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: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:0030684 | preribosome | 3 | 1 |
GO:0030687 | preribosome, large subunit precursor | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
GO:0005634 | nucleus | 5 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: A4HFX5
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: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 |
GO:0000460 | maturation of 5.8S rRNA | 9 | 1 |
GO:0000463 | maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000466 | maturation of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000470 | maturation of LSU-rRNA | 9 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008173 | RNA methyltransferase activity | 4 | 11 |
GO:0008649 | rRNA methyltransferase activity | 5 | 10 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 10 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
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 |
GO:0008171 | O-methyltransferase activity | 5 | 1 |
GO:0008650 | rRNA (uridine-2'-O-)-methyltransferase activity | 6 | 1 |
GO:0016435 | rRNA (guanine) methyltransferase activity | 6 | 1 |
GO:0016436 | rRNA (uridine) methyltransferase activity | 6 | 1 |
GO:0062105 | RNA 2'-O-methyltransferase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 11 | 15 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.407 |
CLV_C14_Caspase3-7 | 349 | 353 | PF00656 | 0.318 |
CLV_C14_Caspase3-7 | 428 | 432 | PF00656 | 0.659 |
CLV_C14_Caspase3-7 | 438 | 442 | PF00656 | 0.651 |
CLV_C14_Caspase3-7 | 516 | 520 | PF00656 | 0.784 |
CLV_C14_Caspase3-7 | 573 | 577 | PF00656 | 0.769 |
CLV_C14_Caspase3-7 | 674 | 678 | PF00656 | 0.780 |
CLV_C14_Caspase3-7 | 686 | 690 | PF00656 | 0.697 |
CLV_C14_Caspase3-7 | 793 | 797 | PF00656 | 0.344 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 705 | 707 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 726 | 728 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 737 | 739 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 791 | 793 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 838 | 840 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 848 | 850 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 856 | 858 | PF00675 | 0.185 |
CLV_NRD_NRD_1 | 859 | 861 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 888 | 890 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 917 | 919 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 925 | 927 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.301 |
CLV_PCSK_FUR_1 | 705 | 709 | PF00082 | 0.643 |
CLV_PCSK_FUR_1 | 857 | 861 | PF00082 | 0.344 |
CLV_PCSK_FUR_1 | 915 | 919 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 660 | 662 | PF00082 | 0.771 |
CLV_PCSK_KEX2_1 | 705 | 707 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 742 | 744 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 791 | 793 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 837 | 839 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 858 | 860 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 917 | 919 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 924 | 926 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 366 | 368 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 589 | 591 | PF00082 | 0.627 |
CLV_PCSK_PC1ET2_1 | 637 | 639 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 660 | 662 | PF00082 | 0.771 |
CLV_PCSK_PC1ET2_1 | 707 | 709 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 742 | 744 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 858 | 860 | PF00082 | 0.328 |
CLV_PCSK_PC1ET2_1 | 924 | 926 | PF00082 | 0.595 |
CLV_PCSK_PC7_1 | 701 | 707 | PF00082 | 0.648 |
CLV_PCSK_PC7_1 | 738 | 744 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.276 |
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 | 0.358 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 728 | 732 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 792 | 796 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 801 | 805 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 823 | 827 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.301 |
CLV_Separin_Metazoa | 721 | 725 | PF03568 | 0.463 |
DEG_APCC_KENBOX_2 | 514 | 518 | PF00400 | 0.553 |
DOC_CKS1_1 | 233 | 238 | PF01111 | 0.537 |
DOC_CYCLIN_RxL_1 | 170 | 180 | PF00134 | 0.495 |
DOC_CYCLIN_RxL_1 | 381 | 388 | PF00134 | 0.328 |
DOC_MAPK_gen_1 | 290 | 299 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 45 | 52 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 608 | 616 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 820 | 828 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 880 | 888 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 45 | 52 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 820 | 828 | PF00069 | 0.328 |
DOC_PP1_RVXF_1 | 311 | 318 | PF00149 | 0.328 |
DOC_PP4_FxxP_1 | 160 | 163 | PF00568 | 0.556 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.439 |
DOC_PP4_FxxP_1 | 211 | 214 | PF00568 | 0.415 |
DOC_PP4_FxxP_1 | 373 | 376 | PF00568 | 0.449 |
DOC_PP4_FxxP_1 | 624 | 627 | PF00568 | 0.615 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 603 | 607 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 845 | 849 | PF00917 | 0.449 |
DOC_USP7_UBL2_3 | 267 | 271 | PF12436 | 0.427 |
DOC_USP7_UBL2_3 | 284 | 288 | PF12436 | 0.204 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.333 |
DOC_USP7_UBL2_3 | 391 | 395 | PF12436 | 0.328 |
DOC_USP7_UBL2_3 | 398 | 402 | PF12436 | 0.328 |
DOC_USP7_UBL2_3 | 4 | 8 | PF12436 | 0.585 |
DOC_USP7_UBL2_3 | 588 | 592 | PF12436 | 0.678 |
DOC_USP7_UBL2_3 | 735 | 739 | PF12436 | 0.362 |
DOC_USP7_UBL2_3 | 898 | 902 | PF12436 | 0.371 |
DOC_USP7_UBL2_3 | 920 | 924 | PF12436 | 0.599 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.712 |
LIG_14-3-3_CanoR_1 | 253 | 258 | PF00244 | 0.223 |
LIG_14-3-3_CanoR_1 | 26 | 34 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 560 | 564 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 646 | 652 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 775 | 780 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.487 |
LIG_APCC_ABBA_1 | 270 | 275 | PF00400 | 0.455 |
LIG_BIR_III_4 | 332 | 336 | PF00653 | 0.483 |
LIG_BRCT_BRCA1_1 | 151 | 155 | PF00533 | 0.470 |
LIG_BRCT_BRCA1_1 | 161 | 165 | PF00533 | 0.480 |
LIG_eIF4E_1 | 907 | 913 | PF01652 | 0.475 |
LIG_FHA_1 | 717 | 723 | PF00498 | 0.585 |
LIG_FHA_1 | 776 | 782 | PF00498 | 0.328 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.423 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.347 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.660 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.661 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.714 |
LIG_FHA_2 | 560 | 566 | PF00498 | 0.720 |
LIG_FHA_2 | 664 | 670 | PF00498 | 0.735 |
LIG_FHA_2 | 716 | 722 | PF00498 | 0.591 |
LIG_FHA_2 | 758 | 764 | PF00498 | 0.344 |
LIG_FHA_2 | 768 | 774 | PF00498 | 0.344 |
LIG_FHA_2 | 827 | 833 | PF00498 | 0.328 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.528 |
LIG_FXI_DFP_1 | 370 | 374 | PF00024 | 0.449 |
LIG_LIR_Apic_2 | 157 | 163 | PF02991 | 0.562 |
LIG_LIR_Apic_2 | 208 | 214 | PF02991 | 0.529 |
LIG_LIR_Apic_2 | 372 | 376 | PF02991 | 0.449 |
LIG_LIR_Apic_2 | 482 | 488 | PF02991 | 0.632 |
LIG_LIR_Apic_2 | 622 | 627 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 162 | 172 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 256 | 263 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 540 | 549 | PF02991 | 0.727 |
LIG_LIR_Gen_1 | 759 | 769 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 256 | 260 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 368 | 373 | PF02991 | 0.223 |
LIG_LIR_Nem_3 | 540 | 546 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 547 | 552 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 759 | 765 | PF02991 | 0.328 |
LIG_MAD2 | 72 | 80 | PF02301 | 0.487 |
LIG_OCRL_FandH_1 | 268 | 280 | PF00620 | 0.223 |
LIG_PCNA_yPIPBox_3 | 608 | 620 | PF02747 | 0.726 |
LIG_PCNA_yPIPBox_3 | 857 | 870 | PF02747 | 0.328 |
LIG_PCNA_yPIPBox_3 | 878 | 892 | PF02747 | 0.363 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.581 |
LIG_PTB_Apo_2 | 618 | 625 | PF02174 | 0.600 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.513 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.456 |
LIG_SH2_SRC | 552 | 555 | PF00017 | 0.615 |
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 | 370 | 373 | PF00017 | 0.223 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 802 | 805 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 907 | 910 | PF00017 | 0.449 |
LIG_SH3_2 | 80 | 85 | PF14604 | 0.487 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.618 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.485 |
LIG_SH3_3 | 821 | 827 | PF00018 | 0.328 |
LIG_TRAF2_1 | 718 | 721 | PF00917 | 0.593 |
LIG_TRAF2_1 | 829 | 832 | PF00917 | 0.363 |
LIG_UBA3_1 | 33 | 39 | PF00899 | 0.501 |
LIG_UBA3_1 | 386 | 393 | PF00899 | 0.328 |
LIG_UBA3_1 | 865 | 874 | PF00899 | 0.328 |
LIG_UBA3_1 | 912 | 920 | 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 | 0.610 |
MOD_CDK_SPxxK_3 | 580 | 587 | PF00069 | 0.700 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.328 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.662 |
MOD_CK1_1 | 650 | 656 | PF00069 | 0.754 |
MOD_CK1_1 | 676 | 682 | PF00069 | 0.656 |
MOD_CK1_1 | 884 | 890 | PF00069 | 0.347 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.466 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.223 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.755 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.815 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.696 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.774 |
MOD_CK2_1 | 676 | 682 | PF00069 | 0.734 |
MOD_CK2_1 | 715 | 721 | PF00069 | 0.584 |
MOD_CK2_1 | 752 | 758 | PF00069 | 0.372 |
MOD_CK2_1 | 826 | 832 | PF00069 | 0.344 |
MOD_Cter_Amidation | 855 | 858 | PF01082 | 0.376 |
MOD_Cter_Amidation | 900 | 903 | PF01082 | 0.387 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.338 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.233 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.276 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.555 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.281 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.599 |
MOD_GlcNHglycan | 649 | 652 | PF01048 | 0.724 |
MOD_GlcNHglycan | 677 | 681 | PF01048 | 0.753 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.381 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.315 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.466 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.703 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.668 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.647 |
MOD_N-GLC_1 | 620 | 625 | PF02516 | 0.606 |
MOD_N-GLC_1 | 745 | 750 | PF02516 | 0.379 |
MOD_N-GLC_1 | 884 | 889 | PF02516 | 0.345 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.531 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.501 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.501 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.714 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.590 |
MOD_NEK2_1 | 795 | 800 | PF00069 | 0.328 |
MOD_NEK2_1 | 891 | 896 | PF00069 | 0.344 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.427 |
MOD_PIKK_1 | 716 | 722 | PF00454 | 0.592 |
MOD_PIKK_1 | 891 | 897 | PF00454 | 0.363 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.377 |
MOD_PKA_2 | 556 | 562 | PF00069 | 0.709 |
MOD_PKA_2 | 645 | 651 | PF00069 | 0.637 |
MOD_PKA_2 | 845 | 851 | PF00069 | 0.449 |
MOD_PKB_1 | 661 | 669 | PF00069 | 0.529 |
MOD_PKB_1 | 699 | 707 | PF00069 | 0.756 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.753 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.598 |
MOD_Plk_1 | 795 | 801 | PF00069 | 0.328 |
MOD_Plk_1 | 884 | 890 | PF00069 | 0.363 |
MOD_Plk_2-3 | 425 | 431 | PF00069 | 0.657 |
MOD_Plk_2-3 | 462 | 468 | PF00069 | 0.630 |
MOD_Plk_2-3 | 685 | 691 | PF00069 | 0.574 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.487 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.492 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.386 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.715 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.487 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.562 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.535 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.449 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.704 |
MOD_SUMO_for_1 | 107 | 110 | PF00179 | 0.487 |
MOD_SUMO_for_1 | 591 | 594 | PF00179 | 0.692 |
MOD_SUMO_for_1 | 815 | 818 | PF00179 | 0.328 |
MOD_SUMO_rev_2 | 220 | 227 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 259 | 269 | PF00179 | 0.344 |
MOD_SUMO_rev_2 | 453 | 458 | PF00179 | 0.553 |
MOD_SUMO_rev_2 | 93 | 99 | PF00179 | 0.487 |
TRG_DiLeu_BaEn_1 | 467 | 472 | PF01217 | 0.686 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.223 |
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 | 638 | 641 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 661 | 664 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 665 | 668 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 705 | 708 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 774 | 777 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 837 | 839 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 857 | 860 | PF00400 | 0.145 |
TRG_ER_diArg_1 | 877 | 880 | PF00400 | 0.145 |
TRG_ER_diArg_1 | 915 | 918 | PF00400 | 0.335 |
TRG_ER_diLys_1 | 922 | 927 | PF00400 | 0.679 |
TRG_NES_CRM1_1 | 494 | 508 | PF08389 | 0.702 |
TRG_NLS_Bipartite_1 | 727 | 746 | PF00514 | 0.385 |
TRG_NLS_Bipartite_1 | 889 | 907 | PF00514 | 0.360 |
TRG_NLS_MonoCore_2 | 389 | 394 | PF00514 | 0.449 |
TRG_NLS_MonoCore_2 | 586 | 591 | PF00514 | 0.738 |
TRG_NLS_MonoCore_2 | 705 | 710 | PF00514 | 0.729 |
TRG_NLS_MonoCore_2 | 856 | 861 | PF00514 | 0.328 |
TRG_NLS_MonoExtC_3 | 390 | 395 | PF00514 | 0.358 |
TRG_NLS_MonoExtC_3 | 397 | 402 | PF00514 | 0.296 |
TRG_NLS_MonoExtC_3 | 5 | 10 | PF00514 | 0.572 |
TRG_NLS_MonoExtC_3 | 587 | 592 | PF00514 | 0.677 |
TRG_NLS_MonoExtC_3 | 635 | 640 | PF00514 | 0.560 |
TRG_NLS_MonoExtC_3 | 660 | 665 | PF00514 | 0.563 |
TRG_NLS_MonoExtC_3 | 856 | 861 | PF00514 | 0.328 |
TRG_NLS_MonoExtC_3 | 901 | 906 | PF00514 | 0.347 |
TRG_NLS_MonoExtN_4 | 390 | 395 | PF00514 | 0.348 |
TRG_NLS_MonoExtN_4 | 398 | 403 | PF00514 | 0.302 |
TRG_NLS_MonoExtN_4 | 4 | 11 | PF00514 | 0.577 |
TRG_NLS_MonoExtN_4 | 584 | 591 | PF00514 | 0.724 |
TRG_NLS_MonoExtN_4 | 634 | 641 | PF00514 | 0.564 |
TRG_NLS_MonoExtN_4 | 658 | 665 | PF00514 | 0.606 |
TRG_NLS_MonoExtN_4 | 705 | 711 | PF00514 | 0.640 |
TRG_NLS_MonoExtN_4 | 739 | 746 | PF00514 | 0.400 |
TRG_NLS_MonoExtN_4 | 857 | 862 | PF00514 | 0.328 |
TRG_NLS_MonoExtN_4 | 902 | 907 | PF00514 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.289 |
TRG_Pf-PMV_PEXEL_1 | 384 | 388 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 407 | 411 | PF00026 | 0.333 |
TRG_Pf-PMV_PEXEL_1 | 47 | 51 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 534 | 538 | PF00026 | 0.680 |
TRG_Pf-PMV_PEXEL_1 | 640 | 644 | PF00026 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 708 | 713 | PF00026 | 0.780 |
TRG_Pf-PMV_PEXEL_1 | 792 | 796 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 867 | 871 | 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 | 64% | 100% |
A0A3S7X0W6 | Leishmania donovani | 91% | 100% |
A4I305 | Leishmania infantum | 91% | 100% |
C9ZJF7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
E9ADH8 | Leishmania major | 90% | 100% |
E9AZA2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BE24 | Trypanosoma cruzi | 60% | 100% |