Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 6 |
Forrest at al. (procyclic) | no | yes: 6 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0010494 | cytoplasmic stress granule | 5 | 1 |
GO:0034399 | nuclear periphery | 2 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0097165 | nuclear stress granule | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9B6I9
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003676 | nucleic acid binding | 3 | 13 |
GO:0003724 | RNA helicase activity | 3 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004386 | helicase activity | 2 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 12 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 13 |
GO:0140657 | ATP-dependent activity | 1 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0003723 | RNA binding | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 902 | 906 | PF00656 | 0.684 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.741 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 741 | 743 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 757 | 759 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 832 | 834 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 876 | 878 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 916 | 918 | PF00675 | 0.695 |
CLV_PCSK_FUR_1 | 318 | 322 | PF00082 | 0.696 |
CLV_PCSK_FUR_1 | 40 | 44 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.715 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.741 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 675 | 677 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 741 | 743 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 757 | 759 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 832 | 834 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 875 | 877 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 916 | 918 | PF00082 | 0.695 |
CLV_PCSK_PC1ET2_1 | 675 | 677 | PF00082 | 0.487 |
CLV_PCSK_PC7_1 | 171 | 177 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 571 | 575 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 607 | 611 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 695 | 699 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 833 | 837 | PF00082 | 0.514 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.715 |
DEG_SPOP_SBC_1 | 690 | 694 | PF00917 | 0.567 |
DOC_ANK_TNKS_1 | 887 | 894 | PF00023 | 0.641 |
DOC_CKS1_1 | 143 | 148 | PF01111 | 0.563 |
DOC_CYCLIN_RxL_1 | 618 | 629 | PF00134 | 0.519 |
DOC_CYCLIN_yCln2_LP_2 | 480 | 486 | PF00134 | 0.497 |
DOC_MAPK_DCC_7 | 770 | 778 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 447 | 455 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 545 | 554 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 679 | 687 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 770 | 778 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 829 | 838 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 502 | 509 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 547 | 556 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 829 | 838 | PF00069 | 0.516 |
DOC_PP1_RVXF_1 | 569 | 576 | PF00149 | 0.562 |
DOC_PP2B_LxvP_1 | 787 | 790 | PF13499 | 0.556 |
DOC_PP4_FxxP_1 | 528 | 531 | PF00568 | 0.519 |
DOC_PP4_FxxP_1 | 798 | 801 | PF00568 | 0.562 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 899 | 903 | PF00917 | 0.880 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 771 | 776 | PF00397 | 0.519 |
LIG_14-3-3_CanoR_1 | 545 | 551 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 571 | 576 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 647 | 654 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 657 | 661 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 689 | 697 | PF00244 | 0.571 |
LIG_APCC_ABBA_1 | 564 | 569 | PF00400 | 0.558 |
LIG_APCC_ABBA_1 | 726 | 731 | PF00400 | 0.558 |
LIG_BIR_III_4 | 115 | 119 | PF00653 | 0.638 |
LIG_BRCT_BRCA1_1 | 662 | 666 | PF00533 | 0.558 |
LIG_Clathr_ClatBox_1 | 727 | 731 | PF01394 | 0.558 |
LIG_CtBP_PxDLS_1 | 462 | 466 | PF00389 | 0.539 |
LIG_EH1_1 | 719 | 727 | PF00400 | 0.562 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.571 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.547 |
LIG_FHA_1 | 772 | 778 | PF00498 | 0.519 |
LIG_FHA_1 | 806 | 812 | PF00498 | 0.538 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.572 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.730 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.662 |
LIG_FHA_2 | 651 | 657 | PF00498 | 0.578 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.683 |
LIG_LIR_Apic_2 | 525 | 531 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 456 | 466 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 474 | 484 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 578 | 585 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 612 | 622 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 646 | 654 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 344 | 348 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 456 | 461 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 474 | 479 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 577 | 583 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 612 | 617 | PF02991 | 0.588 |
LIG_Pex14_2 | 662 | 666 | PF04695 | 0.519 |
LIG_PTAP_UEV_1 | 907 | 912 | PF05743 | 0.672 |
LIG_PTB_Apo_2 | 608 | 615 | PF02174 | 0.522 |
LIG_PTB_Phospho_1 | 608 | 614 | PF10480 | 0.562 |
LIG_SH2_CRK | 458 | 462 | PF00017 | 0.592 |
LIG_SH2_CRK | 494 | 498 | PF00017 | 0.536 |
LIG_SH2_CRK | 503 | 507 | PF00017 | 0.537 |
LIG_SH2_CRK | 535 | 539 | PF00017 | 0.565 |
LIG_SH2_CRK | 581 | 585 | PF00017 | 0.562 |
LIG_SH2_GRB2like | 3 | 6 | PF00017 | 0.633 |
LIG_SH2_NCK_1 | 458 | 462 | PF00017 | 0.533 |
LIG_SH2_NCK_1 | 581 | 585 | PF00017 | 0.562 |
LIG_SH2_SRC | 304 | 307 | PF00017 | 0.645 |
LIG_SH2_STAP1 | 581 | 585 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 807 | 811 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 648 | 651 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 677 | 680 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 683 | 686 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 807 | 810 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 841 | 844 | PF00017 | 0.513 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.663 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.750 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.868 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.570 |
LIG_SH3_3 | 597 | 603 | PF00018 | 0.579 |
LIG_SH3_3 | 905 | 911 | PF00018 | 0.681 |
LIG_Sin3_3 | 477 | 484 | PF02671 | 0.511 |
LIG_SUMO_SIM_par_1 | 505 | 510 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 774 | 781 | PF11976 | 0.519 |
LIG_TRAF2_1 | 224 | 227 | PF00917 | 0.656 |
LIG_TRAF2_1 | 354 | 357 | PF00917 | 0.719 |
LIG_TYR_ITIM | 533 | 538 | PF00017 | 0.521 |
LIG_TYR_ITIM | 579 | 584 | PF00017 | 0.562 |
LIG_UBA3_1 | 670 | 675 | PF00899 | 0.466 |
LIG_WRC_WIRS_1 | 25 | 30 | PF05994 | 0.728 |
LIG_WRC_WIRS_1 | 345 | 350 | PF05994 | 0.733 |
LIG_WRC_WIRS_1 | 614 | 619 | PF05994 | 0.562 |
MOD_CDC14_SPxK_1 | 542 | 545 | PF00782 | 0.569 |
MOD_CDK_SPxK_1 | 539 | 545 | PF00069 | 0.569 |
MOD_CDK_SPxxK_3 | 495 | 502 | PF00069 | 0.408 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.650 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.610 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.568 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.663 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.519 |
MOD_CK1_1 | 749 | 755 | PF00069 | 0.534 |
MOD_CK1_1 | 906 | 912 | PF00069 | 0.761 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.651 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.658 |
MOD_CK2_1 | 650 | 656 | PF00069 | 0.527 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.684 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.686 |
MOD_Cter_Amidation | 217 | 220 | PF01082 | 0.722 |
MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.718 |
MOD_Cter_Amidation | 340 | 343 | PF01082 | 0.732 |
MOD_Cter_Amidation | 40 | 43 | PF01082 | 0.697 |
MOD_Cter_Amidation | 873 | 876 | PF01082 | 0.713 |
MOD_Cter_Amidation | 914 | 917 | PF01082 | 0.696 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.640 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.585 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.651 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.577 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.675 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.567 |
MOD_GlcNHglycan | 356 | 360 | PF01048 | 0.736 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.732 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.661 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.599 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.333 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.374 |
MOD_GlcNHglycan | 55 | 59 | PF01048 | 0.820 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.362 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.378 |
MOD_GlcNHglycan | 888 | 891 | PF01048 | 0.709 |
MOD_GlcNHglycan | 908 | 911 | PF01048 | 0.677 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.616 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.643 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.652 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.668 |
MOD_GSK3_1 | 646 | 653 | PF00069 | 0.568 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.579 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.582 |
MOD_GSK3_1 | 777 | 784 | PF00069 | 0.558 |
MOD_GSK3_1 | 899 | 906 | PF00069 | 0.707 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.648 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.564 |
MOD_N-GLC_1 | 695 | 700 | PF02516 | 0.543 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.545 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.511 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.629 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.530 |
MOD_PIKK_1 | 414 | 420 | PF00454 | 0.643 |
MOD_PIKK_1 | 695 | 701 | PF00454 | 0.559 |
MOD_PKA_1 | 422 | 428 | PF00069 | 0.640 |
MOD_PKA_1 | 571 | 577 | PF00069 | 0.599 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.724 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.661 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.794 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.519 |
MOD_PKA_2 | 646 | 652 | PF00069 | 0.553 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.565 |
MOD_PKA_2 | 906 | 912 | PF00069 | 0.723 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.741 |
MOD_Plk_2-3 | 24 | 30 | PF00069 | 0.673 |
MOD_Plk_2-3 | 650 | 656 | PF00069 | 0.562 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.558 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.662 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.569 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.631 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.722 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.408 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.557 |
MOD_ProDKin_1 | 771 | 777 | PF00069 | 0.519 |
MOD_SUMO_rev_2 | 2 | 10 | PF00179 | 0.719 |
MOD_SUMO_rev_2 | 436 | 441 | PF00179 | 0.594 |
MOD_SUMO_rev_2 | 464 | 473 | PF00179 | 0.498 |
TRG_DiLeu_BaEn_1 | 595 | 600 | PF01217 | 0.519 |
TRG_DiLeu_BaEn_1 | 861 | 866 | PF01217 | 0.575 |
TRG_DiLeu_BaEn_2 | 655 | 661 | PF01217 | 0.516 |
TRG_DiLeu_BaLyEn_6 | 709 | 714 | PF01217 | 0.562 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.590 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 614 | 617 | PF00928 | 0.584 |
TRG_ENDOCYTIC_2 | 648 | 651 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 682 | 685 | PF00928 | 0.396 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 232 | 235 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.717 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 319 | 321 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.724 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.738 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 678 | 680 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 741 | 743 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 832 | 834 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 875 | 877 | PF00400 | 0.763 |
TRG_Pf-PMV_PEXEL_1 | 560 | 565 | PF00026 | 0.359 |
TRG_Pf-PMV_PEXEL_1 | 741 | 746 | PF00026 | 0.399 |
TRG_Pf-PMV_PEXEL_1 | 832 | 837 | PF00026 | 0.521 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCW9 | Leptomonas seymouri | 66% | 100% |
A0A0S4JDN6 | Bodo saltans | 53% | 100% |
A0A3Q8IF94 | Leishmania donovani | 51% | 100% |
A0A3Q8IJ79 | Leishmania donovani | 92% | 100% |
A4HMX7 | Leishmania braziliensis | 79% | 94% |
A4I7K4 | Leishmania infantum | 51% | 100% |
A4IBK1 | Leishmania infantum | 92% | 100% |
E9AFD4 | Leishmania major | 94% | 100% |
E9AYQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B2G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
Q4Q5P5 | Leishmania major | 49% | 100% |