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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 10 |
GO:0030684 | preribosome | 3 | 2 |
GO:0030687 | preribosome, large subunit precursor | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
GO:0005634 | nucleus | 5 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: E9ADH8
Term | Name | Level | Count |
---|---|---|---|
GO:0000154 | rRNA modification | 6 | 10 |
GO:0000451 | rRNA 2'-O-methylation | 6 | 10 |
GO:0000453 | obsolete enzyme-directed rRNA 2'-O-methylation | 7 | 10 |
GO:0000460 | maturation of 5.8S rRNA | 9 | 2 |
GO:0000463 | maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 2 |
GO:0000466 | maturation of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 2 |
GO:0000470 | maturation of LSU-rRNA | 9 | 2 |
GO:0001510 | RNA methylation | 4 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006364 | rRNA processing | 8 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 10 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016072 | rRNA metabolic process | 7 | 12 |
GO:0031167 | rRNA methylation | 5 | 10 |
GO:0032259 | methylation | 2 | 11 |
GO:0034470 | ncRNA processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0043414 | macromolecule methylation | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0051301 | cell division | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008171 | O-methyltransferase activity | 5 | 2 |
GO:0008173 | RNA methyltransferase activity | 4 | 11 |
GO:0008649 | rRNA methyltransferase activity | 5 | 10 |
GO:0008650 | rRNA (uridine-2'-O-)-methyltransferase activity | 6 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 10 |
GO:0016435 | rRNA (guanine) methyltransferase activity | 6 | 2 |
GO:0016436 | rRNA (uridine) methyltransferase activity | 6 | 2 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0062105 | RNA 2'-O-methyltransferase activity | 5 | 2 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140102 | catalytic activity, acting on a rRNA | 4 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 11 | 15 | PF00656 | 0.512 |
CLV_C14_Caspase3-7 | 424 | 428 | PF00656 | 0.649 |
CLV_C14_Caspase3-7 | 434 | 438 | PF00656 | 0.650 |
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.671 |
CLV_C14_Caspase3-7 | 510 | 514 | PF00656 | 0.779 |
CLV_C14_Caspase3-7 | 569 | 573 | PF00656 | 0.758 |
CLV_C14_Caspase3-7 | 589 | 593 | PF00656 | 0.620 |
CLV_C14_Caspase3-7 | 665 | 669 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 683 | 687 | PF00656 | 0.687 |
CLV_C14_Caspase3-7 | 790 | 794 | PF00656 | 0.344 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 656 | 658 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 702 | 704 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 723 | 725 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 734 | 736 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 788 | 790 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 835 | 837 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 845 | 847 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 853 | 855 | PF00675 | 0.185 |
CLV_NRD_NRD_1 | 856 | 858 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 885 | 887 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 914 | 916 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 922 | 924 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.301 |
CLV_PCSK_FUR_1 | 702 | 706 | PF00082 | 0.636 |
CLV_PCSK_FUR_1 | 854 | 858 | PF00082 | 0.344 |
CLV_PCSK_FUR_1 | 912 | 916 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 656 | 658 | PF00082 | 0.773 |
CLV_PCSK_KEX2_1 | 702 | 704 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 739 | 741 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 788 | 790 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 834 | 836 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 855 | 857 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 900 | 902 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 914 | 916 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 921 | 923 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 585 | 587 | PF00082 | 0.643 |
CLV_PCSK_PC1ET2_1 | 656 | 658 | PF00082 | 0.773 |
CLV_PCSK_PC1ET2_1 | 704 | 706 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 739 | 741 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 855 | 857 | PF00082 | 0.328 |
CLV_PCSK_PC1ET2_1 | 900 | 902 | PF00082 | 0.392 |
CLV_PCSK_PC1ET2_1 | 921 | 923 | PF00082 | 0.597 |
CLV_PCSK_PC7_1 | 698 | 704 | PF00082 | 0.644 |
CLV_PCSK_PC7_1 | 735 | 741 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 789 | 793 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 798 | 802 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 820 | 824 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.296 |
DOC_CKS1_1 | 233 | 238 | PF01111 | 0.549 |
DOC_CYCLIN_RxL_1 | 170 | 180 | PF00134 | 0.495 |
DOC_CYCLIN_RxL_1 | 377 | 384 | PF00134 | 0.328 |
DOC_MAPK_gen_1 | 290 | 299 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 323 | 331 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 45 | 52 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 604 | 612 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 817 | 825 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 877 | 885 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 45 | 52 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 817 | 825 | PF00069 | 0.328 |
DOC_PIKK_1 | 450 | 457 | PF02985 | 0.720 |
DOC_PP1_RVXF_1 | 311 | 318 | PF00149 | 0.328 |
DOC_PP4_FxxP_1 | 160 | 163 | PF00568 | 0.562 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.424 |
DOC_PP4_FxxP_1 | 211 | 214 | PF00568 | 0.409 |
DOC_PP4_FxxP_1 | 369 | 372 | PF00568 | 0.449 |
DOC_PP4_FxxP_1 | 620 | 623 | PF00568 | 0.598 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 842 | 846 | PF00917 | 0.449 |
DOC_USP7_UBL2_3 | 267 | 271 | PF12436 | 0.427 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.333 |
DOC_USP7_UBL2_3 | 387 | 391 | PF12436 | 0.328 |
DOC_USP7_UBL2_3 | 394 | 398 | PF12436 | 0.328 |
DOC_USP7_UBL2_3 | 4 | 8 | PF12436 | 0.584 |
DOC_USP7_UBL2_3 | 584 | 588 | PF12436 | 0.697 |
DOC_USP7_UBL2_3 | 732 | 736 | PF12436 | 0.362 |
DOC_USP7_UBL2_3 | 895 | 899 | PF12436 | 0.371 |
DOC_USP7_UBL2_3 | 917 | 921 | PF12436 | 0.597 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.722 |
LIG_14-3-3_CanoR_1 | 26 | 34 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 556 | 560 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 642 | 648 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 724 | 729 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 772 | 777 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 861 | 867 | PF00244 | 0.364 |
LIG_BIR_III_4 | 332 | 336 | PF00653 | 0.483 |
LIG_BIR_III_4 | 522 | 526 | PF00653 | 0.717 |
LIG_BRCT_BRCA1_1 | 161 | 165 | PF00533 | 0.476 |
LIG_eIF4E_1 | 904 | 910 | PF01652 | 0.475 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.558 |
LIG_FHA_1 | 714 | 720 | PF00498 | 0.573 |
LIG_FHA_1 | 773 | 779 | PF00498 | 0.328 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.475 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.381 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.423 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.649 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.656 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.715 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.661 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.623 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.651 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.739 |
LIG_FHA_2 | 713 | 719 | PF00498 | 0.577 |
LIG_FHA_2 | 725 | 731 | PF00498 | 0.551 |
LIG_FHA_2 | 755 | 761 | PF00498 | 0.344 |
LIG_FHA_2 | 765 | 771 | PF00498 | 0.344 |
LIG_FHA_2 | 824 | 830 | PF00498 | 0.328 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.528 |
LIG_FXI_DFP_1 | 366 | 370 | PF00024 | 0.449 |
LIG_LIR_Apic_2 | 157 | 163 | PF02991 | 0.562 |
LIG_LIR_Apic_2 | 208 | 214 | PF02991 | 0.522 |
LIG_LIR_Apic_2 | 368 | 372 | PF02991 | 0.449 |
LIG_LIR_Apic_2 | 478 | 484 | PF02991 | 0.640 |
LIG_LIR_Apic_2 | 618 | 623 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 162 | 172 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 242 | 250 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 256 | 263 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 536 | 545 | PF02991 | 0.733 |
LIG_LIR_Gen_1 | 756 | 766 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 242 | 247 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 256 | 260 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 536 | 542 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 543 | 548 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 756 | 762 | PF02991 | 0.328 |
LIG_MAD2 | 72 | 80 | PF02301 | 0.487 |
LIG_PCNA_yPIPBox_3 | 604 | 616 | PF02747 | 0.701 |
LIG_PCNA_yPIPBox_3 | 854 | 867 | PF02747 | 0.328 |
LIG_PCNA_yPIPBox_3 | 875 | 889 | PF02747 | 0.363 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.581 |
LIG_PTB_Apo_2 | 614 | 621 | PF02174 | 0.577 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.513 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.456 |
LIG_SH2_SRC | 548 | 551 | PF00017 | 0.611 |
LIG_SH2_SRC | 567 | 570 | PF00017 | 0.656 |
LIG_SH2_STAP1 | 244 | 248 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 799 | 802 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 904 | 907 | PF00017 | 0.449 |
LIG_SH3_2 | 80 | 85 | PF14604 | 0.487 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.635 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.487 |
LIG_SH3_3 | 818 | 824 | PF00018 | 0.328 |
LIG_TRAF2_1 | 637 | 640 | PF00917 | 0.646 |
LIG_TRAF2_1 | 715 | 718 | PF00917 | 0.579 |
LIG_TRAF2_1 | 826 | 829 | PF00917 | 0.363 |
LIG_UBA3_1 | 33 | 39 | PF00899 | 0.501 |
LIG_UBA3_1 | 382 | 389 | PF00899 | 0.328 |
LIG_UBA3_1 | 707 | 713 | PF00899 | 0.665 |
LIG_UBA3_1 | 862 | 871 | PF00899 | 0.328 |
LIG_UBA3_1 | 909 | 917 | PF00899 | 0.475 |
LIG_WRC_WIRS_1 | 254 | 259 | PF05994 | 0.413 |
LIG_WRC_WIRS_1 | 87 | 92 | PF05994 | 0.501 |
MOD_CDK_SPK_2 | 232 | 237 | PF00069 | 0.623 |
MOD_CDK_SPxxK_3 | 576 | 583 | PF00069 | 0.713 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.328 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.752 |
MOD_CK1_1 | 673 | 679 | PF00069 | 0.663 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.476 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.412 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.332 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.223 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.746 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.815 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.642 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.648 |
MOD_CK2_1 | 634 | 640 | PF00069 | 0.650 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.776 |
MOD_CK2_1 | 673 | 679 | PF00069 | 0.741 |
MOD_CK2_1 | 712 | 718 | PF00069 | 0.568 |
MOD_CK2_1 | 754 | 760 | PF00069 | 0.337 |
MOD_CK2_1 | 823 | 829 | PF00069 | 0.344 |
MOD_Cter_Amidation | 360 | 363 | PF01082 | 0.359 |
MOD_Cter_Amidation | 852 | 855 | PF01082 | 0.376 |
MOD_Cter_Amidation | 897 | 900 | PF01082 | 0.387 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.339 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.276 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.573 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.287 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.585 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.727 |
MOD_GlcNHglycan | 679 | 683 | PF01048 | 0.740 |
MOD_GlcNHglycan | 746 | 749 | PF01048 | 0.381 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.315 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.476 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.390 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.242 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.667 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.659 |
MOD_GSK3_1 | 744 | 751 | PF00069 | 0.398 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.470 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.398 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.645 |
MOD_N-GLC_1 | 616 | 621 | PF02516 | 0.584 |
MOD_N-GLC_1 | 749 | 754 | PF02516 | 0.425 |
MOD_N-GLC_1 | 881 | 886 | PF02516 | 0.345 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.532 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.501 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.305 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.501 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.712 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.683 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.568 |
MOD_NEK2_1 | 792 | 797 | PF00069 | 0.328 |
MOD_NEK2_1 | 862 | 867 | PF00069 | 0.364 |
MOD_NEK2_1 | 888 | 893 | PF00069 | 0.344 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.434 |
MOD_PIKK_1 | 527 | 533 | PF00454 | 0.561 |
MOD_PIKK_1 | 713 | 719 | PF00454 | 0.578 |
MOD_PIKK_1 | 888 | 894 | PF00454 | 0.363 |
MOD_PKA_1 | 724 | 730 | PF00069 | 0.542 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.377 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.670 |
MOD_PKA_2 | 748 | 754 | PF00069 | 0.242 |
MOD_PKA_2 | 842 | 848 | PF00069 | 0.449 |
MOD_PKB_1 | 696 | 704 | PF00069 | 0.751 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.759 |
MOD_Plk_1 | 616 | 622 | PF00069 | 0.578 |
MOD_Plk_1 | 673 | 679 | PF00069 | 0.718 |
MOD_Plk_1 | 792 | 798 | PF00069 | 0.328 |
MOD_Plk_1 | 881 | 887 | PF00069 | 0.363 |
MOD_Plk_2-3 | 421 | 427 | PF00069 | 0.648 |
MOD_Plk_2-3 | 458 | 464 | PF00069 | 0.614 |
MOD_Plk_2-3 | 670 | 676 | PF00069 | 0.705 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.501 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.494 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.511 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.661 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.487 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.562 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.550 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.449 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.714 |
MOD_SUMO_for_1 | 107 | 110 | PF00179 | 0.482 |
MOD_SUMO_for_1 | 587 | 590 | PF00179 | 0.716 |
MOD_SUMO_for_1 | 812 | 815 | PF00179 | 0.328 |
MOD_SUMO_rev_2 | 259 | 269 | PF00179 | 0.344 |
MOD_SUMO_rev_2 | 93 | 99 | PF00179 | 0.487 |
TRG_DiLeu_BaEn_1 | 463 | 468 | PF01217 | 0.677 |
TRG_DiLeu_BaEn_3 | 639 | 645 | PF01217 | 0.676 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 311 | 313 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 660 | 663 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 702 | 705 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 771 | 774 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 834 | 836 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 854 | 857 | PF00400 | 0.145 |
TRG_ER_diArg_1 | 874 | 877 | PF00400 | 0.145 |
TRG_ER_diArg_1 | 912 | 915 | PF00400 | 0.544 |
TRG_ER_diLys_1 | 919 | 924 | PF00400 | 0.679 |
TRG_NES_CRM1_1 | 490 | 504 | PF08389 | 0.716 |
TRG_NLS_Bipartite_1 | 724 | 743 | PF00514 | 0.622 |
TRG_NLS_Bipartite_1 | 886 | 904 | PF00514 | 0.360 |
TRG_NLS_MonoCore_2 | 385 | 390 | PF00514 | 0.449 |
TRG_NLS_MonoCore_2 | 582 | 587 | PF00514 | 0.756 |
TRG_NLS_MonoCore_2 | 702 | 707 | PF00514 | 0.722 |
TRG_NLS_MonoCore_2 | 853 | 858 | PF00514 | 0.328 |
TRG_NLS_MonoExtC_3 | 386 | 391 | PF00514 | 0.368 |
TRG_NLS_MonoExtC_3 | 393 | 398 | PF00514 | 0.283 |
TRG_NLS_MonoExtC_3 | 5 | 10 | PF00514 | 0.575 |
TRG_NLS_MonoExtC_3 | 583 | 588 | PF00514 | 0.698 |
TRG_NLS_MonoExtC_3 | 853 | 858 | PF00514 | 0.328 |
TRG_NLS_MonoExtC_3 | 898 | 903 | PF00514 | 0.347 |
TRG_NLS_MonoExtN_4 | 386 | 391 | PF00514 | 0.358 |
TRG_NLS_MonoExtN_4 | 394 | 399 | PF00514 | 0.288 |
TRG_NLS_MonoExtN_4 | 4 | 11 | PF00514 | 0.578 |
TRG_NLS_MonoExtN_4 | 580 | 587 | PF00514 | 0.741 |
TRG_NLS_MonoExtN_4 | 702 | 708 | PF00514 | 0.631 |
TRG_NLS_MonoExtN_4 | 736 | 743 | PF00514 | 0.400 |
TRG_NLS_MonoExtN_4 | 854 | 859 | PF00514 | 0.328 |
TRG_NLS_MonoExtN_4 | 899 | 904 | PF00514 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 173 | 177 | PF00026 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 380 | 384 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 403 | 407 | PF00026 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 47 | 51 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 636 | 640 | PF00026 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 705 | 710 | PF00026 | 0.761 |
TRG_Pf-PMV_PEXEL_1 | 789 | 793 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 864 | 868 | PF00026 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5J0 | Leptomonas seymouri | 81% | 97% |
A0A0S4IND8 | Bodo saltans | 60% | 99% |
A0A1X0NSL6 | Trypanosomatidae | 64% | 99% |
A0A3R7KBR5 | Trypanosoma rangeli | 65% | 100% |
A0A3S7X0W6 | Leishmania donovani | 96% | 100% |
A4HFX5 | Leishmania braziliensis | 90% | 100% |
A4I305 | Leishmania infantum | 96% | 100% |
C9ZJF7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
E9AZA2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
V5BE24 | Trypanosoma cruzi | 61% | 100% |