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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016281 | eukaryotic translation initiation factor 4F complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ANB8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006412 | translation | 4 | 1 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043043 | peptide biosynthetic process | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003729 | mRNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 705 | 707 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 739 | 741 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 779 | 781 | PF00675 | 0.622 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.718 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.338 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 702 | 706 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 707 | 711 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 740 | 744 | PF00082 | 0.436 |
CLV_Separin_Metazoa | 251 | 255 | PF03568 | 0.550 |
CLV_Separin_Metazoa | 703 | 707 | PF03568 | 0.503 |
DEG_APCC_DBOX_1 | 504 | 512 | PF00400 | 0.418 |
DEG_APCC_DBOX_1 | 739 | 747 | PF00400 | 0.487 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.735 |
DOC_CKS1_1 | 67 | 72 | PF01111 | 0.641 |
DOC_CYCLIN_yCln2_LP_2 | 67 | 73 | PF00134 | 0.681 |
DOC_MAPK_gen_1 | 186 | 196 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 292 | 299 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 712 | 721 | PF00069 | 0.480 |
DOC_PP1_RVXF_1 | 207 | 213 | PF00149 | 0.519 |
DOC_PP1_RVXF_1 | 284 | 290 | PF00149 | 0.481 |
DOC_PP1_RVXF_1 | 375 | 382 | PF00149 | 0.497 |
DOC_SPAK_OSR1_1 | 610 | 614 | PF12202 | 0.358 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.465 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 618 | 623 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 665 | 670 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 675 | 680 | PF00397 | 0.422 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 197 | 204 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 257 | 261 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 273 | 278 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 494 | 500 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 761 | 765 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.696 |
LIG_Actin_WH2_2 | 690 | 708 | PF00022 | 0.504 |
LIG_APCC_ABBAyCdc20_2 | 147 | 153 | PF00400 | 0.678 |
LIG_BRCT_BRCA1_1 | 683 | 687 | PF00533 | 0.335 |
LIG_BRCT_BRCA1_1 | 730 | 734 | PF00533 | 0.478 |
LIG_CaM_IQ_9 | 284 | 300 | PF13499 | 0.538 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.468 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.370 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.355 |
LIG_FHA_1 | 714 | 720 | PF00498 | 0.415 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.479 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.479 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.519 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.640 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.609 |
LIG_FHA_2 | 656 | 662 | PF00498 | 0.239 |
LIG_FHA_2 | 761 | 767 | PF00498 | 0.488 |
LIG_HCF-1_HBM_1 | 101 | 104 | PF13415 | 0.638 |
LIG_Integrin_isoDGR_2 | 427 | 429 | PF01839 | 0.731 |
LIG_LIR_Gen_1 | 107 | 117 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 220 | 231 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 333 | 343 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 452 | 460 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 510 | 520 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 540 | 551 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 651 | 660 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 684 | 694 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 452 | 456 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 510 | 515 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 540 | 546 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 609 | 614 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 651 | 656 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 684 | 690 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 699 | 704 | PF02991 | 0.407 |
LIG_MLH1_MIPbox_1 | 683 | 687 | PF16413 | 0.412 |
LIG_NRBOX | 317 | 323 | PF00104 | 0.465 |
LIG_NRBOX | 613 | 619 | PF00104 | 0.479 |
LIG_PCNA_PIPBox_1 | 380 | 389 | PF02747 | 0.538 |
LIG_PCNA_PIPBox_1 | 527 | 536 | PF02747 | 0.284 |
LIG_PCNA_yPIPBox_3 | 307 | 318 | PF02747 | 0.587 |
LIG_PCNA_yPIPBox_3 | 377 | 387 | PF02747 | 0.550 |
LIG_Pex14_1 | 491 | 495 | PF04695 | 0.479 |
LIG_Pex14_2 | 734 | 738 | PF04695 | 0.428 |
LIG_REV1ctd_RIR_1 | 209 | 217 | PF16727 | 0.519 |
LIG_RPA_C_Fungi | 744 | 756 | PF08784 | 0.513 |
LIG_SH2_CRK | 335 | 339 | PF00017 | 0.433 |
LIG_SH2_CRK | 620 | 624 | PF00017 | 0.461 |
LIG_SH2_GRB2like | 495 | 498 | PF00017 | 0.490 |
LIG_SH2_GRB2like | 652 | 655 | PF00017 | 0.454 |
LIG_SH2_PTP2 | 227 | 230 | PF00017 | 0.297 |
LIG_SH2_SRC | 356 | 359 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.635 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 692 | 696 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 652 | 655 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 680 | 683 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 722 | 725 | PF00017 | 0.361 |
LIG_SH3_2 | 74 | 79 | PF14604 | 0.495 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.724 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.433 |
LIG_SH3_3 | 431 | 437 | PF00018 | 0.629 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.514 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.693 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.733 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.616 |
LIG_SH3_4 | 62 | 69 | PF00018 | 0.584 |
LIG_SUMO_SIM_anti_2 | 470 | 478 | PF11976 | 0.424 |
LIG_SUMO_SIM_anti_2 | 482 | 487 | PF11976 | 0.404 |
LIG_SUMO_SIM_anti_2 | 582 | 587 | PF11976 | 0.316 |
LIG_SUMO_SIM_anti_2 | 638 | 644 | PF11976 | 0.491 |
LIG_SUMO_SIM_anti_2 | 766 | 775 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 470 | 478 | PF11976 | 0.547 |
LIG_SUMO_SIM_par_1 | 715 | 720 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 766 | 775 | PF11976 | 0.470 |
LIG_TRAF2_1 | 200 | 203 | PF00917 | 0.433 |
LIG_TRAF2_1 | 442 | 445 | PF00917 | 0.709 |
LIG_TRAF2_1 | 537 | 540 | PF00917 | 0.552 |
LIG_TRAF2_1 | 81 | 84 | PF00917 | 0.768 |
LIG_TRAF2_2 | 599 | 604 | PF00917 | 0.658 |
LIG_TYR_ITSM | 331 | 338 | PF00017 | 0.433 |
LIG_UBA3_1 | 511 | 518 | PF00899 | 0.439 |
LIG_UBA3_1 | 530 | 536 | PF00899 | 0.357 |
LIG_UBA3_1 | 542 | 548 | PF00899 | 0.485 |
LIG_UBA3_1 | 735 | 741 | PF00899 | 0.347 |
LIG_WRC_WIRS_1 | 686 | 691 | PF05994 | 0.343 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.570 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.433 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.725 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.516 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.369 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.644 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.409 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.243 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.335 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.433 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.421 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.433 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.448 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.545 |
MOD_CK2_1 | 760 | 766 | PF00069 | 0.478 |
MOD_CK2_1 | 768 | 774 | PF00069 | 0.447 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.676 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.617 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.438 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.430 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.649 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.786 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.548 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.355 |
MOD_GlcNHglycan | 756 | 759 | PF01048 | 0.474 |
MOD_GlcNHglycan | 82 | 88 | PF01048 | 0.729 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.588 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.402 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.520 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.479 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.692 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.512 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.241 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.695 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.673 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.333 |
MOD_N-GLC_1 | 417 | 422 | PF02516 | 0.727 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.313 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.343 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.439 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.332 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.340 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.433 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.437 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.484 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.407 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.390 |
MOD_NEK2_1 | 728 | 733 | PF00069 | 0.513 |
MOD_NEK2_1 | 760 | 765 | PF00069 | 0.513 |
MOD_NEK2_2 | 218 | 223 | PF00069 | 0.315 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.763 |
MOD_PIKK_1 | 696 | 702 | PF00454 | 0.504 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.323 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.441 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.415 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.712 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.699 |
MOD_PKA_2 | 760 | 766 | PF00069 | 0.516 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.693 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.675 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.333 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.415 |
MOD_Plk_1 | 503 | 509 | PF00069 | 0.533 |
MOD_Plk_1 | 648 | 654 | PF00069 | 0.480 |
MOD_Plk_1 | 765 | 771 | PF00069 | 0.536 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.687 |
MOD_Plk_2-3 | 142 | 148 | PF00069 | 0.693 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.418 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.774 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.433 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.415 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.671 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.488 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.533 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.475 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.491 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.597 |
MOD_Plk_4 | 648 | 654 | PF00069 | 0.356 |
MOD_Plk_4 | 713 | 719 | PF00069 | 0.429 |
MOD_Plk_4 | 765 | 771 | PF00069 | 0.461 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.433 |
MOD_ProDKin_1 | 618 | 624 | PF00069 | 0.445 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.686 |
MOD_ProDKin_1 | 665 | 671 | PF00069 | 0.533 |
MOD_ProDKin_1 | 675 | 681 | PF00069 | 0.415 |
MOD_SUMO_for_1 | 187 | 190 | PF00179 | 0.297 |
MOD_SUMO_for_1 | 77 | 80 | PF00179 | 0.747 |
MOD_SUMO_rev_2 | 160 | 168 | PF00179 | 0.532 |
MOD_SUMO_rev_2 | 592 | 599 | PF00179 | 0.566 |
MOD_SUMO_rev_2 | 600 | 607 | PF00179 | 0.541 |
TRG_DiLeu_BaEn_3 | 242 | 248 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 701 | 704 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 505 | 508 | PF00400 | 0.407 |
TRG_NES_CRM1_1 | 185 | 198 | PF08389 | 0.357 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEC9 | Leptomonas seymouri | 71% | 100% |
A0A0S4J374 | Bodo saltans | 28% | 90% |
A0A1X0NQC6 | Trypanosomatidae | 45% | 100% |
A0A3R7KDY4 | Trypanosoma rangeli | 40% | 100% |
A0A3S7WRD0 | Leishmania donovani | 97% | 100% |
A4H696 | Leishmania braziliensis | 90% | 100% |
A4HUL9 | Leishmania infantum | 97% | 100% |
C9ZVP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
Q4QHA6 | Leishmania major | 95% | 100% |
V5BTU8 | Trypanosoma cruzi | 39% | 100% |