Translation, eukaryotic translation initiation factor 3 subunit a
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 2 |
Forrest at al. (procyclic) | yes | yes: 2 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005852 | eukaryotic translation initiation factor 3 complex | 2 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043614 | multi-eIF complex | 3 | 1 |
GO:0071540 | eukaryotic translation initiation factor 3 complex, eIF3e | 3 | 1 |
GO:0071541 | eukaryotic translation initiation factor 3 complex, eIF3m | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HX65
Term | Name | Level | Count |
---|---|---|---|
GO:0001732 | formation of cytoplasmic translation initiation complex | 7 | 1 |
GO:0002183 | cytoplasmic translational initiation | 4 | 1 |
GO:0002188 | translation reinitiation | 5 | 1 |
GO:0006413 | translational initiation | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003729 | mRNA binding | 5 | 1 |
GO:0003743 | translation initiation factor activity | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0008135 | translation factor activity, RNA binding | 3 | 10 |
GO:0045182 | translation regulator activity | 1 | 10 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 29 | 33 | PF00656 | 0.435 |
CLV_C14_Caspase3-7 | 490 | 494 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 626 | 628 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 663 | 665 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 669 | 671 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 690 | 692 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 718 | 720 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 723 | 725 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 745 | 747 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 769 | 771 | PF00675 | 0.638 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 662 | 664 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 690 | 692 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 718 | 720 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 723 | 725 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 756 | 758 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 769 | 771 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 537 | 539 | PF00082 | 0.687 |
CLV_PCSK_PC1ET2_1 | 582 | 584 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 662 | 664 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 690 | 692 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 747 | 749 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 756 | 758 | PF00082 | 0.465 |
CLV_PCSK_PC7_1 | 719 | 725 | PF00082 | 0.586 |
CLV_PCSK_PC7_1 | 743 | 749 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 623 | 627 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 728 | 732 | PF00082 | 0.524 |
CLV_Separin_Metazoa | 624 | 628 | PF03568 | 0.530 |
CLV_Separin_Metazoa | 71 | 75 | PF03568 | 0.499 |
DEG_APCC_DBOX_1 | 329 | 337 | PF00400 | 0.345 |
DEG_APCC_DBOX_1 | 433 | 441 | PF00400 | 0.454 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.673 |
DEG_SPOP_SBC_1 | 532 | 536 | PF00917 | 0.663 |
DEG_SPOP_SBC_1 | 552 | 556 | PF00917 | 0.491 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.479 |
DOC_MAPK_DCC_7 | 39 | 48 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 109 | 117 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 277 | 287 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 92 | 101 | PF00069 | 0.418 |
DOC_MAPK_RevD_3 | 127 | 141 | PF00069 | 0.471 |
DOC_PP1_RVXF_1 | 165 | 172 | PF00149 | 0.490 |
DOC_PP2B_LxvP_1 | 686 | 689 | PF13499 | 0.429 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.475 |
DOC_PP4_FxxP_1 | 362 | 365 | PF00568 | 0.550 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.265 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.556 |
DOC_USP7_UBL2_3 | 319 | 323 | PF12436 | 0.535 |
DOC_USP7_UBL2_3 | 577 | 581 | PF12436 | 0.550 |
DOC_USP7_UBL2_3 | 628 | 632 | PF12436 | 0.460 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.496 |
LIG_14-3-3_CanoR_1 | 10 | 16 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 202 | 209 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 485 | 490 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 524 | 531 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 551 | 560 | PF00244 | 0.515 |
LIG_Actin_WH2_2 | 65 | 83 | PF00022 | 0.506 |
LIG_AP2alpha_2 | 346 | 348 | PF02296 | 0.607 |
LIG_BRCT_BRCA1_1 | 295 | 299 | PF00533 | 0.441 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.405 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.529 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.527 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.460 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.452 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.409 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.545 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.446 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.554 |
LIG_FHA_2 | 700 | 706 | PF00498 | 0.621 |
LIG_IRF3_LxIS_1 | 190 | 197 | PF10401 | 0.432 |
LIG_LIR_Apic_2 | 186 | 190 | PF02991 | 0.435 |
LIG_LIR_Apic_2 | 359 | 365 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 282 | 292 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 398 | 407 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 443 | 454 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 501 | 510 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 522 | 533 | PF02991 | 0.686 |
LIG_LIR_Nem_3 | 282 | 287 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 346 | 351 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 443 | 449 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 501 | 506 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 522 | 528 | PF02991 | 0.686 |
LIG_NRBOX | 247 | 253 | PF00104 | 0.447 |
LIG_NRBOX | 653 | 659 | PF00104 | 0.443 |
LIG_PCNA_yPIPBox_3 | 167 | 181 | PF02747 | 0.462 |
LIG_PCNA_yPIPBox_3 | 350 | 362 | PF02747 | 0.599 |
LIG_PCNA_yPIPBox_3 | 91 | 102 | PF02747 | 0.452 |
LIG_Pex14_2 | 741 | 745 | PF04695 | 0.613 |
LIG_RPA_C_Fungi | 548 | 560 | PF08784 | 0.566 |
LIG_SH2_GRB2like | 464 | 467 | PF00017 | 0.479 |
LIG_SH2_GRB2like | 502 | 505 | PF00017 | 0.544 |
LIG_SH2_NCK_1 | 382 | 386 | PF00017 | 0.388 |
LIG_SH2_PTP2 | 446 | 449 | PF00017 | 0.479 |
LIG_SH2_SRC | 446 | 449 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 679 | 683 | PF00017 | 0.561 |
LIG_SH2_STAT3 | 558 | 561 | PF00017 | 0.563 |
LIG_SH2_STAT3 | 694 | 697 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 713 | 716 | PF00017 | 0.587 |
LIG_SUMO_SIM_anti_2 | 282 | 289 | PF11976 | 0.467 |
LIG_SUMO_SIM_anti_2 | 49 | 56 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 192 | 198 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 469 | 477 | PF11976 | 0.499 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.529 |
LIG_UBA3_1 | 372 | 379 | PF00899 | 0.494 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.543 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.450 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.372 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.538 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.481 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.711 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.557 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.562 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.498 |
MOD_CK2_1 | 699 | 705 | PF00069 | 0.618 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.359 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.417 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.421 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.496 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.657 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.542 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.556 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.480 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.410 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.461 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.407 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.580 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.479 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.460 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.651 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.733 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.543 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.423 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.350 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.564 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.409 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.460 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.470 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.490 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.525 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.660 |
MOD_NEK2_1 | 741 | 746 | PF00069 | 0.629 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.461 |
MOD_NEK2_2 | 173 | 178 | PF00069 | 0.448 |
MOD_NEK2_2 | 300 | 305 | PF00069 | 0.398 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.355 |
MOD_PIKK_1 | 598 | 604 | PF00454 | 0.582 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.450 |
MOD_PK_1 | 553 | 559 | PF00069 | 0.536 |
MOD_PKA_1 | 167 | 173 | PF00069 | 0.477 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.506 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.567 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.685 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.466 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.468 |
MOD_PKB_1 | 551 | 559 | PF00069 | 0.537 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.424 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.354 |
MOD_Plk_1 | 474 | 480 | PF00069 | 0.540 |
MOD_Plk_1 | 526 | 532 | PF00069 | 0.687 |
MOD_Plk_1 | 638 | 644 | PF00069 | 0.546 |
MOD_Plk_1 | 652 | 658 | PF00069 | 0.312 |
MOD_Plk_1 | 741 | 747 | PF00069 | 0.543 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.436 |
MOD_Plk_2-3 | 476 | 482 | PF00069 | 0.549 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.479 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.405 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.456 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.559 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.468 |
MOD_Plk_4 | 638 | 644 | PF00069 | 0.486 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.491 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.559 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.508 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.487 |
MOD_SUMO_for_1 | 596 | 599 | PF00179 | 0.557 |
MOD_SUMO_rev_2 | 20 | 30 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 570 | 578 | PF00179 | 0.588 |
MOD_SUMO_rev_2 | 667 | 673 | PF00179 | 0.580 |
TRG_DiLeu_BaEn_1 | 49 | 54 | PF01217 | 0.454 |
TRG_DiLeu_BaEn_1 | 65 | 70 | PF01217 | 0.336 |
TRG_DiLeu_BaEn_1 | 653 | 658 | PF01217 | 0.416 |
TRG_DiLeu_BaEn_1 | 759 | 764 | PF01217 | 0.482 |
TRG_DiLeu_BaEn_2 | 229 | 235 | PF01217 | 0.496 |
TRG_DiLeu_BaEn_4 | 766 | 772 | PF01217 | 0.619 |
TRG_DiLeu_BaLyEn_6 | 149 | 154 | PF01217 | 0.455 |
TRG_DiLeu_LyEn_5 | 653 | 658 | PF01217 | 0.517 |
TRG_DiLeu_LyEn_5 | 759 | 764 | PF01217 | 0.619 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 525 | 528 | PF00928 | 0.685 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 150 | 152 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 745 | 748 | PF00400 | 0.699 |
TRG_ER_diArg_1 | 768 | 770 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 99 | 102 | PF00400 | 0.512 |
TRG_NES_CRM1_1 | 49 | 62 | PF08389 | 0.467 |
TRG_NLS_MonoExtC_3 | 661 | 667 | PF00514 | 0.558 |
TRG_NLS_MonoExtN_4 | 743 | 750 | PF00514 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 607 | 612 | PF00026 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 762 | 766 | PF00026 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 769 | 774 | PF00026 | 0.651 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGW0 | Leptomonas seymouri | 76% | 100% |
A0A0S4IU09 | Bodo saltans | 23% | 95% |
A0A1X0NTC2 | Trypanosomatidae | 34% | 100% |
A0A3Q8IDU4 | Leishmania donovani | 100% | 100% |
A0A422NFC9 | Trypanosoma rangeli | 33% | 100% |
A4H8U7 | Leishmania braziliensis | 93% | 100% |
C9ZTS8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9ARC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q4QEJ8 | Leishmania major | 98% | 100% |
V5D8P7 | Trypanosoma cruzi | 32% | 100% |