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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QB84
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0008213 | protein alkylation | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016570 | histone modification | 5 | 2 |
GO:0016571 | histone methylation | 5 | 2 |
GO:0018022 | peptidyl-lysine methylation | 5 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018205 | peptidyl-lysine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032259 | methylation | 2 | 3 |
GO:0034968 | histone lysine methylation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043414 | macromolecule methylation | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0008168 | methyltransferase activity | 4 | 3 |
GO:0008170 | N-methyltransferase activity | 5 | 2 |
GO:0008276 | protein methyltransferase activity | 3 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 2 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 2 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 3 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 2 |
GO:0042054 | histone methyltransferase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 414 | 418 | PF00656 | 0.753 |
CLV_C14_Caspase3-7 | 464 | 468 | PF00656 | 0.605 |
CLV_C14_Caspase3-7 | 492 | 496 | PF00656 | 0.558 |
CLV_C14_Caspase3-7 | 622 | 626 | PF00656 | 0.751 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 735 | 737 | PF00675 | 0.444 |
CLV_PCSK_FUR_1 | 246 | 250 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 600 | 602 | PF00082 | 0.530 |
CLV_PCSK_PC7_1 | 244 | 250 | PF00082 | 0.687 |
CLV_PCSK_PC7_1 | 596 | 602 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 615 | 619 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 736 | 740 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.592 |
DEG_APCC_DBOX_1 | 152 | 160 | PF00400 | 0.628 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.648 |
DEG_SCF_FBW7_1 | 821 | 828 | PF00400 | 0.706 |
DEG_SPOP_SBC_1 | 123 | 127 | PF00917 | 0.539 |
DEG_SPOP_SBC_1 | 333 | 337 | PF00917 | 0.696 |
DEG_SPOP_SBC_1 | 358 | 362 | PF00917 | 0.692 |
DEG_SPOP_SBC_1 | 458 | 462 | PF00917 | 0.731 |
DOC_CYCLIN_RxL_1 | 227 | 240 | PF00134 | 0.669 |
DOC_CYCLIN_RxL_1 | 733 | 741 | PF00134 | 0.429 |
DOC_MAPK_gen_1 | 219 | 226 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 248 | 258 | PF00069 | 0.718 |
DOC_PP1_RVXF_1 | 363 | 370 | PF00149 | 0.565 |
DOC_PP2B_LxvP_1 | 805 | 808 | PF13499 | 0.592 |
DOC_PP4_FxxP_1 | 786 | 789 | PF00568 | 0.641 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 814 | 818 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.788 |
DOC_USP7_UBL2_3 | 55 | 59 | PF12436 | 0.487 |
DOC_USP7_UBL2_3 | 74 | 78 | PF12436 | 0.579 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 779 | 784 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 810 | 815 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 817 | 822 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 128 | 134 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 153 | 163 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 359 | 364 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 452 | 458 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 505 | 510 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 541 | 548 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 588 | 592 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 615 | 620 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 736 | 745 | PF00244 | 0.364 |
LIG_APCC_ABBA_1 | 677 | 682 | PF00400 | 0.489 |
LIG_BIR_III_2 | 495 | 499 | PF00653 | 0.665 |
LIG_BRCT_BRCA1_1 | 137 | 141 | PF00533 | 0.544 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.695 |
LIG_BRCT_BRCA1_1 | 370 | 374 | PF00533 | 0.469 |
LIG_CSL_BTD_1 | 822 | 825 | PF09270 | 0.536 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.607 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.654 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.717 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.716 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.599 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.587 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.747 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.608 |
LIG_FHA_2 | 722 | 728 | PF00498 | 0.661 |
LIG_FHA_2 | 826 | 832 | PF00498 | 0.637 |
LIG_Integrin_RGD_1 | 189 | 191 | PF01839 | 0.590 |
LIG_LIR_Gen_1 | 133 | 144 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 368 | 377 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 567 | 576 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 650 | 660 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 720 | 729 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 133 | 139 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 319 | 324 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 368 | 372 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 567 | 573 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 589 | 594 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 650 | 656 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 664 | 668 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 720 | 726 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 740 | 745 | PF02991 | 0.231 |
LIG_LYPXL_S_1 | 320 | 324 | PF13949 | 0.431 |
LIG_LYPXL_yS_3 | 321 | 324 | PF13949 | 0.440 |
LIG_NRBOX | 605 | 611 | PF00104 | 0.575 |
LIG_PTB_Apo_2 | 39 | 46 | PF02174 | 0.505 |
LIG_PTB_Phospho_1 | 39 | 45 | PF10480 | 0.418 |
LIG_SH2_GRB2like | 685 | 688 | PF00017 | 0.476 |
LIG_SH2_NCK_1 | 723 | 727 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 570 | 574 | PF00017 | 0.570 |
LIG_SH2_STAP1 | 708 | 712 | PF00017 | 0.576 |
LIG_SH2_STAT3 | 668 | 671 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 652 | 655 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 685 | 688 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 723 | 726 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 801 | 804 | PF00017 | 0.434 |
LIG_SH3_1 | 801 | 807 | PF00018 | 0.465 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.713 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.493 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.700 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.734 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.702 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.729 |
LIG_SH3_3 | 768 | 774 | PF00018 | 0.699 |
LIG_SH3_3 | 801 | 807 | PF00018 | 0.487 |
LIG_SUMO_SIM_anti_2 | 490 | 495 | PF11976 | 0.584 |
LIG_SUMO_SIM_anti_2 | 577 | 584 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 489 | 495 | PF11976 | 0.599 |
LIG_TRAF2_1 | 11 | 14 | PF00917 | 0.659 |
LIG_TRAF2_1 | 714 | 717 | PF00917 | 0.576 |
LIG_TRAF2_1 | 828 | 831 | PF00917 | 0.623 |
LIG_TYR_ITIM | 721 | 726 | PF00017 | 0.544 |
LIG_UBA3_1 | 477 | 484 | PF00899 | 0.630 |
LIG_WW_1 | 807 | 810 | PF00397 | 0.462 |
MOD_CDC14_SPxK_1 | 813 | 816 | PF00782 | 0.692 |
MOD_CDK_SPxK_1 | 810 | 816 | PF00069 | 0.686 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.680 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.692 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.737 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.610 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.611 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.726 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.787 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.693 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.731 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.651 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.718 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.469 |
MOD_CK1_1 | 817 | 823 | PF00069 | 0.745 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.625 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.308 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.594 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.757 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.767 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.718 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.614 |
MOD_CK2_1 | 721 | 727 | PF00069 | 0.576 |
MOD_CK2_1 | 825 | 831 | PF00069 | 0.656 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.761 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.644 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.497 |
MOD_GlcNHglycan | 309 | 313 | PF01048 | 0.495 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.636 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.514 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.695 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.706 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.675 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.463 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.463 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.575 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.522 |
MOD_GlcNHglycan | 771 | 774 | PF01048 | 0.693 |
MOD_GlcNHglycan | 775 | 778 | PF01048 | 0.712 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.751 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.658 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.536 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.704 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.568 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.639 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.491 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.758 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.738 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.740 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.686 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.627 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.740 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.624 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.692 |
MOD_GSK3_1 | 717 | 724 | PF00069 | 0.575 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.675 |
MOD_GSK3_1 | 810 | 817 | PF00069 | 0.711 |
MOD_GSK3_1 | 819 | 826 | PF00069 | 0.654 |
MOD_GSK3_1 | 835 | 842 | PF00069 | 0.424 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.799 |
MOD_N-GLC_1 | 578 | 583 | PF02516 | 0.476 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.474 |
MOD_N-GLC_1 | 686 | 691 | PF02516 | 0.276 |
MOD_N-GLC_2 | 44 | 46 | PF02516 | 0.593 |
MOD_N-GLC_2 | 693 | 695 | PF02516 | 0.276 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.668 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.512 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.496 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.743 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.612 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.476 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.652 |
MOD_NEK2_1 | 738 | 743 | PF00069 | 0.434 |
MOD_NEK2_1 | 809 | 814 | PF00069 | 0.740 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.805 |
MOD_PIKK_1 | 667 | 673 | PF00454 | 0.469 |
MOD_PKA_1 | 210 | 216 | PF00069 | 0.709 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.625 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.546 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.715 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.760 |
MOD_PKA_2 | 587 | 593 | PF00069 | 0.491 |
MOD_PKA_2 | 749 | 755 | PF00069 | 0.517 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.636 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.585 |
MOD_Plk_1 | 578 | 584 | PF00069 | 0.495 |
MOD_Plk_1 | 586 | 592 | PF00069 | 0.468 |
MOD_Plk_1 | 681 | 687 | PF00069 | 0.476 |
MOD_Plk_1 | 835 | 841 | PF00069 | 0.449 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.771 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.439 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.585 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.792 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.496 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.479 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.667 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.508 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.472 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.788 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.803 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.594 |
MOD_ProDKin_1 | 779 | 785 | PF00069 | 0.707 |
MOD_ProDKin_1 | 810 | 816 | PF00069 | 0.708 |
MOD_ProDKin_1 | 817 | 823 | PF00069 | 0.636 |
MOD_SUMO_for_1 | 111 | 114 | PF00179 | 0.591 |
MOD_SUMO_rev_2 | 420 | 427 | PF00179 | 0.631 |
MOD_SUMO_rev_2 | 826 | 834 | PF00179 | 0.434 |
TRG_DiLeu_BaEn_1 | 368 | 373 | PF01217 | 0.398 |
TRG_DiLeu_BaEn_1 | 787 | 792 | PF01217 | 0.612 |
TRG_DiLeu_BaEn_4 | 254 | 260 | PF01217 | 0.729 |
TRG_DiLeu_BaLyEn_6 | 226 | 231 | PF01217 | 0.596 |
TRG_DiLeu_BaLyEn_6 | 473 | 478 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 786 | 791 | PF01217 | 0.617 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.586 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 723 | 726 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 742 | 745 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 243 | 246 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.624 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 500 | 502 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 563 | 566 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 734 | 736 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 841 | 844 | PF00400 | 0.616 |
TRG_NLS_MonoExtC_3 | 206 | 211 | PF00514 | 0.726 |
TRG_Pf-PMV_PEXEL_1 | 365 | 370 | PF00026 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 476 | 480 | PF00026 | 0.445 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEZ6 | Leptomonas seymouri | 49% | 100% |
A0A1X0NYH3 | Trypanosomatidae | 30% | 100% |
A0A3R7KV16 | Trypanosoma rangeli | 31% | 100% |
A0A3S7WXM7 | Leishmania donovani | 87% | 100% |
A4I0D0 | Leishmania infantum | 87% | 100% |
C9ZV40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AW94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 98% |
V5ARQ1 | Trypanosoma cruzi | 30% | 100% |