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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B2N9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006378 | mRNA polyadenylation | 7 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0043022 | ribosome binding | 4 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.749 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 657 | 659 | PF00675 | 0.515 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.741 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 657 | 659 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 308 | 310 | PF00082 | 0.365 |
CLV_PCSK_PC7_1 | 304 | 310 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 647 | 651 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.280 |
DEG_APCC_DBOX_1 | 110 | 118 | PF00400 | 0.512 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.557 |
DOC_ANK_TNKS_1 | 325 | 332 | PF00023 | 0.598 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.571 |
DOC_CYCLIN_RxL_1 | 225 | 236 | PF00134 | 0.329 |
DOC_MAPK_gen_1 | 326 | 334 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 395 | 405 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 664 | 672 | PF00069 | 0.354 |
DOC_MAPK_MEF2A_6 | 27 | 35 | PF00069 | 0.451 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.778 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 560 | 565 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 111 | 115 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 244 | 249 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 273 | 282 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 326 | 334 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 386 | 396 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 515 | 523 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 573 | 578 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 62 | 68 | PF00244 | 0.775 |
LIG_14-3-3_CanoR_1 | 638 | 648 | PF00244 | 0.503 |
LIG_APCC_ABBA_1 | 650 | 655 | PF00400 | 0.380 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.492 |
LIG_BRCT_BRCA1_1 | 644 | 648 | PF00533 | 0.377 |
LIG_deltaCOP1_diTrp_1 | 124 | 134 | PF00928 | 0.446 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.537 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.460 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.331 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.267 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.397 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.381 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.457 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.690 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.343 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.373 |
LIG_FHA_1 | 667 | 673 | PF00498 | 0.437 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.747 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.490 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.734 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.623 |
LIG_FHA_2 | 475 | 481 | PF00498 | 0.438 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.528 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.550 |
LIG_LIR_Gen_1 | 181 | 192 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 2 | 9 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 243 | 254 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 411 | 419 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 444 | 452 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 505 | 514 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 518 | 528 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 582 | 590 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 615 | 623 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 379 | 383 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 477 | 482 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 505 | 510 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 518 | 523 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 582 | 586 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 597 | 603 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 615 | 621 | PF02991 | 0.497 |
LIG_NRBOX | 509 | 515 | PF00104 | 0.456 |
LIG_Pex14_2 | 366 | 370 | PF04695 | 0.457 |
LIG_RPA_C_Fungi | 321 | 333 | PF08784 | 0.535 |
LIG_SH2_CRK | 412 | 416 | PF00017 | 0.403 |
LIG_SH2_PTP2 | 424 | 427 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 412 | 416 | PF00017 | 0.403 |
LIG_SH2_STAP1 | 583 | 587 | PF00017 | 0.334 |
LIG_SH2_STAP1 | 603 | 607 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 618 | 622 | PF00017 | 0.384 |
LIG_SH2_STAT3 | 592 | 595 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.447 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.524 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.566 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.652 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.691 |
LIG_SUMO_SIM_anti_2 | 619 | 624 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 266 | 272 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 371 | 379 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 619 | 624 | PF11976 | 0.423 |
LIG_TRAF2_1 | 430 | 433 | PF00917 | 0.557 |
LIG_TRAF2_1 | 449 | 452 | PF00917 | 0.713 |
LIG_TYR_ITIM | 410 | 415 | PF00017 | 0.412 |
LIG_UBA3_1 | 302 | 308 | PF00899 | 0.516 |
LIG_UBA3_1 | 396 | 402 | PF00899 | 0.453 |
LIG_UBA3_1 | 510 | 517 | PF00899 | 0.415 |
LIG_WRC_WIRS_1 | 663 | 668 | PF05994 | 0.514 |
LIG_WW_3 | 194 | 198 | PF00397 | 0.530 |
MOD_CDC14_SPxK_1 | 24 | 27 | PF00782 | 0.466 |
MOD_CDC14_SPxK_1 | 287 | 290 | PF00782 | 0.459 |
MOD_CDK_SPxK_1 | 21 | 27 | PF00069 | 0.473 |
MOD_CDK_SPxK_1 | 284 | 290 | PF00069 | 0.479 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.603 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.575 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.532 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.624 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.421 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.729 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.524 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.652 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.567 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.763 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.672 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.634 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.575 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.727 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.561 |
MOD_CK2_1 | 474 | 480 | PF00069 | 0.473 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.473 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.492 |
MOD_CMANNOS | 574 | 577 | PF00535 | 0.456 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.421 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.612 |
MOD_GlcNHglycan | 349 | 353 | PF01048 | 0.812 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.647 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.672 |
MOD_GlcNHglycan | 471 | 475 | PF01048 | 0.482 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.648 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.665 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.613 |
MOD_GlcNHglycan | 637 | 641 | PF01048 | 0.565 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.739 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.616 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.754 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.677 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.526 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.593 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.437 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.621 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.656 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.769 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.605 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.448 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.530 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.441 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.484 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.795 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.558 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.646 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.639 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.383 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.428 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.322 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.301 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.546 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.528 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.555 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.521 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.449 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.516 |
MOD_NEK2_2 | 110 | 115 | PF00069 | 0.358 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.448 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.683 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.835 |
MOD_PK_1 | 244 | 250 | PF00069 | 0.444 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.586 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.642 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.336 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.472 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.565 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.716 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.515 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.500 |
MOD_PKA_2 | 611 | 617 | PF00069 | 0.428 |
MOD_PKB_1 | 678 | 686 | PF00069 | 0.492 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.467 |
MOD_Plk_2-3 | 401 | 407 | PF00069 | 0.317 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.457 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.544 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.479 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.572 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.762 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.565 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.596 |
MOD_ProDKin_1 | 560 | 566 | PF00069 | 0.720 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.725 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.628 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.705 |
MOD_SUMO_for_1 | 33 | 36 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 30 | 35 | PF00179 | 0.606 |
TRG_DiLeu_BaEn_1 | 509 | 514 | PF01217 | 0.448 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 583 | 586 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 618 | 621 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 653 | 656 | PF00928 | 0.370 |
TRG_ER_diArg_1 | 103 | 105 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 589 | 592 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 656 | 658 | PF00400 | 0.497 |
TRG_NES_CRM1_1 | 394 | 408 | PF08389 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 290 | 294 | PF00026 | 0.684 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PGR3 | Leptomonas seymouri | 50% | 92% |
A0A1X0NVZ4 | Trypanosomatidae | 31% | 100% |
A0A3Q8IG45 | Leishmania donovani | 83% | 100% |
A0A3R7NTQ6 | Trypanosoma rangeli | 30% | 100% |
A4HKA1 | Leishmania braziliensis | 69% | 100% |
A4I7T1 | Leishmania infantum | 83% | 100% |
D0A9Z2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
Q4Q5G8 | Leishmania major | 83% | 99% |
V5BQR4 | Trypanosoma cruzi | 28% | 100% |