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 | 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: A4H3W4
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 | 275 | 279 | PF00656 | 0.437 |
CLV_C14_Caspase3-7 | 303 | 307 | PF00656 | 0.528 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.543 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.649 |
CLV_Separin_Metazoa | 44 | 48 | PF03568 | 0.488 |
DEG_APCC_KENBOX_2 | 474 | 478 | PF00400 | 0.363 |
DEG_Kelch_Keap1_1 | 208 | 213 | PF01344 | 0.376 |
DEG_SCF_TRCP1_1 | 306 | 312 | PF00400 | 0.363 |
DOC_ANK_TNKS_1 | 383 | 390 | PF00023 | 0.454 |
DOC_CDC14_PxL_1 | 736 | 744 | PF14671 | 0.399 |
DOC_CKS1_1 | 498 | 503 | PF01111 | 0.471 |
DOC_CKS1_1 | 572 | 577 | PF01111 | 0.476 |
DOC_CYCLIN_RxL_1 | 238 | 248 | PF00134 | 0.283 |
DOC_CYCLIN_yClb1_LxF_4 | 288 | 294 | PF00134 | 0.428 |
DOC_CYCLIN_yCln2_LP_2 | 556 | 562 | PF00134 | 0.548 |
DOC_CYCLIN_yCln2_LP_2 | 762 | 768 | PF00134 | 0.454 |
DOC_MAPK_DCC_7 | 760 | 768 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 491 | 498 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 591 | 598 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 259 | 266 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 645 | 652 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 785 | 793 | PF00069 | 0.468 |
DOC_PP1_RVXF_1 | 137 | 143 | PF00149 | 0.649 |
DOC_PP1_RVXF_1 | 390 | 396 | PF00149 | 0.479 |
DOC_PP1_RVXF_1 | 483 | 490 | PF00149 | 0.533 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.525 |
DOC_PP2B_LxvP_1 | 686 | 689 | PF13499 | 0.256 |
DOC_PP2B_LxvP_1 | 737 | 740 | PF13499 | 0.381 |
DOC_PP4_FxxP_1 | 157 | 160 | PF00568 | 0.304 |
DOC_PP4_FxxP_1 | 373 | 376 | PF00568 | 0.482 |
DOC_PP4_FxxP_1 | 617 | 620 | PF00568 | 0.393 |
DOC_PP4_FxxP_1 | 83 | 86 | PF00568 | 0.545 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 777 | 781 | PF00917 | 0.611 |
DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.476 |
DOC_USP7_UBL2_3 | 544 | 548 | PF12436 | 0.545 |
DOC_USP7_UBL2_3 | 88 | 92 | PF12436 | 0.543 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.429 |
LIG_14-3-3_CanoR_1 | 253 | 262 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 392 | 396 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 626 | 632 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 701 | 710 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 87 | 94 | PF00244 | 0.604 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.749 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.315 |
LIG_BRCT_BRCA1_1 | 19 | 23 | PF00533 | 0.668 |
LIG_BRCT_BRCA1_1 | 309 | 313 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 513 | 517 | PF00533 | 0.601 |
LIG_BRCT_BRCA1_1 | 772 | 776 | PF00533 | 0.300 |
LIG_CSL_BTD_1 | 96 | 99 | PF09270 | 0.340 |
LIG_deltaCOP1_diTrp_1 | 712 | 717 | PF00928 | 0.451 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.485 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.569 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.466 |
LIG_FHA_1 | 724 | 730 | PF00498 | 0.483 |
LIG_FHA_1 | 782 | 788 | PF00498 | 0.496 |
LIG_FHA_1 | 823 | 829 | PF00498 | 0.453 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.338 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.210 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.432 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.437 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.580 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.424 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.304 |
LIG_LIR_Apic_2 | 154 | 160 | PF02991 | 0.297 |
LIG_LIR_Apic_2 | 80 | 86 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 434 | 445 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 597 | 607 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 712 | 723 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 733 | 743 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 771 | 779 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 295 | 301 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 443 | 447 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 597 | 603 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 678 | 682 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 694 | 700 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 712 | 718 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 733 | 739 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 771 | 775 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 818 | 823 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.486 |
LIG_LYPXL_yS_3 | 679 | 682 | PF13949 | 0.370 |
LIG_PDZ_Class_2 | 851 | 856 | PF00595 | 0.342 |
LIG_Pex14_2 | 228 | 232 | PF04695 | 0.361 |
LIG_PTB_Apo_2 | 335 | 342 | PF02174 | 0.364 |
LIG_PTB_Phospho_1 | 335 | 341 | PF10480 | 0.363 |
LIG_SH2_CRK | 444 | 448 | PF00017 | 0.472 |
LIG_SH2_CRK | 494 | 498 | PF00017 | 0.494 |
LIG_SH2_CRK | 697 | 701 | PF00017 | 0.538 |
LIG_SH2_NCK_1 | 123 | 127 | PF00017 | 0.672 |
LIG_SH2_NCK_1 | 444 | 448 | PF00017 | 0.494 |
LIG_SH2_PTP2 | 324 | 327 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 772 | 776 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 736 | 739 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 836 | 839 | PF00017 | 0.494 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.504 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.742 |
LIG_SH3_3 | 622 | 628 | PF00018 | 0.213 |
LIG_SH3_3 | 641 | 647 | PF00018 | 0.401 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.706 |
LIG_SH3_3 | 818 | 824 | PF00018 | 0.504 |
LIG_SH3_4 | 326 | 333 | PF00018 | 0.441 |
LIG_SUMO_SIM_anti_2 | 595 | 600 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 213 | 219 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 539 | 545 | PF11976 | 0.571 |
LIG_SUMO_SIM_par_1 | 680 | 685 | PF11976 | 0.406 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.815 |
LIG_TRAF2_1 | 795 | 798 | PF00917 | 0.274 |
LIG_TRAF2_1 | 830 | 833 | PF00917 | 0.555 |
LIG_TRFH_1 | 736 | 740 | PF08558 | 0.373 |
LIG_TYR_ITIM | 162 | 167 | PF00017 | 0.344 |
LIG_UBA3_1 | 486 | 492 | PF00899 | 0.483 |
LIG_WRC_WIRS_1 | 173 | 178 | PF05994 | 0.359 |
LIG_WRC_WIRS_1 | 188 | 193 | PF05994 | 0.415 |
MOD_CDK_SPxK_1 | 497 | 503 | PF00069 | 0.492 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.638 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.327 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.484 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.542 |
MOD_CK1_1 | 780 | 786 | PF00069 | 0.633 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.432 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.307 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.449 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.476 |
MOD_CK2_1 | 780 | 786 | PF00069 | 0.404 |
MOD_CK2_1 | 827 | 833 | PF00069 | 0.507 |
MOD_GlcNHglycan | 208 | 213 | PF01048 | 0.334 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.519 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.289 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.280 |
MOD_GlcNHglycan | 476 | 480 | PF01048 | 0.266 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.336 |
MOD_GlcNHglycan | 810 | 813 | PF01048 | 0.435 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.378 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.399 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.482 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.474 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.662 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.483 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.451 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.407 |
MOD_GSK3_1 | 777 | 784 | PF00069 | 0.580 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.505 |
MOD_LATS_1 | 194 | 200 | PF00433 | 0.166 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.639 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.323 |
MOD_N-GLC_1 | 701 | 706 | PF02516 | 0.432 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.638 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.277 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.501 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.490 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.478 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.393 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.364 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.530 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.449 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.478 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.540 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.552 |
MOD_PIKK_1 | 564 | 570 | PF00454 | 0.499 |
MOD_PIKK_1 | 705 | 711 | PF00454 | 0.493 |
MOD_PIKK_1 | 827 | 833 | PF00454 | 0.527 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.455 |
MOD_PKA_2 | 700 | 706 | PF00069 | 0.496 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.535 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.685 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.354 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.476 |
MOD_Plk_1 | 594 | 600 | PF00069 | 0.459 |
MOD_Plk_1 | 648 | 654 | PF00069 | 0.380 |
MOD_Plk_1 | 745 | 751 | PF00069 | 0.486 |
MOD_Plk_1 | 770 | 776 | PF00069 | 0.290 |
MOD_Plk_2-3 | 179 | 185 | PF00069 | 0.277 |
MOD_Plk_2-3 | 34 | 40 | PF00069 | 0.674 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.619 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.337 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.652 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.498 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.481 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.404 |
MOD_Plk_4 | 648 | 654 | PF00069 | 0.372 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.474 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.626 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.485 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.479 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.514 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.428 |
MOD_SUMO_for_1 | 325 | 328 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 478 | 487 | PF00179 | 0.554 |
MOD_SUMO_rev_2 | 539 | 546 | PF00179 | 0.526 |
TRG_DiLeu_BaEn_1 | 158 | 163 | PF01217 | 0.331 |
TRG_DiLeu_BaEn_2 | 223 | 229 | PF01217 | 0.255 |
TRG_DiLeu_BaEn_4 | 158 | 164 | PF01217 | 0.336 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 679 | 682 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 736 | 739 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 772 | 775 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 320 | 323 | PF00400 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 423 | 427 | PF00026 | 0.290 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 30% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 29% | 87% |
A0A0N1IGQ2 | Leptomonas seymouri | 30% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 35% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 31% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 72% | 100% |
A0A0N1PCA9 | Leptomonas seymouri | 31% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 26% | 96% |
A0A0N1PFI4 | Leptomonas seymouri | 36% | 100% |
A0A0S4JLK6 | Bodo saltans | 28% | 100% |
A0A0S4JS70 | Bodo saltans | 26% | 100% |
A0A0S4KGT2 | Bodo saltans | 38% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 27% | 70% |
A0A1X0NJK2 | Trypanosomatidae | 34% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 31% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 32% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 31% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 48% | 100% |
A0A1X0NW84 | Trypanosomatidae | 36% | 100% |
A0A1X0NW85 | Trypanosomatidae | 36% | 100% |
A0A1X0NW89 | Trypanosomatidae | 43% | 99% |
A0A1X0NWA6 | Trypanosomatidae | 28% | 98% |
A0A1X0NWW1 | Trypanosomatidae | 39% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 41% | 94% |
A0A3Q8IDD4 | Leishmania donovani | 31% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 27% | 100% |
A0A3S5H5A5 | Leishmania donovani | 85% | 100% |
A0A3S5ISG2 | Trypanosoma rangeli | 32% | 100% |
A0A3S7WW13 | Leishmania donovani | 28% | 77% |
A0A3S7WW18 | Leishmania donovani | 40% | 100% |
A0A3S7WW41 | Leishmania donovani | 30% | 100% |
A0A3S7WW71 | Leishmania donovani | 34% | 100% |
A0A3S7X430 | Leishmania donovani | 31% | 100% |
A0A3S7X438 | Leishmania donovani | 33% | 91% |
A0A3S7X460 | Leishmania donovani | 30% | 100% |
A0A3S7X463 | Leishmania donovani | 30% | 91% |
A0A3S7X470 | Leishmania donovani | 33% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 43% | 93% |
A0A422MYX0 | Trypanosoma rangeli | 36% | 100% |
A4HE81 | Leishmania braziliensis | 30% | 100% |
A4HJ14 | Leishmania braziliensis | 31% | 100% |
A4HJ21 | Leishmania braziliensis | 29% | 96% |
A4HJ22 | Leishmania braziliensis | 31% | 90% |
A4HJ24 | Leishmania braziliensis | 33% | 100% |
A4HS39 | Leishmania infantum | 85% | 100% |
A4HYN0 | Leishmania infantum | 40% | 100% |
A4HYW1 | Leishmania infantum | 41% | 84% |
A4HYW2 | Leishmania infantum | 34% | 100% |
A4HYW3 | Leishmania infantum | 30% | 100% |
A4HYW4 | Leishmania infantum | 28% | 86% |
A4I1J4 | Leishmania infantum | 31% | 100% |
A4I6E4 | Leishmania infantum | 33% | 100% |
A4I6E6 | Leishmania infantum | 30% | 100% |
A4I6F0 | Leishmania infantum | 33% | 91% |
A4I6K4 | Leishmania infantum | 31% | 100% |
A4I6K5 | Leishmania infantum | 30% | 91% |
A4I6K6 | Leishmania infantum | 27% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 79% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 91% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AIH1 | Leishmania braziliensis | 40% | 100% |
E9AIH3 | Leishmania braziliensis | 34% | 100% |
E9AIH4 | Leishmania braziliensis | 30% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 92% |
E9AUQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 91% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
Q4Q6L7 | Leishmania major | 30% | 100% |
Q4Q6L9 | Leishmania major | 33% | 100% |
Q4Q6M0 | Leishmania major | 33% | 100% |
Q4Q6M2 | Leishmania major | 27% | 100% |
Q4Q6M3 | Leishmania major | 29% | 100% |
Q4Q6M4 | Leishmania major | 33% | 100% |
Q4Q9U3 | Leishmania major | 31% | 98% |
Q4QCS6 | Leishmania major | 30% | 100% |
Q4QCS7 | Leishmania major | 33% | 91% |
Q4QCS8 | Leishmania major | 40% | 100% |
Q4QCS9 | Leishmania major | 41% | 100% |
Q9U0T9 | Leishmania major | 84% | 100% |
V5AYJ1 | Trypanosoma cruzi | 30% | 100% |
V5B5I4 | Trypanosoma cruzi | 43% | 100% |
V5BA05 | Trypanosoma cruzi | 40% | 100% |
V5BEL3 | Trypanosoma cruzi | 36% | 100% |
V5BII7 | Trypanosoma cruzi | 28% | 69% |
V5BN20 | Trypanosoma cruzi | 31% | 100% |
V5D5V8 | Trypanosoma cruzi | 29% | 100% |
V5D9Y2 | Trypanosoma cruzi | 46% | 100% |
V5DES7 | Trypanosoma cruzi | 32% | 100% |