Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | yes | yes: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IJ90
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0019538 | protein metabolic process | 3 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
GO:0016579 | protein deubiquitination | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0070646 | protein modification by small protein removal | 5 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0005488 | binding | 1 | 11 |
GO:0008233 | peptidase activity | 3 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
GO:0004843 | cysteine-type deubiquitinase activity | 5 | 1 |
GO:0008234 | cysteine-type peptidase activity | 4 | 1 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 1 |
GO:0101005 | deubiquitinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.507 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.469 |
CLV_PCSK_FUR_1 | 153 | 157 | PF00082 | 0.664 |
CLV_PCSK_FUR_1 | 566 | 570 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.870 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.630 |
CLV_PCSK_PC1ET2_1 | 388 | 390 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 565 | 567 | PF00082 | 0.673 |
CLV_PCSK_PC1ET2_1 | 568 | 570 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.796 |
DEG_APCC_DBOX_1 | 220 | 228 | PF00400 | 0.593 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.657 |
DEG_SCF_FBW7_2 | 226 | 233 | PF00400 | 0.578 |
DEG_SCF_TRCP1_1 | 578 | 584 | PF00400 | 0.707 |
DEG_SPOP_SBC_1 | 146 | 150 | PF00917 | 0.717 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.739 |
DEG_SPOP_SBC_1 | 33 | 37 | PF00917 | 0.863 |
DOC_CKS1_1 | 227 | 232 | PF01111 | 0.603 |
DOC_CKS1_1 | 301 | 306 | PF01111 | 0.505 |
DOC_CKS1_1 | 95 | 100 | PF01111 | 0.476 |
DOC_CYCLIN_RxL_1 | 605 | 614 | PF00134 | 0.635 |
DOC_CYCLIN_yCln2_LP_2 | 612 | 618 | PF00134 | 0.648 |
DOC_MAPK_gen_1 | 478 | 486 | PF00069 | 0.638 |
DOC_MAPK_gen_1 | 49 | 58 | PF00069 | 0.598 |
DOC_MAPK_gen_1 | 69 | 78 | PF00069 | 0.497 |
DOC_MAPK_HePTP_8 | 68 | 80 | PF00069 | 0.600 |
DOC_MAPK_MEF2A_6 | 478 | 486 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 71 | 80 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 84 | 92 | PF00069 | 0.436 |
DOC_MIT_MIM_1 | 387 | 397 | PF04212 | 0.613 |
DOC_PIKK_1 | 369 | 377 | PF02985 | 0.595 |
DOC_PP1_RVXF_1 | 55 | 61 | PF00149 | 0.620 |
DOC_PP2B_LxvP_1 | 90 | 93 | PF13499 | 0.547 |
DOC_PP4_FxxP_1 | 207 | 210 | PF00568 | 0.644 |
DOC_PP4_FxxP_1 | 420 | 423 | PF00568 | 0.575 |
DOC_PP4_FxxP_1 | 448 | 451 | PF00568 | 0.503 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.826 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 585 | 589 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.879 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.792 |
DOC_USP7_UBL2_3 | 335 | 339 | PF12436 | 0.709 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.836 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 535 | 540 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.801 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 667 | 672 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.463 |
LIG_14-3-3_CanoR_1 | 100 | 108 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 162 | 170 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 221 | 225 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 264 | 273 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 49 | 58 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 505 | 510 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 569 | 576 | PF00244 | 0.780 |
LIG_14-3-3_CanoR_1 | 619 | 627 | PF00244 | 0.771 |
LIG_14-3-3_CanoR_1 | 648 | 657 | PF00244 | 0.784 |
LIG_14-3-3_CanoR_1 | 84 | 88 | PF00244 | 0.577 |
LIG_deltaCOP1_diTrp_1 | 492 | 498 | PF00928 | 0.587 |
LIG_eIF4E_1 | 527 | 533 | PF01652 | 0.477 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.748 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.592 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.878 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.784 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.646 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.510 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.592 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.637 |
LIG_FHA_2 | 523 | 529 | PF00498 | 0.569 |
LIG_GSK3_LRP6_1 | 667 | 673 | PF00069 | 0.740 |
LIG_IRF3_LxIS_1 | 394 | 400 | PF10401 | 0.596 |
LIG_LIR_Apic_2 | 184 | 189 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 104 | 114 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 441 | 452 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 492 | 498 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 601 | 611 | PF02991 | 0.712 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.703 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 453 | 457 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 492 | 497 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 525 | 530 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 531 | 536 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 601 | 606 | PF02991 | 0.712 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.503 |
LIG_NRBOX | 3 | 9 | PF00104 | 0.563 |
LIG_NRBOX | 554 | 560 | PF00104 | 0.640 |
LIG_PCNA_yPIPBox_3 | 180 | 194 | PF02747 | 0.588 |
LIG_PDZ_Class_2 | 675 | 680 | PF00595 | 0.710 |
LIG_Pex14_1 | 494 | 498 | PF04695 | 0.544 |
LIG_PTB_Apo_2 | 414 | 421 | PF02174 | 0.575 |
LIG_SH2_CRK | 444 | 448 | PF00017 | 0.559 |
LIG_SH2_NCK_1 | 301 | 305 | PF00017 | 0.616 |
LIG_SH2_NCK_1 | 542 | 546 | PF00017 | 0.471 |
LIG_SH2_SRC | 542 | 545 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 444 | 448 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.499 |
LIG_SH3_1 | 665 | 671 | PF00018 | 0.838 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.612 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.535 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.597 |
LIG_SH3_3 | 604 | 610 | PF00018 | 0.748 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.709 |
LIG_SH3_3 | 639 | 645 | PF00018 | 0.796 |
LIG_SH3_3 | 660 | 666 | PF00018 | 0.790 |
LIG_SUMO_SIM_anti_2 | 86 | 92 | PF11976 | 0.544 |
LIG_TRAF2_1 | 373 | 376 | PF00917 | 0.659 |
LIG_TRAF2_1 | 489 | 492 | PF00917 | 0.647 |
LIG_TYR_ITIM | 540 | 545 | PF00017 | 0.455 |
LIG_TYR_ITSM | 523 | 530 | PF00017 | 0.554 |
LIG_WRC_WIRS_1 | 182 | 187 | PF05994 | 0.573 |
LIG_WRC_WIRS_1 | 190 | 195 | PF05994 | 0.617 |
MOD_CDC14_SPxK_1 | 66 | 69 | PF00782 | 0.582 |
MOD_CDK_SPxK_1 | 63 | 69 | PF00069 | 0.575 |
MOD_CDK_SPxK_1 | 94 | 100 | PF00069 | 0.456 |
MOD_CDK_SPxxK_3 | 94 | 101 | PF00069 | 0.456 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.693 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.704 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.690 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.498 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.583 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.387 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.834 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.758 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.721 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.841 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.544 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.550 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.526 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.594 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.808 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.784 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.780 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.706 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.780 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.731 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.674 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.733 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.590 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.745 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.808 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.781 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.617 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.716 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.692 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.758 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.751 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.695 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.584 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.784 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.770 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.875 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.714 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.827 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.817 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.725 |
MOD_LATS_1 | 343 | 349 | PF00433 | 0.658 |
MOD_N-GLC_1 | 569 | 574 | PF02516 | 0.743 |
MOD_N-GLC_1 | 601 | 606 | PF02516 | 0.712 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.556 |
MOD_N-GLC_1 | 637 | 642 | PF02516 | 0.837 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.812 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.746 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.706 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.596 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.506 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.653 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.589 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.713 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.463 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.583 |
MOD_PK_1 | 118 | 124 | PF00069 | 0.590 |
MOD_PKA_1 | 100 | 106 | PF00069 | 0.502 |
MOD_PKA_1 | 333 | 339 | PF00069 | 0.616 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.502 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.593 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.636 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.870 |
MOD_PKA_2 | 620 | 626 | PF00069 | 0.901 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.562 |
MOD_PKB_1 | 646 | 654 | PF00069 | 0.826 |
MOD_Plk_1 | 601 | 607 | PF00069 | 0.750 |
MOD_Plk_2-3 | 370 | 376 | PF00069 | 0.559 |
MOD_Plk_2-3 | 463 | 469 | PF00069 | 0.520 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.697 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.650 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.642 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.582 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.564 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.583 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.675 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.837 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.541 |
MOD_ProDKin_1 | 535 | 541 | PF00069 | 0.582 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.495 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.809 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.575 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.763 |
MOD_ProDKin_1 | 667 | 673 | PF00069 | 0.795 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.456 |
TRG_DiLeu_BaEn_1 | 159 | 164 | PF01217 | 0.664 |
TRG_DiLeu_BaEn_2 | 202 | 208 | PF01217 | 0.674 |
TRG_DiLeu_BaEn_4 | 159 | 165 | PF01217 | 0.753 |
TRG_DiLeu_BaLyEn_6 | 386 | 391 | PF01217 | 0.621 |
TRG_DiLeu_BaLyEn_6 | 607 | 612 | PF01217 | 0.628 |
TRG_DiLeu_LyEn_5 | 159 | 164 | PF01217 | 0.664 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.675 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.625 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.545 |
TRG_ER_diArg_1 | 152 | 155 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.737 |
TRG_ER_diArg_1 | 618 | 621 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 645 | 648 | PF00400 | 0.789 |
TRG_NLS_MonoExtC_3 | 564 | 569 | PF00514 | 0.623 |
TRG_Pf-PMV_PEXEL_1 | 413 | 418 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 609 | 614 | PF00026 | 0.872 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5V7 | Leptomonas seymouri | 56% | 100% |
A0A1X0NIV4 | Trypanosomatidae | 32% | 87% |
A0A3R7MGK1 | Trypanosoma rangeli | 38% | 98% |
A4HMG1 | Leishmania braziliensis | 69% | 100% |
A4IB32 | Leishmania infantum | 100% | 100% |
C9ZNN0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 74% |
E9AEW2 | Leishmania major | 94% | 100% |
E9B618 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BC93 | Trypanosoma cruzi | 37% | 100% |