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. | yes | 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. | yes | 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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
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:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0097165 | nuclear stress granule | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
Related structures:
AlphaFold database: E9AFD4
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 3 |
GO:0003724 | RNA helicase activity | 3 | 10 |
GO:0003743 | translation initiation factor activity | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004386 | helicase activity | 2 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0008135 | translation factor activity, RNA binding | 3 | 10 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion 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:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.649 |
CLV_C14_Caspase3-7 | 899 | 903 | PF00656 | 0.759 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.730 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.802 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.753 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 675 | 677 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 737 | 739 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 753 | 755 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 828 | 830 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 872 | 874 | PF00675 | 0.749 |
CLV_NRD_NRD_1 | 913 | 915 | PF00675 | 0.772 |
CLV_PCSK_FUR_1 | 314 | 318 | PF00082 | 0.717 |
CLV_PCSK_FUR_1 | 40 | 44 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.802 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.753 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 675 | 677 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 737 | 739 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 753 | 755 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 828 | 830 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 871 | 873 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 913 | 915 | PF00082 | 0.772 |
CLV_PCSK_PC1ET2_1 | 671 | 673 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 691 | 695 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 829 | 833 | PF00082 | 0.540 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.737 |
DEG_SPOP_SBC_1 | 686 | 690 | PF00917 | 0.707 |
DOC_ANK_TNKS_1 | 883 | 890 | PF00023 | 0.719 |
DOC_CYCLIN_RxL_1 | 614 | 625 | PF00134 | 0.596 |
DOC_CYCLIN_yCln2_LP_2 | 476 | 482 | PF00134 | 0.522 |
DOC_MAPK_DCC_7 | 766 | 774 | PF00069 | 0.630 |
DOC_MAPK_gen_1 | 541 | 550 | PF00069 | 0.596 |
DOC_MAPK_gen_1 | 675 | 683 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 766 | 774 | PF00069 | 0.661 |
DOC_MAPK_gen_1 | 825 | 834 | PF00069 | 0.583 |
DOC_MAPK_MEF2A_6 | 498 | 505 | PF00069 | 0.610 |
DOC_MAPK_MEF2A_6 | 543 | 552 | PF00069 | 0.596 |
DOC_MAPK_MEF2A_6 | 825 | 834 | PF00069 | 0.542 |
DOC_PP1_RVXF_1 | 565 | 572 | PF00149 | 0.596 |
DOC_PP2B_LxvP_1 | 783 | 786 | PF13499 | 0.732 |
DOC_PP4_FxxP_1 | 168 | 171 | PF00568 | 0.706 |
DOC_PP4_FxxP_1 | 524 | 527 | PF00568 | 0.596 |
DOC_PP4_FxxP_1 | 794 | 797 | PF00568 | 0.596 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.765 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 535 | 540 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 767 | 772 | PF00397 | 0.596 |
LIG_14-3-3_CanoR_1 | 541 | 547 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 567 | 572 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 643 | 650 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 653 | 657 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 685 | 693 | PF00244 | 0.709 |
LIG_APCC_ABBA_1 | 560 | 565 | PF00400 | 0.681 |
LIG_APCC_ABBA_1 | 722 | 727 | PF00400 | 0.681 |
LIG_BIR_III_4 | 115 | 119 | PF00653 | 0.718 |
LIG_BRCT_BRCA1_1 | 658 | 662 | PF00533 | 0.681 |
LIG_Clathr_ClatBox_1 | 723 | 727 | PF01394 | 0.681 |
LIG_CtBP_PxDLS_1 | 458 | 462 | PF00389 | 0.559 |
LIG_EH1_1 | 715 | 723 | PF00400 | 0.596 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.681 |
LIG_FHA_1 | 688 | 694 | PF00498 | 0.698 |
LIG_FHA_1 | 768 | 774 | PF00498 | 0.596 |
LIG_FHA_1 | 802 | 808 | PF00498 | 0.596 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.744 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.728 |
LIG_FHA_2 | 647 | 653 | PF00498 | 0.596 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.740 |
LIG_LIR_Apic_2 | 165 | 171 | PF02991 | 0.710 |
LIG_LIR_Apic_2 | 323 | 329 | PF02991 | 0.734 |
LIG_LIR_Apic_2 | 521 | 527 | PF02991 | 0.681 |
LIG_LIR_Gen_1 | 452 | 462 | PF02991 | 0.712 |
LIG_LIR_Gen_1 | 470 | 480 | PF02991 | 0.656 |
LIG_LIR_Gen_1 | 574 | 581 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 608 | 618 | PF02991 | 0.669 |
LIG_LIR_Gen_1 | 642 | 650 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 340 | 344 | PF02991 | 0.752 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.740 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 573 | 579 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 608 | 613 | PF02991 | 0.677 |
LIG_Pex14_2 | 658 | 662 | PF04695 | 0.596 |
LIG_PTAP_UEV_1 | 904 | 909 | PF05743 | 0.745 |
LIG_PTB_Apo_2 | 604 | 611 | PF02174 | 0.596 |
LIG_PTB_Phospho_1 | 604 | 610 | PF10480 | 0.596 |
LIG_SH2_CRK | 326 | 330 | PF00017 | 0.736 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.605 |
LIG_SH2_CRK | 490 | 494 | PF00017 | 0.659 |
LIG_SH2_CRK | 499 | 503 | PF00017 | 0.518 |
LIG_SH2_CRK | 531 | 535 | PF00017 | 0.647 |
LIG_SH2_CRK | 577 | 581 | PF00017 | 0.599 |
LIG_SH2_GRB2like | 3 | 6 | PF00017 | 0.705 |
LIG_SH2_NCK_1 | 378 | 382 | PF00017 | 0.651 |
LIG_SH2_NCK_1 | 454 | 458 | PF00017 | 0.602 |
LIG_SH2_NCK_1 | 577 | 581 | PF00017 | 0.596 |
LIG_SH2_SRC | 237 | 240 | PF00017 | 0.694 |
LIG_SH2_SRC | 300 | 303 | PF00017 | 0.716 |
LIG_SH2_SRC | 378 | 381 | PF00017 | 0.658 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.738 |
LIG_SH2_STAP1 | 577 | 581 | PF00017 | 0.596 |
LIG_SH2_STAP1 | 803 | 807 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.737 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 673 | 676 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 679 | 682 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 803 | 806 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 837 | 840 | PF00017 | 0.551 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.658 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.715 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.770 |
LIG_SH3_3 | 548 | 554 | PF00018 | 0.725 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.681 |
LIG_SH3_3 | 902 | 908 | PF00018 | 0.745 |
LIG_Sin3_3 | 473 | 480 | PF02671 | 0.536 |
LIG_SUMO_SIM_par_1 | 148 | 155 | PF11976 | 0.658 |
LIG_SUMO_SIM_par_1 | 501 | 506 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 770 | 777 | PF11976 | 0.596 |
LIG_TRAF2_1 | 224 | 227 | PF00917 | 0.734 |
LIG_TRAF2_1 | 350 | 353 | PF00917 | 0.705 |
LIG_TRAF2_1 | 374 | 377 | PF00917 | 0.708 |
LIG_TYR_ITIM | 529 | 534 | PF00017 | 0.596 |
LIG_TYR_ITIM | 575 | 580 | PF00017 | 0.596 |
LIG_UBA3_1 | 666 | 671 | PF00899 | 0.491 |
LIG_WRC_WIRS_1 | 25 | 30 | PF05994 | 0.742 |
LIG_WRC_WIRS_1 | 341 | 346 | PF05994 | 0.749 |
LIG_WRC_WIRS_1 | 610 | 615 | PF05994 | 0.596 |
MOD_CDC14_SPxK_1 | 538 | 541 | PF00782 | 0.596 |
MOD_CDK_SPxK_1 | 535 | 541 | PF00069 | 0.596 |
MOD_CDK_SPxxK_3 | 491 | 498 | PF00069 | 0.554 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.711 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.622 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.720 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.729 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.596 |
MOD_CK1_1 | 745 | 751 | PF00069 | 0.596 |
MOD_CK1_1 | 903 | 909 | PF00069 | 0.718 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.719 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.730 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.745 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.741 |
MOD_Cter_Amidation | 217 | 220 | PF01082 | 0.734 |
MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.741 |
MOD_Cter_Amidation | 336 | 339 | PF01082 | 0.758 |
MOD_Cter_Amidation | 40 | 43 | PF01082 | 0.770 |
MOD_Cter_Amidation | 869 | 872 | PF01082 | 0.727 |
MOD_Cter_Amidation | 911 | 914 | PF01082 | 0.772 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.714 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.642 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.747 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.732 |
MOD_GlcNHglycan | 352 | 356 | PF01048 | 0.758 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.719 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.735 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.638 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.417 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.437 |
MOD_GlcNHglycan | 55 | 59 | PF01048 | 0.759 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.396 |
MOD_GlcNHglycan | 658 | 661 | PF01048 | 0.481 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.680 |
MOD_GlcNHglycan | 884 | 887 | PF01048 | 0.766 |
MOD_GlcNHglycan | 905 | 908 | PF01048 | 0.739 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.684 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.705 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.720 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.641 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.743 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.639 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.633 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.700 |
MOD_GSK3_1 | 773 | 780 | PF00069 | 0.681 |
MOD_GSK3_1 | 896 | 903 | PF00069 | 0.762 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.732 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.716 |
MOD_N-GLC_1 | 691 | 696 | PF02516 | 0.688 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.781 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.596 |
MOD_NEK2_1 | 639 | 644 | PF00069 | 0.609 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.599 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.596 |
MOD_PIKK_1 | 691 | 697 | PF00454 | 0.681 |
MOD_PKA_1 | 418 | 424 | PF00069 | 0.661 |
MOD_PKA_1 | 567 | 573 | PF00069 | 0.704 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.745 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.672 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.661 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.725 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.596 |
MOD_PKA_2 | 642 | 648 | PF00069 | 0.639 |
MOD_PKA_2 | 652 | 658 | PF00069 | 0.633 |
MOD_PKA_2 | 903 | 909 | PF00069 | 0.746 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.748 |
MOD_Plk_2-3 | 24 | 30 | PF00069 | 0.744 |
MOD_Plk_2-3 | 646 | 652 | PF00069 | 0.596 |
MOD_Plk_4 | 652 | 658 | PF00069 | 0.681 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.732 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.706 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.763 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.778 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.540 |
MOD_ProDKin_1 | 535 | 541 | PF00069 | 0.596 |
MOD_ProDKin_1 | 767 | 773 | PF00069 | 0.596 |
MOD_SUMO_rev_2 | 2 | 10 | PF00179 | 0.741 |
MOD_SUMO_rev_2 | 432 | 437 | PF00179 | 0.589 |
MOD_SUMO_rev_2 | 460 | 469 | PF00179 | 0.556 |
TRG_DiLeu_BaEn_1 | 591 | 596 | PF01217 | 0.596 |
TRG_DiLeu_BaEn_1 | 857 | 862 | PF01217 | 0.595 |
TRG_DiLeu_BaLyEn_6 | 705 | 710 | PF01217 | 0.596 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.725 |
TRG_ENDOCYTIC_2 | 531 | 534 | PF00928 | 0.647 |
TRG_ENDOCYTIC_2 | 577 | 580 | PF00928 | 0.599 |
TRG_ENDOCYTIC_2 | 610 | 613 | PF00928 | 0.669 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.596 |
TRG_ENDOCYTIC_2 | 678 | 681 | PF00928 | 0.522 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.729 |
TRG_ER_diArg_1 | 232 | 235 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.740 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 329 | 332 | PF00400 | 0.681 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.770 |
TRG_ER_diArg_1 | 417 | 419 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 674 | 676 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 737 | 739 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 828 | 830 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 871 | 873 | PF00400 | 0.816 |
TRG_Pf-PMV_PEXEL_1 | 556 | 561 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 737 | 742 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 828 | 833 | PF00026 | 0.642 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IF94 | Leishmania donovani | 51% | 100% |
A0A3Q8IJ79 | Leishmania donovani | 94% | 100% |
A4HMX7 | Leishmania braziliensis | 91% | 100% |
A4I7K4 | Leishmania infantum | 51% | 100% |
A4IBK1 | Leishmania infantum | 94% | 100% |
E9B2G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9B6I9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q5P5 | Leishmania major | 49% | 100% |