Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3S5H6I6
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008033 | tRNA processing | 8 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0034470 | ncRNA processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0031119 | tRNA pseudouridine synthesis | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0009982 | pseudouridine synthase activity | 4 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.745 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.243 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.614 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.675 |
CLV_PCSK_PC7_1 | 640 | 646 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.625 |
DEG_APCC_DBOX_1 | 315 | 323 | PF00400 | 0.741 |
DEG_MDM2_SWIB_1 | 181 | 188 | PF02201 | 0.487 |
DEG_SCF_FBW7_1 | 657 | 664 | PF00400 | 0.468 |
DOC_ANK_TNKS_1 | 535 | 542 | PF00023 | 0.519 |
DOC_CKS1_1 | 635 | 640 | PF01111 | 0.410 |
DOC_MAPK_DCC_7 | 250 | 260 | PF00069 | 0.659 |
DOC_MAPK_FxFP_2 | 32 | 35 | PF00069 | 0.579 |
DOC_MAPK_FxFP_2 | 461 | 464 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 582 | 590 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 649 | 659 | PF00069 | 0.426 |
DOC_MAPK_JIP1_4 | 542 | 548 | PF00069 | 0.364 |
DOC_MAPK_MEF2A_6 | 251 | 260 | PF00069 | 0.658 |
DOC_MAPK_MEF2A_6 | 530 | 537 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 583 | 592 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 689 | 696 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 701 | 709 | PF00069 | 0.378 |
DOC_PP1_RVXF_1 | 602 | 609 | PF00149 | 0.378 |
DOC_PP2B_LxvP_1 | 99 | 102 | PF13499 | 0.792 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.544 |
DOC_PP4_FxxP_1 | 461 | 464 | PF00568 | 0.410 |
DOC_PP4_FxxP_1 | 548 | 551 | PF00568 | 0.428 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.480 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 433 | 438 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 505 | 510 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 634 | 639 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 657 | 662 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 688 | 693 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.564 |
LIG_14-3-3_CanoR_1 | 179 | 184 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 250 | 258 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 27 | 31 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 289 | 298 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 341 | 349 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 362 | 369 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 406 | 412 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 431 | 440 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 555 | 561 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 582 | 590 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 594 | 600 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 644 | 648 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 652 | 658 | PF00244 | 0.400 |
LIG_APCC_ABBA_1 | 258 | 263 | PF00400 | 0.641 |
LIG_APCC_ABBAyCdc20_2 | 680 | 686 | PF00400 | 0.391 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.724 |
LIG_BIR_III_4 | 263 | 267 | PF00653 | 0.566 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.382 |
LIG_BRCT_BRCA1_1 | 28 | 32 | PF00533 | 0.499 |
LIG_BRCT_BRCA1_1 | 435 | 439 | PF00533 | 0.414 |
LIG_Clathr_ClatBox_1 | 668 | 672 | PF01394 | 0.406 |
LIG_CtBP_PxDLS_1 | 44 | 48 | PF00389 | 0.509 |
LIG_eIF4E_1 | 145 | 151 | PF01652 | 0.526 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.565 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.690 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.718 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.554 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.492 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.519 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.464 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.433 |
LIG_FHA_1 | 700 | 706 | PF00498 | 0.341 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.613 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.630 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.479 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.448 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.731 |
LIG_FXI_DFP_1 | 714 | 718 | PF00024 | 0.407 |
LIG_LIR_Apic_2 | 29 | 35 | PF02991 | 0.530 |
LIG_LIR_Apic_2 | 374 | 378 | PF02991 | 0.403 |
LIG_LIR_Apic_2 | 547 | 551 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 502 | 512 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 502 | 507 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 664 | 669 | PF02991 | 0.489 |
LIG_MYND_1 | 467 | 471 | PF01753 | 0.589 |
LIG_NRBOX | 693 | 699 | PF00104 | 0.399 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.488 |
LIG_Pex14_2 | 544 | 548 | PF04695 | 0.393 |
LIG_Rb_pABgroove_1 | 26 | 34 | PF01858 | 0.568 |
LIG_SH2_CRK | 369 | 373 | PF00017 | 0.374 |
LIG_SH2_CRK | 375 | 379 | PF00017 | 0.392 |
LIG_SH2_CRK | 603 | 607 | PF00017 | 0.374 |
LIG_SH2_NCK_1 | 369 | 373 | PF00017 | 0.409 |
LIG_SH2_NCK_1 | 375 | 379 | PF00017 | 0.427 |
LIG_SH2_SRC | 261 | 264 | PF00017 | 0.632 |
LIG_SH2_SRC | 373 | 376 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 132 | 136 | PF00017 | 0.620 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.630 |
LIG_SH2_STAP1 | 369 | 373 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 678 | 681 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.606 |
LIG_SH3_2 | 477 | 482 | PF14604 | 0.582 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.425 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.492 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.686 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.689 |
LIG_SUMO_SIM_par_1 | 491 | 496 | PF11976 | 0.684 |
LIG_SUMO_SIM_par_1 | 667 | 673 | PF11976 | 0.450 |
LIG_TRAF2_1 | 393 | 396 | PF00917 | 0.681 |
LIG_TRAF2_1 | 449 | 452 | PF00917 | 0.363 |
LIG_TYR_ITIM | 367 | 372 | PF00017 | 0.379 |
LIG_WRC_WIRS_1 | 445 | 450 | PF05994 | 0.496 |
LIG_WW_3 | 35 | 39 | PF00397 | 0.578 |
MOD_CDC14_SPxK_1 | 550 | 553 | PF00782 | 0.446 |
MOD_CDK_SPK_2 | 74 | 79 | PF00069 | 0.534 |
MOD_CDK_SPxK_1 | 547 | 553 | PF00069 | 0.426 |
MOD_CDK_SPxK_1 | 634 | 640 | PF00069 | 0.411 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.677 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.593 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.751 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.589 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.729 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.552 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.645 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.484 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.594 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.396 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.497 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.743 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.585 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.679 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.691 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.625 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.724 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.727 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.698 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.393 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.474 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.671 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.767 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.495 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.390 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.672 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.686 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.581 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.458 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.428 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.378 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.477 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.568 |
MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.520 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.435 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.515 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.426 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.661 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.408 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.363 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.517 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.433 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.435 |
MOD_NEK2_2 | 409 | 414 | PF00069 | 0.521 |
MOD_NEK2_2 | 586 | 591 | PF00069 | 0.480 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.617 |
MOD_PIKK_1 | 431 | 437 | PF00454 | 0.400 |
MOD_PIKK_1 | 670 | 676 | PF00454 | 0.368 |
MOD_PKA_1 | 250 | 256 | PF00069 | 0.481 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.661 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.407 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.651 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.590 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.687 |
MOD_PKA_2 | 554 | 560 | PF00069 | 0.560 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.434 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.452 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.471 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.462 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.651 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.506 |
MOD_Plk_1 | 586 | 592 | PF00069 | 0.455 |
MOD_Plk_2-3 | 554 | 560 | PF00069 | 0.524 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.592 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.532 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.408 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.596 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.406 |
MOD_Plk_4 | 674 | 680 | PF00069 | 0.390 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.507 |
MOD_ProDKin_1 | 433 | 439 | PF00069 | 0.402 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.748 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.539 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.426 |
MOD_ProDKin_1 | 634 | 640 | PF00069 | 0.411 |
MOD_ProDKin_1 | 657 | 663 | PF00069 | 0.455 |
MOD_ProDKin_1 | 688 | 694 | PF00069 | 0.460 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.559 |
MOD_SUMO_for_1 | 209 | 212 | PF00179 | 0.586 |
MOD_SUMO_rev_2 | 596 | 600 | PF00179 | 0.549 |
TRG_DiLeu_BaEn_2 | 539 | 545 | PF01217 | 0.534 |
TRG_DiLeu_BaLyEn_6 | 454 | 459 | PF01217 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 649 | 654 | PF01217 | 0.541 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.379 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 249 | 251 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 561 | 563 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 581 | 583 | PF00400 | 0.240 |
TRG_ER_diArg_1 | 649 | 652 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.630 |
TRG_NES_CRM1_1 | 211 | 223 | PF08389 | 0.567 |
TRG_NES_CRM1_1 | 703 | 716 | PF08389 | 0.407 |
TRG_NLS_MonoExtN_4 | 285 | 292 | PF00514 | 0.689 |
TRG_Pf-PMV_PEXEL_1 | 536 | 540 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 611 | 615 | PF00026 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 629 | 634 | PF00026 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HW55 | Leptomonas seymouri | 67% | 96% |
A0A0S4IV39 | Bodo saltans | 37% | 90% |
A0A1X0NVE2 | Trypanosomatidae | 44% | 100% |
A0A422MV99 | Trypanosoma rangeli | 45% | 100% |
A4H6H8 | Leishmania braziliensis | 83% | 100% |
A4HUW4 | Leishmania infantum | 100% | 100% |
D0A7I9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9ANJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QH27 | Leishmania major | 95% | 100% |
V5BW97 | Trypanosoma cruzi | 45% | 100% |