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: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005643 | nuclear pore | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IBN9
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 10 |
GO:0051301 | cell division | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 469 | 473 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 602 | 606 | PF00656 | 0.279 |
CLV_C14_Caspase3-7 | 631 | 635 | PF00656 | 0.279 |
CLV_C14_Caspase3-7 | 774 | 778 | PF00656 | 0.556 |
CLV_MEL_PAP_1 | 364 | 370 | PF00089 | 0.540 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 698 | 700 | PF00675 | 0.642 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 697 | 699 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 462 | 464 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 697 | 699 | PF00082 | 0.578 |
CLV_PCSK_PC7_1 | 694 | 700 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.261 |
DEG_APCC_DBOX_1 | 236 | 244 | PF00400 | 0.543 |
DEG_APCC_DBOX_1 | 264 | 272 | PF00400 | 0.516 |
DEG_SPOP_SBC_1 | 296 | 300 | PF00917 | 0.548 |
DEG_SPOP_SBC_1 | 675 | 679 | PF00917 | 0.442 |
DEG_SPOP_SBC_1 | 793 | 797 | PF00917 | 0.470 |
DOC_CYCLIN_RxL_1 | 549 | 558 | PF00134 | 0.410 |
DOC_CYCLIN_RxL_1 | 55 | 63 | PF00134 | 0.500 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 264 | 272 | PF00134 | 0.408 |
DOC_MAPK_gen_1 | 461 | 467 | PF00069 | 0.595 |
DOC_MAPK_gen_1 | 560 | 567 | PF00069 | 0.377 |
DOC_MAPK_gen_1 | 662 | 672 | PF00069 | 0.279 |
DOC_MAPK_JIP1_4 | 662 | 668 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 662 | 670 | PF00069 | 0.279 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.580 |
DOC_PP2B_LxvP_1 | 287 | 290 | PF13499 | 0.517 |
DOC_PP2B_LxvP_1 | 525 | 528 | PF13499 | 0.558 |
DOC_PP2B_LxvP_1 | 554 | 557 | PF13499 | 0.410 |
DOC_PP2B_LxvP_1 | 607 | 610 | PF13499 | 0.279 |
DOC_PP2B_LxvP_1 | 810 | 813 | PF13499 | 0.468 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.297 |
DOC_USP7_MATH_1 | 676 | 680 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 749 | 753 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 785 | 789 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 793 | 797 | PF00917 | 0.526 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 751 | 756 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 777 | 782 | PF00397 | 0.720 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.770 |
LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 161 | 165 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 187 | 196 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 374 | 384 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 624 | 630 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 698 | 705 | PF00244 | 0.619 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.578 |
LIG_BRCT_BRCA1_1 | 225 | 229 | PF00533 | 0.390 |
LIG_Clathr_ClatBox_1 | 274 | 278 | PF01394 | 0.497 |
LIG_Clathr_ClatBox_1 | 310 | 314 | PF01394 | 0.307 |
LIG_CSL_BTD_1 | 15 | 18 | PF09270 | 0.481 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.651 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.436 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.553 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.563 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.574 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.375 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.385 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.536 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.488 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.641 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.428 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.245 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.624 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.464 |
LIG_FHA_1 | 713 | 719 | PF00498 | 0.529 |
LIG_FHA_1 | 732 | 738 | PF00498 | 0.427 |
LIG_FHA_1 | 757 | 763 | PF00498 | 0.567 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.693 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.483 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.508 |
LIG_FHA_2 | 612 | 618 | PF00498 | 0.351 |
LIG_FHA_2 | 629 | 635 | PF00498 | 0.187 |
LIG_FHA_2 | 793 | 799 | PF00498 | 0.728 |
LIG_Integrin_isoDGR_2 | 122 | 124 | PF01839 | 0.589 |
LIG_Integrin_RGD_1 | 775 | 777 | PF01839 | 0.560 |
LIG_LIR_Gen_1 | 176 | 185 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 493 | 501 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 72 | 81 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 493 | 498 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.535 |
LIG_MAD2 | 643 | 651 | PF02301 | 0.161 |
LIG_MYND_1 | 751 | 755 | PF01753 | 0.629 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.438 |
LIG_NRBOX | 238 | 244 | PF00104 | 0.323 |
LIG_NRBOX | 625 | 631 | PF00104 | 0.279 |
LIG_Pex14_1 | 75 | 79 | PF04695 | 0.410 |
LIG_PTAP_UEV_1 | 436 | 441 | PF05743 | 0.517 |
LIG_Rb_pABgroove_1 | 582 | 590 | PF01858 | 0.306 |
LIG_SH2_CRK | 101 | 105 | PF00017 | 0.483 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.622 |
LIG_SH2_CRK | 495 | 499 | PF00017 | 0.415 |
LIG_SH2_SRC | 811 | 814 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 495 | 499 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 729 | 732 | PF00017 | 0.609 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.618 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.496 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.661 |
LIG_SH3_3 | 657 | 663 | PF00018 | 0.410 |
LIG_SH3_3 | 745 | 751 | PF00018 | 0.661 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.480 |
LIG_SUMO_SIM_anti_2 | 270 | 276 | PF11976 | 0.483 |
LIG_SUMO_SIM_anti_2 | 278 | 284 | PF11976 | 0.421 |
LIG_SUMO_SIM_anti_2 | 422 | 429 | PF11976 | 0.398 |
LIG_SUMO_SIM_anti_2 | 517 | 524 | PF11976 | 0.521 |
LIG_SUMO_SIM_anti_2 | 568 | 574 | PF11976 | 0.279 |
LIG_SUMO_SIM_anti_2 | 642 | 649 | PF11976 | 0.395 |
LIG_SUMO_SIM_anti_2 | 715 | 721 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 308 | 315 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 422 | 429 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 517 | 524 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 642 | 649 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 714 | 721 | PF11976 | 0.571 |
LIG_WRC_WIRS_1 | 350 | 355 | PF05994 | 0.465 |
LIG_WW_3 | 608 | 612 | PF00397 | 0.279 |
LIG_WW_3 | 747 | 751 | PF00397 | 0.603 |
MOD_CDK_SPxxK_3 | 230 | 237 | PF00069 | 0.504 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.677 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.531 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.520 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.676 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.571 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.279 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.306 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.386 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.646 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.616 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.442 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.464 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.438 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.563 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.410 |
MOD_CK2_1 | 751 | 757 | PF00069 | 0.571 |
MOD_Cter_Amidation | 550 | 553 | PF01082 | 0.306 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.536 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.680 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.545 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.745 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.282 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.317 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.613 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.629 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.753 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.580 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.607 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.544 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.544 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.473 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.576 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.673 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.684 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.685 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.308 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.511 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.407 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.294 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.248 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.406 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.537 |
MOD_N-GLC_1 | 618 | 623 | PF02516 | 0.402 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.644 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.567 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.601 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.410 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.517 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.568 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.635 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.354 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.539 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.357 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.481 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.476 |
MOD_PIKK_1 | 628 | 634 | PF00454 | 0.410 |
MOD_PKA_1 | 444 | 450 | PF00069 | 0.532 |
MOD_PKA_1 | 698 | 704 | PF00069 | 0.617 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.606 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.509 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.542 |
MOD_PKA_2 | 612 | 618 | PF00069 | 0.322 |
MOD_PKA_2 | 698 | 704 | PF00069 | 0.617 |
MOD_PKA_2 | 749 | 755 | PF00069 | 0.676 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.396 |
MOD_Plk_1 | 622 | 628 | PF00069 | 0.279 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.518 |
MOD_Plk_2-3 | 270 | 276 | PF00069 | 0.482 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.406 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.606 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.362 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.499 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.374 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.409 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.560 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.639 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.297 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.279 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.556 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.490 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.434 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.596 |
MOD_ProDKin_1 | 751 | 757 | PF00069 | 0.673 |
MOD_ProDKin_1 | 777 | 783 | PF00069 | 0.724 |
TRG_DiLeu_BaEn_1 | 176 | 181 | PF01217 | 0.509 |
TRG_DiLeu_BaEn_1 | 270 | 275 | PF01217 | 0.379 |
TRG_DiLeu_BaEn_1 | 314 | 319 | PF01217 | 0.365 |
TRG_DiLeu_BaEn_1 | 721 | 726 | PF01217 | 0.543 |
TRG_DiLeu_BaEn_4 | 176 | 182 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 238 | 243 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 495 | 498 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 142 | 145 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 389 | 391 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 552 | 554 | PF00400 | 0.297 |
TRG_ER_diArg_1 | 560 | 562 | PF00400 | 0.296 |
TRG_ER_diArg_1 | 610 | 613 | PF00400 | 0.326 |
TRG_NES_CRM1_1 | 510 | 524 | PF08389 | 0.532 |
TRG_NLS_Bipartite_1 | 444 | 465 | PF00514 | 0.504 |
TRG_NLS_MonoExtC_3 | 460 | 466 | PF00514 | 0.510 |
TRG_NLS_MonoExtC_3 | 696 | 702 | PF00514 | 0.580 |
TRG_NLS_MonoExtN_4 | 694 | 701 | PF00514 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 135 | 140 | PF00026 | 0.631 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.559 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4E7 | Leptomonas seymouri | 51% | 100% |
A0A1X0NXH5 | Trypanosomatidae | 33% | 100% |
A0A3R7NWG6 | Trypanosoma rangeli | 34% | 100% |
A4HZ08 | Leishmania infantum | 99% | 100% |
C9ZIP1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AIL0 | Leishmania braziliensis | 76% | 100% |
E9AUU2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QCP1 | Leishmania major | 93% | 100% |
V5BCV9 | Trypanosoma cruzi | 34% | 100% |