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. | yes | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
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: A0A3Q8IJ79
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003724 | RNA helicase activity | 3 | 11 |
GO:0003743 | translation initiation factor activity | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004386 | helicase activity | 2 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008135 | translation factor activity, RNA binding | 3 | 11 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0045182 | translation regulator activity | 1 | 11 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003723 | RNA binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 893 | 897 | PF00656 | 0.790 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.776 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.784 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.810 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.777 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.769 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.864 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.793 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.777 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 670 | 672 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 732 | 734 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 748 | 750 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 823 | 825 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 867 | 869 | PF00675 | 0.785 |
CLV_NRD_NRD_1 | 907 | 909 | PF00675 | 0.832 |
CLV_PCSK_FUR_1 | 309 | 313 | PF00082 | 0.734 |
CLV_PCSK_FUR_1 | 40 | 44 | PF00082 | 0.799 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.776 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.784 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.810 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.777 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.864 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.793 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.777 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 666 | 668 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 670 | 672 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 732 | 734 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 748 | 750 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 823 | 825 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 866 | 868 | PF00082 | 0.772 |
CLV_PCSK_KEX2_1 | 907 | 909 | PF00082 | 0.832 |
CLV_PCSK_PC1ET2_1 | 666 | 668 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 686 | 690 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 824 | 828 | PF00082 | 0.570 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.774 |
DEG_SPOP_SBC_1 | 681 | 685 | PF00917 | 0.675 |
DOC_ANK_TNKS_1 | 879 | 886 | PF00023 | 0.739 |
DOC_CYCLIN_RxL_1 | 609 | 620 | PF00134 | 0.615 |
DOC_CYCLIN_yCln2_LP_2 | 471 | 477 | PF00134 | 0.554 |
DOC_MAPK_DCC_7 | 761 | 769 | PF00069 | 0.642 |
DOC_MAPK_gen_1 | 438 | 446 | PF00069 | 0.641 |
DOC_MAPK_gen_1 | 536 | 545 | PF00069 | 0.615 |
DOC_MAPK_gen_1 | 670 | 678 | PF00069 | 0.529 |
DOC_MAPK_gen_1 | 761 | 769 | PF00069 | 0.637 |
DOC_MAPK_gen_1 | 820 | 829 | PF00069 | 0.625 |
DOC_MAPK_MEF2A_6 | 493 | 500 | PF00069 | 0.615 |
DOC_MAPK_MEF2A_6 | 538 | 547 | PF00069 | 0.615 |
DOC_MAPK_MEF2A_6 | 820 | 829 | PF00069 | 0.572 |
DOC_PP1_RVXF_1 | 560 | 567 | PF00149 | 0.615 |
DOC_PP2B_LxvP_1 | 778 | 781 | PF13499 | 0.653 |
DOC_PP4_FxxP_1 | 163 | 166 | PF00568 | 0.771 |
DOC_PP4_FxxP_1 | 519 | 522 | PF00568 | 0.615 |
DOC_PP4_FxxP_1 | 789 | 792 | PF00568 | 0.615 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.791 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 762 | 767 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 536 | 542 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 562 | 567 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 638 | 645 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 648 | 652 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 680 | 688 | PF00244 | 0.674 |
LIG_APCC_ABBA_1 | 555 | 560 | PF00400 | 0.653 |
LIG_APCC_ABBA_1 | 717 | 722 | PF00400 | 0.653 |
LIG_BRCT_BRCA1_1 | 653 | 657 | PF00533 | 0.653 |
LIG_Clathr_ClatBox_1 | 718 | 722 | PF01394 | 0.653 |
LIG_CtBP_PxDLS_1 | 453 | 457 | PF00389 | 0.614 |
LIG_EH1_1 | 710 | 718 | PF00400 | 0.615 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.653 |
LIG_FHA_1 | 683 | 689 | PF00498 | 0.631 |
LIG_FHA_1 | 763 | 769 | PF00498 | 0.606 |
LIG_FHA_1 | 797 | 803 | PF00498 | 0.615 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.784 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.748 |
LIG_FHA_2 | 642 | 648 | PF00498 | 0.621 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.795 |
LIG_LIR_Apic_2 | 160 | 166 | PF02991 | 0.782 |
LIG_LIR_Apic_2 | 318 | 324 | PF02991 | 0.869 |
LIG_LIR_Apic_2 | 516 | 522 | PF02991 | 0.653 |
LIG_LIR_Gen_1 | 447 | 457 | PF02991 | 0.682 |
LIG_LIR_Gen_1 | 465 | 475 | PF02991 | 0.721 |
LIG_LIR_Gen_1 | 569 | 576 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 603 | 613 | PF02991 | 0.708 |
LIG_LIR_Gen_1 | 637 | 645 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.730 |
LIG_LIR_Nem_3 | 335 | 339 | PF02991 | 0.782 |
LIG_LIR_Nem_3 | 447 | 452 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 465 | 470 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 568 | 574 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 603 | 608 | PF02991 | 0.710 |
LIG_Pex14_2 | 653 | 657 | PF04695 | 0.615 |
LIG_PTAP_UEV_1 | 898 | 903 | PF05743 | 0.782 |
LIG_PTB_Apo_2 | 599 | 606 | PF02174 | 0.615 |
LIG_PTB_Phospho_1 | 599 | 605 | PF10480 | 0.615 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.877 |
LIG_SH2_CRK | 449 | 453 | PF00017 | 0.640 |
LIG_SH2_CRK | 485 | 489 | PF00017 | 0.669 |
LIG_SH2_CRK | 494 | 498 | PF00017 | 0.617 |
LIG_SH2_CRK | 526 | 530 | PF00017 | 0.615 |
LIG_SH2_CRK | 572 | 576 | PF00017 | 0.615 |
LIG_SH2_GRB2like | 3 | 6 | PF00017 | 0.728 |
LIG_SH2_NCK_1 | 449 | 453 | PF00017 | 0.640 |
LIG_SH2_NCK_1 | 572 | 576 | PF00017 | 0.615 |
LIG_SH2_SRC | 232 | 235 | PF00017 | 0.717 |
LIG_SH2_SRC | 295 | 298 | PF00017 | 0.743 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.750 |
LIG_SH2_STAP1 | 572 | 576 | PF00017 | 0.615 |
LIG_SH2_STAP1 | 798 | 802 | PF00017 | 0.615 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.769 |
LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 668 | 671 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 674 | 677 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 798 | 801 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 832 | 835 | PF00017 | 0.581 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.735 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.687 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.682 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.843 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.675 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.653 |
LIG_SH3_3 | 896 | 902 | PF00018 | 0.785 |
LIG_Sin3_3 | 468 | 475 | PF02671 | 0.567 |
LIG_SUMO_SIM_par_1 | 496 | 501 | PF11976 | 0.585 |
LIG_SUMO_SIM_par_1 | 765 | 772 | PF11976 | 0.577 |
LIG_TRAF2_1 | 219 | 222 | PF00917 | 0.771 |
LIG_TRAF2_1 | 369 | 372 | PF00917 | 0.760 |
LIG_TYR_ITIM | 524 | 529 | PF00017 | 0.615 |
LIG_TYR_ITIM | 570 | 575 | PF00017 | 0.615 |
LIG_UBA3_1 | 661 | 666 | PF00899 | 0.517 |
LIG_WRC_WIRS_1 | 25 | 30 | PF05994 | 0.782 |
LIG_WRC_WIRS_1 | 336 | 341 | PF05994 | 0.781 |
LIG_WRC_WIRS_1 | 605 | 610 | PF05994 | 0.615 |
MOD_CDC14_SPxK_1 | 533 | 536 | PF00782 | 0.620 |
MOD_CDK_SPxK_1 | 530 | 536 | PF00069 | 0.620 |
MOD_CDK_SPxxK_3 | 486 | 493 | PF00069 | 0.518 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.737 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.653 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.758 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.615 |
MOD_CK1_1 | 740 | 746 | PF00069 | 0.615 |
MOD_CK1_1 | 897 | 903 | PF00069 | 0.782 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.735 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.752 |
MOD_CK2_1 | 641 | 647 | PF00069 | 0.575 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.822 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.796 |
MOD_Cter_Amidation | 212 | 215 | PF01082 | 0.770 |
MOD_Cter_Amidation | 267 | 270 | PF01082 | 0.764 |
MOD_Cter_Amidation | 331 | 334 | PF01082 | 0.784 |
MOD_Cter_Amidation | 40 | 43 | PF01082 | 0.799 |
MOD_Cter_Amidation | 864 | 867 | PF01082 | 0.757 |
MOD_Cter_Amidation | 905 | 908 | PF01082 | 0.806 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.638 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.725 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.635 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.737 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.755 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.758 |
MOD_GlcNHglycan | 347 | 351 | PF01048 | 0.786 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.767 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.699 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.772 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.426 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.400 |
MOD_GlcNHglycan | 55 | 59 | PF01048 | 0.802 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.507 |
MOD_GlcNHglycan | 653 | 656 | PF01048 | 0.427 |
MOD_GlcNHglycan | 880 | 883 | PF01048 | 0.798 |
MOD_GlcNHglycan | 899 | 902 | PF01048 | 0.883 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.727 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.739 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.667 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.769 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.675 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.635 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.667 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.653 |
MOD_GSK3_1 | 890 | 897 | PF00069 | 0.792 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.783 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.746 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.627 |
MOD_N-GLC_1 | 686 | 691 | PF02516 | 0.653 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.763 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.615 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.620 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.716 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.586 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.738 |
MOD_PIKK_1 | 686 | 692 | PF00454 | 0.647 |
MOD_PKA_1 | 413 | 419 | PF00069 | 0.710 |
MOD_PKA_1 | 562 | 568 | PF00069 | 0.725 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.778 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.710 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.699 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.615 |
MOD_PKA_2 | 637 | 643 | PF00069 | 0.675 |
MOD_PKA_2 | 647 | 653 | PF00069 | 0.635 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.783 |
MOD_PKA_2 | 897 | 903 | PF00069 | 0.782 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.703 |
MOD_Plk_2-3 | 24 | 30 | PF00069 | 0.784 |
MOD_Plk_2-3 | 641 | 647 | PF00069 | 0.615 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.653 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.765 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.720 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.771 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.779 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.514 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.617 |
MOD_ProDKin_1 | 762 | 768 | PF00069 | 0.615 |
MOD_SUMO_rev_2 | 2 | 10 | PF00179 | 0.773 |
MOD_SUMO_rev_2 | 427 | 432 | PF00179 | 0.622 |
MOD_SUMO_rev_2 | 455 | 464 | PF00179 | 0.585 |
TRG_DiLeu_BaEn_1 | 586 | 591 | PF01217 | 0.615 |
TRG_DiLeu_BaEn_1 | 852 | 857 | PF01217 | 0.629 |
TRG_DiLeu_BaEn_2 | 646 | 652 | PF01217 | 0.548 |
TRG_DiLeu_BaLyEn_6 | 700 | 705 | PF01217 | 0.615 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.696 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.615 |
TRG_ENDOCYTIC_2 | 572 | 575 | PF00928 | 0.615 |
TRG_ENDOCYTIC_2 | 605 | 608 | PF00928 | 0.649 |
TRG_ENDOCYTIC_2 | 639 | 642 | PF00928 | 0.662 |
TRG_ENDOCYTIC_2 | 673 | 676 | PF00928 | 0.506 |
TRG_ER_diArg_1 | 214 | 216 | PF00400 | 0.765 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.772 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 303 | 305 | PF00400 | 0.800 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.730 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.820 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.799 |
TRG_ER_diArg_1 | 412 | 414 | PF00400 | 0.798 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 669 | 671 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 732 | 734 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 823 | 825 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 866 | 868 | PF00400 | 0.808 |
TRG_Pf-PMV_PEXEL_1 | 551 | 556 | PF00026 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 732 | 737 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 823 | 828 | PF00026 | 0.703 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JDN6 | Bodo saltans | 52% | 100% |
A0A3Q8IF94 | Leishmania donovani | 51% | 100% |
A4HMX7 | Leishmania braziliensis | 80% | 95% |
A4I7K4 | Leishmania infantum | 51% | 100% |
A4IBK1 | Leishmania infantum | 99% | 100% |
E9AFD4 | Leishmania major | 94% | 100% |
E9B2G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9B6I9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q5P5 | Leishmania major | 49% | 100% |