_1 | 324 | 327 | PF00568 | 0.592 |
DOC_PP4_FxxP_1 | 404 | 407 | PF00568 | 0.553 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.550 |
DOC_USP7_MATH_2 | 357 | 363 | PF00917 | 0.604 |
DOC_USP7_UBL2_3 | 467 | 471 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 621 | 625 | PF12436 | 0.576 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.851 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 660 | 665 | PF00397 | 0.470 |
LIG_14-3-3_CanoR_1 | 129 | 135 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 286 | 294 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 423 | 427 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 713 | 722 | PF00244 | 0.597 |
LIG_Actin_WH2_2 | 434 | 451 | PF00022 | 0.631 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.892 |
LIG_BIR_III_2 | 597 | 601 | PF00653 | 0.450 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.583 |
LIG_BRCT_BRCA1_1 | 771 | 775 | PF00533 | 0.542 |
LIG_Clathr_ClatBox_1 | 795 | 799 | PF01394 | 0.632 |
LIG_CtBP_PxDLS_1 | 357 | 361 | PF00389 | 0.453 |
LIG_deltaCOP1_diTrp_1 | 584 | 589 | PF00928 | 0.544 |
LIG_deltaCOP1_diTrp_1 | 717 | 721 | PF00928 | 0.503 |
LIG_eIF4E_1 | 546 | 552 | PF01652 | 0.567 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.653 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.406 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.548 |
LIG_FHA_1 | 647 | 653 | PF00498 | 0.499 |
LIG_FHA_1 | 666 | 672 | PF00498 | 0.515 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.484 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.568 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.890 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.561 |
LIG_LIR_Apic_2 | 189 | 194 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 466 | 477 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 492 | 499 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 510 | 521 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 544 | 552 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 665 | 671 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 716 | 727 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 466 | 472 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 475 | 479 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 510 | 516 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 544 | 549 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 665 | 670 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 684 | 688 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 698 | 704 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 716 | 722 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 772 | 778 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 786 | 791 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 9 | 13 | PF02991 | 0.576 |
LIG_Pex14_2 | 616 | 620 | PF04695 | 0.546 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.543 |
LIG_SH2_CRK | 476 | 480 | PF00017 | 0.543 |
LIG_SH2_CRK | 524 | 528 | PF00017 | 0.565 |
LIG_SH2_CRK | 546 | 550 | PF00017 | 0.548 |
LIG_SH2_CRK | 685 | 689 | PF00017 | 0.467 |
LIG_SH2_CRK | 701 | 705 | PF00017 | 0.549 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.859 |
LIG_SH2_GRB2like | 282 | 285 | PF00017 | 0.596 |
LIG_SH2_GRB2like | 626 | 629 | PF00017 | 0.512 |
LIG_SH2_NCK_1 | 546 | 550 | PF00017 | 0.563 |
LIG_SH2_NCK_1 | 86 | 90 | PF00017 | 0.592 |
LIG_SH2_NCK_1 | 93 | 97 | PF00017 | 0.585 |
LIG_SH2_PTP2 | 738 | 741 | PF00017 | 0.457 |
LIG_SH2_SRC | 440 | 443 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 450 | 454 | PF00017 | 0.579 |
LIG_SH2_STAP1 | 640 | 644 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.913 |
LIG_SH2_STAP1 | 93 | 97 | PF00017 | 0.585 |
LIG_SH2_STAT3 | 45 | 48 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 738 | 741 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 756 | 759 | PF00017 | 0.424 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.737 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.391 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.591 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.619 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.783 |
LIG_SH3_3 | 658 | 664 | PF00018 | 0.448 |
LIG_SH3_3 | 747 | 753 | PF00018 | 0.668 |
LIG_SH3_3 | 795 | 801 | PF00018 | 0.530 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.771 |
LIG_SH3_5 | 638 | 642 | PF00018 | 0.497 |
LIG_SUMO_SIM_anti_2 | 726 | 731 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 654 | 660 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 686 | 691 | PF11976 | 0.445 |
LIG_TRAF2_1 | 69 | 72 | PF00917 | 0.901 |
LIG_TYR_ITIM | 196 | 201 | PF00017 | 0.406 |
LIG_TYR_ITIM | 683 | 688 | PF00017 | 0.545 |
LIG_UBA3_1 | 196 | 204 | PF00899 | 0.423 |
LIG_UBA3_1 | 615 | 621 | PF00899 | 0.450 |
LIG_UBA3_1 | 729 | 737 | PF00899 | 0.521 |
LIG_WRPW_2 | 344 | 347 | PF00400 | 0.450 |
MOD_CDK_SPxK_1 | 527 | 533 | PF00069 | 0.560 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.567 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.558 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.558 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.791 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.539 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.606 |
MOD_CK2_1 | 688 | 694 | PF00069 | 0.467 |
MOD_CMANNOS | 617 | 620 | PF00535 | 0.345 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.635 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.608 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.370 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.412 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.342 |
MOD_GlcNHglycan | 584 | 588 | PF01048 | 0.399 |
MOD_GlcNHglycan | 653 | 656 | PF01048 | 0.564 |
MOD_GlcNHglycan | 707 | 710 | PF01048 | 0.498 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.543 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.553 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.503 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.392 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.410 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.776 |
MOD_N-GLC_1 | 705 | 710 | PF02516 | 0.467 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.572 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.349 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.464 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.566 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.579 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.552 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.610 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.545 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.487 |
MOD_NEK2_2 | 493 | 498 | PF00069 | 0.633 |
MOD_NEK2_2 | 769 | 774 | PF00069 | 0.629 |
MOD_OFUCOSY | 183 | 190 | PF10250 | 0.260 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.611 |
MOD_PIKK_1 | 669 | 675 | PF00454 | 0.432 |
MOD_PIKK_1 | 813 | 819 | PF00454 | 0.600 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.530 |
MOD_PKA_2 | 712 | 718 | PF00069 | 0.611 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.656 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.400 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.361 |
MOD_Plk_1 | 499 | 505 | PF00069 | 0.579 |
MOD_Plk_1 | 725 | 731 | PF00069 | 0.442 |
MOD_Plk_1 | 769 | 775 | PF00069 | 0.512 |
MOD_Plk_2-3 | 501 | 507 | PF00069 | 0.594 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.658 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.781 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.549 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.579 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.609 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.566 |
MOD_Plk_4 | 725 | 731 | PF00069 | 0.494 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.682 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.852 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.554 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.472 |
MOD_SUMO_for_1 | 789 | 792 | PF00179 | 0.504 |
MOD_SUMO_rev_2 | 500 | 509 | PF00179 | 0.551 |
MOD_SUMO_rev_2 | 561 | 570 | PF00179 | 0.594 |
TRG_DiLeu_BaEn_2 | 256 | 262 | PF01217 | 0.326 |
TRG_DiLeu_BaEn_4 | 15 | 21 | PF01217 | 0.581 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 557 | 560 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 685 | 688 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 701 | 704 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 738 | 741 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.881 |
TRG_ER_diArg_1 | 126 | 129 | PF00400 | 0.732 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.864 |
TRG_Pf-PMV_PEXEL_1 | 287 | 291 | PF00026 | 0.632 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 34% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 29% | 84% |
A0A0N1IGQ2 | Leptomonas seymouri | 32% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 40% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 33% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 40% | 96% |
A0A0N1PCA9 | Leptomonas seymouri | 35% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 28% | 92% |
A0A0N1PFI4 | Leptomonas seymouri | 35% | 100% |
A0A0S4JLK6 | Bodo saltans | 27% | 100% |
A0A0S4JS70 | Bodo saltans | 25% | 100% |
A0A0S4KGT2 | Bodo saltans | 40% | 100% |
A0A0S4KKP7 | Bodo saltans | 24% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 28% | 67% |
A0A1X0NJK2 | Trypanosomatidae | 31% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 36% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 32% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 32% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 42% | 97% |
A0A1X0NW84 | Trypanosomatidae | 39% | 100% |
A0A1X0NW85 | Trypanosomatidae | 39% | 100% |
A0A1X0NW89 | Trypanosomatidae | 54% | 95% |
A0A1X0NWA6 | Trypanosomatidae | 30% | 94% |
A0A1X0NWW1 | Trypanosomatidae | 40% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 95% | 90% |
A0A3Q8IDD4 | Leishmania donovani | 33% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 25% | 100% |
A0A3S5H5A5 | Leishmania donovani | 41% | 96% |
A0A3S5ISG2 | Trypanosoma rangeli | 31% | 100% |
A0A3S7WW13 | Leishmania donovani | 27% | 74% |
A0A3S7WW18 | Leishmania donovani | 95% | 100% |
A0A3S7WW41 | Leishmania donovani | 35% | 100% |
A0A3S7WW71 | Leishmania donovani | 39% | 100% |
A0A3S7X430 | Leishmania donovani | 33% | 100% |
A0A3S7X438 | Leishmania donovani | 30% | 88% |
A0A3S7X460 | Leishmania donovani | 35% | 100% |
A0A3S7X463 | Leishmania donovani | 27% | 88% |
A0A3S7X470 | Leishmania donovani | 35% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 52% | 89% |
A0A422MYX0 | Trypanosoma rangeli | 39% | 100% |
A4H3W4 | Leishmania braziliensis | 40% | 96% |
A4HE81 | Leishmania braziliensis | 34% | 100% |
A4HJ14 | Leishmania braziliensis | 34% | 100% |
A4HJ22 | Leishmania braziliensis | 32% | 87% |
A4HJ24 | Leishmania braziliensis | 34% | 100% |
A4HS39 | Leishmania infantum | 41% | 96% |
A4HYN0 | Leishmania infantum | 95% | 100% |
A4HYW1 | Leishmania infantum | 95% | 81% |
A4HYW2 | Leishmania infantum | 39% | 100% |
A4HYW3 | Leishmania infantum | 35% | 100% |
A4HYW4 | Leishmania infantum | 28% | 82% |
A4I1J4 | Leishmania infantum | 33% | 100% |
A4I6E4 | Leishmania infantum | 35% | 100% |
A4I6E6 | Leishmania infantum | 35% | 100% |
A4I6F0 | Leishmania infantum | 30% | 88% |
A4I6K4 | Leishmania infantum | 33% | 100% |
A4I6K5 | Leishmania infantum | 27% | 88% |
A4I6K6 | Leishmania infantum | 25% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 76% |
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) | 31% | 96% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 96% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 87% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AIH1 | Leishmania braziliensis | 83% | 100% |
E9AIH3 | Leishmania braziliensis | 39% | 100% |
E9AIH4 | Leishmania braziliensis | 35% | 100% |
E9AIH6 | Leishmania braziliensis | 28% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 88% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 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% | 88% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 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 | 27% | 100% |
Q4Q6M4 | Leishmania major | 33% | 100% |
Q4Q9U3 | Leishmania major | 34% | 100% |
Q4QCS6 | Leishmania major | 35% | 100% |
Q4QCS7 | Leishmania major | 39% | 100% |
Q4QCS9 | Leishmania major | 100% | 100% |
Q9U0T9 | Leishmania major | 41% | 96% |
V5AYJ1 | Trypanosoma cruzi | 31% | 100% |
V5B5I4 | Trypanosoma cruzi | 49% | 98% |
V5BA05 | Trypanosoma cruzi | 41% | 100% |
V5BEL3 | Trypanosoma cruzi | 36% | 100% |
V5BII7 | Trypanosoma cruzi | 29% | 67% |
V5BN20 | Trypanosoma cruzi | 35% | 100% |
V5D9Y2 | Trypanosoma cruzi | 40% | 97% |
V5DES7 | Trypanosoma cruzi | 31% | 100% |