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. | yes | 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: A0A3S7X0W6
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 | 0.510 |
CLV_C14_Caspase3-7 | 425 | 429 | PF00656 | 0.642 |
CLV_C14_Caspase3-7 | 435 | 439 | PF00656 | 0.649 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.667 |
CLV_C14_Caspase3-7 | 511 | 515 | PF00656 | 0.781 |
CLV_C14_Caspase3-7 | 570 | 574 | PF00656 | 0.758 |
CLV_C14_Caspase3-7 | 684 | 688 | PF00656 | 0.688 |
CLV_C14_Caspase3-7 | 728 | 732 | PF00656 | 0.513 |
CLV_C14_Caspase3-7 | 791 | 795 | PF00656 | 0.344 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 657 | 659 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 703 | 705 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 724 | 726 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 735 | 737 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 789 | 791 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 836 | 838 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 846 | 848 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 854 | 856 | PF00675 | 0.185 |
CLV_NRD_NRD_1 | 857 | 859 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 886 | 888 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 915 | 917 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 923 | 925 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.301 |
CLV_PCSK_FUR_1 | 703 | 707 | PF00082 | 0.621 |
CLV_PCSK_FUR_1 | 855 | 859 | PF00082 | 0.344 |
CLV_PCSK_FUR_1 | 913 | 917 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 634 | 636 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 657 | 659 | PF00082 | 0.763 |
CLV_PCSK_KEX2_1 | 703 | 705 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 740 | 742 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 789 | 791 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 835 | 837 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 856 | 858 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 901 | 903 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 915 | 917 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 922 | 924 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 363 | 365 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 586 | 588 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 634 | 636 | PF00082 | 0.575 |
CLV_PCSK_PC1ET2_1 | 657 | 659 | PF00082 | 0.763 |
CLV_PCSK_PC1ET2_1 | 705 | 707 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 740 | 742 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 856 | 858 | PF00082 | 0.328 |
CLV_PCSK_PC1ET2_1 | 901 | 903 | PF00082 | 0.392 |
CLV_PCSK_PC1ET2_1 | 922 | 924 | PF00082 | 0.592 |
CLV_PCSK_PC7_1 | 699 | 705 | PF00082 | 0.636 |
CLV_PCSK_PC7_1 | 736 | 742 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 790 | 794 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 799 | 803 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 821 | 825 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.301 |
DOC_CYCLIN_RxL_1 | 170 | 180 | PF00134 | 0.495 |
DOC_CYCLIN_RxL_1 | 378 | 385 | PF00134 | 0.328 |
DOC_MAPK_gen_1 | 290 | 299 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 323 | 331 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 45 | 52 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 605 | 613 | PF00069 | 0.578 |
DOC_MAPK_gen_1 | 818 | 826 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 878 | 886 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 45 | 52 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 818 | 826 | PF00069 | 0.328 |
DOC_PIKK_1 | 451 | 458 | PF02985 | 0.717 |
DOC_PP1_RVXF_1 | 311 | 318 | PF00149 | 0.328 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.530 |
DOC_PP4_FxxP_1 | 160 | 163 | PF00568 | 0.562 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.444 |
DOC_PP4_FxxP_1 | 211 | 214 | PF00568 | 0.422 |
DOC_PP4_FxxP_1 | 370 | 373 | PF00568 | 0.449 |
DOC_PP4_FxxP_1 | 621 | 624 | PF00568 | 0.605 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 843 | 847 | PF00917 | 0.449 |
DOC_USP7_UBL2_3 | 267 | 271 | PF12436 | 0.434 |
DOC_USP7_UBL2_3 | 284 | 288 | PF12436 | 0.187 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.333 |
DOC_USP7_UBL2_3 | 388 | 392 | PF12436 | 0.328 |
DOC_USP7_UBL2_3 | 395 | 399 | PF12436 | 0.328 |
DOC_USP7_UBL2_3 | 4 | 8 | PF12436 | 0.581 |
DOC_USP7_UBL2_3 | 585 | 589 | PF12436 | 0.680 |
DOC_USP7_UBL2_3 | 733 | 737 | PF12436 | 0.362 |
DOC_USP7_UBL2_3 | 896 | 900 | PF12436 | 0.371 |
DOC_USP7_UBL2_3 | 918 | 922 | PF12436 | 0.593 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.703 |
LIG_14-3-3_CanoR_1 | 26 | 34 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 557 | 561 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 635 | 640 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 643 | 649 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 725 | 730 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 773 | 778 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 862 | 868 | PF00244 | 0.364 |
LIG_BIR_III_4 | 332 | 336 | PF00653 | 0.483 |
LIG_BRCT_BRCA1_1 | 161 | 165 | PF00533 | 0.476 |
LIG_eIF4E_1 | 905 | 911 | PF01652 | 0.475 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.262 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.563 |
LIG_FHA_1 | 774 | 780 | PF00498 | 0.328 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.475 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.384 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.641 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.656 |
LIG_FHA_2 | 479 | 485 | PF00498 | 0.727 |
LIG_FHA_2 | 557 | 563 | PF00498 | 0.704 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.643 |
LIG_FHA_2 | 661 | 667 | PF00498 | 0.734 |
LIG_FHA_2 | 714 | 720 | PF00498 | 0.568 |
LIG_FHA_2 | 726 | 732 | PF00498 | 0.542 |
LIG_FHA_2 | 756 | 762 | PF00498 | 0.344 |
LIG_FHA_2 | 766 | 772 | PF00498 | 0.344 |
LIG_FHA_2 | 825 | 831 | PF00498 | 0.328 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.524 |
LIG_FXI_DFP_1 | 367 | 371 | PF00024 | 0.449 |
LIG_LIR_Apic_2 | 157 | 163 | PF02991 | 0.562 |
LIG_LIR_Apic_2 | 208 | 214 | PF02991 | 0.536 |
LIG_LIR_Apic_2 | 369 | 373 | PF02991 | 0.449 |
LIG_LIR_Apic_2 | 479 | 485 | PF02991 | 0.652 |
LIG_LIR_Apic_2 | 619 | 624 | PF02991 | 0.599 |
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 | 537 | 546 | PF02991 | 0.728 |
LIG_LIR_Gen_1 | 757 | 767 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.449 |
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 | 0.421 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 544 | 549 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 757 | 763 | PF02991 | 0.328 |
LIG_MAD2 | 72 | 80 | PF02301 | 0.487 |
LIG_PCNA_yPIPBox_3 | 605 | 617 | PF02747 | 0.722 |
LIG_PCNA_yPIPBox_3 | 855 | 868 | PF02747 | 0.328 |
LIG_PCNA_yPIPBox_3 | 876 | 890 | PF02747 | 0.363 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.581 |
LIG_PTB_Apo_2 | 615 | 622 | PF02174 | 0.593 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.528 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.432 |
LIG_SH2_SRC | 549 | 552 | PF00017 | 0.591 |
LIG_SH2_SRC | 568 | 571 | PF00017 | 0.659 |
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 | 549 | 552 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 800 | 803 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 905 | 908 | PF00017 | 0.449 |
LIG_SH3_2 | 80 | 85 | PF14604 | 0.487 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.642 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.487 |
LIG_SH3_3 | 819 | 825 | PF00018 | 0.328 |
LIG_TRAF2_1 | 638 | 641 | PF00917 | 0.634 |
LIG_TRAF2_1 | 716 | 719 | PF00917 | 0.570 |
LIG_TRAF2_1 | 827 | 830 | PF00917 | 0.363 |
LIG_UBA3_1 | 33 | 39 | PF00899 | 0.501 |
LIG_UBA3_1 | 383 | 390 | PF00899 | 0.328 |
LIG_UBA3_1 | 708 | 714 | PF00899 | 0.664 |
LIG_UBA3_1 | 863 | 872 | PF00899 | 0.328 |
LIG_UBA3_1 | 910 | 918 | PF00899 | 0.475 |
LIG_WRC_WIRS_1 | 254 | 259 | PF05994 | 0.413 |
LIG_WRC_WIRS_1 | 87 | 92 | PF05994 | 0.501 |
MOD_CDK_SPxxK_3 | 577 | 584 | PF00069 | 0.693 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.328 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.752 |
MOD_CK1_1 | 674 | 680 | PF00069 | 0.659 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.468 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.332 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.343 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.395 |
MOD_CK2_1 | 478 | 484 | PF00069 | 0.756 |
MOD_CK2_1 | 515 | 521 | PF00069 | 0.817 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.683 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.663 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.643 |
MOD_CK2_1 | 660 | 666 | PF00069 | 0.771 |
MOD_CK2_1 | 674 | 680 | PF00069 | 0.736 |
MOD_CK2_1 | 713 | 719 | PF00069 | 0.559 |
MOD_CK2_1 | 755 | 761 | PF00069 | 0.337 |
MOD_CK2_1 | 824 | 830 | PF00069 | 0.344 |
MOD_Cter_Amidation | 361 | 364 | PF01082 | 0.359 |
MOD_Cter_Amidation | 853 | 856 | PF01082 | 0.376 |
MOD_Cter_Amidation | 898 | 901 | PF01082 | 0.387 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.339 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.272 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.559 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.287 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.801 |
MOD_GlcNHglycan | 680 | 684 | PF01048 | 0.740 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.381 |
MOD_GlcNHglycan | 752 | 755 | PF01048 | 0.315 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.474 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.390 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.570 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.689 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.678 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.659 |
MOD_GSK3_1 | 745 | 752 | PF00069 | 0.398 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.470 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.398 |
MOD_N-GLC_1 | 417 | 422 | PF02516 | 0.628 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.596 |
MOD_N-GLC_1 | 743 | 748 | PF02516 | 0.379 |
MOD_N-GLC_1 | 750 | 755 | PF02516 | 0.425 |
MOD_N-GLC_1 | 882 | 887 | PF02516 | 0.345 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.519 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.487 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.305 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.489 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.722 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.580 |
MOD_NEK2_1 | 793 | 798 | PF00069 | 0.328 |
MOD_NEK2_1 | 863 | 868 | PF00069 | 0.364 |
MOD_NEK2_1 | 889 | 894 | PF00069 | 0.344 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.434 |
MOD_PIKK_1 | 714 | 720 | PF00454 | 0.570 |
MOD_PIKK_1 | 889 | 895 | PF00454 | 0.363 |
MOD_PKA_1 | 725 | 731 | PF00069 | 0.529 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.377 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.698 |
MOD_PKA_2 | 843 | 849 | PF00069 | 0.449 |
MOD_PKB_1 | 697 | 705 | PF00069 | 0.745 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.530 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.769 |
MOD_Plk_1 | 617 | 623 | PF00069 | 0.588 |
MOD_Plk_1 | 674 | 680 | PF00069 | 0.714 |
MOD_Plk_1 | 793 | 799 | PF00069 | 0.328 |
MOD_Plk_1 | 882 | 888 | PF00069 | 0.363 |
MOD_Plk_2-3 | 422 | 428 | PF00069 | 0.638 |
MOD_Plk_2-3 | 459 | 465 | PF00069 | 0.614 |
MOD_Plk_2-3 | 671 | 677 | PF00069 | 0.697 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.487 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.482 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.702 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.487 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.562 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.449 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.695 |
MOD_SUMO_for_1 | 107 | 110 | PF00179 | 0.487 |
MOD_SUMO_for_1 | 588 | 591 | PF00179 | 0.708 |
MOD_SUMO_for_1 | 813 | 816 | 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 | 464 | 469 | PF01217 | 0.668 |
TRG_DiLeu_BaEn_3 | 640 | 646 | PF01217 | 0.673 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.432 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 311 | 313 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 661 | 664 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 703 | 706 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 772 | 775 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 835 | 837 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 855 | 858 | PF00400 | 0.145 |
TRG_ER_diArg_1 | 875 | 878 | PF00400 | 0.145 |
TRG_ER_diArg_1 | 913 | 916 | PF00400 | 0.546 |
TRG_ER_diLys_1 | 920 | 925 | PF00400 | 0.678 |
TRG_NES_CRM1_1 | 491 | 505 | PF08389 | 0.720 |
TRG_NLS_Bipartite_1 | 725 | 744 | PF00514 | 0.385 |
TRG_NLS_Bipartite_1 | 887 | 905 | PF00514 | 0.360 |
TRG_NLS_MonoCore_2 | 386 | 391 | PF00514 | 0.449 |
TRG_NLS_MonoCore_2 | 583 | 588 | PF00514 | 0.737 |
TRG_NLS_MonoCore_2 | 703 | 708 | PF00514 | 0.710 |
TRG_NLS_MonoCore_2 | 854 | 859 | PF00514 | 0.328 |
TRG_NLS_MonoExtC_3 | 387 | 392 | PF00514 | 0.358 |
TRG_NLS_MonoExtC_3 | 394 | 399 | PF00514 | 0.296 |
TRG_NLS_MonoExtC_3 | 5 | 10 | PF00514 | 0.570 |
TRG_NLS_MonoExtC_3 | 584 | 589 | PF00514 | 0.680 |
TRG_NLS_MonoExtC_3 | 632 | 637 | PF00514 | 0.571 |
TRG_NLS_MonoExtC_3 | 854 | 859 | PF00514 | 0.328 |
TRG_NLS_MonoExtC_3 | 899 | 904 | PF00514 | 0.347 |
TRG_NLS_MonoExtN_4 | 387 | 392 | PF00514 | 0.348 |
TRG_NLS_MonoExtN_4 | 395 | 400 | PF00514 | 0.302 |
TRG_NLS_MonoExtN_4 | 4 | 11 | PF00514 | 0.573 |
TRG_NLS_MonoExtN_4 | 581 | 588 | PF00514 | 0.722 |
TRG_NLS_MonoExtN_4 | 631 | 638 | PF00514 | 0.567 |
TRG_NLS_MonoExtN_4 | 703 | 709 | PF00514 | 0.620 |
TRG_NLS_MonoExtN_4 | 737 | 744 | PF00514 | 0.400 |
TRG_NLS_MonoExtN_4 | 855 | 860 | PF00514 | 0.328 |
TRG_NLS_MonoExtN_4 | 900 | 905 | 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 | 381 | 385 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 404 | 408 | PF00026 | 0.332 |
TRG_Pf-PMV_PEXEL_1 | 47 | 51 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 637 | 641 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 706 | 711 | PF00026 | 0.759 |
TRG_Pf-PMV_PEXEL_1 | 790 | 794 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 865 | 869 | PF00026 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5J0 | Leptomonas seymouri | 82% | 97% |
A0A0S4IND8 | Bodo saltans | 60% | 99% |
A0A1X0NSL6 | Trypanosomatidae | 64% | 99% |
A0A3R7KBR5 | Trypanosoma rangeli | 64% | 100% |
A4HFX5 | Leishmania braziliensis | 91% | 100% |
A4I305 | Leishmania infantum | 100% | 100% |
C9ZJF7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9ADH8 | Leishmania major | 96% | 100% |
E9AZA2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
V5BE24 | Trypanosoma cruzi | 60% | 100% |