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 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AW94
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008213 | protein alkylation | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016571 | histone methylation | 5 | 1 |
GO:0018022 | peptidyl-lysine methylation | 5 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032259 | methylation | 2 | 2 |
GO:0034968 | histone lysine methylation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008168 | methyltransferase activity | 4 | 2 |
GO:0008170 | N-methyltransferase activity | 5 | 1 |
GO:0008276 | protein methyltransferase activity | 3 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 1 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 1 |
GO:0042054 | histone methyltransferase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 232 | 236 | PF00656 | 0.412 |
CLV_C14_Caspase3-7 | 286 | 290 | PF00656 | 0.472 |
CLV_C14_Caspase3-7 | 430 | 434 | PF00656 | 0.712 |
CLV_C14_Caspase3-7 | 480 | 484 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 508 | 512 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 642 | 646 | PF00656 | 0.569 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 751 | 753 | PF00675 | 0.392 |
CLV_PCSK_FUR_1 | 263 | 267 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 517 | 519 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 616 | 618 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 750 | 752 | PF00082 | 0.377 |
CLV_PCSK_PC1ET2_1 | 616 | 618 | PF00082 | 0.324 |
CLV_PCSK_PC7_1 | 259 | 265 | PF00082 | 0.554 |
CLV_PCSK_PC7_1 | 612 | 618 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 752 | 756 | PF00082 | 0.375 |
DEG_APCC_DBOX_1 | 160 | 168 | PF00400 | 0.627 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.497 |
DEG_ODPH_VHL_1 | 651 | 664 | PF01847 | 0.364 |
DEG_SCF_FBW7_1 | 837 | 844 | PF00400 | 0.574 |
DEG_SPOP_SBC_1 | 349 | 353 | PF00917 | 0.554 |
DEG_SPOP_SBC_1 | 374 | 378 | PF00917 | 0.552 |
DOC_CKS1_1 | 838 | 843 | PF01111 | 0.426 |
DOC_CYCLIN_RxL_1 | 241 | 254 | PF00134 | 0.541 |
DOC_CYCLIN_RxL_1 | 749 | 757 | PF00134 | 0.375 |
DOC_MAPK_gen_1 | 233 | 240 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 263 | 273 | PF00069 | 0.575 |
DOC_PP1_RVXF_1 | 379 | 386 | PF00149 | 0.520 |
DOC_PP2B_LxvP_1 | 821 | 824 | PF13499 | 0.566 |
DOC_PP4_FxxP_1 | 452 | 455 | PF00568 | 0.479 |
DOC_PP4_FxxP_1 | 802 | 805 | PF00568 | 0.642 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 697 | 701 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 785 | 789 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 810 | 814 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 824 | 828 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 832 | 836 | PF00917 | 0.671 |
DOC_USP7_MATH_2 | 488 | 494 | PF00917 | 0.465 |
DOC_USP7_UBL2_3 | 224 | 228 | PF12436 | 0.561 |
DOC_USP7_UBL2_3 | 74 | 78 | PF12436 | 0.536 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 795 | 800 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 837 | 842 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 136 | 142 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 284 | 288 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 375 | 380 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 406 | 416 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 604 | 608 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 630 | 636 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 784 | 788 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 851 | 856 | PF00244 | 0.460 |
LIG_Actin_WH2_2 | 237 | 254 | PF00022 | 0.392 |
LIG_APCC_ABBA_1 | 693 | 698 | PF00400 | 0.442 |
LIG_BIR_III_2 | 511 | 515 | PF00653 | 0.557 |
LIG_BRCT_BRCA1_1 | 145 | 149 | PF00533 | 0.410 |
LIG_BRCT_BRCA1_1 | 386 | 390 | PF00533 | 0.409 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.570 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.388 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.550 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.659 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.483 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.462 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.410 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.675 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.682 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.539 |
LIG_FHA_2 | 738 | 744 | PF00498 | 0.661 |
LIG_FHA_2 | 842 | 848 | PF00498 | 0.530 |
LIG_LIR_Apic_2 | 449 | 455 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 560 | 566 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 583 | 592 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 666 | 676 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 736 | 745 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 560 | 564 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 583 | 589 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 605 | 610 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 666 | 672 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 680 | 684 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 736 | 742 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 757 | 761 | PF02991 | 0.367 |
LIG_LYPXL_S_1 | 336 | 340 | PF13949 | 0.369 |
LIG_LYPXL_yS_3 | 337 | 340 | PF13949 | 0.377 |
LIG_NRBOX | 621 | 627 | PF00104 | 0.474 |
LIG_PTB_Apo_2 | 39 | 46 | PF02174 | 0.451 |
LIG_PTB_Phospho_1 | 39 | 45 | PF10480 | 0.344 |
LIG_SH2_CRK | 561 | 565 | PF00017 | 0.412 |
LIG_SH2_GRB2like | 701 | 704 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 739 | 743 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 586 | 590 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 724 | 728 | PF00017 | 0.474 |
LIG_SH2_STAT3 | 684 | 687 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.712 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 668 | 671 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 701 | 704 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 739 | 742 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 817 | 820 | PF00017 | 0.408 |
LIG_SH3_1 | 817 | 823 | PF00018 | 0.430 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.457 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.697 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.736 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.364 |
LIG_SH3_3 | 728 | 734 | PF00018 | 0.498 |
LIG_SH3_3 | 784 | 790 | PF00018 | 0.695 |
LIG_SH3_3 | 817 | 823 | PF00018 | 0.453 |
LIG_SUMO_SIM_anti_2 | 506 | 511 | PF11976 | 0.515 |
LIG_SUMO_SIM_anti_2 | 593 | 600 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 504 | 511 | PF11976 | 0.549 |
LIG_TRAF2_1 | 11 | 14 | PF00917 | 0.600 |
LIG_TRAF2_1 | 653 | 656 | PF00917 | 0.364 |
LIG_TRAF2_1 | 730 | 733 | PF00917 | 0.474 |
LIG_TRAF2_1 | 844 | 847 | PF00917 | 0.617 |
LIG_TYR_ITIM | 737 | 742 | PF00017 | 0.371 |
MOD_CDK_SPK_2 | 580 | 585 | PF00069 | 0.508 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.751 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.642 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.636 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.726 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.457 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.601 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.712 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.706 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.724 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.670 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.691 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.268 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.597 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.641 |
MOD_CK1_1 | 827 | 833 | PF00069 | 0.502 |
MOD_CK1_1 | 839 | 845 | PF00069 | 0.652 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.596 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.328 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.530 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.696 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.560 |
MOD_CK2_1 | 527 | 533 | PF00069 | 0.755 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.577 |
MOD_CK2_1 | 737 | 743 | PF00069 | 0.419 |
MOD_CK2_1 | 841 | 847 | PF00069 | 0.548 |
MOD_DYRK1A_RPxSP_1 | 284 | 288 | PF00069 | 0.472 |
MOD_DYRK1A_RPxSP_1 | 580 | 584 | PF00069 | 0.401 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.707 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.711 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.644 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.442 |
MOD_GlcNHglycan | 325 | 329 | PF01048 | 0.438 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.624 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.652 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.537 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.646 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.642 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.419 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.731 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.184 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.691 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.727 |
MOD_GlcNHglycan | 746 | 749 | PF01048 | 0.542 |
MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.477 |
MOD_GlcNHglycan | 787 | 790 | PF01048 | 0.683 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.594 |
MOD_GlcNHglycan | 834 | 837 | PF01048 | 0.585 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.786 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.595 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.489 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.700 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.522 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.600 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.471 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.733 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.668 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.524 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.668 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.433 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.639 |
MOD_GSK3_1 | 733 | 740 | PF00069 | 0.442 |
MOD_GSK3_1 | 785 | 792 | PF00069 | 0.657 |
MOD_GSK3_1 | 826 | 833 | PF00069 | 0.650 |
MOD_GSK3_1 | 837 | 844 | PF00069 | 0.555 |
MOD_GSK3_1 | 847 | 854 | PF00069 | 0.420 |
MOD_N-GLC_1 | 594 | 599 | PF02516 | 0.264 |
MOD_N-GLC_1 | 702 | 707 | PF02516 | 0.264 |
MOD_N-GLC_2 | 44 | 46 | PF02516 | 0.453 |
MOD_N-GLC_2 | 709 | 711 | PF02516 | 0.264 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.672 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.460 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.524 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.514 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.742 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.579 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.525 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.599 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.294 |
MOD_NEK2_1 | 754 | 759 | PF00069 | 0.376 |
MOD_NEK2_1 | 825 | 830 | PF00069 | 0.715 |
MOD_NEK2_2 | 435 | 440 | PF00069 | 0.482 |
MOD_NEK2_2 | 810 | 815 | PF00069 | 0.439 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.437 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.793 |
MOD_PIKK_1 | 683 | 689 | PF00454 | 0.326 |
MOD_PKA_1 | 224 | 230 | PF00069 | 0.642 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.596 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.613 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.566 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.481 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.725 |
MOD_PKA_2 | 603 | 609 | PF00069 | 0.298 |
MOD_PKA_2 | 765 | 771 | PF00069 | 0.475 |
MOD_PKA_2 | 783 | 789 | PF00069 | 0.610 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.471 |
MOD_Plk_1 | 594 | 600 | PF00069 | 0.280 |
MOD_Plk_1 | 697 | 703 | PF00069 | 0.264 |
MOD_Plk_1 | 810 | 816 | PF00069 | 0.613 |
MOD_Plk_2-3 | 490 | 496 | PF00069 | 0.461 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.385 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.375 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.785 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.681 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.288 |
MOD_Plk_4 | 697 | 703 | PF00069 | 0.269 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.505 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.459 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.533 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.638 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.668 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.510 |
MOD_ProDKin_1 | 795 | 801 | PF00069 | 0.571 |
MOD_ProDKin_1 | 837 | 843 | PF00069 | 0.496 |
TRG_DiLeu_BaEn_1 | 384 | 389 | PF01217 | 0.332 |
TRG_DiLeu_BaEn_1 | 803 | 808 | PF01217 | 0.596 |
TRG_DiLeu_BaEn_3 | 176 | 182 | PF01217 | 0.393 |
TRG_DiLeu_BaLyEn_6 | 802 | 807 | PF01217 | 0.605 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.651 |
TRG_ENDOCYTIC_2 | 586 | 589 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 611 | 614 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 739 | 742 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 758 | 761 | PF00928 | 0.357 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 257 | 260 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 263 | 266 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 516 | 518 | PF00400 | 0.744 |
TRG_ER_diArg_1 | 579 | 582 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 750 | 752 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 857 | 860 | PF00400 | 0.498 |
TRG_NLS_MonoExtC_3 | 220 | 225 | PF00514 | 0.578 |
TRG_NLS_MonoExtC_3 | 76 | 81 | PF00514 | 0.531 |
TRG_NLS_MonoExtN_4 | 74 | 81 | PF00514 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 381 | 386 | PF00026 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 517 | 522 | PF00026 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEZ6 | Leptomonas seymouri | 49% | 100% |
A0A1X0NYH3 | Trypanosomatidae | 33% | 100% |
A0A3R7KV16 | Trypanosoma rangeli | 30% | 100% |
A0A3S7WXM7 | Leishmania donovani | 85% | 100% |
A4I0D0 | Leishmania infantum | 85% | 100% |
C9ZV40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
Q4QB84 | Leishmania major | 82% | 98% |
V5ARQ1 | Trypanosoma cruzi | 30% | 100% |