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: 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: 92 |
NetGPI | no | yes: 0, no: 94 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0005737 | cytoplasm | 2 | 3 |
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: E9AIH3
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 95 |
GO:0006807 | nitrogen compound metabolic process | 2 | 95 |
GO:0008152 | metabolic process | 1 | 95 |
GO:0019538 | protein metabolic process | 3 | 95 |
GO:0043170 | macromolecule metabolic process | 3 | 95 |
GO:0044238 | primary metabolic process | 2 | 95 |
GO:0071704 | organic substance metabolic process | 2 | 95 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 95 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 95 |
GO:0004175 | endopeptidase activity | 4 | 95 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 95 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 95 |
GO:0008233 | peptidase activity | 3 | 95 |
GO:0008234 | cysteine-type peptidase activity | 4 | 95 |
GO:0016787 | hydrolase activity | 2 | 95 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 95 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.435 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.498 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.434 |
CLV_PCSK_PC1ET2_1 | 453 | 455 | PF00082 | 0.265 |
CLV_PCSK_PC1ET2_1 | 538 | 540 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 670 | 674 | PF00082 | 0.459 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.695 |
DOC_CKS1_1 | 380 | 385 | PF01111 | 0.456 |
DOC_CYCLIN_yCln2_LP_2 | 620 | 626 | PF00134 | 0.397 |
DOC_MAPK_FxFP_2 | 177 | 180 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 524 | 531 | PF00069 | 0.384 |
DOC_MAPK_HePTP_8 | 521 | 533 | PF00069 | 0.255 |
DOC_MAPK_MEF2A_6 | 524 | 533 | PF00069 | 0.353 |
DOC_MAPK_MEF2A_6 | 628 | 637 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 670 | 678 | PF00069 | 0.490 |
DOC_PP1_RVXF_1 | 169 | 175 | PF00149 | 0.392 |
DOC_PP1_RVXF_1 | 632 | 638 | PF00149 | 0.359 |
DOC_PP1_RVXF_1 | 67 | 73 | PF00149 | 0.198 |
DOC_PP2B_LxvP_1 | 602 | 605 | PF13499 | 0.330 |
DOC_PP2B_PxIxI_1 | 673 | 679 | PF00149 | 0.473 |
DOC_PP4_FxxP_1 | 177 | 180 | PF00568 | 0.501 |
DOC_PP4_FxxP_1 | 254 | 257 | PF00568 | 0.457 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.464 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.449 |
DOC_USP7_MATH_2 | 180 | 186 | PF00917 | 0.469 |
DOC_USP7_UBL2_3 | 317 | 321 | PF12436 | 0.454 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 574 | 579 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.302 |
LIG_14-3-3_CanoR_1 | 273 | 277 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 437 | 447 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 56 | 60 | PF00244 | 0.273 |
LIG_14-3-3_CanoR_1 | 606 | 615 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 97 | 103 | PF00244 | 0.355 |
LIG_AP2alpha_1 | 174 | 178 | PF02296 | 0.338 |
LIG_APCC_ABBA_1 | 588 | 593 | PF00400 | 0.392 |
LIG_BIR_III_2 | 36 | 40 | PF00653 | 0.359 |
LIG_deltaCOP1_diTrp_1 | 446 | 451 | PF00928 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 481 | 489 | PF00928 | 0.462 |
LIG_eIF4E_1 | 407 | 413 | PF01652 | 0.483 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.324 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.414 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.458 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.449 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.461 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.319 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.494 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.315 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.378 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.452 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.452 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.411 |
LIG_FHA_2 | 515 | 521 | PF00498 | 0.377 |
LIG_FHA_2 | 658 | 664 | PF00498 | 0.433 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.232 |
LIG_LIR_Apic_2 | 176 | 181 | PF02991 | 0.443 |
LIG_LIR_Apic_2 | 25 | 31 | PF02991 | 0.473 |
LIG_LIR_Apic_2 | 252 | 257 | PF02991 | 0.459 |
LIG_LIR_Apic_2 | 445 | 450 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 139 | 148 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 149 | 158 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 316 | 326 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 360 | 368 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 417 | 426 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 509 | 519 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 577 | 588 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 599 | 608 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 609 | 618 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 648 | 658 | PF02991 | 0.461 |
LIG_LIR_LC3C_4 | 599 | 604 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 139 | 143 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 288 | 293 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 309 | 314 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 360 | 365 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 417 | 421 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 466 | 470 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 509 | 514 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 577 | 583 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 589 | 594 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 599 | 604 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 609 | 614 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 648 | 653 | PF02991 | 0.445 |
LIG_LYPXL_SIV_4 | 406 | 414 | PF13949 | 0.433 |
LIG_Pex14_2 | 174 | 178 | PF04695 | 0.450 |
LIG_Pex14_2 | 349 | 353 | PF04695 | 0.442 |
LIG_Pex14_2 | 478 | 482 | PF04695 | 0.455 |
LIG_PTB_Apo_2 | 370 | 377 | PF02174 | 0.392 |
LIG_PTB_Apo_2 | 90 | 97 | PF02174 | 0.164 |
LIG_PTB_Phospho_1 | 370 | 376 | PF10480 | 0.392 |
LIG_PTB_Phospho_1 | 90 | 96 | PF10480 | 0.164 |
LIG_SH2_CRK | 319 | 323 | PF00017 | 0.453 |
LIG_SH2_CRK | 326 | 330 | PF00017 | 0.455 |
LIG_SH2_CRK | 371 | 375 | PF00017 | 0.486 |
LIG_SH2_CRK | 418 | 422 | PF00017 | 0.469 |
LIG_SH2_CRK | 580 | 584 | PF00017 | 0.436 |
LIG_SH2_GRB2like | 371 | 374 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 151 | 155 | PF00017 | 0.517 |
LIG_SH2_NCK_1 | 319 | 323 | PF00017 | 0.472 |
LIG_SH2_NCK_1 | 407 | 411 | PF00017 | 0.472 |
LIG_SH2_NCK_1 | 461 | 465 | PF00017 | 0.489 |
LIG_SH2_SRC | 290 | 293 | PF00017 | 0.460 |
LIG_SH2_SRC | 376 | 379 | PF00017 | 0.448 |
LIG_SH2_SRC | 624 | 627 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 429 | 433 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 502 | 506 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 601 | 604 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 677 | 680 | PF00017 | 0.463 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.356 |
LIG_SH3_5 | 500 | 504 | PF00018 | 0.389 |
LIG_SUMO_SIM_par_1 | 547 | 552 | PF11976 | 0.382 |
LIG_TYR_ITSM | 147 | 154 | PF00017 | 0.529 |
LIG_UBA3_1 | 191 | 195 | PF00899 | 0.451 |
LIG_UBA3_1 | 364 | 369 | PF00899 | 0.472 |
LIG_UBA3_1 | 45 | 52 | PF00899 | 0.318 |
MOD_CDK_SPxK_1 | 379 | 385 | PF00069 | 0.475 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.468 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.482 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.443 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.466 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.457 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.358 |
MOD_CK2_1 | 657 | 663 | PF00069 | 0.439 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.278 |
MOD_GlcNHglycan | 340 | 344 | PF01048 | 0.270 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.624 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.288 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.405 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.251 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.261 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.485 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.488 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.454 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.345 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.364 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.332 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.318 |
MOD_LATS_1 | 367 | 373 | PF00433 | 0.355 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.255 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.319 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.297 |
MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.418 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.340 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.470 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.460 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.506 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.471 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.356 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.261 |
MOD_NEK2_2 | 98 | 103 | PF00069 | 0.291 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.338 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.504 |
MOD_PIKK_1 | 531 | 537 | PF00454 | 0.364 |
MOD_PIKK_1 | 606 | 612 | PF00454 | 0.425 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.344 |
MOD_PKA_1 | 459 | 465 | PF00069 | 0.496 |
MOD_PKA_1 | 538 | 544 | PF00069 | 0.416 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.435 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.367 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.415 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.315 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.335 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.500 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.323 |
MOD_Plk_1 | 586 | 592 | PF00069 | 0.360 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.550 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.381 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.452 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.467 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.484 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.429 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.470 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.457 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.406 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.395 |
MOD_Plk_4 | 677 | 683 | PF00069 | 0.383 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.320 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.324 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.465 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.456 |
MOD_ProDKin_1 | 574 | 580 | PF00069 | 0.421 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.301 |
MOD_SUMO_for_1 | 143 | 146 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 176 | 186 | PF00179 | 0.452 |
TRG_DiLeu_BaEn_1 | 408 | 413 | PF01217 | 0.512 |
TRG_DiLeu_BaEn_2 | 105 | 111 | PF01217 | 0.243 |
TRG_DiLeu_BaLyEn_6 | 429 | 434 | PF01217 | 0.517 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 580 | 583 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 601 | 604 | PF00928 | 0.317 |
TRG_ER_diArg_1 | 504 | 507 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 523 | 525 | PF00400 | 0.202 |
TRG_NES_CRM1_1 | 187 | 200 | PF08389 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 638 | 643 | PF00026 | 0.371 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 35% | 98% |
A0A0N1I8N2 | Leptomonas seymouri | 28% | 70% |
A0A0N1IGQ2 | Leptomonas seymouri | 32% | 97% |
A0A0N1ILF1 | Leptomonas seymouri | 87% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 34% | 88% |
A0A0N1P9P1 | Leptomonas seymouri | 36% | 81% |
A0A0N1PCA9 | Leptomonas seymouri | 36% | 93% |
A0A0N1PE91 | Leptomonas seymouri | 24% | 77% |
A0A0N1PFI4 | Leptomonas seymouri | 33% | 89% |
A0A0S4JLK6 | Bodo saltans | 29% | 85% |
A0A0S4JS70 | Bodo saltans | 25% | 89% |
A0A0S4KGT2 | Bodo saltans | 36% | 91% |
A0A0S4KKP7 | Bodo saltans | 26% | 92% |
A0A1X0NJ61 | Trypanosomatidae | 34% | 100% |
A0A1X0NJK2 | Trypanosomatidae | 33% | 91% |
A0A1X0NJX8 | Trypanosomatidae | 36% | 88% |
A0A1X0NKT7 | Trypanosomatidae | 31% | 86% |
A0A1X0NKX8 | Trypanosomatidae | 33% | 84% |
A0A1X0NMT3 | Trypanosomatidae | 39% | 81% |
A0A1X0NW84 | Trypanosomatidae | 60% | 99% |
A0A1X0NW85 | Trypanosomatidae | 41% | 100% |
A0A1X0NW89 | Trypanosomatidae | 43% | 80% |
A0A1X0NWA6 | Trypanosomatidae | 27% | 79% |
A0A1X0NWW1 | Trypanosomatidae | 42% | 95% |
A0A3Q8IBS3 | Leishmania donovani | 40% | 75% |
A0A3Q8IDD4 | Leishmania donovani | 32% | 97% |
A0A3S5H5A5 | Leishmania donovani | 37% | 80% |
A0A3S5ISG2 | Trypanosoma rangeli | 33% | 89% |
A0A3S7WW18 | Leishmania donovani | 40% | 84% |
A0A3S7WW41 | Leishmania donovani | 33% | 92% |
A0A3S7WW71 | Leishmania donovani | 91% | 100% |
A0A3S7X430 | Leishmania donovani | 34% | 88% |
A0A3S7X438 | Leishmania donovani | 30% | 73% |
A0A3S7X460 | Leishmania donovani | 34% | 88% |
A0A3S7X463 | Leishmania donovani | 26% | 73% |
A0A3S7X470 | Leishmania donovani | 32% | 95% |
A0A422MYU1 | Trypanosoma rangeli | 40% | 75% |
A0A422MYX0 | Trypanosoma rangeli | 41% | 94% |
A4H3W4 | Leishmania braziliensis | 34% | 100% |
A4HE81 | Leishmania braziliensis | 33% | 100% |
A4HFH7 | Leishmania braziliensis | 22% | 100% |
A4HJ14 | Leishmania braziliensis | 35% | 100% |
A4HJ21 | Leishmania braziliensis | 25% | 100% |
A4HJ22 | Leishmania braziliensis | 30% | 100% |
A4HJ23 | Leishmania braziliensis | 32% | 97% |
A4HJ24 | Leishmania braziliensis | 34% | 100% |
A4HS39 | Leishmania infantum | 37% | 80% |
A4HYN0 | Leishmania infantum | 40% | 84% |
A4HYW1 | Leishmania infantum | 40% | 68% |
A4HYW2 | Leishmania infantum | 91% | 100% |
A4HYW3 | Leishmania infantum | 33% | 92% |
A4HYW4 | Leishmania infantum | 28% | 69% |
A4I1J4 | Leishmania infantum | 33% | 97% |
A4I6E4 | Leishmania infantum | 32% | 95% |
A4I6E6 | Leishmania infantum | 34% | 88% |
A4I6F0 | Leishmania infantum | 30% | 73% |
A4I6K4 | Leishmania infantum | 34% | 88% |
A4I6K5 | Leishmania infantum | 26% | 73% |
A4I6K6 | Leishmania infantum | 23% | 91% |
A8MX76 | Homo sapiens | 25% | 100% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 94% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 87% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 81% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 85% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 80% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 95% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 73% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 87% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 97% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 97% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AIH1 | Leishmania braziliensis | 40% | 100% |
E9AIH4 | Leishmania braziliensis | 34% | 92% |
E9AIH6 | Leishmania braziliensis | 31% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 86% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 74% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 92% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 97% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 88% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 73% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 91% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 97% |
O08688 | Mus musculus | 26% | 100% |
O15484 | Homo sapiens | 26% | 100% |
Q4Q6L7 | Leishmania major | 34% | 100% |
Q4Q6L9 | Leishmania major | 31% | 100% |
Q4Q6M0 | Leishmania major | 31% | 100% |
Q4Q6M2 | Leishmania major | 23% | 100% |
Q4Q6M3 | Leishmania major | 26% | 100% |
Q4Q6M4 | Leishmania major | 35% | 100% |
Q4Q9U3 | Leishmania major | 33% | 100% |
Q4QCS6 | Leishmania major | 33% | 100% |
Q4QCS7 | Leishmania major | 91% | 100% |
Q4QCS8 | Leishmania major | 39% | 100% |
Q4QCS9 | Leishmania major | 39% | 100% |
Q8R4C0 | Rattus norvegicus | 26% | 100% |
Q9U0T9 | Leishmania major | 35% | 100% |
V5AYJ1 | Trypanosoma cruzi | 32% | 96% |
V5B5I4 | Trypanosoma cruzi | 41% | 82% |
V5BA05 | Trypanosoma cruzi | 42% | 100% |
V5BEL3 | Trypanosoma cruzi | 61% | 99% |
V5BN20 | Trypanosoma cruzi | 36% | 89% |
V5D5V8 | Trypanosoma cruzi | 29% | 93% |
V5D9Y2 | Trypanosoma cruzi | 36% | 81% |
V5DES7 | Trypanosoma cruzi | 32% | 87% |