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: 103 |
NetGPI | no | yes: 0, no: 105 |
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: A0A3Q8IDD4
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 106 |
GO:0006807 | nitrogen compound metabolic process | 2 | 106 |
GO:0008152 | metabolic process | 1 | 106 |
GO:0019538 | protein metabolic process | 3 | 106 |
GO:0043170 | macromolecule metabolic process | 3 | 106 |
GO:0044238 | primary metabolic process | 2 | 106 |
GO:0071704 | organic substance metabolic process | 2 | 106 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 106 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 106 |
GO:0004175 | endopeptidase activity | 4 | 106 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 106 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 106 |
GO:0008233 | peptidase activity | 3 | 106 |
GO:0008234 | cysteine-type peptidase activity | 4 | 106 |
GO:0016787 | hydrolase activity | 2 | 106 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 106 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 547 | 551 | PF00656 | 0.512 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 691 | 693 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.561 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.574 |
CLV_Separin_Metazoa | 74 | 78 | PF03568 | 0.279 |
DEG_MDM2_SWIB_1 | 475 | 482 | PF02201 | 0.569 |
DEG_SCF_TRCP1_1 | 80 | 85 | PF00400 | 0.282 |
DOC_AGCK_PIF_2 | 343 | 348 | PF00069 | 0.471 |
DOC_CKS1_1 | 381 | 386 | PF01111 | 0.580 |
DOC_CYCLIN_RxL_1 | 360 | 368 | PF00134 | 0.659 |
DOC_MAPK_gen_1 | 157 | 167 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 208 | 216 | PF00069 | 0.681 |
DOC_MAPK_gen_1 | 375 | 381 | PF00069 | 0.563 |
DOC_MAPK_gen_1 | 600 | 610 | PF00069 | 0.570 |
DOC_MAPK_gen_1 | 624 | 631 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.673 |
DOC_MAPK_MEF2A_6 | 552 | 560 | PF00069 | 0.424 |
DOC_PP2B_LxvP_1 | 608 | 611 | PF13499 | 0.466 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.426 |
DOC_USP7_UBL2_3 | 12 | 16 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 123 | 127 | PF12436 | 0.559 |
DOC_USP7_UBL2_3 | 209 | 213 | PF12436 | 0.652 |
DOC_USP7_UBL2_3 | 250 | 254 | PF12436 | 0.692 |
DOC_USP7_UBL2_3 | 316 | 320 | PF12436 | 0.583 |
DOC_USP7_UBL2_3 | 390 | 394 | PF12436 | 0.648 |
DOC_USP7_UBL2_3 | 96 | 100 | PF12436 | 0.498 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 663 | 668 | PF00397 | 0.481 |
LIG_14-3-3_CanoR_1 | 593 | 598 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 612 | 622 | PF00244 | 0.540 |
LIG_Actin_WH2_2 | 374 | 392 | PF00022 | 0.649 |
LIG_BIR_III_2 | 10 | 14 | PF00653 | 0.751 |
LIG_BRCT_BRCA1_1 | 482 | 486 | PF00533 | 0.578 |
LIG_BRCT_BRCA1_1 | 489 | 493 | PF00533 | 0.574 |
LIG_deltaCOP1_diTrp_1 | 308 | 313 | PF00928 | 0.649 |
LIG_deltaCOP1_diTrp_1 | 42 | 46 | PF00928 | 0.355 |
LIG_deltaCOP1_diTrp_1 | 443 | 448 | PF00928 | 0.579 |
LIG_deltaCOP1_diTrp_1 | 478 | 486 | PF00928 | 0.587 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.593 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.435 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.642 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.521 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.445 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.462 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.599 |
LIG_IRF3_LxIS_1 | 273 | 278 | PF10401 | 0.665 |
LIG_LIR_Apic_2 | 196 | 202 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 308 | 318 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 324 | 333 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 510 | 519 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 550 | 560 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 701 | 706 | PF02991 | 0.707 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 478 | 482 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 501 | 505 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 510 | 514 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 527 | 533 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 550 | 556 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 596 | 601 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 701 | 705 | PF02991 | 0.653 |
LIG_LYPXL_yS_3 | 458 | 461 | PF13949 | 0.537 |
LIG_MLH1_MIPbox_1 | 482 | 486 | PF16413 | 0.629 |
LIG_PCNA_yPIPBox_3 | 267 | 281 | PF02747 | 0.552 |
LIG_Pex14_2 | 348 | 352 | PF04695 | 0.575 |
LIG_Pex14_2 | 475 | 479 | PF04695 | 0.577 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.488 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.576 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.584 |
LIG_SH2_CRK | 505 | 509 | PF00017 | 0.453 |
LIG_SH2_CRK | 553 | 557 | PF00017 | 0.500 |
LIG_SH2_NCK_1 | 318 | 322 | PF00017 | 0.629 |
LIG_SH2_PTP2 | 533 | 536 | PF00017 | 0.499 |
LIG_SH2_SRC | 289 | 292 | PF00017 | 0.588 |
LIG_SH2_SRC | 627 | 630 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 318 | 322 | PF00017 | 0.613 |
LIG_SH2_STAP1 | 503 | 507 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 553 | 557 | PF00017 | 0.421 |
LIG_SH2_STAT3 | 332 | 335 | PF00017 | 0.657 |
LIG_SH2_STAT3 | 587 | 590 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.472 |
LIG_SH3_3 | 577 | 583 | PF00018 | 0.579 |
LIG_SH3_4 | 12 | 19 | PF00018 | 0.612 |
LIG_SUMO_SIM_anti_2 | 517 | 524 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 282 | 288 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 556 | 562 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 627 | 633 | PF11976 | 0.545 |
LIG_TYR_ITIM | 109 | 114 | PF00017 | 0.286 |
LIG_UBA3_1 | 216 | 223 | PF00899 | 0.480 |
LIG_UBA3_1 | 35 | 40 | PF00899 | 0.452 |
LIG_UBA3_1 | 520 | 526 | PF00899 | 0.327 |
LIG_WRC_WIRS_1 | 508 | 513 | PF05994 | 0.610 |
LIG_WRC_WIRS_1 | 659 | 664 | PF05994 | 0.552 |
MOD_CDK_SPK_2 | 218 | 223 | PF00069 | 0.649 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.425 |
MOD_CK1_1 | 669 | 675 | PF00069 | 0.606 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.572 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.577 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.485 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.411 |
MOD_CMANNOS | 476 | 479 | PF00535 | 0.378 |
MOD_Cter_Amidation | 693 | 696 | PF01082 | 0.689 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.477 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.657 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.441 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.396 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.408 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.386 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.433 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.570 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.444 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.612 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.589 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.619 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.463 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.584 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.530 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.458 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.494 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.383 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.427 |
MOD_N-GLC_1 | 524 | 529 | PF02516 | 0.549 |
MOD_N-GLC_1 | 565 | 570 | PF02516 | 0.582 |
MOD_N-GLC_1 | 574 | 579 | PF02516 | 0.529 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.427 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.530 |
MOD_N-GLC_2 | 3 | 5 | PF02516 | 0.533 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.602 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.579 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.639 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.586 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.570 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.507 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.634 |
MOD_NEK2_2 | 532 | 537 | PF00069 | 0.552 |
MOD_NEK2_2 | 86 | 91 | PF00069 | 0.412 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.625 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.640 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.615 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.528 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.455 |
MOD_PIKK_1 | 525 | 531 | PF00454 | 0.521 |
MOD_PIKK_1 | 565 | 571 | PF00454 | 0.659 |
MOD_PIKK_1 | 630 | 636 | PF00454 | 0.612 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.578 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.592 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.615 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.603 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.518 |
MOD_Plk_4 | 669 | 675 | PF00069 | 0.618 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.445 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.562 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.443 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.592 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.599 |
MOD_ProDKin_1 | 663 | 669 | PF00069 | 0.485 |
MOD_SUMO_for_1 | 11 | 14 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 10 | 17 | PF00179 | 0.602 |
MOD_SUMO_rev_2 | 368 | 378 | PF00179 | 0.612 |
MOD_SUMO_rev_2 | 417 | 424 | PF00179 | 0.625 |
MOD_SUMO_rev_2 | 547 | 554 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 89 | 98 | PF00179 | 0.484 |
TRG_DiLeu_BaEn_1 | 374 | 379 | PF01217 | 0.658 |
TRG_DiLeu_BaLyEn_6 | 151 | 156 | PF01217 | 0.379 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.603 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 533 | 536 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 598 | 601 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.434 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 493 | 495 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 611 | 613 | PF00400 | 0.538 |
TRG_NLS_Bipartite_1 | 612 | 628 | PF00514 | 0.629 |
TRG_NLS_MonoExtC_3 | 361 | 367 | PF00514 | 0.474 |
TRG_NLS_MonoExtC_3 | 691 | 696 | PF00514 | 0.635 |
TRG_NLS_MonoExtN_4 | 623 | 628 | PF00514 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 140 | 144 | PF00026 | 0.672 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 36% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 28% | 72% |
A0A0N1IGQ2 | Leptomonas seymouri | 70% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 34% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 33% | 90% |
A0A0N1P9P1 | Leptomonas seymouri | 31% | 83% |
A0A0N1PCA9 | Leptomonas seymouri | 29% | 96% |
A0A0N1PE91 | Leptomonas seymouri | 23% | 79% |
A0A0N1PFI4 | Leptomonas seymouri | 32% | 91% |
A0A0S4JLK6 | Bodo saltans | 33% | 87% |
A0A0S4JS70 | Bodo saltans | 24% | 92% |
A0A0S4KGT2 | Bodo saltans | 39% | 94% |
A0A1X0NJ61 | Trypanosomatidae | 46% | 100% |
A0A1X0NJK2 | Trypanosomatidae | 33% | 93% |
A0A1X0NJX8 | Trypanosomatidae | 34% | 91% |
A0A1X0NKT7 | Trypanosomatidae | 28% | 89% |
A0A1X0NKX8 | Trypanosomatidae | 32% | 86% |
A0A1X0NMT3 | Trypanosomatidae | 33% | 83% |
A0A1X0NW84 | Trypanosomatidae | 34% | 100% |
A0A1X0NW85 | Trypanosomatidae | 31% | 100% |
A0A1X0NW89 | Trypanosomatidae | 34% | 82% |
A0A1X0NWA6 | Trypanosomatidae | 27% | 81% |
A0A1X0NWW1 | Trypanosomatidae | 34% | 98% |
A0A3Q8IBS3 | Leishmania donovani | 34% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 25% | 94% |
A0A3S5H5A5 | Leishmania donovani | 31% | 83% |
A0A3S5ISG2 | Trypanosoma rangeli | 32% | 91% |
A0A3S7WW18 | Leishmania donovani | 34% | 86% |
A0A3S7WW41 | Leishmania donovani | 29% | 95% |
A0A3S7WW71 | Leishmania donovani | 35% | 100% |
A0A3S7X430 | Leishmania donovani | 33% | 90% |
A0A3S7X438 | Leishmania donovani | 29% | 75% |
A0A3S7X460 | Leishmania donovani | 35% | 91% |
A0A3S7X463 | Leishmania donovani | 28% | 75% |
A0A3S7X470 | Leishmania donovani | 32% | 98% |
A0A422MYU1 | Trypanosoma rangeli | 32% | 77% |
A0A422MYX0 | Trypanosoma rangeli | 33% | 97% |
A4H3W4 | Leishmania braziliensis | 31% | 100% |
A4HE81 | Leishmania braziliensis | 84% | 100% |
A4HJ14 | Leishmania braziliensis | 33% | 100% |
A4HJ21 | Leishmania braziliensis | 25% | 79% |
A4HJ22 | Leishmania braziliensis | 31% | 100% |
A4HJ23 | Leishmania braziliensis | 31% | 97% |
A4HJ24 | Leishmania braziliensis | 36% | 100% |
A4HS39 | Leishmania infantum | 31% | 100% |
A4HYN0 | Leishmania infantum | 34% | 100% |
A4HYW1 | Leishmania infantum | 34% | 70% |
A4HYW2 | Leishmania infantum | 34% | 100% |
A4HYW3 | Leishmania infantum | 29% | 100% |
A4HYW4 | Leishmania infantum | 26% | 71% |
A4I1J4 | Leishmania infantum | 100% | 100% |
A4I6E4 | Leishmania infantum | 32% | 100% |
A4I6E6 | Leishmania infantum | 35% | 100% |
A4I6F0 | Leishmania infantum | 29% | 100% |
A4I6K4 | Leishmania infantum | 33% | 100% |
A4I6K5 | Leishmania infantum | 28% | 75% |
A4I6K6 | Leishmania infantum | 25% | 100% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 96% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 89% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 83% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 88% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 82% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AIH1 | Leishmania braziliensis | 34% | 100% |
E9AIH3 | Leishmania braziliensis | 32% | 100% |
E9AIH4 | Leishmania braziliensis | 29% | 100% |
E9AIH6 | Leishmania braziliensis | 24% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 99% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 75% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
Q4Q6L7 | Leishmania major | 34% | 100% |
Q4Q6L9 | Leishmania major | 32% | 100% |
Q4Q6M0 | Leishmania major | 29% | 100% |
Q4Q6M2 | Leishmania major | 22% | 100% |
Q4Q6M3 | Leishmania major | 28% | 76% |
Q4Q6M4 | Leishmania major | 33% | 100% |
Q4Q9U3 | Leishmania major | 97% | 100% |
Q4QCS6 | Leishmania major | 29% | 100% |
Q4QCS7 | Leishmania major | 34% | 100% |
Q4QCS8 | Leishmania major | 33% | 100% |
Q4QCS9 | Leishmania major | 33% | 100% |
Q9U0T9 | Leishmania major | 30% | 100% |
V5AYJ1 | Trypanosoma cruzi | 35% | 99% |
V5B5I4 | Trypanosoma cruzi | 34% | 84% |
V5BA05 | Trypanosoma cruzi | 34% | 100% |
V5BEL3 | Trypanosoma cruzi | 34% | 100% |
V5BN20 | Trypanosoma cruzi | 32% | 91% |
V5D5V8 | Trypanosoma cruzi | 28% | 95% |
V5D9Y2 | Trypanosoma cruzi | 30% | 83% |
V5DES7 | Trypanosoma cruzi | 32% | 89% |