Uncharacterized Protein, Uncharacterized
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 6 |
GO:0031931 | TORC1 complex | 4 | 8 |
GO:0031932 | TORC2 complex | 4 | 8 |
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0038201 | TOR complex | 3 | 8 |
GO:0043226 | organelle | 2 | 6 |
GO:0043228 | non-membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0140535 | intracellular protein-containing complex | 2 | 8 |
GO:1990904 | ribonucleoprotein complex | 2 | 6 |
GO:0005737 | cytoplasm | 2 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HYB8
Term | Name | Level | Count |
---|---|---|---|
GO:0007165 | signal transduction | 2 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0031929 | TOR signaling | 4 | 8 |
GO:0035556 | intracellular signal transduction | 3 | 8 |
GO:0050789 | regulation of biological process | 2 | 8 |
GO:0050794 | regulation of cellular process | 3 | 8 |
GO:0065007 | biological regulation | 1 | 8 |
GO:0032956 | regulation of actin cytoskeleton organization | 5 | 1 |
GO:0032970 | regulation of actin filament-based process | 4 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 632 | 636 | PF00656 | 0.511 |
CLV_C14_Caspase3-7 | 678 | 682 | PF00656 | 0.675 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 806 | 808 | PF00675 | 0.518 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 805 | 807 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 805 | 807 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 743 | 747 | PF00082 | 0.191 |
DEG_APCC_DBOX_1 | 295 | 303 | PF00400 | 0.410 |
DOC_CKS1_1 | 371 | 376 | PF01111 | 0.532 |
DOC_MAPK_MEF2A_6 | 188 | 195 | PF00069 | 0.291 |
DOC_MAPK_MEF2A_6 | 549 | 556 | PF00069 | 0.281 |
DOC_MAPK_MEF2A_6 | 794 | 801 | PF00069 | 0.322 |
DOC_PP1_RVXF_1 | 329 | 335 | PF00149 | 0.261 |
DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.416 |
DOC_PP4_FxxP_1 | 575 | 578 | PF00568 | 0.288 |
DOC_SPAK_OSR1_1 | 574 | 578 | PF12202 | 0.284 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.315 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 706 | 710 | PF00917 | 0.508 |
DOC_USP7_UBL2_3 | 395 | 399 | PF12436 | 0.556 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.307 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.288 |
DOC_WW_Pin1_4 | 681 | 686 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 718 | 723 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 729 | 734 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 24 | 30 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 354 | 359 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 413 | 417 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 502 | 508 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 783 | 788 | PF00244 | 0.378 |
LIG_Actin_WH2_2 | 569 | 584 | PF00022 | 0.342 |
LIG_APCC_ABBAyCdc20_2 | 27 | 33 | PF00400 | 0.371 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.352 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.386 |
LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.351 |
LIG_BRCT_BRCA1_1 | 785 | 789 | PF00533 | 0.399 |
LIG_eIF4E_1 | 550 | 556 | PF01652 | 0.334 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.469 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.567 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.740 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.366 |
LIG_FHA_1 | 642 | 648 | PF00498 | 0.704 |
LIG_FHA_1 | 791 | 797 | PF00498 | 0.317 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.436 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.276 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.631 |
LIG_IRF3_LxIS_1 | 577 | 584 | PF10401 | 0.313 |
LIG_LIR_Apic_2 | 227 | 232 | PF02991 | 0.281 |
LIG_LIR_Apic_2 | 38 | 43 | PF02991 | 0.398 |
LIG_LIR_Apic_2 | 392 | 397 | PF02991 | 0.548 |
LIG_LIR_Apic_2 | 432 | 436 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 104 | 115 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 168 | 175 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 307 | 316 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 44 | 55 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 539 | 548 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 738 | 745 | PF02991 | 0.175 |
LIG_LIR_LC3C_4 | 443 | 447 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 307 | 311 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 539 | 544 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 715 | 719 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 738 | 742 | PF02991 | 0.287 |
LIG_Pex14_1 | 753 | 757 | PF04695 | 0.397 |
LIG_REV1ctd_RIR_1 | 182 | 192 | PF16727 | 0.266 |
LIG_SH2_CRK | 308 | 312 | PF00017 | 0.350 |
LIG_SH2_CRK | 394 | 398 | PF00017 | 0.718 |
LIG_SH2_CRK | 433 | 437 | PF00017 | 0.586 |
LIG_SH2_CRK | 548 | 552 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 11 | 15 | PF00017 | 0.287 |
LIG_SH2_STAT3 | 11 | 14 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.314 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.705 |
LIG_SH3_3 | 607 | 613 | PF00018 | 0.564 |
LIG_SUMO_SIM_anti_2 | 3 | 8 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 3 | 8 | PF11976 | 0.337 |
LIG_TRAF2_1 | 285 | 288 | PF00917 | 0.489 |
LIG_TYR_ITSM | 43 | 50 | PF00017 | 0.359 |
LIG_WRC_WIRS_1 | 26 | 31 | PF05994 | 0.359 |
LIG_WRC_WIRS_1 | 61 | 66 | PF05994 | 0.397 |
LIG_WRC_WIRS_1 | 713 | 718 | PF05994 | 0.509 |
LIG_WRC_WIRS_1 | 96 | 101 | PF05994 | 0.391 |
LIG_WW_1 | 93 | 96 | PF00397 | 0.423 |
MOD_CDC14_SPxK_1 | 211 | 214 | PF00782 | 0.328 |
MOD_CDC14_SPxK_1 | 392 | 395 | PF00782 | 0.591 |
MOD_CDC14_SPxK_1 | 396 | 399 | PF00782 | 0.599 |
MOD_CDK_SPK_2 | 681 | 686 | PF00069 | 0.510 |
MOD_CDK_SPxK_1 | 208 | 214 | PF00069 | 0.306 |
MOD_CDK_SPxK_1 | 389 | 395 | PF00069 | 0.589 |
MOD_CDK_SPxxK_3 | 208 | 215 | PF00069 | 0.369 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.591 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.483 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.420 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.299 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.313 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.537 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.534 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.661 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.495 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.623 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.530 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.642 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.511 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.615 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.458 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.570 |
MOD_CK1_1 | 758 | 764 | PF00069 | 0.429 |
MOD_CK1_1 | 769 | 775 | PF00069 | 0.438 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.694 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.290 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.537 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.599 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.571 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.618 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.353 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.603 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.484 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.432 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.279 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.372 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.500 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.498 |
MOD_GlcNHglycan | 307 | 311 | PF01048 | 0.389 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.580 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.736 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.558 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.526 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.445 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.418 |
MOD_GlcNHglycan | 459 | 463 | PF01048 | 0.695 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.649 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.668 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.522 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.330 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.686 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.487 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.502 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.615 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.503 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.260 |
MOD_GlcNHglycan | 708 | 711 | PF01048 | 0.659 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.503 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.576 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.530 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.358 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.399 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.338 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.254 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.472 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.571 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.708 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.602 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.708 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.562 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.586 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.335 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.407 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.519 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.400 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.513 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.620 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.583 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.589 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.469 |
MOD_GSK3_1 | 765 | 772 | PF00069 | 0.438 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.586 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.277 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.299 |
MOD_N-GLC_1 | 429 | 434 | PF02516 | 0.560 |
MOD_N-GLC_1 | 500 | 505 | PF02516 | 0.602 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.289 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.600 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.611 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.421 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.345 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.442 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.450 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.378 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.576 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.572 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.583 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.268 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.608 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.467 |
MOD_NEK2_1 | 763 | 768 | PF00069 | 0.401 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.313 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.552 |
MOD_PIKK_1 | 608 | 614 | PF00454 | 0.554 |
MOD_PIKK_1 | 641 | 647 | PF00454 | 0.732 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.370 |
MOD_PK_1 | 339 | 345 | PF00069 | 0.461 |
MOD_PK_1 | 783 | 789 | PF00069 | 0.393 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.483 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.485 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.519 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.496 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.455 |
MOD_PKA_2 | 616 | 622 | PF00069 | 0.609 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.298 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.353 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.461 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.574 |
MOD_Plk_1 | 568 | 574 | PF00069 | 0.314 |
MOD_Plk_1 | 769 | 775 | PF00069 | 0.441 |
MOD_Plk_2-3 | 726 | 732 | PF00069 | 0.544 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.364 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.405 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.246 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.608 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.379 |
MOD_Plk_4 | 785 | 791 | PF00069 | 0.375 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.308 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.530 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.548 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.736 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.555 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.287 |
MOD_ProDKin_1 | 681 | 687 | PF00069 | 0.621 |
MOD_ProDKin_1 | 718 | 724 | PF00069 | 0.541 |
MOD_ProDKin_1 | 729 | 735 | PF00069 | 0.546 |
MOD_SUMO_for_1 | 518 | 521 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 237 | 245 | PF00179 | 0.458 |
TRG_DiLeu_BaEn_1 | 168 | 173 | PF01217 | 0.387 |
TRG_DiLeu_BaLyEn_6 | 356 | 361 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 708 | 713 | PF01217 | 0.535 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 214 | 216 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 806 | 808 | PF00400 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 194 | 198 | PF00026 | 0.379 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7T2 | Leptomonas seymouri | 55% | 100% |
A0A1X0P678 | Trypanosomatidae | 35% | 100% |
A0A3S7WVI8 | Leishmania donovani | 100% | 100% |
A4HA53 | Leishmania braziliensis | 71% | 98% |
E9AS52 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QDB4 | Leishmania major | 91% | 100% |