Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 3 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 2, no: 102 |
NetGPI | no | yes: 0, no: 104 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0020038 | subpellicular network | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9AIH1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 105 |
GO:0006807 | nitrogen compound metabolic process | 2 | 105 |
GO:0008152 | metabolic process | 1 | 105 |
GO:0019538 | protein metabolic process | 3 | 105 |
GO:0043170 | macromolecule metabolic process | 3 | 105 |
GO:0044238 | primary metabolic process | 2 | 105 |
GO:0071704 | organic substance metabolic process | 2 | 105 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 105 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 105 |
GO:0004175 | endopeptidase activity | 4 | 105 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 105 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 105 |
GO:0008233 | peptidase activity | 3 | 105 |
GO:0008234 | cysteine-type peptidase activity | 4 | 105 |
GO:0016787 | hydrolase activity | 2 | 105 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 105 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 300 | 304 | PF00656 | 0.550 |
CLV_C14_Caspase3-7 | 375 | 379 | PF00656 | 0.504 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 669 | 671 | PF00675 | 0.460 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 669 | 671 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 769 | 771 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 799 | 801 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 769 | 771 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 799 | 801 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.234 |
DEG_MDM2_SWIB_1 | 609 | 616 | PF02201 | 0.523 |
DEG_SIAH_1 | 114 | 122 | PF03145 | 0.451 |
DOC_ANK_TNKS_1 | 799 | 806 | PF00023 | 0.339 |
DOC_CYCLIN_yCln2_LP_2 | 740 | 746 | PF00134 | 0.655 |
DOC_PP1_RVXF_1 | 338 | 345 | PF00149 | 0.434 |
DOC_PP1_RVXF_1 | 416 | 422 | PF00149 | 0.533 |
DOC_PP1_RVXF_1 | 573 | 580 | PF00149 | 0.592 |
DOC_PP4_FxxP_1 | 186 | 189 | PF00568 | 0.351 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.528 |
DOC_PP4_FxxP_1 | 319 | 322 | PF00568 | 0.576 |
DOC_PP4_FxxP_1 | 399 | 402 | PF00568 | 0.537 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.651 |
DOC_USP7_MATH_2 | 352 | 358 | PF00917 | 0.588 |
DOC_USP7_UBL2_3 | 462 | 466 | PF12436 | 0.532 |
DOC_USP7_UBL2_3 | 614 | 618 | PF12436 | 0.560 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 653 | 658 | PF00397 | 0.443 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 281 | 289 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 418 | 422 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 706 | 715 | PF00244 | 0.597 |
LIG_Actin_WH2_2 | 429 | 446 | PF00022 | 0.615 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.560 |
LIG_BRCT_BRCA1_1 | 764 | 768 | PF00533 | 0.521 |
LIG_Clathr_ClatBox_1 | 788 | 792 | PF01394 | 0.618 |
LIG_CtBP_PxDLS_1 | 352 | 356 | PF00389 | 0.437 |
LIG_deltaCOP1_diTrp_1 | 710 | 714 | PF00928 | 0.487 |
LIG_eIF4E_1 | 540 | 546 | PF01652 | 0.551 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.690 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.390 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.472 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.561 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.468 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.549 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.545 |
LIG_FHA_2 | 586 | 592 | PF00498 | 0.612 |
LIG_LIR_Apic_2 | 184 | 189 | PF02991 | 0.346 |
LIG_LIR_Apic_2 | 19 | 24 | PF02991 | 0.529 |
LIG_LIR_Apic_2 | 90 | 96 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 15 | 24 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 461 | 472 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 487 | 494 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 709 | 720 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 15 | 21 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 202 | 206 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 219 | 223 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 433 | 438 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 461 | 467 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 470 | 474 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 612 | 616 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 656 | 662 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 676 | 681 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 692 | 697 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 709 | 715 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 765 | 771 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 779 | 784 | PF02991 | 0.514 |
LIG_PDZ_Class_3 | 811 | 816 | PF00595 | 0.544 |
LIG_Pex14_2 | 609 | 613 | PF04695 | 0.530 |
LIG_SH2_CRK | 223 | 227 | PF00017 | 0.369 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.527 |
LIG_SH2_CRK | 471 | 475 | PF00017 | 0.527 |
LIG_SH2_CRK | 518 | 522 | PF00017 | 0.547 |
LIG_SH2_CRK | 678 | 682 | PF00017 | 0.456 |
LIG_SH2_CRK | 694 | 698 | PF00017 | 0.533 |
LIG_SH2_CRK | 93 | 97 | PF00017 | 0.560 |
LIG_SH2_GRB2like | 277 | 280 | PF00017 | 0.601 |
LIG_SH2_GRB2like | 619 | 622 | PF00017 | 0.496 |
LIG_SH2_NCK_1 | 100 | 104 | PF00017 | 0.531 |
LIG_SH2_NCK_1 | 540 | 544 | PF00017 | 0.547 |
LIG_SH2_NCK_1 | 93 | 97 | PF00017 | 0.553 |
LIG_SH2_PTP2 | 731 | 734 | PF00017 | 0.436 |
LIG_SH2_SRC | 100 | 103 | PF00017 | 0.516 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.495 |
LIG_SH2_SRC | 435 | 438 | PF00017 | 0.546 |
LIG_SH2_SRC | 558 | 561 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 100 | 104 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 212 | 216 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 445 | 449 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 633 | 637 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 77 | 81 | PF00017 | 0.824 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.809 |
LIG_SH2_STAT5 | 731 | 734 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 749 | 752 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.830 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.375 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.575 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.603 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.454 |
LIG_SH3_3 | 651 | 657 | PF00018 | 0.427 |
LIG_SH3_3 | 740 | 746 | PF00018 | 0.639 |
LIG_SH3_3 | 788 | 794 | PF00018 | 0.512 |
LIG_SH3_5 | 631 | 635 | PF00018 | 0.481 |
LIG_SUMO_SIM_anti_2 | 719 | 724 | PF11976 | 0.428 |
LIG_SUMO_SIM_anti_2 | 763 | 768 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 647 | 653 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 679 | 684 | PF11976 | 0.435 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.540 |
LIG_TRAF2_1 | 76 | 79 | PF00917 | 0.838 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.515 |
LIG_TYR_ITIM | 191 | 196 | PF00017 | 0.388 |
LIG_TYR_ITIM | 516 | 521 | PF00017 | 0.598 |
LIG_UBA3_1 | 191 | 200 | PF00899 | 0.405 |
LIG_UBA3_1 | 722 | 730 | PF00899 | 0.496 |
LIG_WW_1 | 59 | 62 | PF00397 | 0.855 |
MOD_CDK_SPxK_1 | 521 | 527 | PF00069 | 0.544 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.736 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.553 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.571 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.542 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.523 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.592 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.426 |
MOD_CMANNOS | 610 | 613 | PF00535 | 0.331 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.621 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.356 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.360 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.366 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.326 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.384 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.545 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.473 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.673 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.689 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.547 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.516 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.430 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.522 |
MOD_GSK3_1 | 706 | 713 | PF00069 | 0.477 |
MOD_N-GLC_1 | 206 | 211 | PF02516 | 0.379 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.393 |
MOD_N-GLC_1 | 673 | 678 | PF02516 | 0.662 |
MOD_N-GLC_1 | 698 | 703 | PF02516 | 0.449 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.568 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.334 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.550 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.566 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.536 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.594 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.529 |
MOD_NEK2_1 | 698 | 703 | PF00069 | 0.472 |
MOD_NEK2_2 | 206 | 211 | PF00069 | 0.344 |
MOD_OFUCOSY | 178 | 185 | PF10250 | 0.244 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.595 |
MOD_PIKK_1 | 662 | 668 | PF00454 | 0.408 |
MOD_PIKK_1 | 806 | 812 | PF00454 | 0.602 |
MOD_PKA_1 | 199 | 205 | PF00069 | 0.469 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.514 |
MOD_PKA_2 | 705 | 711 | PF00069 | 0.642 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.639 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.384 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.346 |
MOD_Plk_1 | 27 | 33 | PF00069 | 0.693 |
MOD_Plk_1 | 494 | 500 | PF00069 | 0.570 |
MOD_Plk_1 | 718 | 724 | PF00069 | 0.430 |
MOD_Plk_1 | 762 | 768 | PF00069 | 0.479 |
MOD_Plk_2-3 | 162 | 168 | PF00069 | 0.603 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.649 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.532 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.564 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.598 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.550 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.536 |
MOD_Plk_4 | 762 | 768 | PF00069 | 0.522 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.641 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.538 |
MOD_ProDKin_1 | 653 | 659 | PF00069 | 0.449 |
MOD_SUMO_for_1 | 782 | 785 | PF00179 | 0.487 |
MOD_SUMO_rev_2 | 555 | 564 | PF00179 | 0.578 |
MOD_SUMO_rev_2 | 676 | 681 | PF00179 | 0.525 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 518 | 521 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 678 | 681 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 694 | 697 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 731 | 734 | PF00928 | 0.371 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.729 |
TRG_ER_diArg_1 | 567 | 570 | PF00400 | 0.563 |
TRG_NLS_MonoExtN_4 | 198 | 203 | PF00514 | 0.294 |
TRG_Pf-PMV_PEXEL_1 | 282 | 286 | PF00026 | 0.651 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 35% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 28% | 83% |
A0A0N1IGQ2 | Leptomonas seymouri | 32% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 41% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 34% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 41% | 96% |
A0A0N1PCA9 | Leptomonas seymouri | 35% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 27% | 92% |
A0A0N1PFI4 | Leptomonas seymouri | 36% | 100% |
A0A0S4JLK6 | Bodo saltans | 28% | 100% |
A0A0S4KGT2 | Bodo saltans | 40% | 100% |
A0A0S4KKP7 | Bodo saltans | 25% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 30% | 67% |
A0A1X0NJK2 | Trypanosomatidae | 32% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 36% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 30% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 32% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 41% | 96% |
A0A1X0NW84 | Trypanosomatidae | 40% | 100% |
A0A1X0NW85 | Trypanosomatidae | 39% | 100% |
A0A1X0NW89 | Trypanosomatidae | 55% | 95% |
A0A1X0NWA6 | Trypanosomatidae | 29% | 94% |
A0A1X0NWW1 | Trypanosomatidae | 40% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 85% | 90% |
A0A3Q8IDD4 | Leishmania donovani | 34% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 25% | 100% |
A0A3S5H5A5 | Leishmania donovani | 41% | 95% |
A0A3S5ISG2 | Trypanosoma rangeli | 32% | 100% |
A0A3S7WW13 | Leishmania donovani | 27% | 74% |
A0A3S7WW18 | Leishmania donovani | 84% | 99% |
A0A3S7WW41 | Leishmania donovani | 36% | 100% |
A0A3S7WW71 | Leishmania donovani | 39% | 100% |
A0A3S7X430 | Leishmania donovani | 34% | 100% |
A0A3S7X438 | Leishmania donovani | 29% | 87% |
A0A3S7X460 | Leishmania donovani | 35% | 100% |
A0A3S7X463 | Leishmania donovani | 27% | 87% |
A0A3S7X470 | Leishmania donovani | 34% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 53% | 89% |
A0A422MYX0 | Trypanosoma rangeli | 39% | 100% |
A4H3W4 | Leishmania braziliensis | 40% | 100% |
A4HE81 | Leishmania braziliensis | 34% | 100% |
A4HJ14 | Leishmania braziliensis | 35% | 100% |
A4HJ22 | Leishmania braziliensis | 30% | 100% |
A4HJ24 | Leishmania braziliensis | 35% | 100% |
A4HS39 | Leishmania infantum | 41% | 95% |
A4HYN0 | Leishmania infantum | 84% | 99% |
A4HYW1 | Leishmania infantum | 85% | 80% |
A4HYW2 | Leishmania infantum | 39% | 100% |
A4HYW3 | Leishmania infantum | 36% | 100% |
A4HYW4 | Leishmania infantum | 27% | 82% |
A4I1J4 | Leishmania infantum | 34% | 100% |
A4I6E4 | Leishmania infantum | 34% | 100% |
A4I6E6 | Leishmania infantum | 35% | 100% |
A4I6F0 | Leishmania infantum | 29% | 87% |
A4I6K4 | Leishmania infantum | 34% | 100% |
A4I6K5 | Leishmania infantum | 27% | 87% |
A4I6K6 | Leishmania infantum | 26% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 76% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 96% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 95% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 87% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AIH3 | Leishmania braziliensis | 40% | 100% |
E9AIH4 | Leishmania braziliensis | 36% | 100% |
E9AIH6 | Leishmania braziliensis | 27% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 87% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 87% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
Q4Q6L7 | Leishmania major | 35% | 100% |
Q4Q6L9 | Leishmania major | 33% | 100% |
Q4Q6M0 | Leishmania major | 30% | 100% |
Q4Q6M2 | Leishmania major | 29% | 100% |
Q4Q6M3 | Leishmania major | 28% | 100% |
Q4Q6M4 | Leishmania major | 35% | 100% |
Q4Q9U3 | Leishmania major | 34% | 100% |
Q4QCS6 | Leishmania major | 36% | 100% |
Q4QCS7 | Leishmania major | 40% | 100% |
Q4QCS8 | Leishmania major | 83% | 99% |
Q4QCS9 | Leishmania major | 84% | 100% |
Q9U0T9 | Leishmania major | 41% | 100% |
V5AYJ1 | Trypanosoma cruzi | 31% | 100% |
V5B5I4 | Trypanosoma cruzi | 54% | 97% |
V5BA05 | Trypanosoma cruzi | 41% | 100% |
V5BEL3 | Trypanosoma cruzi | 36% | 100% |
V5BII7 | Trypanosoma cruzi | 30% | 66% |
V5BN20 | Trypanosoma cruzi | 36% | 100% |
V5D9Y2 | Trypanosoma cruzi | 42% | 96% |
V5DES7 | Trypanosoma cruzi | 32% | 100% |