| 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: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005654 | nucleoplasm | 2 | 1 |
| GO:0005681 | spliceosomal complex | 3 | 1 |
| GO:0032991 | protein-containing complex | 1 | 1 |
| GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
| GO:0140513 | nuclear protein-containing complex | 2 | 1 |
| GO:1902494 | catalytic complex | 2 | 1 |
| GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HPE9
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000390 | spliceosomal complex disassembly | 7 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0016043 | cellular component organization | 3 | 1 |
| GO:0022411 | cellular component disassembly | 4 | 1 |
| GO:0032984 | protein-containing complex disassembly | 5 | 1 |
| GO:0032988 | ribonucleoprotein complex disassembly | 6 | 1 |
| GO:0043933 | protein-containing complex organization | 4 | 1 |
| GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 12 |
| GO:0003676 | nucleic acid binding | 3 | 12 |
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0004386 | helicase activity | 2 | 12 |
| GO:0005488 | binding | 1 | 12 |
| GO:0005524 | ATP binding | 5 | 12 |
| GO:0016787 | hydrolase activity | 2 | 11 |
| GO:0017076 | purine nucleotide binding | 4 | 12 |
| GO:0030554 | adenyl nucleotide binding | 5 | 12 |
| GO:0032553 | ribonucleotide binding | 3 | 12 |
| GO:0032555 | purine ribonucleotide binding | 4 | 12 |
| GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
| GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
| GO:0036094 | small molecule binding | 2 | 12 |
| GO:0043167 | ion binding | 2 | 12 |
| GO:0043168 | anion binding | 3 | 12 |
| GO:0097159 | organic cyclic compound binding | 2 | 12 |
| GO:0097367 | carbohydrate derivative binding | 2 | 12 |
| GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
| GO:0140657 | ATP-dependent activity | 1 | 12 |
| GO:1901265 | nucleoside phosphate binding | 3 | 12 |
| GO:1901363 | heterocyclic compound binding | 2 | 12 |
| GO:0003723 | RNA binding | 4 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 46 | 50 | PF00656 | 0.498 |
| CLV_C14_Caspase3-7 | 77 | 81 | PF00656 | 0.696 |
| CLV_C14_Caspase3-7 | 882 | 886 | PF00656 | 0.410 |
| CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.313 |
| CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.560 |
| CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.592 |
| CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.510 |
| CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.503 |
| CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.635 |
| CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.210 |
| CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.280 |
| CLV_NRD_NRD_1 | 652 | 654 | PF00675 | 0.331 |
| CLV_NRD_NRD_1 | 687 | 689 | PF00675 | 0.210 |
| CLV_NRD_NRD_1 | 888 | 890 | PF00675 | 0.312 |
| CLV_NRD_NRD_1 | 944 | 946 | PF00675 | 0.517 |
| CLV_NRD_NRD_1 | 960 | 962 | PF00675 | 0.212 |
| CLV_NRD_NRD_1 | 974 | 976 | PF00675 | 0.302 |
| CLV_NRD_NRD_1 | 989 | 991 | PF00675 | 0.165 |
| CLV_PCSK_KEX2_1 | 1017 | 1019 | PF00082 | 0.312 |
| CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.496 |
| CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.592 |
| CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.551 |
| CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.227 |
| CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.264 |
| CLV_PCSK_KEX2_1 | 870 | 872 | PF00082 | 0.221 |
| CLV_PCSK_KEX2_1 | 888 | 890 | PF00082 | 0.210 |
| CLV_PCSK_KEX2_1 | 944 | 946 | PF00082 | 0.446 |
| CLV_PCSK_KEX2_1 | 974 | 976 | PF00082 | 0.277 |
| CLV_PCSK_KEX2_1 | 989 | 991 | PF00082 | 0.210 |
| CLV_PCSK_PC1ET2_1 | 1017 | 1019 | PF00082 | 0.312 |
| CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.595 |
| CLV_PCSK_PC1ET2_1 | 870 | 872 | PF00082 | 0.221 |
| CLV_PCSK_SKI1_1 | 1006 | 1010 | PF00082 | 0.221 |
| CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.501 |
| CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.604 |
| CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.477 |
| CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.215 |
| CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.201 |
| CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.163 |
| CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.221 |
| CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.458 |
| CLV_PCSK_SKI1_1 | 689 | 693 | PF00082 | 0.210 |
| CLV_PCSK_SKI1_1 | 761 | 765 | PF00082 | 0.405 |
| CLV_PCSK_SKI1_1 | 845 | 849 | PF00082 | 0.210 |
| CLV_PCSK_SKI1_1 | 871 | 875 | PF00082 | 0.210 |
| CLV_PCSK_SKI1_1 | 939 | 943 | PF00082 | 0.488 |
| CLV_PCSK_SKI1_1 | 962 | 966 | PF00082 | 0.211 |
| CLV_Separin_Metazoa | 649 | 653 | PF03568 | 0.512 |
| DEG_APCC_DBOX_1 | 608 | 616 | PF00400 | 0.451 |
| DEG_APCC_DBOX_1 | 776 | 784 | PF00400 | 0.329 |
| DEG_APCC_DBOX_1 | 934 | 942 | PF00400 | 0.357 |
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.716 |
| DEG_SCF_FBW7_1 | 826 | 832 | PF00400 | 0.512 |
| DOC_CKS1_1 | 655 | 660 | PF01111 | 0.512 |
| DOC_CKS1_1 | 826 | 831 | PF01111 | 0.421 |
| DOC_CYCLIN_RxL_1 | 842 | 852 | PF00134 | 0.410 |
| DOC_MAPK_gen_1 | 184 | 190 | PF00069 | 0.538 |
| DOC_MAPK_gen_1 | 421 | 428 | PF00069 | 0.441 |
| DOC_PP4_FxxP_1 | 400 | 403 | PF00568 | 0.665 |
| DOC_PP4_FxxP_1 | 874 | 877 | PF00568 | 0.410 |
| DOC_PP4_FxxP_1 | 891 | 894 | PF00568 | 0.318 |
| DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.493 |
| DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.582 |
| DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.596 |
| DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.575 |
| DOC_USP7_MATH_1 | 697 | 701 | PF00917 | 0.410 |
| DOC_USP7_MATH_1 | 807 | 811 | PF00917 | 0.443 |
| DOC_USP7_MATH_1 | 829 | 833 | PF00917 | 0.461 |
| DOC_USP7_MATH_1 | 841 | 845 | PF00917 | 0.378 |
| DOC_USP7_MATH_2 | 672 | 678 | PF00917 | 0.435 |
| DOC_USP7_UBL2_3 | 185 | 189 | PF12436 | 0.679 |
| DOC_WW_Pin1_4 | 1055 | 1060 | PF00397 | 0.585 |
| DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.641 |
| DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.488 |
| DOC_WW_Pin1_4 | 654 | 659 | PF00397 | 0.512 |
| DOC_WW_Pin1_4 | 680 | 685 | PF00397 | 0.410 |
| DOC_WW_Pin1_4 | 825 | 830 | PF00397 | 0.421 |
| LIG_14-3-3_CanoR_1 | 413 | 417 | PF00244 | 0.370 |
| LIG_14-3-3_CanoR_1 | 529 | 533 | PF00244 | 0.410 |
| LIG_14-3-3_CanoR_1 | 541 | 551 | PF00244 | 0.410 |
| LIG_14-3-3_CanoR_1 | 652 | 658 | PF00244 | 0.466 |
| LIG_14-3-3_CanoR_1 | 756 | 763 | PF00244 | 0.354 |
| LIG_14-3-3_CanoR_1 | 777 | 781 | PF00244 | 0.458 |
| LIG_14-3-3_CanoR_1 | 961 | 970 | PF00244 | 0.410 |
| LIG_14-3-3_CanoR_1 | 981 | 987 | PF00244 | 0.440 |
| LIG_Actin_WH2_2 | 505 | 521 | PF00022 | 0.410 |
| LIG_APCC_ABBAyCdc20_2 | 1006 | 1012 | PF00400 | 0.410 |
| LIG_BRCT_BRCA1_1 | 582 | 586 | PF00533 | 0.478 |
| LIG_BRCT_BRCA1_1 | 676 | 680 | PF00533 | 0.421 |
| LIG_Clathr_ClatBox_1 | 1024 | 1028 | PF01394 | 0.435 |
| LIG_Clathr_ClatBox_1 | 794 | 798 | PF01394 | 0.342 |
| LIG_deltaCOP1_diTrp_1 | 915 | 922 | PF00928 | 0.346 |
| LIG_EH1_1 | 431 | 439 | PF00400 | 0.262 |
| LIG_FHA_1 | 1020 | 1026 | PF00498 | 0.512 |
| LIG_FHA_1 | 1056 | 1062 | PF00498 | 0.577 |
| LIG_FHA_1 | 286 | 292 | PF00498 | 0.426 |
| LIG_FHA_1 | 433 | 439 | PF00498 | 0.431 |
| LIG_FHA_1 | 444 | 450 | PF00498 | 0.421 |
| LIG_FHA_1 | 501 | 507 | PF00498 | 0.413 |
| LIG_FHA_1 | 543 | 549 | PF00498 | 0.410 |
| LIG_FHA_1 | 590 | 596 | PF00498 | 0.380 |
| LIG_FHA_1 | 603 | 609 | PF00498 | 0.344 |
| LIG_FHA_1 | 763 | 769 | PF00498 | 0.439 |
| LIG_FHA_1 | 782 | 788 | PF00498 | 0.435 |
| LIG_FHA_2 | 1 | 7 | PF00498 | 0.455 |
| LIG_FHA_2 | 1014 | 1020 | PF00498 | 0.410 |
| LIG_FHA_2 | 316 | 322 | PF00498 | 0.430 |
| LIG_FHA_2 | 368 | 374 | PF00498 | 0.585 |
| LIG_FHA_2 | 406 | 412 | PF00498 | 0.501 |
| LIG_FHA_2 | 42 | 48 | PF00498 | 0.597 |
| LIG_FHA_2 | 630 | 636 | PF00498 | 0.410 |
| LIG_FHA_2 | 769 | 775 | PF00498 | 0.357 |
| LIG_FHA_2 | 847 | 853 | PF00498 | 0.410 |
| LIG_FHA_2 | 953 | 959 | PF00498 | 0.591 |
| LIG_FHA_2 | 983 | 989 | PF00498 | 0.415 |
| LIG_HCF-1_HBM_1 | 455 | 458 | PF13415 | 0.421 |
| LIG_LIR_Apic_2 | 991 | 996 | PF02991 | 0.421 |
| LIG_LIR_Gen_1 | 29 | 39 | PF02991 | 0.488 |
| LIG_LIR_Gen_1 | 546 | 556 | PF02991 | 0.421 |
| LIG_LIR_Gen_1 | 980 | 988 | PF02991 | 0.415 |
| LIG_LIR_Nem_3 | 1055 | 1060 | PF02991 | 0.585 |
| LIG_LIR_Nem_3 | 29 | 35 | PF02991 | 0.390 |
| LIG_LIR_Nem_3 | 496 | 502 | PF02991 | 0.421 |
| LIG_LIR_Nem_3 | 524 | 530 | PF02991 | 0.432 |
| LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.410 |
| LIG_LIR_Nem_3 | 573 | 579 | PF02991 | 0.332 |
| LIG_LIR_Nem_3 | 704 | 710 | PF02991 | 0.426 |
| LIG_LIR_Nem_3 | 980 | 986 | PF02991 | 0.415 |
| LIG_NRP_CendR_1 | 1077 | 1080 | PF00754 | 0.553 |
| LIG_PCNA_PIPBox_1 | 115 | 124 | PF02747 | 0.443 |
| LIG_Pex14_2 | 576 | 580 | PF04695 | 0.310 |
| LIG_PTB_Apo_2 | 239 | 246 | PF02174 | 0.586 |
| LIG_PTB_Apo_2 | 702 | 709 | PF02174 | 0.410 |
| LIG_PTB_Phospho_1 | 702 | 708 | PF10480 | 0.435 |
| LIG_Rb_LxCxE_1 | 56 | 77 | PF01857 | 0.503 |
| LIG_Rb_LxCxE_1 | 849 | 864 | PF01857 | 0.512 |
| LIG_SH2_CRK | 1040 | 1044 | PF00017 | 0.381 |
| LIG_SH2_CRK | 122 | 126 | PF00017 | 0.475 |
| LIG_SH2_CRK | 255 | 259 | PF00017 | 0.497 |
| LIG_SH2_CRK | 530 | 534 | PF00017 | 0.410 |
| LIG_SH2_PTP2 | 983 | 986 | PF00017 | 0.435 |
| LIG_SH2_PTP2 | 993 | 996 | PF00017 | 0.383 |
| LIG_SH2_SRC | 817 | 820 | PF00017 | 0.410 |
| LIG_SH2_SRC | 993 | 996 | PF00017 | 0.421 |
| LIG_SH2_STAP1 | 495 | 499 | PF00017 | 0.410 |
| LIG_SH2_STAP1 | 530 | 534 | PF00017 | 0.410 |
| LIG_SH2_STAP1 | 905 | 909 | PF00017 | 0.328 |
| LIG_SH2_STAT3 | 161 | 164 | PF00017 | 0.581 |
| LIG_SH2_STAT3 | 357 | 360 | PF00017 | 0.572 |
| LIG_SH2_STAT5 | 1007 | 1010 | PF00017 | 0.418 |
| LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.424 |
| LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.428 |
| LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.417 |
| LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.513 |
| LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.321 |
| LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.221 |
| LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.300 |
| LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.473 |
| LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.419 |
| LIG_SH2_STAT5 | 758 | 761 | PF00017 | 0.340 |
| LIG_SH2_STAT5 | 817 | 820 | PF00017 | 0.410 |
| LIG_SH2_STAT5 | 968 | 971 | PF00017 | 0.444 |
| LIG_SH2_STAT5 | 983 | 986 | PF00017 | 0.401 |
| LIG_SH2_STAT5 | 993 | 996 | PF00017 | 0.426 |
| LIG_SH3_3 | 108 | 114 | PF00018 | 0.638 |
| LIG_SH3_3 | 652 | 658 | PF00018 | 0.480 |
| LIG_SH3_5 | 603 | 607 | PF00018 | 0.353 |
| LIG_SUMO_SIM_anti_2 | 531 | 537 | PF11976 | 0.423 |
| LIG_SUMO_SIM_anti_2 | 661 | 666 | PF11976 | 0.477 |
| LIG_SUMO_SIM_anti_2 | 897 | 903 | PF11976 | 0.410 |
| LIG_SUMO_SIM_par_1 | 1022 | 1028 | PF11976 | 0.423 |
| LIG_SUMO_SIM_par_1 | 434 | 441 | PF11976 | 0.438 |
| LIG_SUMO_SIM_par_1 | 531 | 537 | PF11976 | 0.410 |
| LIG_SUMO_SIM_par_1 | 856 | 864 | PF11976 | 0.431 |
| LIG_TRAF2_1 | 107 | 110 | PF00917 | 0.715 |
| LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.608 |
| LIG_TRAF2_1 | 191 | 194 | PF00917 | 0.626 |
| LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.410 |
| LIG_TRAF2_1 | 408 | 411 | PF00917 | 0.553 |
| LIG_TRAF2_1 | 43 | 46 | PF00917 | 0.628 |
| LIG_TRAF2_1 | 632 | 635 | PF00917 | 0.410 |
| LIG_TYR_ITIM | 1008 | 1013 | PF00017 | 0.262 |
| LIG_UBA3_1 | 1024 | 1030 | PF00899 | 0.445 |
| LIG_WW_1 | 1004 | 1007 | PF00397 | 0.281 |
| MOD_CDK_SPxxK_3 | 1055 | 1062 | PF00069 | 0.576 |
| MOD_CDK_SPxxK_3 | 266 | 273 | PF00069 | 0.484 |
| MOD_CK1_1 | 1063 | 1069 | PF00069 | 0.433 |
| MOD_CK1_1 | 176 | 182 | PF00069 | 0.571 |
| MOD_CK1_1 | 443 | 449 | PF00069 | 0.278 |
| MOD_CK1_1 | 504 | 510 | PF00069 | 0.247 |
| MOD_CK1_1 | 542 | 548 | PF00069 | 0.247 |
| MOD_CK1_1 | 982 | 988 | PF00069 | 0.390 |
| MOD_CK2_1 | 1013 | 1019 | PF00069 | 0.260 |
| MOD_CK2_1 | 149 | 155 | PF00069 | 0.606 |
| MOD_CK2_1 | 177 | 183 | PF00069 | 0.674 |
| MOD_CK2_1 | 188 | 194 | PF00069 | 0.637 |
| MOD_CK2_1 | 315 | 321 | PF00069 | 0.587 |
| MOD_CK2_1 | 340 | 346 | PF00069 | 0.453 |
| MOD_CK2_1 | 367 | 373 | PF00069 | 0.604 |
| MOD_CK2_1 | 405 | 411 | PF00069 | 0.509 |
| MOD_CK2_1 | 41 | 47 | PF00069 | 0.580 |
| MOD_CK2_1 | 61 | 67 | PF00069 | 0.260 |
| MOD_CK2_1 | 629 | 635 | PF00069 | 0.247 |
| MOD_CK2_1 | 807 | 813 | PF00069 | 0.447 |
| MOD_Cter_Amidation | 394 | 397 | PF01082 | 0.624 |
| MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.534 |
| MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.596 |
| MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.524 |
| MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.247 |
| MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.247 |
| MOD_GlcNHglycan | 711 | 714 | PF01048 | 0.277 |
| MOD_GlcNHglycan | 742 | 745 | PF01048 | 0.341 |
| MOD_GlcNHglycan | 809 | 812 | PF01048 | 0.380 |
| MOD_GSK3_1 | 1066 | 1073 | PF00069 | 0.434 |
| MOD_GSK3_1 | 167 | 174 | PF00069 | 0.724 |
| MOD_GSK3_1 | 286 | 293 | PF00069 | 0.622 |
| MOD_GSK3_1 | 315 | 322 | PF00069 | 0.497 |
| MOD_GSK3_1 | 351 | 358 | PF00069 | 0.711 |
| MOD_GSK3_1 | 359 | 366 | PF00069 | 0.672 |
| MOD_GSK3_1 | 41 | 48 | PF00069 | 0.596 |
| MOD_GSK3_1 | 440 | 447 | PF00069 | 0.294 |
| MOD_GSK3_1 | 500 | 507 | PF00069 | 0.252 |
| MOD_GSK3_1 | 594 | 601 | PF00069 | 0.495 |
| MOD_GSK3_1 | 607 | 614 | PF00069 | 0.348 |
| MOD_GSK3_1 | 697 | 704 | PF00069 | 0.245 |
| MOD_GSK3_1 | 825 | 832 | PF00069 | 0.322 |
| MOD_GSK3_1 | 835 | 842 | PF00069 | 0.216 |
| MOD_GSK3_1 | 911 | 918 | PF00069 | 0.494 |
| MOD_GSK3_1 | 975 | 982 | PF00069 | 0.390 |
| MOD_LATS_1 | 539 | 545 | PF00433 | 0.323 |
| MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.580 |
| MOD_N-GLC_1 | 952 | 957 | PF02516 | 0.499 |
| MOD_NEK2_1 | 1013 | 1018 | PF00069 | 0.296 |
| MOD_NEK2_1 | 177 | 182 | PF00069 | 0.676 |
| MOD_NEK2_1 | 243 | 248 | PF00069 | 0.584 |
| MOD_NEK2_1 | 340 | 345 | PF00069 | 0.440 |
| MOD_NEK2_1 | 390 | 395 | PF00069 | 0.469 |
| MOD_NEK2_1 | 523 | 528 | PF00069 | 0.273 |
| MOD_NEK2_1 | 565 | 570 | PF00069 | 0.390 |
| MOD_NEK2_1 | 667 | 672 | PF00069 | 0.266 |
| MOD_NEK2_1 | 776 | 781 | PF00069 | 0.481 |
| MOD_NEK2_2 | 329 | 334 | PF00069 | 0.442 |
| MOD_PIKK_1 | 258 | 264 | PF00454 | 0.617 |
| MOD_PIKK_1 | 315 | 321 | PF00454 | 0.695 |
| MOD_PIKK_1 | 356 | 362 | PF00454 | 0.497 |
| MOD_PIKK_1 | 41 | 47 | PF00454 | 0.614 |
| MOD_PIKK_1 | 444 | 450 | PF00454 | 0.247 |
| MOD_PIKK_1 | 464 | 470 | PF00454 | 0.118 |
| MOD_PIKK_1 | 732 | 738 | PF00454 | 0.247 |
| MOD_PIKK_1 | 839 | 845 | PF00454 | 0.262 |
| MOD_PKA_2 | 1013 | 1019 | PF00069 | 0.390 |
| MOD_PKA_2 | 1046 | 1052 | PF00069 | 0.566 |
| MOD_PKA_2 | 1070 | 1076 | PF00069 | 0.448 |
| MOD_PKA_2 | 412 | 418 | PF00069 | 0.348 |
| MOD_PKA_2 | 528 | 534 | PF00069 | 0.247 |
| MOD_PKA_2 | 776 | 782 | PF00069 | 0.464 |
| MOD_PKA_2 | 931 | 937 | PF00069 | 0.345 |
| MOD_PKA_2 | 960 | 966 | PF00069 | 0.323 |
| MOD_PKB_1 | 498 | 506 | PF00069 | 0.262 |
| MOD_Plk_1 | 14 | 20 | PF00069 | 0.454 |
| MOD_Plk_1 | 154 | 160 | PF00069 | 0.516 |
| MOD_Plk_1 | 335 | 341 | PF00069 | 0.606 |
| MOD_Plk_1 | 523 | 529 | PF00069 | 0.247 |
| MOD_Plk_1 | 539 | 545 | PF00069 | 0.247 |
| MOD_Plk_1 | 697 | 703 | PF00069 | 0.247 |
| MOD_Plk_2-3 | 127 | 133 | PF00069 | 0.332 |
| MOD_Plk_2-3 | 335 | 341 | PF00069 | 0.606 |
| MOD_Plk_2-3 | 367 | 373 | PF00069 | 0.644 |
| MOD_Plk_4 | 139 | 145 | PF00069 | 0.614 |
| MOD_Plk_4 | 14 | 20 | PF00069 | 0.536 |
| MOD_Plk_4 | 244 | 250 | PF00069 | 0.609 |
| MOD_Plk_4 | 359 | 365 | PF00069 | 0.624 |
| MOD_Plk_4 | 432 | 438 | PF00069 | 0.271 |
| MOD_Plk_4 | 528 | 534 | PF00069 | 0.247 |
| MOD_Plk_4 | 594 | 600 | PF00069 | 0.467 |
| MOD_Plk_4 | 611 | 617 | PF00069 | 0.247 |
| MOD_Plk_4 | 776 | 782 | PF00069 | 0.464 |
| MOD_Plk_4 | 843 | 849 | PF00069 | 0.247 |
| MOD_Plk_4 | 858 | 864 | PF00069 | 0.247 |
| MOD_Plk_4 | 897 | 903 | PF00069 | 0.343 |
| MOD_Plk_4 | 995 | 1001 | PF00069 | 0.390 |
| MOD_ProDKin_1 | 1055 | 1061 | PF00069 | 0.580 |
| MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.637 |
| MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.487 |
| MOD_ProDKin_1 | 654 | 660 | PF00069 | 0.390 |
| MOD_ProDKin_1 | 680 | 686 | PF00069 | 0.247 |
| MOD_ProDKin_1 | 825 | 831 | PF00069 | 0.262 |
| MOD_SUMO_for_1 | 420 | 423 | PF00179 | 0.432 |
| MOD_SUMO_rev_2 | 1023 | 1032 | PF00179 | 0.390 |
| MOD_SUMO_rev_2 | 142 | 152 | PF00179 | 0.597 |
| MOD_SUMO_rev_2 | 180 | 187 | PF00179 | 0.627 |
| TRG_DiLeu_BaEn_1 | 1028 | 1033 | PF01217 | 0.262 |
| TRG_DiLeu_BaEn_2 | 234 | 240 | PF01217 | 0.518 |
| TRG_DiLeu_BaEn_4 | 154 | 160 | PF01217 | 0.625 |
| TRG_DiLeu_BaEn_4 | 193 | 199 | PF01217 | 0.476 |
| TRG_DiLeu_BaEn_4 | 235 | 241 | PF01217 | 0.476 |
| TRG_ENDOCYTIC_2 | 1010 | 1013 | PF00928 | 0.249 |
| TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.432 |
| TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.394 |
| TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.247 |
| TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.281 |
| TRG_ENDOCYTIC_2 | 983 | 986 | PF00928 | 0.247 |
| TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.562 |
| TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.517 |
| TRG_ER_diArg_1 | 469 | 471 | PF00400 | 0.247 |
| TRG_ER_diArg_1 | 651 | 653 | PF00400 | 0.323 |
| TRG_ER_diArg_1 | 875 | 878 | PF00400 | 0.247 |
| TRG_ER_diArg_1 | 974 | 976 | PF00400 | 0.307 |
| TRG_ER_diLys_1 | 1076 | 1080 | PF00400 | 0.595 |
| TRG_NES_CRM1_1 | 119 | 135 | PF08389 | 0.313 |
| TRG_NES_CRM1_1 | 774 | 786 | PF08389 | 0.453 |
| TRG_NLS_MonoCore_2 | 395 | 400 | PF00514 | 0.611 |
| TRG_NLS_MonoExtC_3 | 1075 | 1080 | PF00514 | 0.588 |
| TRG_NLS_MonoExtN_4 | 1074 | 1080 | PF00514 | 0.583 |
| TRG_Pf-PMV_PEXEL_1 | 1030 | 1034 | PF00026 | 0.341 |
| TRG_Pf-PMV_PEXEL_1 | 350 | 355 | PF00026 | 0.695 |
| TRG_Pf-PMV_PEXEL_1 | 926 | 930 | PF00026 | 0.343 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P8Y1 | Leptomonas seymouri | 34% | 100% |
| A0A0N1I0Z0 | Leptomonas seymouri | 83% | 99% |
| A0A0N1PEU4 | Leptomonas seymouri | 35% | 100% |
| A0A0S4JCY8 | Bodo saltans | 55% | 100% |
| A0A1X0NKY7 | Trypanosomatidae | 60% | 100% |
| A0A3Q8II71 | Leishmania donovani | 34% | 100% |
| A0A3Q8IJ24 | Leishmania donovani | 35% | 100% |
| A0A3S7XB01 | Leishmania donovani | 95% | 99% |
| A0A422MXB1 | Trypanosoma rangeli | 61% | 100% |
| A4HAT8 | Leishmania braziliensis | 34% | 100% |
| A4HNU7 | Leishmania braziliensis | 35% | 100% |
| A4IA06 | Leishmania infantum | 33% | 100% |
| A4ICJ0 | Leishmania infantum | 95% | 99% |
| A4ICP7 | Leishmania infantum | 35% | 100% |
| B4JT42 | Drosophila grimshawi | 28% | 75% |
| D0A3F8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
| E9ASK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
| E9AT60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 99% |
| E9B512 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
| O60114 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 76% |
| Q09530 | Caenorhabditis elegans | 42% | 90% |
| Q296Q5 | Drosophila pseudoobscura pseudoobscura | 28% | 75% |
| Q38953 | Arabidopsis thaliana | 47% | 92% |
| Q4Q1D7 | Leishmania major | 94% | 100% |
| Q4Q1Y9 | Leishmania major | 34% | 100% |
| Q4Q2X4 | Leishmania major | 34% | 100% |
| Q54F05 | Dictyostelium discoideum | 43% | 93% |
| Q9HDY4 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 91% |
| Q9VF26 | Drosophila melanogaster | 27% | 75% |
| V5BPV3 | Trypanosoma cruzi | 62% | 100% |
| V5BV22 | Trypanosoma cruzi | 37% | 100% |