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. | no | yes: 38 |
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 | yes | yes: 1, no: 95 |
NetGPI | no | yes: 0, no: 96 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0016020 | membrane | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
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 |
Related structures:
AlphaFold database: Q4Q6L7
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 97 |
GO:0006807 | nitrogen compound metabolic process | 2 | 97 |
GO:0008152 | metabolic process | 1 | 97 |
GO:0019538 | protein metabolic process | 3 | 97 |
GO:0043170 | macromolecule metabolic process | 3 | 97 |
GO:0044238 | primary metabolic process | 2 | 97 |
GO:0071704 | organic substance metabolic process | 2 | 97 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 97 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 97 |
GO:0004175 | endopeptidase activity | 4 | 97 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 97 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 97 |
GO:0008233 | peptidase activity | 3 | 97 |
GO:0008234 | cysteine-type peptidase activity | 4 | 97 |
GO:0016787 | hydrolase activity | 2 | 97 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 97 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 513 | 517 | PF00656 | 0.505 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 662 | 664 | PF00675 | 0.375 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 232 | 234 | PF00082 | 0.269 |
CLV_PCSK_PC1ET2_1 | 706 | 708 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.296 |
DEG_APCC_DBOX_1 | 462 | 470 | PF00400 | 0.515 |
DEG_MDM2_SWIB_1 | 510 | 518 | PF02201 | 0.437 |
DEG_SCF_FBW7_1 | 659 | 665 | PF00400 | 0.485 |
DOC_AGCK_PIF_1 | 376 | 381 | PF00069 | 0.502 |
DOC_ANK_TNKS_1 | 152 | 159 | PF00023 | 0.276 |
DOC_CKS1_1 | 414 | 419 | PF01111 | 0.448 |
DOC_CKS1_1 | 659 | 664 | PF01111 | 0.366 |
DOC_CYCLIN_RxL_1 | 556 | 566 | PF00134 | 0.480 |
DOC_CYCLIN_RxL_1 | 580 | 590 | PF00134 | 0.473 |
DOC_MAPK_DCC_7 | 196 | 205 | PF00069 | 0.414 |
DOC_MAPK_DCC_7 | 457 | 466 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 232 | 240 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 404 | 414 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 556 | 563 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 668 | 677 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 712 | 719 | PF00069 | 0.537 |
DOC_MAPK_HePTP_8 | 454 | 466 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 196 | 205 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 457 | 466 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 623 | 631 | PF00069 | 0.456 |
DOC_MAPK_RevD_3 | 543 | 557 | PF00069 | 0.473 |
DOC_PP2B_LxvP_1 | 342 | 345 | PF13499 | 0.440 |
DOC_PP4_FxxP_1 | 286 | 289 | PF00568 | 0.452 |
DOC_PP4_FxxP_1 | 459 | 462 | PF00568 | 0.492 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.481 |
DOC_USP7_UBL2_3 | 137 | 141 | PF12436 | 0.446 |
DOC_USP7_UBL2_3 | 279 | 283 | PF12436 | 0.564 |
DOC_USP7_UBL2_3 | 349 | 353 | PF12436 | 0.450 |
DOC_USP7_UBL2_3 | 485 | 489 | PF12436 | 0.483 |
DOC_USP7_UBL2_3 | 552 | 556 | PF12436 | 0.421 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.318 |
LIG_14-3-3_CanoR_1 | 110 | 114 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 497 | 505 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 663 | 672 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 685 | 691 | PF00244 | 0.434 |
LIG_APCC_ABBAyCdc20_2 | 79 | 85 | PF00400 | 0.341 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.511 |
LIG_CSL_BTD_1 | 342 | 345 | PF09270 | 0.444 |
LIG_deltaCOP1_diTrp_1 | 477 | 483 | PF00928 | 0.441 |
LIG_deltaCOP1_diTrp_1 | 513 | 521 | PF00928 | 0.460 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.437 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.502 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.384 |
LIG_FHA_2 | 716 | 722 | PF00498 | 0.462 |
LIG_IRF3_LxIS_1 | 581 | 588 | PF10401 | 0.403 |
LIG_LIR_Apic_2 | 230 | 234 | PF02991 | 0.441 |
LIG_LIR_Apic_2 | 284 | 289 | PF02991 | 0.453 |
LIG_LIR_Apic_2 | 49 | 55 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 132 | 139 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 21 | 28 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 348 | 359 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 450 | 459 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 615 | 625 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 236 | 240 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 348 | 354 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 357 | 361 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 374 | 379 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 450 | 454 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 579 | 585 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 683 | 687 | PF02991 | 0.418 |
LIG_MLH1_MIPbox_1 | 395 | 399 | PF16413 | 0.514 |
LIG_MYND_3 | 344 | 348 | PF01753 | 0.344 |
LIG_NRBOX | 4 | 10 | PF00104 | 0.398 |
LIG_PCNA_yPIPBox_3 | 310 | 323 | PF02747 | 0.403 |
LIG_Pex14_2 | 381 | 385 | PF04695 | 0.438 |
LIG_Pex14_2 | 510 | 514 | PF04695 | 0.447 |
LIG_Pex14_2 | 538 | 542 | PF04695 | 0.413 |
LIG_REV1ctd_RIR_1 | 396 | 404 | PF16727 | 0.463 |
LIG_SH2_CRK | 326 | 330 | PF00017 | 0.569 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.447 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.448 |
LIG_SH2_CRK | 451 | 455 | PF00017 | 0.463 |
LIG_SH2_CRK | 52 | 56 | PF00017 | 0.319 |
LIG_SH2_CRK | 536 | 540 | PF00017 | 0.326 |
LIG_SH2_CRK | 582 | 586 | PF00017 | 0.393 |
LIG_SH2_PTP2 | 237 | 240 | PF00017 | 0.474 |
LIG_SH2_PTP2 | 639 | 642 | PF00017 | 0.396 |
LIG_SH2_SRC | 237 | 240 | PF00017 | 0.472 |
LIG_SH2_SRC | 410 | 413 | PF00017 | 0.436 |
LIG_SH2_SRC | 639 | 642 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 340 | 344 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 617 | 621 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 104 | 107 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.334 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.290 |
LIG_SH3_3 | 572 | 578 | PF00018 | 0.526 |
LIG_SH3_3 | 608 | 614 | PF00018 | 0.455 |
LIG_SH3_3 | 672 | 678 | PF00018 | 0.390 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.442 |
LIG_SUMO_SIM_anti_2 | 2 | 8 | PF11976 | 0.602 |
LIG_SUMO_SIM_anti_2 | 271 | 278 | PF11976 | 0.465 |
LIG_SUMO_SIM_par_1 | 410 | 416 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 585 | 590 | PF11976 | 0.351 |
LIG_SUMO_SIM_par_1 | 600 | 607 | PF11976 | 0.409 |
LIG_TRFH_1 | 10 | 14 | PF08558 | 0.385 |
LIG_UBA3_1 | 561 | 568 | PF00899 | 0.379 |
LIG_WRC_WIRS_1 | 19 | 24 | PF05994 | 0.372 |
LIG_WRC_WIRS_1 | 378 | 383 | PF05994 | 0.486 |
LIG_WRC_WIRS_1 | 687 | 692 | PF05994 | 0.427 |
MOD_CDK_SPK_2 | 113 | 118 | PF00069 | 0.388 |
MOD_CDK_SPK_2 | 658 | 663 | PF00069 | 0.407 |
MOD_CDK_SPxK_1 | 658 | 664 | PF00069 | 0.425 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.574 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.585 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.435 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.429 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.513 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.418 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.537 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.453 |
MOD_CK2_1 | 715 | 721 | PF00069 | 0.398 |
MOD_CMANNOS | 511 | 514 | PF00535 | 0.249 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.456 |
MOD_GlcNHglycan | 252 | 256 | PF01048 | 0.283 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.286 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.264 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.318 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.591 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.297 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.605 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.500 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.457 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.471 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.496 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.498 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.435 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.318 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.504 |
MOD_N-GLC_1 | 485 | 490 | PF02516 | 0.281 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.290 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.459 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.463 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.465 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.523 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.318 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.309 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.420 |
MOD_NEK2_1 | 670 | 675 | PF00069 | 0.357 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.421 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.279 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.273 |
MOD_NEK2_2 | 109 | 114 | PF00069 | 0.334 |
MOD_NEK2_2 | 715 | 720 | PF00069 | 0.250 |
MOD_OFUCOSY | 674 | 681 | PF10250 | 0.217 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.389 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.540 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.635 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.440 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.582 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.525 |
MOD_PIKK_1 | 563 | 569 | PF00454 | 0.350 |
MOD_PKA_1 | 663 | 669 | PF00069 | 0.536 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.329 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.508 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.496 |
MOD_PKA_2 | 662 | 668 | PF00069 | 0.374 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.394 |
MOD_Plk_1 | 653 | 659 | PF00069 | 0.438 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.300 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.302 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.478 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.491 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.443 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.489 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.470 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.492 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.455 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.332 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.525 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.421 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.463 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.448 |
MOD_ProDKin_1 | 658 | 664 | PF00069 | 0.322 |
MOD_SUMO_for_1 | 551 | 554 | PF00179 | 0.378 |
MOD_SUMO_for_1 | 57 | 60 | PF00179 | 0.280 |
MOD_SUMO_rev_2 | 161 | 169 | PF00179 | 0.446 |
MOD_SUMO_rev_2 | 271 | 281 | PF00179 | 0.524 |
TRG_DiLeu_BaLyEn_6 | 342 | 347 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 462 | 467 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 582 | 585 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 617 | 620 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.333 |
TRG_ER_diArg_1 | 214 | 216 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 462 | 465 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.489 |
TRG_NLS_MonoExtN_4 | 194 | 200 | PF00514 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 67% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 28% | 74% |
A0A0N1IGQ2 | Leptomonas seymouri | 34% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 34% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 35% | 93% |
A0A0N1P9P1 | Leptomonas seymouri | 33% | 86% |
A0A0N1PCA9 | Leptomonas seymouri | 29% | 99% |
A0A0N1PE91 | Leptomonas seymouri | 24% | 82% |
A0A0N1PFI4 | Leptomonas seymouri | 33% | 94% |
A0A0S4JLK6 | Bodo saltans | 29% | 90% |
A0A0S4JS70 | Bodo saltans | 26% | 95% |
A0A0S4KGT2 | Bodo saltans | 39% | 97% |
A0A1X0NJ61 | Trypanosomatidae | 39% | 100% |
A0A1X0NJK2 | Trypanosomatidae | 44% | 96% |
A0A1X0NJX8 | Trypanosomatidae | 34% | 94% |
A0A1X0NKT7 | Trypanosomatidae | 30% | 92% |
A0A1X0NKX8 | Trypanosomatidae | 32% | 89% |
A0A1X0NMT3 | Trypanosomatidae | 35% | 86% |
A0A1X0NW84 | Trypanosomatidae | 35% | 100% |
A0A1X0NW85 | Trypanosomatidae | 33% | 100% |
A0A1X0NW89 | Trypanosomatidae | 34% | 85% |
A0A1X0NWA6 | Trypanosomatidae | 25% | 84% |
A0A1X0NWW1 | Trypanosomatidae | 34% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 35% | 80% |
A0A3Q8IDD4 | Leishmania donovani | 34% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 25% | 97% |
A0A3S5H5A5 | Leishmania donovani | 31% | 86% |
A0A3S5ISG2 | Trypanosoma rangeli | 34% | 95% |
A0A3S7WW13 | Leishmania donovani | 27% | 66% |
A0A3S7WW18 | Leishmania donovani | 35% | 89% |
A0A3S7WW41 | Leishmania donovani | 31% | 99% |
A0A3S7WW71 | Leishmania donovani | 34% | 100% |
A0A3S7X430 | Leishmania donovani | 34% | 93% |
A0A3S7X438 | Leishmania donovani | 31% | 78% |
A0A3S7X460 | Leishmania donovani | 93% | 94% |
A0A3S7X463 | Leishmania donovani | 27% | 78% |
A0A3S7X470 | Leishmania donovani | 33% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 35% | 80% |
A0A422MYX0 | Trypanosoma rangeli | 33% | 100% |
A4H3W4 | Leishmania braziliensis | 30% | 86% |
A4HE81 | Leishmania braziliensis | 35% | 100% |
A4HJ14 | Leishmania braziliensis | 33% | 93% |
A4HJ21 | Leishmania braziliensis | 25% | 82% |
A4HJ22 | Leishmania braziliensis | 30% | 77% |
A4HJ23 | Leishmania braziliensis | 33% | 100% |
A4HJ24 | Leishmania braziliensis | 81% | 100% |
A4HS39 | Leishmania infantum | 31% | 86% |
A4HYN0 | Leishmania infantum | 35% | 89% |
A4HYW1 | Leishmania infantum | 35% | 72% |
A4HYW2 | Leishmania infantum | 34% | 100% |
A4HYW3 | Leishmania infantum | 31% | 99% |
A4HYW4 | Leishmania infantum | 27% | 73% |
A4I1J4 | Leishmania infantum | 34% | 100% |
A4I6E4 | Leishmania infantum | 33% | 100% |
A4I6E6 | Leishmania infantum | 93% | 94% |
A4I6F0 | Leishmania infantum | 31% | 78% |
A4I6K4 | Leishmania infantum | 34% | 93% |
A4I6K5 | Leishmania infantum | 28% | 78% |
A4I6K6 | Leishmania infantum | 25% | 97% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 68% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 92% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 86% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 91% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 86% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 78% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 93% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AIH1 | Leishmania braziliensis | 35% | 90% |
E9AIH3 | Leishmania braziliensis | 34% | 100% |
E9AIH4 | Leishmania braziliensis | 30% | 99% |
E9AIH6 | Leishmania braziliensis | 28% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 92% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 78% |
E9AUQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 99% |
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% | 93% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 78% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 97% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
O08688 | Mus musculus | 27% | 100% |
O15484 | Homo sapiens | 26% | 100% |
Q4Q6L9 | Leishmania major | 33% | 100% |
Q4Q6M0 | Leishmania major | 30% | 78% |
Q4Q6M2 | Leishmania major | 23% | 97% |
Q4Q6M3 | Leishmania major | 28% | 79% |
Q4Q6M4 | Leishmania major | 34% | 86% |
Q4Q9U3 | Leishmania major | 35% | 100% |
Q4QCS6 | Leishmania major | 31% | 99% |
Q4QCS7 | Leishmania major | 34% | 100% |
Q4QCS8 | Leishmania major | 35% | 89% |
Q4QCS9 | Leishmania major | 35% | 100% |
Q8R4C0 | Rattus norvegicus | 26% | 100% |
Q9U0T9 | Leishmania major | 30% | 86% |
V5AYJ1 | Trypanosoma cruzi | 41% | 100% |
V5B5I4 | Trypanosoma cruzi | 33% | 87% |
V5BA05 | Trypanosoma cruzi | 36% | 100% |
V5BEL3 | Trypanosoma cruzi | 34% | 100% |
V5BN20 | Trypanosoma cruzi | 35% | 95% |
V5D5V8 | Trypanosoma cruzi | 28% | 99% |
V5D9Y2 | Trypanosoma cruzi | 34% | 86% |
V5DES7 | Trypanosoma cruzi | 35% | 92% |