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 | 4 |
GO:0005868 | cytoplasmic dynein complex | 4 | 4 |
GO:0005874 | microtubule | 6 | 4 |
GO:0005875 | microtubule associated complex | 2 | 4 |
GO:0030286 | dynein complex | 3 | 4 |
GO:0032991 | protein-containing complex | 1 | 4 |
GO:0099080 | supramolecular complex | 2 | 4 |
GO:0099081 | supramolecular polymer | 3 | 4 |
GO:0099512 | supramolecular fiber | 4 | 4 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:1902494 | catalytic complex | 2 | 4 |
Related structures:
AlphaFold database: A4H7V5
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 4 |
GO:0007018 | microtubule-based movement | 3 | 4 |
GO:0009987 | cellular process | 1 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 4 |
GO:0005488 | binding | 1 | 4 |
GO:0005524 | ATP binding | 5 | 4 |
GO:0017076 | purine nucleotide binding | 4 | 4 |
GO:0030554 | adenyl nucleotide binding | 5 | 4 |
GO:0032553 | ribonucleotide binding | 3 | 4 |
GO:0032555 | purine ribonucleotide binding | 4 | 4 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 4 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 4 |
GO:0036094 | small molecule binding | 2 | 4 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043168 | anion binding | 3 | 4 |
GO:0097159 | organic cyclic compound binding | 2 | 4 |
GO:0097367 | carbohydrate derivative binding | 2 | 4 |
GO:1901265 | nucleoside phosphate binding | 3 | 4 |
GO:1901363 | heterocyclic compound binding | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 490 | 494 | PF00656 | 0.414 |
CLV_C14_Caspase3-7 | 525 | 529 | PF00656 | 0.281 |
CLV_MEL_PAP_1 | 593 | 599 | PF00089 | 0.612 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.497 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 230 | 232 | PF00082 | 0.456 |
CLV_PCSK_PC7_1 | 231 | 237 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 587 | 591 | PF00082 | 0.506 |
DEG_APCC_DBOX_1 | 564 | 572 | PF00400 | 0.484 |
DEG_APCC_DBOX_1 | 586 | 594 | PF00400 | 0.272 |
DEG_SPOP_SBC_1 | 475 | 479 | PF00917 | 0.542 |
DOC_ANK_TNKS_1 | 695 | 702 | PF00023 | 0.483 |
DOC_CDC14_PxL_1 | 115 | 123 | PF14671 | 0.446 |
DOC_CKS1_1 | 301 | 306 | PF01111 | 0.525 |
DOC_CKS1_1 | 702 | 707 | PF01111 | 0.644 |
DOC_CYCLIN_RxL_1 | 120 | 130 | PF00134 | 0.464 |
DOC_CYCLIN_yCln2_LP_2 | 11 | 17 | PF00134 | 0.457 |
DOC_CYCLIN_yCln2_LP_2 | 116 | 122 | PF00134 | 0.569 |
DOC_CYCLIN_yCln2_LP_2 | 506 | 512 | PF00134 | 0.431 |
DOC_PP1_RVXF_1 | 233 | 240 | PF00149 | 0.529 |
DOC_PP2B_LxvP_1 | 11 | 14 | PF13499 | 0.458 |
DOC_PP2B_LxvP_1 | 116 | 119 | PF13499 | 0.566 |
DOC_PP2B_LxvP_1 | 203 | 206 | PF13499 | 0.685 |
DOC_PP2B_LxvP_1 | 361 | 364 | PF13499 | 0.504 |
DOC_PP2B_LxvP_1 | 506 | 509 | PF13499 | 0.452 |
DOC_PP2B_LxvP_1 | 554 | 557 | PF13499 | 0.571 |
DOC_PP2B_LxvP_1 | 684 | 687 | PF13499 | 0.711 |
DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.453 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 589 | 593 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 690 | 694 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 736 | 740 | PF00917 | 0.486 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 701 | 706 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.634 |
LIG_14-3-3_CanoR_1 | 105 | 114 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 175 | 179 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 355 | 362 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 370 | 376 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 41 | 46 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 507 | 515 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 565 | 569 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 596 | 600 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 645 | 653 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 696 | 703 | PF00244 | 0.665 |
LIG_Actin_WH2_2 | 547 | 563 | PF00022 | 0.577 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.450 |
LIG_BRCT_BRCA1_1 | 280 | 284 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.762 |
LIG_Clathr_ClatBox_1 | 400 | 404 | PF01394 | 0.392 |
LIG_DLG_GKlike_1 | 43 | 50 | PF00625 | 0.474 |
LIG_EH_1 | 614 | 618 | PF12763 | 0.514 |
LIG_eIF4E_1 | 608 | 614 | PF01652 | 0.631 |
LIG_EVH1_2 | 87 | 91 | PF00568 | 0.457 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.454 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.669 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.476 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.674 |
LIG_FHA_2 | 523 | 529 | PF00498 | 0.400 |
LIG_FHA_2 | 695 | 701 | PF00498 | 0.674 |
LIG_LIR_Apic_2 | 5 | 9 | PF02991 | 0.453 |
LIG_LIR_Apic_2 | 727 | 733 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 416 | 427 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 724 | 734 | PF02991 | 0.717 |
LIG_LIR_Gen_1 | 742 | 748 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 80 | 91 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 724 | 729 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 742 | 748 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.690 |
LIG_NRBOX | 567 | 573 | PF00104 | 0.291 |
LIG_PDZ_Class_3 | 743 | 748 | PF00595 | 0.524 |
LIG_Pex14_1 | 79 | 83 | PF04695 | 0.456 |
LIG_Pex14_1 | 85 | 89 | PF04695 | 0.440 |
LIG_Pex14_2 | 487 | 491 | PF04695 | 0.415 |
LIG_Pex14_2 | 617 | 621 | PF04695 | 0.273 |
LIG_PTB_Apo_2 | 612 | 619 | PF02174 | 0.538 |
LIG_PTB_Phospho_1 | 612 | 618 | PF10480 | 0.538 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.685 |
LIG_SH2_GRB2like | 608 | 611 | PF00017 | 0.703 |
LIG_SH2_NCK_1 | 298 | 302 | PF00017 | 0.646 |
LIG_SH2_SRC | 608 | 611 | PF00017 | 0.703 |
LIG_SH2_STAP1 | 608 | 612 | PF00017 | 0.663 |
LIG_SH2_STAT3 | 329 | 332 | PF00017 | 0.547 |
LIG_SH2_STAT3 | 715 | 718 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 624 | 627 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 715 | 718 | PF00017 | 0.520 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.763 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.641 |
LIG_SH3_3 | 673 | 679 | PF00018 | 0.594 |
LIG_SH3_3 | 684 | 690 | PF00018 | 0.737 |
LIG_SH3_3 | 699 | 705 | PF00018 | 0.663 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.455 |
LIG_SUMO_SIM_anti_2 | 395 | 402 | PF11976 | 0.382 |
LIG_SUMO_SIM_anti_2 | 662 | 668 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 146 | 154 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 398 | 404 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 43 | 49 | PF11976 | 0.475 |
LIG_TRAF2_1 | 138 | 141 | PF00917 | 0.521 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.530 |
MOD_CDC14_SPxK_1 | 31 | 34 | PF00782 | 0.460 |
MOD_CDK_SPK_2 | 167 | 172 | PF00069 | 0.525 |
MOD_CDK_SPK_2 | 300 | 305 | PF00069 | 0.524 |
MOD_CDK_SPK_2 | 36 | 41 | PF00069 | 0.467 |
MOD_CDK_SPK_2 | 95 | 100 | PF00069 | 0.486 |
MOD_CDK_SPxK_1 | 28 | 34 | PF00069 | 0.465 |
MOD_CDK_SPxK_1 | 501 | 507 | PF00069 | 0.496 |
MOD_CDK_SPxxK_3 | 36 | 43 | PF00069 | 0.468 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.504 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.673 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.768 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.660 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.454 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.634 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.631 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.507 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.471 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.645 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.602 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.565 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.448 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.594 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.572 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.654 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.522 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.516 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.481 |
MOD_CK2_1 | 694 | 700 | PF00069 | 0.663 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.486 |
MOD_Cter_Amidation | 228 | 231 | PF01082 | 0.428 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.450 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.474 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.695 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.471 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.818 |
MOD_GlcNHglycan | 277 | 283 | PF01048 | 0.439 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.632 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.652 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.546 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.644 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.580 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.620 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.574 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.616 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.426 |
MOD_GlcNHglycan | 692 | 695 | PF01048 | 0.562 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.743 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.473 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.723 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.739 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.786 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.660 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.379 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.411 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.722 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.489 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.491 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.468 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.519 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.707 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.582 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.378 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.678 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.524 |
MOD_N-GLC_1 | 179 | 184 | PF02516 | 0.522 |
MOD_N-GLC_1 | 501 | 506 | PF02516 | 0.651 |
MOD_N-GLC_1 | 635 | 640 | PF02516 | 0.626 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.588 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.457 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.587 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.542 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.418 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.595 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.467 |
MOD_NEK2_1 | 595 | 600 | PF00069 | 0.490 |
MOD_NEK2_1 | 670 | 675 | PF00069 | 0.626 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.451 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.490 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.431 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.585 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.640 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.665 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.342 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.466 |
MOD_PIKK_1 | 573 | 579 | PF00454 | 0.479 |
MOD_PKA_1 | 370 | 376 | PF00069 | 0.524 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.734 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.762 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.362 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.504 |
MOD_PKA_2 | 564 | 570 | PF00069 | 0.429 |
MOD_PKA_2 | 595 | 601 | PF00069 | 0.608 |
MOD_PKA_2 | 695 | 701 | PF00069 | 0.679 |
MOD_PKB_1 | 41 | 49 | PF00069 | 0.474 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.520 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.669 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.484 |
MOD_Plk_1 | 487 | 493 | PF00069 | 0.491 |
MOD_Plk_1 | 635 | 641 | PF00069 | 0.627 |
MOD_Plk_1 | 721 | 727 | PF00069 | 0.408 |
MOD_Plk_2-3 | 541 | 547 | PF00069 | 0.389 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.444 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.475 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.399 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.452 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.517 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.683 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.768 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.465 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.624 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.443 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.467 |
MOD_ProDKin_1 | 701 | 707 | PF00069 | 0.574 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.634 |
MOD_SUMO_rev_2 | 451 | 460 | PF00179 | 0.539 |
TRG_DiLeu_BaEn_1 | 546 | 551 | PF01217 | 0.588 |
TRG_DiLeu_BaEn_1 | 680 | 685 | PF01217 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.443 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.685 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 618 | 621 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.578 |
TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 369 | 371 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAQ5 | Leptomonas seymouri | 58% | 100% |
A0A1X0NMR8 | Trypanosomatidae | 29% | 100% |
A0A3Q8I9X0 | Leishmania donovani | 77% | 100% |
A0A422NDE3 | Trypanosoma rangeli | 27% | 100% |
A4HW81 | Leishmania infantum | 76% | 100% |
D0A9A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9APY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4QFJ9 | Leishmania major | 75% | 100% |
V5BID0 | Trypanosoma cruzi | 28% | 100% |