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) | no | yes: 0 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QG60
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 2 |
GO:0002940 | tRNA N2-guanine methylation | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006399 | tRNA metabolic process | 7 | 2 |
GO:0006400 | tRNA modification | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008033 | tRNA processing | 8 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009451 | RNA modification | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0030488 | tRNA methylation | 5 | 2 |
GO:0032259 | methylation | 2 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043414 | macromolecule methylation | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004809 | tRNA (guanine-N2-)-methyltransferase activity | 6 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008170 | N-methyltransferase activity | 5 | 12 |
GO:0008173 | RNA methyltransferase activity | 4 | 12 |
GO:0008175 | tRNA methyltransferase activity | 5 | 12 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
GO:0016423 | tRNA (guanine) methyltransferase activity | 6 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 280 | 284 | PF00656 | 0.307 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.660 |
CLV_C14_Caspase3-7 | 709 | 713 | PF00656 | 0.737 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 691 | 693 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.328 |
CLV_PCSK_FUR_1 | 396 | 400 | PF00082 | 0.604 |
CLV_PCSK_FUR_1 | 431 | 435 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.781 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.794 |
CLV_PCSK_KEX2_1 | 690 | 692 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.687 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.795 |
CLV_PCSK_PC7_1 | 391 | 397 | PF00082 | 0.659 |
CLV_PCSK_PC7_1 | 433 | 439 | PF00082 | 0.778 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.587 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.323 |
DEG_APCC_DBOX_1 | 546 | 554 | PF00400 | 0.427 |
DEG_SCF_FBW7_2 | 652 | 659 | PF00400 | 0.526 |
DEG_SPOP_SBC_1 | 487 | 491 | PF00917 | 0.318 |
DOC_CKS1_1 | 574 | 579 | PF01111 | 0.323 |
DOC_CKS1_1 | 653 | 658 | PF01111 | 0.524 |
DOC_CYCLIN_RxL_1 | 310 | 322 | PF00134 | 0.307 |
DOC_CYCLIN_RxL_1 | 647 | 655 | PF00134 | 0.588 |
DOC_CYCLIN_yCln2_LP_2 | 505 | 511 | PF00134 | 0.364 |
DOC_MAPK_DCC_7 | 330 | 338 | PF00069 | 0.310 |
DOC_MAPK_DCC_7 | 601 | 610 | PF00069 | 0.319 |
DOC_MAPK_gen_1 | 269 | 279 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 327 | 335 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 330 | 338 | PF00069 | 0.310 |
DOC_MAPK_MEF2A_6 | 541 | 550 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 601 | 610 | PF00069 | 0.319 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.459 |
DOC_PP4_FxxP_1 | 331 | 334 | PF00568 | 0.415 |
DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.307 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 643 | 647 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.646 |
DOC_USP7_UBL2_3 | 637 | 641 | PF12436 | 0.646 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.307 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 652 | 657 | PF00397 | 0.484 |
LIG_14-3-3_CanoR_1 | 379 | 389 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 467 | 471 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 530 | 536 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 89 | 95 | PF00244 | 0.415 |
LIG_Actin_WH2_2 | 101 | 119 | PF00022 | 0.308 |
LIG_Actin_WH2_2 | 76 | 93 | PF00022 | 0.454 |
LIG_APCC_ABBA_1 | 336 | 341 | PF00400 | 0.307 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.557 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.434 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.371 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.436 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.398 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.364 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.307 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.307 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.359 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.679 |
LIG_GSK3_LRP6_1 | 573 | 578 | PF00069 | 0.312 |
LIG_IRF3_LxIS_1 | 75 | 82 | PF10401 | 0.422 |
LIG_LIR_Apic_2 | 374 | 380 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 567 | 575 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 85 | 95 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 567 | 571 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.364 |
LIG_LYPXL_yS_3 | 157 | 160 | PF13949 | 0.427 |
LIG_NRBOX | 519 | 525 | PF00104 | 0.307 |
LIG_PCNA_yPIPBox_3 | 241 | 252 | PF02747 | 0.368 |
LIG_PTB_Apo_2 | 124 | 131 | PF02174 | 0.427 |
LIG_PTB_Apo_2 | 144 | 151 | PF02174 | 0.123 |
LIG_PTB_Phospho_1 | 124 | 130 | PF10480 | 0.427 |
LIG_PTB_Phospho_1 | 144 | 150 | PF10480 | 0.123 |
LIG_REV1ctd_RIR_1 | 345 | 353 | PF16727 | 0.364 |
LIG_SH2_CRK | 10 | 14 | PF00017 | 0.528 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.427 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.323 |
LIG_SH2_CRK | 510 | 514 | PF00017 | 0.323 |
LIG_SH2_NCK_1 | 10 | 14 | PF00017 | 0.497 |
LIG_SH2_NCK_1 | 510 | 514 | PF00017 | 0.307 |
LIG_SH2_NCK_1 | 69 | 73 | PF00017 | 0.307 |
LIG_SH2_PTP2 | 568 | 571 | PF00017 | 0.427 |
LIG_SH2_SRC | 130 | 133 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.576 |
LIG_SH2_STAT3 | 366 | 369 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 560 | 563 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.411 |
LIG_SH3_2 | 462 | 467 | PF14604 | 0.573 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.425 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.630 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.416 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.562 |
LIG_SH3_3 | 551 | 557 | PF00018 | 0.335 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.220 |
LIG_SUMO_SIM_anti_2 | 103 | 109 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 80 | 85 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 250 | 255 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 82 | 88 | PF11976 | 0.454 |
LIG_TRAF2_1 | 390 | 393 | PF00917 | 0.608 |
LIG_TRAF2_1 | 412 | 415 | PF00917 | 0.738 |
LIG_TRAF2_1 | 54 | 57 | PF00917 | 0.729 |
LIG_TRAF2_1 | 549 | 552 | PF00917 | 0.323 |
LIG_TRFH_1 | 559 | 563 | PF08558 | 0.454 |
LIG_TYR_ITIM | 155 | 160 | PF00017 | 0.454 |
LIG_UBA3_1 | 609 | 617 | PF00899 | 0.374 |
MOD_CDC14_SPxK_1 | 464 | 467 | PF00782 | 0.688 |
MOD_CDK_SPK_2 | 185 | 190 | PF00069 | 0.659 |
MOD_CDK_SPxK_1 | 461 | 467 | PF00069 | 0.651 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.560 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.323 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.463 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.590 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.370 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.707 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.307 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.631 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.711 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.422 |
MOD_Cter_Amidation | 221 | 224 | PF01082 | 0.624 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.307 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.674 |
MOD_GlcNHglycan | 233 | 237 | PF01048 | 0.459 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.312 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.310 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.427 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.427 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.437 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.676 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.614 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.315 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.658 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.801 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.532 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.322 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.305 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.620 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.599 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.341 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.550 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.648 |
MOD_LATS_1 | 296 | 302 | PF00433 | 0.307 |
MOD_N-GLC_1 | 51 | 56 | PF02516 | 0.727 |
MOD_N-GLC_1 | 682 | 687 | PF02516 | 0.439 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.306 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.321 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.307 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.364 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.409 |
MOD_NEK2_2 | 236 | 241 | PF00069 | 0.220 |
MOD_NEK2_2 | 334 | 339 | PF00069 | 0.307 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.314 |
MOD_PIKK_1 | 588 | 594 | PF00454 | 0.307 |
MOD_PK_1 | 77 | 83 | PF00069 | 0.307 |
MOD_PKA_1 | 37 | 43 | PF00069 | 0.591 |
MOD_PKA_1 | 433 | 439 | PF00069 | 0.661 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.638 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.700 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.609 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.359 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.325 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.323 |
MOD_PKA_2 | 672 | 678 | PF00069 | 0.583 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.374 |
MOD_PKB_1 | 431 | 439 | PF00069 | 0.658 |
MOD_PKB_1 | 96 | 104 | PF00069 | 0.427 |
MOD_Plk_1 | 627 | 633 | PF00069 | 0.613 |
MOD_Plk_1 | 660 | 666 | PF00069 | 0.411 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.318 |
MOD_Plk_2-3 | 103 | 109 | PF00069 | 0.392 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.376 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.389 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.294 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.524 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.648 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.307 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.630 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.503 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.323 |
MOD_ProDKin_1 | 652 | 658 | PF00069 | 0.489 |
MOD_SUMO_rev_2 | 410 | 419 | PF00179 | 0.745 |
TRG_DiLeu_BaLyEn_6 | 239 | 244 | PF01217 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 331 | 336 | PF01217 | 0.307 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 568 | 571 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 431 | 434 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 569 | 572 | PF00400 | 0.304 |
TRG_ER_diArg_1 | 670 | 673 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 689 | 692 | PF00400 | 0.706 |
TRG_ER_diArg_1 | 89 | 92 | PF00400 | 0.318 |
TRG_ER_diArg_1 | 95 | 98 | PF00400 | 0.305 |
TRG_NLS_MonoExtC_3 | 638 | 643 | PF00514 | 0.699 |
TRG_NLS_MonoExtN_4 | 34 | 41 | PF00514 | 0.480 |
TRG_NLS_MonoExtN_4 | 637 | 643 | PF00514 | 0.672 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.364 |
TRG_Pf-PMV_PEXEL_1 | 269 | 273 | PF00026 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF43 | Leptomonas seymouri | 67% | 98% |
A0A0S4IT52 | Bodo saltans | 48% | 100% |
A0A1X0NNC1 | Trypanosomatidae | 49% | 95% |
A0A3R7KAT5 | Trypanosoma rangeli | 52% | 100% |
A0A3S7WSL8 | Leishmania donovani | 93% | 99% |
A4H782 | Leishmania braziliensis | 80% | 98% |
A4HVM2 | Leishmania infantum | 93% | 99% |
D0A6N2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 99% |
E9APB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
Q4R6C7 | Macaca fascicularis | 21% | 100% |
V5BB27 | Trypanosoma cruzi | 53% | 99% |