Nucleic acid binding, rRNA biogenesis -like
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 |
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: A4HYP7
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 | 150 | 154 | PF00656 | 0.552 |
CLV_C14_Caspase3-7 | 434 | 438 | PF00656 | 0.507 |
CLV_C14_Caspase3-7 | 726 | 730 | PF00656 | 0.586 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 657 | 659 | PF00675 | 0.442 |
CLV_PCSK_FUR_1 | 426 | 430 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 587 | 589 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 592 | 594 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 603 | 605 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 640 | 642 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 709 | 711 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.392 |
CLV_PCSK_PC1ET2_1 | 587 | 589 | PF00082 | 0.385 |
CLV_PCSK_PC1ET2_1 | 592 | 594 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 603 | 605 | PF00082 | 0.398 |
CLV_PCSK_PC1ET2_1 | 640 | 642 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 709 | 711 | PF00082 | 0.316 |
CLV_PCSK_PC7_1 | 588 | 594 | PF00082 | 0.380 |
CLV_PCSK_PC7_1 | 636 | 642 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 593 | 597 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 628 | 632 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 669 | 673 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.443 |
CLV_Separin_Metazoa | 98 | 102 | PF03568 | 0.498 |
DEG_SCF_FBW7_1 | 237 | 244 | PF00400 | 0.505 |
DOC_CYCLIN_RxL_1 | 51 | 61 | PF00134 | 0.418 |
DOC_CYCLIN_RxL_1 | 688 | 696 | PF00134 | 0.418 |
DOC_MAPK_gen_1 | 106 | 116 | PF00069 | 0.336 |
DOC_MAPK_gen_1 | 552 | 560 | PF00069 | 0.360 |
DOC_MAPK_gen_1 | 572 | 580 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 603 | 611 | PF00069 | 0.353 |
DOC_MAPK_MEF2A_6 | 109 | 116 | PF00069 | 0.339 |
DOC_MAPK_MEF2A_6 | 573 | 582 | PF00069 | 0.405 |
DOC_PP1_RVXF_1 | 689 | 696 | PF00149 | 0.420 |
DOC_PP2B_PxIxI_1 | 327 | 333 | PF00149 | 0.261 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 639 | 643 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.630 |
DOC_USP7_UBL2_3 | 592 | 596 | PF12436 | 0.410 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 620 | 625 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.377 |
LIG_14-3-3_CanoR_1 | 139 | 146 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 204 | 214 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 41 | 47 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 572 | 576 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 691 | 696 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 710 | 716 | PF00244 | 0.247 |
LIG_14-3-3_CanoR_1 | 80 | 85 | PF00244 | 0.380 |
LIG_Actin_WH2_2 | 576 | 594 | PF00022 | 0.429 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.707 |
LIG_BIR_III_4 | 75 | 79 | PF00653 | 0.500 |
LIG_BRCT_BRCA1_1 | 523 | 527 | PF00533 | 0.386 |
LIG_Clathr_ClatBox_1 | 538 | 542 | PF01394 | 0.230 |
LIG_Clathr_ClatBox_1 | 81 | 85 | PF01394 | 0.440 |
LIG_DLG_GKlike_1 | 691 | 698 | PF00625 | 0.467 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.722 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.454 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.335 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.437 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.552 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.258 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.373 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.458 |
LIG_FHA_1 | 663 | 669 | PF00498 | 0.447 |
LIG_FHA_1 | 688 | 694 | PF00498 | 0.412 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.525 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.423 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.380 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.406 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.473 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.469 |
LIG_FHA_2 | 447 | 453 | PF00498 | 0.549 |
LIG_FHA_2 | 592 | 598 | PF00498 | 0.491 |
LIG_FHA_2 | 647 | 653 | PF00498 | 0.460 |
LIG_FHA_2 | 699 | 705 | PF00498 | 0.428 |
LIG_FHA_2 | 712 | 718 | PF00498 | 0.438 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.511 |
LIG_GBD_Chelix_1 | 52 | 60 | PF00786 | 0.368 |
LIG_Integrin_isoDGR_2 | 626 | 628 | PF01839 | 0.346 |
LIG_Integrin_RGD_1 | 175 | 177 | PF01839 | 0.515 |
LIG_LIR_Apic_2 | 95 | 99 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 452 | 462 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 574 | 583 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 690 | 698 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 88 | 97 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 465 | 471 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 574 | 578 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 642 | 648 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 690 | 695 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.405 |
LIG_PCNA_PIPBox_1 | 686 | 695 | PF02747 | 0.428 |
LIG_PCNA_yPIPBox_3 | 498 | 507 | PF02747 | 0.460 |
LIG_PCNA_yPIPBox_3 | 528 | 539 | PF02747 | 0.271 |
LIG_PCNA_yPIPBox_3 | 683 | 693 | PF02747 | 0.400 |
LIG_Pex14_1 | 390 | 394 | PF04695 | 0.522 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.349 |
LIG_SH2_GRB2like | 510 | 513 | PF00017 | 0.292 |
LIG_SH2_SRC | 510 | 513 | PF00017 | 0.378 |
LIG_SH2_SRC | 715 | 718 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 221 | 225 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 394 | 398 | PF00017 | 0.585 |
LIG_SH2_STAT3 | 648 | 651 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 648 | 651 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 715 | 718 | PF00017 | 0.378 |
LIG_SH3_1 | 308 | 314 | PF00018 | 0.378 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.340 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.352 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.516 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.649 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.456 |
LIG_SUMO_SIM_anti_2 | 319 | 325 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 329 | 335 | PF11976 | 0.451 |
LIG_SUMO_SIM_anti_2 | 608 | 613 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 261 | 271 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 579 | 584 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 80 | 85 | PF11976 | 0.420 |
LIG_TRAF2_1 | 450 | 453 | PF00917 | 0.444 |
LIG_TRAF2_1 | 649 | 652 | PF00917 | 0.483 |
LIG_TYR_ITIM | 508 | 513 | PF00017 | 0.293 |
LIG_UBA3_1 | 630 | 637 | PF00899 | 0.405 |
LIG_WRC_WIRS_1 | 158 | 163 | PF05994 | 0.709 |
LIG_WRC_WIRS_1 | 692 | 697 | PF05994 | 0.374 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.515 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.677 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.697 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.678 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.330 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.622 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.443 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.476 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.483 |
MOD_CK2_1 | 711 | 717 | PF00069 | 0.391 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.514 |
MOD_Cter_Amidation | 585 | 588 | PF01082 | 0.483 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.572 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.539 |
MOD_GlcNHglycan | 153 | 157 | PF01048 | 0.670 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.668 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.662 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.413 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.574 |
MOD_GlcNHglycan | 364 | 368 | PF01048 | 0.682 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.663 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.707 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.636 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.388 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.671 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.441 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.449 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.423 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.481 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.572 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.658 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.484 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.344 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.546 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.694 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.601 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.658 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.527 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.353 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.470 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.337 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.398 |
MOD_GSK3_1 | 711 | 718 | PF00069 | 0.439 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.397 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.351 |
MOD_N-GLC_1 | 462 | 467 | PF02516 | 0.348 |
MOD_N-GLC_1 | 678 | 683 | PF02516 | 0.434 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.709 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.354 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.661 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.458 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.486 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.448 |
MOD_NEK2_1 | 678 | 683 | PF00069 | 0.469 |
MOD_NEK2_1 | 711 | 716 | PF00069 | 0.512 |
MOD_NEK2_1 | 723 | 728 | PF00069 | 0.615 |
MOD_NEK2_2 | 250 | 255 | PF00069 | 0.441 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.431 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.526 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.440 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.632 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.381 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.412 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.473 |
MOD_Plk_1 | 462 | 468 | PF00069 | 0.342 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.476 |
MOD_Plk_1 | 605 | 611 | PF00069 | 0.444 |
MOD_Plk_2-3 | 571 | 577 | PF00069 | 0.402 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.461 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.364 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.424 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.342 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.389 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.618 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.429 |
MOD_ProDKin_1 | 620 | 626 | PF00069 | 0.454 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.374 |
MOD_SUMO_rev_2 | 304 | 310 | PF00179 | 0.505 |
TRG_DiLeu_BaEn_1 | 453 | 458 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_1 | 499 | 504 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 103 | 108 | PF01217 | 0.445 |
TRG_DiLeu_BaLyEn_6 | 52 | 57 | PF01217 | 0.397 |
TRG_DiLeu_BaLyEn_6 | 77 | 82 | PF01217 | 0.389 |
TRG_DiLeu_LyEn_5 | 453 | 458 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.339 |
TRG_ER_diArg_1 | 100 | 102 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 426 | 429 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 527 | 529 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.449 |
TRG_NES_CRM1_1 | 502 | 514 | PF08389 | 0.300 |
TRG_Pf-PMV_PEXEL_1 | 101 | 105 | PF00026 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 217 | 222 | PF00026 | 0.323 |
TRG_Pf-PMV_PEXEL_1 | 430 | 434 | PF00026 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 533 | 537 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 593 | 597 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 628 | 632 | PF00026 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 669 | 673 | PF00026 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 691 | 696 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 80 | 85 | PF00026 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9P1 | Leptomonas seymouri | 71% | 100% |
A0A0S4J3E1 | Bodo saltans | 42% | 100% |
A0A1X0NXS8 | Trypanosomatidae | 43% | 100% |
A0A3Q8IBQ3 | Leishmania donovani | 99% | 99% |
A0A3R7KD39 | Trypanosoma rangeli | 49% | 100% |
C9ZI84 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AIC1 | Leishmania braziliensis | 83% | 100% |
E9AUK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QCX6 | Leishmania major | 94% | 100% |
V5BQT5 | Trypanosoma cruzi | 50% | 100% |