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:0005730 | nucleolus | 5 | 1 |
GO:0030684 | preribosome | 3 | 1 |
GO:0032040 | small-subunit processome | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 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:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AIC1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006364 | rRNA processing | 8 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016072 | rRNA metabolic process | 7 | 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: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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.374 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.508 |
CLV_C14_Caspase3-7 | 735 | 739 | PF00656 | 0.663 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 665 | 667 | PF00675 | 0.494 |
CLV_PCSK_FUR_1 | 434 | 438 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 595 | 597 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 600 | 602 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 611 | 613 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 648 | 650 | PF00082 | 0.523 |
CLV_PCSK_PC7_1 | 596 | 602 | PF00082 | 0.393 |
CLV_PCSK_PC7_1 | 644 | 650 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 601 | 605 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.551 |
CLV_Separin_Metazoa | 98 | 102 | PF03568 | 0.535 |
DEG_SCF_FBW7_1 | 240 | 247 | PF00400 | 0.619 |
DEG_SPOP_SBC_1 | 378 | 382 | PF00917 | 0.645 |
DOC_CYCLIN_RxL_1 | 696 | 704 | PF00134 | 0.432 |
DOC_MAPK_gen_1 | 106 | 116 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 560 | 568 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 580 | 588 | PF00069 | 0.201 |
DOC_MAPK_gen_1 | 611 | 619 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 109 | 116 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 214 | 221 | PF00069 | 0.340 |
DOC_MAPK_MEF2A_6 | 337 | 345 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 359 | 366 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 581 | 590 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 63 | 71 | PF00069 | 0.348 |
DOC_PP1_RVXF_1 | 697 | 704 | PF00149 | 0.433 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 647 | 651 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.588 |
DOC_USP7_UBL2_3 | 600 | 604 | PF12436 | 0.427 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.466 |
LIG_14-3-3_CanoR_1 | 139 | 146 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 20 | 30 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 284 | 289 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 41 | 47 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 699 | 704 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 80 | 85 | PF00244 | 0.473 |
LIG_Actin_WH2_2 | 584 | 602 | PF00022 | 0.446 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.755 |
LIG_BIR_III_4 | 75 | 79 | PF00653 | 0.581 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.373 |
LIG_BRCT_BRCA1_1 | 531 | 535 | PF00533 | 0.405 |
LIG_Clathr_ClatBox_1 | 81 | 85 | PF01394 | 0.552 |
LIG_DLG_GKlike_1 | 699 | 706 | PF00625 | 0.495 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.389 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.559 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.576 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.416 |
LIG_FHA_1 | 500 | 506 | PF00498 | 0.386 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.398 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.494 |
LIG_FHA_1 | 696 | 702 | PF00498 | 0.438 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.528 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.346 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.498 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.640 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.571 |
LIG_FHA_2 | 600 | 606 | PF00498 | 0.531 |
LIG_FHA_2 | 653 | 659 | PF00498 | 0.486 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.467 |
LIG_FHA_2 | 720 | 726 | PF00498 | 0.265 |
LIG_FHA_2 | 728 | 734 | PF00498 | 0.384 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.603 |
LIG_GBD_Chelix_1 | 52 | 60 | PF00786 | 0.472 |
LIG_Integrin_isoDGR_2 | 634 | 636 | PF01839 | 0.363 |
LIG_LIR_Apic_2 | 95 | 99 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 332 | 341 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 400 | 406 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 460 | 470 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 698 | 706 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 88 | 97 | PF02991 | 0.490 |
LIG_LIR_LC3C_4 | 322 | 327 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 332 | 336 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 460 | 465 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 473 | 479 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 650 | 656 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 698 | 703 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.510 |
LIG_OCRL_FandH_1 | 702 | 714 | PF00620 | 0.287 |
LIG_PCNA_PIPBox_1 | 694 | 703 | PF02747 | 0.442 |
LIG_PCNA_yPIPBox_3 | 506 | 515 | PF02747 | 0.420 |
LIG_PCNA_yPIPBox_3 | 691 | 701 | PF02747 | 0.408 |
LIG_Pex14_1 | 398 | 402 | PF04695 | 0.608 |
LIG_Pex14_2 | 329 | 333 | PF04695 | 0.316 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.424 |
LIG_SH2_GRB2like | 518 | 521 | PF00017 | 0.304 |
LIG_SH2_SRC | 518 | 521 | PF00017 | 0.398 |
LIG_SH2_SRC | 723 | 726 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 224 | 228 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 402 | 406 | PF00017 | 0.634 |
LIG_SH2_STAT3 | 656 | 659 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 556 | 559 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 723 | 726 | PF00017 | 0.397 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.397 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.398 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.634 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.458 |
LIG_SH3_3 | 731 | 737 | PF00018 | 0.423 |
LIG_SUMO_SIM_anti_2 | 322 | 328 | PF11976 | 0.501 |
LIG_SUMO_SIM_anti_2 | 616 | 621 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 264 | 274 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 285 | 295 | PF11976 | 0.693 |
LIG_SUMO_SIM_par_1 | 587 | 592 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 80 | 85 | PF11976 | 0.518 |
LIG_TRAF2_1 | 458 | 461 | PF00917 | 0.445 |
LIG_TRAF2_1 | 657 | 660 | PF00917 | 0.420 |
LIG_TYR_ITIM | 516 | 521 | PF00017 | 0.304 |
LIG_UBA3_1 | 29 | 37 | PF00899 | 0.369 |
LIG_UBA3_1 | 638 | 645 | PF00899 | 0.429 |
LIG_WRC_WIRS_1 | 158 | 163 | PF05994 | 0.657 |
LIG_WRC_WIRS_1 | 700 | 705 | PF05994 | 0.377 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.558 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.787 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.443 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.635 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.526 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.513 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.327 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.479 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.587 |
MOD_CK2_1 | 654 | 660 | PF00069 | 0.421 |
MOD_CK2_1 | 708 | 714 | PF00069 | 0.469 |
MOD_CK2_1 | 719 | 725 | PF00069 | 0.420 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.651 |
MOD_Cter_Amidation | 593 | 596 | PF01082 | 0.511 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.608 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.557 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.660 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.721 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.708 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.478 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.619 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.686 |
MOD_GlcNHglycan | 332 | 336 | PF01048 | 0.354 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.776 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.407 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.403 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.521 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.579 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.710 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.578 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.398 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.618 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.630 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.526 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.638 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.646 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.560 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.359 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.418 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.371 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.394 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.482 |
MOD_LATS_1 | 169 | 175 | PF00433 | 0.511 |
MOD_N-GLC_1 | 231 | 236 | PF02516 | 0.432 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.684 |
MOD_N-GLC_1 | 470 | 475 | PF02516 | 0.351 |
MOD_N-GLC_1 | 686 | 691 | PF02516 | 0.438 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.760 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.485 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.582 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.564 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.526 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.533 |
MOD_NEK2_1 | 706 | 711 | PF00069 | 0.524 |
MOD_NEK2_2 | 253 | 258 | PF00069 | 0.509 |
MOD_PIKK_1 | 474 | 480 | PF00454 | 0.452 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.630 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.600 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.695 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.439 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.623 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.348 |
MOD_Plk_1 | 527 | 533 | PF00069 | 0.513 |
MOD_Plk_1 | 613 | 619 | PF00069 | 0.503 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.540 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.422 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.471 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.372 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.510 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.489 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.716 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.776 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.462 |
MOD_SUMO_for_1 | 235 | 238 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 307 | 313 | PF00179 | 0.590 |
TRG_DiLeu_BaEn_1 | 461 | 466 | PF01217 | 0.436 |
TRG_DiLeu_BaEn_1 | 507 | 512 | PF01217 | 0.465 |
TRG_DiLeu_BaEn_1 | 660 | 665 | PF01217 | 0.335 |
TRG_DiLeu_BaLyEn_6 | 103 | 108 | PF01217 | 0.588 |
TRG_DiLeu_BaLyEn_6 | 77 | 82 | PF01217 | 0.455 |
TRG_DiLeu_LyEn_5 | 461 | 466 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.584 |
TRG_ENDOCYTIC_2 | 518 | 521 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.405 |
TRG_ER_diArg_1 | 100 | 102 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 535 | 537 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.517 |
TRG_NES_CRM1_1 | 510 | 522 | PF08389 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 220 | 225 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 438 | 442 | PF00026 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 541 | 545 | PF00026 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 601 | 605 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 636 | 640 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 677 | 681 | PF00026 | 0.356 |
TRG_Pf-PMV_PEXEL_1 | 699 | 704 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 80 | 85 | PF00026 | 0.429 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9P1 | Leptomonas seymouri | 68% | 100% |
A0A0S4J3E1 | Bodo saltans | 42% | 100% |
A0A1X0NXS8 | Trypanosomatidae | 48% | 100% |
A0A3Q8IBQ3 | Leishmania donovani | 84% | 100% |
A0A3R7KD39 | Trypanosoma rangeli | 55% | 100% |
A4HYP7 | Leishmania infantum | 83% | 100% |
C9ZI84 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9AUK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QCX6 | Leishmania major | 84% | 100% |
V5BQT5 | Trypanosoma cruzi | 53% | 100% |