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: 1, no: 93 |
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: A0A3Q8IJT4
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 | 200 | 204 | PF00656 | 0.540 |
CLV_C14_Caspase3-7 | 376 | 380 | PF00656 | 0.477 |
CLV_C14_Caspase3-7 | 448 | 452 | PF00656 | 0.552 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.278 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.296 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 392 | 394 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 465 | 467 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 684 | 688 | PF00082 | 0.472 |
CLV_Separin_Metazoa | 365 | 369 | PF03568 | 0.367 |
DEG_SCF_FBW7_1 | 84 | 89 | PF00400 | 0.192 |
DEG_SPOP_SBC_1 | 573 | 577 | PF00917 | 0.663 |
DOC_CYCLIN_yCln2_LP_2 | 348 | 354 | PF00134 | 0.380 |
DOC_CYCLIN_yCln2_LP_2 | 698 | 704 | PF00134 | 0.317 |
DOC_MAPK_gen_1 | 181 | 190 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 181 | 190 | PF00069 | 0.268 |
DOC_MAPK_MEF2A_6 | 536 | 544 | PF00069 | 0.400 |
DOC_PP2B_LxvP_1 | 18 | 21 | PF13499 | 0.318 |
DOC_PP2B_LxvP_1 | 328 | 331 | PF13499 | 0.505 |
DOC_PP2B_LxvP_1 | 348 | 351 | PF13499 | 0.365 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.460 |
DOC_PP4_FxxP_1 | 232 | 235 | PF00568 | 0.432 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.486 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.384 |
DOC_USP7_UBL2_3 | 335 | 339 | PF12436 | 0.481 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 718 | 723 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.380 |
LIG_14-3-3_CanoR_1 | 133 | 143 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 166 | 175 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 213 | 219 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 25 | 31 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 477 | 483 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 53 | 61 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 536 | 541 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 68 | 73 | PF00244 | 0.306 |
LIG_Actin_WH2_2 | 363 | 380 | PF00022 | 0.545 |
LIG_APCC_ABBA_1 | 427 | 432 | PF00400 | 0.542 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.725 |
LIG_BRCT_BRCA1_1 | 598 | 602 | PF00533 | 0.631 |
LIG_CSL_BTD_1 | 328 | 331 | PF09270 | 0.505 |
LIG_deltaCOP1_diTrp_1 | 469 | 475 | PF00928 | 0.474 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.353 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.493 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.530 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.501 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.477 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.385 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.692 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.544 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.380 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.659 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.501 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.397 |
LIG_FHA_1 | 697 | 703 | PF00498 | 0.446 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.519 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.511 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.373 |
LIG_GBD_Chelix_1 | 653 | 661 | PF00786 | 0.233 |
LIG_LIR_Apic_2 | 203 | 209 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 343 | 352 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 469 | 478 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 692 | 703 | PF02991 | 0.491 |
LIG_LIR_LC3C_4 | 424 | 428 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 469 | 474 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 692 | 698 | PF02991 | 0.488 |
LIG_MYND_1 | 235 | 239 | PF01753 | 0.375 |
LIG_MYND_3 | 330 | 334 | PF01753 | 0.386 |
LIG_NRBOX | 586 | 592 | PF00104 | 0.230 |
LIG_Pex14_1 | 408 | 412 | PF04695 | 0.540 |
LIG_Pex14_2 | 355 | 359 | PF04695 | 0.481 |
LIG_RPA_C_Fungi | 381 | 393 | PF08784 | 0.171 |
LIG_SH2_CRK | 33 | 37 | PF00017 | 0.377 |
LIG_SH2_NCK_1 | 430 | 434 | PF00017 | 0.351 |
LIG_SH2_PTP2 | 185 | 188 | PF00017 | 0.335 |
LIG_SH2_PTP2 | 206 | 209 | PF00017 | 0.447 |
LIG_SH2_PTP2 | 641 | 644 | PF00017 | 0.438 |
LIG_SH2_SRC | 206 | 209 | PF00017 | 0.397 |
LIG_SH2_SRC | 218 | 221 | PF00017 | 0.375 |
LIG_SH2_SRC | 430 | 433 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 623 | 627 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 655 | 659 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 641 | 644 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 655 | 658 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.395 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.516 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.579 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.393 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.645 |
LIG_SUMO_SIM_anti_2 | 424 | 432 | PF11976 | 0.497 |
LIG_SUMO_SIM_par_1 | 424 | 432 | PF11976 | 0.498 |
LIG_SUMO_SIM_par_1 | 539 | 545 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 699 | 707 | PF11976 | 0.474 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.534 |
LIG_TRAF2_1 | 492 | 495 | PF00917 | 0.185 |
LIG_TRAF2_1 | 97 | 100 | PF00917 | 0.451 |
LIG_TYR_ITIM | 183 | 188 | PF00017 | 0.315 |
LIG_TYR_ITIM | 428 | 433 | PF00017 | 0.189 |
LIG_TYR_ITSM | 65 | 72 | PF00017 | 0.193 |
MOD_CDK_SPK_2 | 718 | 723 | PF00069 | 0.549 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.487 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.333 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.319 |
MOD_CK1_1 | 593 | 599 | PF00069 | 0.527 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.504 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.449 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.676 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.402 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.322 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.471 |
MOD_CK2_1 | 703 | 709 | PF00069 | 0.496 |
MOD_Cter_Amidation | 280 | 283 | PF01082 | 0.281 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.644 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.343 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.374 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.407 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.529 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.599 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.623 |
MOD_GlcNHglycan | 709 | 713 | PF01048 | 0.550 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.449 |
MOD_GlcNHglycan | 739 | 742 | PF01048 | 0.530 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.399 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.503 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.314 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.365 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.375 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.569 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.533 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.401 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.394 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.647 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.509 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.449 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.615 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.332 |
MOD_LATS_1 | 291 | 297 | PF00433 | 0.185 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.327 |
MOD_N-GLC_1 | 696 | 701 | PF02516 | 0.540 |
MOD_N-GLC_2 | 123 | 125 | PF02516 | 0.181 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.414 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.501 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.356 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.415 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.387 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.480 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.394 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.338 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.404 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.545 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.456 |
MOD_NEK2_1 | 703 | 708 | PF00069 | 0.488 |
MOD_NEK2_1 | 737 | 742 | PF00069 | 0.524 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.530 |
MOD_NEK2_2 | 201 | 206 | PF00069 | 0.417 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.510 |
MOD_PIKK_1 | 416 | 422 | PF00454 | 0.470 |
MOD_PIKK_1 | 531 | 537 | PF00454 | 0.545 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.398 |
MOD_PIKK_1 | 565 | 571 | PF00454 | 0.559 |
MOD_PIKK_1 | 578 | 584 | PF00454 | 0.655 |
MOD_PIKK_1 | 696 | 702 | PF00454 | 0.621 |
MOD_PK_1 | 536 | 542 | PF00069 | 0.263 |
MOD_PKA_1 | 464 | 470 | PF00069 | 0.457 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.541 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.401 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.435 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.349 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.363 |
MOD_PKA_2 | 675 | 681 | PF00069 | 0.506 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.424 |
MOD_Plk_1 | 542 | 548 | PF00069 | 0.374 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.339 |
MOD_Plk_1 | 704 | 710 | PF00069 | 0.457 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.446 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.358 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.349 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.340 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.345 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.343 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.176 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.544 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.400 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.303 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.363 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.401 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.436 |
MOD_Plk_4 | 669 | 675 | PF00069 | 0.662 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.480 |
MOD_ProDKin_1 | 718 | 724 | PF00069 | 0.424 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.380 |
MOD_SUMO_rev_2 | 104 | 113 | PF00179 | 0.388 |
MOD_SUMO_rev_2 | 89 | 97 | PF00179 | 0.410 |
TRG_DiLeu_BaEn_1 | 109 | 114 | PF01217 | 0.401 |
TRG_DiLeu_BaEn_1 | 485 | 490 | PF01217 | 0.193 |
TRG_DiLeu_BaLyEn_6 | 328 | 333 | PF01217 | 0.413 |
TRG_DiLeu_BaLyEn_6 | 390 | 395 | PF01217 | 0.362 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 618 | 621 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.445 |
TRG_ER_diArg_1 | 131 | 133 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 268 | 270 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 395 | 398 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 475 | 477 | PF00400 | 0.419 |
TRG_Pf-PMV_PEXEL_1 | 393 | 397 | PF00026 | 0.410 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 23% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 32% | 77% |
A0A0N1IGQ2 | Leptomonas seymouri | 23% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 23% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 27% | 96% |
A0A0N1P9P1 | Leptomonas seymouri | 26% | 88% |
A0A0N1PCA9 | Leptomonas seymouri | 25% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 51% | 85% |
A0A0N1PFI4 | Leptomonas seymouri | 26% | 97% |
A0A0S4JLK6 | Bodo saltans | 24% | 93% |
A0A0S4KGT2 | Bodo saltans | 27% | 100% |
A0A1X0NJ61 | Trypanosomatidae | 25% | 100% |
A0A1X0NJK2 | Trypanosomatidae | 24% | 99% |
A0A1X0NJX8 | Trypanosomatidae | 29% | 97% |
A0A1X0NKX8 | Trypanosomatidae | 28% | 92% |
A0A1X0NMT3 | Trypanosomatidae | 25% | 89% |
A0A1X0NW84 | Trypanosomatidae | 25% | 100% |
A0A1X0NW85 | Trypanosomatidae | 24% | 100% |
A0A1X0NW89 | Trypanosomatidae | 27% | 87% |
A0A1X0NWA6 | Trypanosomatidae | 24% | 86% |
A0A1X0NWW1 | Trypanosomatidae | 25% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 26% | 100% |
A0A3Q8IDD4 | Leishmania donovani | 25% | 100% |
A0A3S5H5A5 | Leishmania donovani | 27% | 88% |
A0A3S5ISG2 | Trypanosoma rangeli | 26% | 97% |
A0A3S7WW18 | Leishmania donovani | 26% | 92% |
A0A3S7WW41 | Leishmania donovani | 25% | 100% |
A0A3S7WW71 | Leishmania donovani | 22% | 100% |
A0A3S7X430 | Leishmania donovani | 27% | 96% |
A0A3S7X438 | Leishmania donovani | 27% | 80% |
A0A3S7X460 | Leishmania donovani | 24% | 97% |
A0A3S7X470 | Leishmania donovani | 27% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 25% | 82% |
A0A422MYX0 | Trypanosoma rangeli | 25% | 100% |
A4H3W4 | Leishmania braziliensis | 27% | 88% |
A4HE81 | Leishmania braziliensis | 24% | 100% |
A4HJ14 | Leishmania braziliensis | 28% | 100% |
A4HJ21 | Leishmania braziliensis | 75% | 100% |
A4HJ22 | Leishmania braziliensis | 28% | 80% |
A4HJ24 | Leishmania braziliensis | 24% | 100% |
A4HS39 | Leishmania infantum | 27% | 100% |
A4HYN0 | Leishmania infantum | 25% | 100% |
A4HYW1 | Leishmania infantum | 26% | 100% |
A4HYW2 | Leishmania infantum | 22% | 93% |
A4HYW3 | Leishmania infantum | 25% | 100% |
A4I1J4 | Leishmania infantum | 25% | 100% |
A4I6E4 | Leishmania infantum | 27% | 100% |
A4I6E6 | Leishmania infantum | 24% | 100% |
A4I6F0 | Leishmania infantum | 27% | 100% |
A4I6K4 | Leishmania infantum | 27% | 100% |
A4I6K6 | Leishmania infantum | 99% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 70% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 95% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 88% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 94% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 88% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AIH1 | Leishmania braziliensis | 25% | 100% |
E9AIH4 | Leishmania braziliensis | 25% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 94% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q6L7 | Leishmania major | 25% | 100% |
Q4Q6L9 | Leishmania major | 27% | 100% |
Q4Q6M0 | Leishmania major | 28% | 100% |
Q4Q6M2 | Leishmania major | 90% | 100% |
Q4Q6M4 | Leishmania major | 28% | 100% |
Q4Q9U3 | Leishmania major | 25% | 100% |
Q4QCS6 | Leishmania major | 24% | 100% |
Q4QCS7 | Leishmania major | 22% | 93% |
Q4QCS8 | Leishmania major | 25% | 100% |
Q4QCS9 | Leishmania major | 26% | 100% |
Q9U0T9 | Leishmania major | 27% | 100% |
V5AYJ1 | Trypanosoma cruzi | 23% | 100% |
V5B5I4 | Trypanosoma cruzi | 26% | 90% |
V5BA05 | Trypanosoma cruzi | 25% | 100% |
V5BEL3 | Trypanosoma cruzi | 23% | 100% |
V5BN20 | Trypanosoma cruzi | 26% | 97% |
V5D5V8 | Trypanosoma cruzi | 25% | 100% |
V5DES7 | Trypanosoma cruzi | 26% | 95% |