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 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0000428 | DNA-directed RNA polymerase complex | 4 | 1 |
GO:0005658 | alpha DNA polymerase:primase complex | 4 | 1 |
GO:0030880 | RNA polymerase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0042575 | DNA polymerase complex | 3 | 1 |
GO:0055029 | nuclear DNA-directed RNA polymerase complex | 3 | 1 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HKF9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006260 | DNA replication | 5 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0006270 | DNA replication initiation | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 559 | 563 | PF00656 | 0.798 |
CLV_C14_Caspase3-7 | 660 | 664 | PF00656 | 0.694 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 709 | 711 | PF00675 | 0.538 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 709 | 711 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 597 | 599 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.411 |
DEG_APCC_DBOX_1 | 172 | 180 | PF00400 | 0.320 |
DEG_APCC_DBOX_1 | 282 | 290 | PF00400 | 0.539 |
DEG_APCC_DBOX_1 | 380 | 388 | PF00400 | 0.449 |
DEG_APCC_DBOX_1 | 412 | 420 | PF00400 | 0.423 |
DEG_APCC_DBOX_1 | 597 | 605 | PF00400 | 0.538 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.676 |
DEG_SPOP_SBC_1 | 563 | 567 | PF00917 | 0.680 |
DOC_CDC14_PxL_1 | 517 | 525 | PF14671 | 0.561 |
DOC_CKS1_1 | 30 | 35 | PF01111 | 0.621 |
DOC_CYCLIN_RxL_1 | 25 | 32 | PF00134 | 0.476 |
DOC_CYCLIN_RxL_1 | 417 | 425 | PF00134 | 0.449 |
DOC_MAPK_MEF2A_6 | 247 | 254 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 518 | 525 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 8 | 17 | PF00069 | 0.581 |
DOC_MAPK_NFAT4_5 | 247 | 255 | PF00069 | 0.322 |
DOC_MAPK_RevD_3 | 694 | 710 | PF00069 | 0.509 |
DOC_PP1_RVXF_1 | 331 | 337 | PF00149 | 0.420 |
DOC_PP2B_LxvP_1 | 503 | 506 | PF13499 | 0.363 |
DOC_PP2B_LxvP_1 | 624 | 627 | PF13499 | 0.760 |
DOC_PP4_FxxP_1 | 129 | 132 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 294 | 297 | PF00568 | 0.399 |
DOC_PP4_FxxP_1 | 371 | 374 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.533 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 686 | 691 | PF00397 | 0.646 |
LIG_14-3-3_CanoR_1 | 214 | 220 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 251 | 255 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 351 | 358 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 49 | 55 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 709 | 718 | PF00244 | 0.508 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.318 |
LIG_BRCT_BRCA1_1 | 688 | 692 | PF00533 | 0.631 |
LIG_Clathr_ClatBox_1 | 16 | 20 | PF01394 | 0.719 |
LIG_eIF4E_1 | 410 | 416 | PF01652 | 0.449 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.327 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.453 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.685 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.449 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.387 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.539 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.635 |
LIG_FHA_1 | 634 | 640 | PF00498 | 0.652 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.641 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.569 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.337 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.490 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.710 |
LIG_Integrin_isoDGR_2 | 500 | 502 | PF01839 | 0.475 |
LIG_Integrin_RGD_1 | 555 | 557 | PF01839 | 0.679 |
LIG_LIR_Apic_2 | 128 | 132 | PF02991 | 0.459 |
LIG_LIR_Apic_2 | 293 | 297 | PF02991 | 0.513 |
LIG_LIR_Apic_2 | 526 | 530 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 187 | 196 | PF02991 | 0.706 |
LIG_LIR_Gen_1 | 390 | 399 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 573 | 584 | PF02991 | 0.655 |
LIG_LIR_Gen_1 | 98 | 109 | PF02991 | 0.528 |
LIG_LIR_LC3C_4 | 363 | 367 | PF02991 | 0.223 |
LIG_LIR_LC3C_4 | 674 | 679 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 159 | 163 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.697 |
LIG_LIR_Nem_3 | 260 | 265 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 390 | 394 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 396 | 401 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 573 | 579 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.521 |
LIG_LYPXL_L_2 | 265 | 274 | PF13949 | 0.307 |
LIG_LYPXL_S_1 | 265 | 269 | PF13949 | 0.286 |
LIG_LYPXL_yS_3 | 266 | 269 | PF13949 | 0.288 |
LIG_NRBOX | 12 | 18 | PF00104 | 0.594 |
LIG_PDZ_Class_2 | 723 | 728 | PF00595 | 0.590 |
LIG_Pex14_1 | 576 | 580 | PF04695 | 0.736 |
LIG_Pex14_2 | 371 | 375 | PF04695 | 0.449 |
LIG_SH2_CRK | 504 | 508 | PF00017 | 0.330 |
LIG_SH2_CRK | 59 | 63 | PF00017 | 0.679 |
LIG_SH2_NCK_1 | 441 | 445 | PF00017 | 0.449 |
LIG_SH2_PTP2 | 527 | 530 | PF00017 | 0.464 |
LIG_SH2_SRC | 441 | 444 | PF00017 | 0.449 |
LIG_SH2_SRC | 527 | 530 | PF00017 | 0.690 |
LIG_SH2_SRC | 638 | 641 | PF00017 | 0.598 |
LIG_SH2_STAP1 | 255 | 259 | PF00017 | 0.446 |
LIG_SH2_STAT3 | 161 | 164 | PF00017 | 0.306 |
LIG_SH2_STAT3 | 255 | 258 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.598 |
LIG_SH3_2 | 300 | 305 | PF14604 | 0.641 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.563 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.564 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.408 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.543 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.371 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.409 |
LIG_SH3_3 | 431 | 437 | PF00018 | 0.339 |
LIG_SH3_3 | 696 | 702 | PF00018 | 0.443 |
LIG_SH3_4 | 106 | 113 | PF00018 | 0.544 |
LIG_SUMO_SIM_anti_2 | 363 | 368 | PF11976 | 0.361 |
LIG_SUMO_SIM_anti_2 | 674 | 680 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 420 | 425 | PF11976 | 0.344 |
LIG_TRAF2_1 | 229 | 232 | PF00917 | 0.718 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.638 |
LIG_UBA3_1 | 415 | 420 | PF00899 | 0.449 |
LIG_UBA3_1 | 534 | 538 | PF00899 | 0.638 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.596 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.615 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.401 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.386 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.586 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.403 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.652 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.543 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.691 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.660 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.528 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.622 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.365 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.250 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.667 |
MOD_GlcNHglycan | 145 | 149 | PF01048 | 0.611 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.706 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.733 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.676 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.226 |
MOD_GlcNHglycan | 345 | 349 | PF01048 | 0.475 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.623 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.716 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.744 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.803 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.728 |
MOD_GlcNHglycan | 581 | 585 | PF01048 | 0.608 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.741 |
MOD_GlcNHglycan | 64 | 68 | PF01048 | 0.584 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.538 |
MOD_GlcNHglycan | 713 | 716 | PF01048 | 0.463 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.567 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.580 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.657 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.493 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.595 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.621 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.342 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.348 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.516 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.693 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.684 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.582 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.642 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.315 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.717 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.566 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.503 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.739 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.438 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.454 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.607 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.355 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.312 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.441 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.449 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.556 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.541 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.629 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.728 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.644 |
MOD_NEK2_2 | 487 | 492 | PF00069 | 0.449 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.404 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.578 |
MOD_PIKK_1 | 428 | 434 | PF00454 | 0.328 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.696 |
MOD_PK_1 | 214 | 220 | PF00069 | 0.487 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.620 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.394 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.398 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.291 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.358 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.539 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.675 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.744 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.701 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.298 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.350 |
MOD_Plk_1 | 428 | 434 | PF00069 | 0.315 |
MOD_Plk_1 | 697 | 703 | PF00069 | 0.430 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.392 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.648 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.343 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.619 |
MOD_ProDKin_1 | 686 | 692 | PF00069 | 0.640 |
MOD_SUMO_for_1 | 105 | 108 | PF00179 | 0.669 |
MOD_SUMO_for_1 | 44 | 47 | PF00179 | 0.463 |
MOD_SUMO_for_1 | 599 | 602 | PF00179 | 0.659 |
MOD_SUMO_rev_2 | 533 | 540 | PF00179 | 0.673 |
TRG_DiLeu_BaLyEn_6 | 306 | 311 | PF01217 | 0.713 |
TRG_DiLeu_BaLyEn_6 | 411 | 416 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.649 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.229 |
TRG_ER_diArg_1 | 342 | 344 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 552 | 555 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 708 | 710 | PF00400 | 0.538 |
TRG_NLS_MonoExtC_3 | 596 | 602 | PF00514 | 0.654 |
TRG_NLS_MonoExtN_4 | 595 | 601 | PF00514 | 0.725 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAT5 | Leptomonas seymouri | 62% | 100% |
A0A0S4JBE4 | Bodo saltans | 28% | 100% |
A0A1X0NW10 | Trypanosomatidae | 42% | 100% |
A0A3Q8IL35 | Leishmania donovani | 76% | 100% |
A0A3R7NGI8 | Trypanosoma rangeli | 43% | 100% |
A4I7Y7 | Leishmania infantum | 76% | 100% |
D0AA49 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B2U8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q5A8 | Leishmania major | 76% | 99% |
V5DFV4 | Trypanosoma cruzi | 42% | 100% |