| 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 | 2 |
| GO:0005681 | spliceosomal complex | 3 | 2 |
| GO:0032991 | protein-containing complex | 1 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
| GO:0140513 | nuclear protein-containing complex | 2 | 2 |
| GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4Q1Y9
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000375 | RNA splicing, via transesterification reactions | 8 | 2 |
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
| GO:0006396 | RNA processing | 6 | 2 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
| GO:0008152 | metabolic process | 1 | 2 |
| GO:0008380 | RNA splicing | 7 | 2 |
| GO:0009987 | cellular process | 1 | 2 |
| GO:0016070 | RNA metabolic process | 5 | 2 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
| GO:0043170 | macromolecule metabolic process | 3 | 2 |
| GO:0044237 | cellular metabolic process | 2 | 2 |
| GO:0044238 | primary metabolic process | 2 | 2 |
| GO:0046483 | heterocycle metabolic process | 3 | 2 |
| GO:0071704 | organic substance metabolic process | 2 | 2 |
| GO:0090304 | nucleic acid metabolic process | 4 | 2 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 12 |
| GO:0003676 | nucleic acid binding | 3 | 12 |
| GO:0003723 | RNA binding | 4 | 2 |
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0004386 | helicase activity | 2 | 12 |
| GO:0005488 | binding | 1 | 12 |
| GO:0005524 | ATP binding | 5 | 12 |
| 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:0016787 | hydrolase activity | 2 | 9 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 612 | 616 | PF00656 | 0.369 |
| CLV_C14_Caspase3-7 | 772 | 776 | PF00656 | 0.671 |
| CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.549 |
| CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.450 |
| CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.304 |
| CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.262 |
| CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.252 |
| CLV_NRD_NRD_1 | 500 | 502 | PF00675 | 0.256 |
| CLV_NRD_NRD_1 | 646 | 648 | PF00675 | 0.275 |
| CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.571 |
| CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.647 |
| CLV_NRD_NRD_1 | 838 | 840 | PF00675 | 0.542 |
| CLV_NRD_NRD_1 | 863 | 865 | PF00675 | 0.642 |
| CLV_NRD_NRD_1 | 899 | 901 | PF00675 | 0.556 |
| CLV_NRD_NRD_1 | 936 | 938 | PF00675 | 0.589 |
| CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.479 |
| CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.272 |
| CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.278 |
| CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.252 |
| CLV_PCSK_KEX2_1 | 646 | 648 | PF00082 | 0.275 |
| CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.631 |
| CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.628 |
| CLV_PCSK_KEX2_1 | 838 | 840 | PF00082 | 0.646 |
| CLV_PCSK_KEX2_1 | 899 | 901 | PF00082 | 0.506 |
| CLV_PCSK_KEX2_1 | 903 | 905 | PF00082 | 0.384 |
| CLV_PCSK_KEX2_1 | 938 | 940 | PF00082 | 0.653 |
| CLV_PCSK_PC1ET2_1 | 243 | 245 | PF00082 | 0.272 |
| CLV_PCSK_PC1ET2_1 | 903 | 905 | PF00082 | 0.422 |
| CLV_PCSK_PC1ET2_1 | 938 | 940 | PF00082 | 0.653 |
| CLV_PCSK_PC7_1 | 369 | 375 | PF00082 | 0.336 |
| CLV_PCSK_PC7_1 | 899 | 905 | PF00082 | 0.455 |
| CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.555 |
| CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.527 |
| CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.329 |
| CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.642 |
| CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.253 |
| CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.277 |
| CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.262 |
| CLV_PCSK_SKI1_1 | 569 | 573 | PF00082 | 0.413 |
| CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.338 |
| CLV_PCSK_SKI1_1 | 742 | 746 | PF00082 | 0.396 |
| CLV_PCSK_SKI1_1 | 748 | 752 | PF00082 | 0.358 |
| CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.670 |
| CLV_PCSK_SKI1_1 | 803 | 807 | PF00082 | 0.369 |
| CLV_PCSK_SKI1_1 | 904 | 908 | PF00082 | 0.530 |
| CLV_Separin_Metazoa | 587 | 591 | PF03568 | 0.389 |
| DEG_APCC_DBOX_1 | 198 | 206 | PF00400 | 0.319 |
| DEG_APCC_DBOX_1 | 747 | 755 | PF00400 | 0.399 |
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.609 |
| DEG_SPOP_SBC_1 | 99 | 103 | PF00917 | 0.549 |
| DOC_AGCK_PIF_1 | 571 | 576 | PF00069 | 0.493 |
| DOC_CKS1_1 | 246 | 251 | PF01111 | 0.555 |
| DOC_CYCLIN_RxL_1 | 240 | 248 | PF00134 | 0.524 |
| DOC_CYCLIN_RxL_1 | 318 | 330 | PF00134 | 0.476 |
| DOC_CYCLIN_RxL_1 | 800 | 807 | PF00134 | 0.420 |
| DOC_CYCLIN_yCln2_LP_2 | 246 | 252 | PF00134 | 0.545 |
| DOC_MAPK_DCC_7 | 469 | 477 | PF00069 | 0.498 |
| DOC_MAPK_gen_1 | 204 | 214 | PF00069 | 0.459 |
| DOC_MAPK_gen_1 | 286 | 293 | PF00069 | 0.462 |
| DOC_MAPK_gen_1 | 373 | 380 | PF00069 | 0.450 |
| DOC_MAPK_gen_1 | 887 | 896 | PF00069 | 0.389 |
| DOC_MAPK_HePTP_8 | 886 | 898 | PF00069 | 0.472 |
| DOC_MAPK_MEF2A_6 | 207 | 215 | PF00069 | 0.441 |
| DOC_MAPK_MEF2A_6 | 373 | 382 | PF00069 | 0.450 |
| DOC_MAPK_MEF2A_6 | 469 | 478 | PF00069 | 0.462 |
| DOC_MAPK_MEF2A_6 | 756 | 765 | PF00069 | 0.549 |
| DOC_MAPK_MEF2A_6 | 887 | 896 | PF00069 | 0.396 |
| DOC_PP1_RVXF_1 | 310 | 316 | PF00149 | 0.450 |
| DOC_PP1_RVXF_1 | 322 | 328 | PF00149 | 0.450 |
| DOC_PP2B_LxvP_1 | 476 | 479 | PF13499 | 0.462 |
| DOC_PP2B_LxvP_1 | 614 | 617 | PF13499 | 0.425 |
| DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.612 |
| DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.540 |
| DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.562 |
| DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.450 |
| DOC_USP7_MATH_1 | 769 | 773 | PF00917 | 0.650 |
| DOC_USP7_MATH_1 | 837 | 841 | PF00917 | 0.698 |
| DOC_USP7_MATH_1 | 846 | 850 | PF00917 | 0.534 |
| DOC_USP7_MATH_1 | 911 | 915 | PF00917 | 0.442 |
| DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.746 |
| DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.526 |
| DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.452 |
| DOC_WW_Pin1_4 | 868 | 873 | PF00397 | 0.732 |
| LIG_14-3-3_CanoR_1 | 138 | 148 | PF00244 | 0.734 |
| LIG_14-3-3_CanoR_1 | 190 | 194 | PF00244 | 0.403 |
| LIG_14-3-3_CanoR_1 | 244 | 249 | PF00244 | 0.553 |
| LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.475 |
| LIG_14-3-3_CanoR_1 | 357 | 367 | PF00244 | 0.457 |
| LIG_14-3-3_CanoR_1 | 558 | 564 | PF00244 | 0.462 |
| LIG_14-3-3_CanoR_1 | 569 | 576 | PF00244 | 0.399 |
| LIG_14-3-3_CanoR_1 | 590 | 600 | PF00244 | 0.345 |
| LIG_14-3-3_CanoR_1 | 640 | 644 | PF00244 | 0.462 |
| LIG_14-3-3_CanoR_1 | 87 | 95 | PF00244 | 0.720 |
| LIG_14-3-3_CanoR_1 | 899 | 906 | PF00244 | 0.469 |
| LIG_Actin_WH2_2 | 356 | 371 | PF00022 | 0.450 |
| LIG_Actin_WH2_2 | 710 | 727 | PF00022 | 0.414 |
| LIG_AP2alpha_1 | 392 | 396 | PF02296 | 0.471 |
| LIG_BIR_III_4 | 261 | 265 | PF00653 | 0.389 |
| LIG_BRCT_BRCA1_1 | 100 | 104 | PF00533 | 0.521 |
| LIG_BRCT_BRCA1_1 | 392 | 396 | PF00533 | 0.385 |
| LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.675 |
| LIG_BRCT_BRCA1_1 | 806 | 810 | PF00533 | 0.390 |
| LIG_BRCT_BRCA1_1 | 856 | 860 | PF00533 | 0.423 |
| LIG_BRCT_BRCA1_2 | 392 | 398 | PF00533 | 0.517 |
| LIG_Clathr_ClatBox_1 | 608 | 612 | PF01394 | 0.380 |
| LIG_FHA_1 | 101 | 107 | PF00498 | 0.545 |
| LIG_FHA_1 | 221 | 227 | PF00498 | 0.459 |
| LIG_FHA_1 | 317 | 323 | PF00498 | 0.469 |
| LIG_FHA_1 | 359 | 365 | PF00498 | 0.475 |
| LIG_FHA_1 | 406 | 412 | PF00498 | 0.413 |
| LIG_FHA_1 | 498 | 504 | PF00498 | 0.459 |
| LIG_FHA_1 | 617 | 623 | PF00498 | 0.413 |
| LIG_FHA_1 | 712 | 718 | PF00498 | 0.460 |
| LIG_FHA_1 | 800 | 806 | PF00498 | 0.336 |
| LIG_FHA_1 | 854 | 860 | PF00498 | 0.465 |
| LIG_FHA_1 | 869 | 875 | PF00498 | 0.723 |
| LIG_FHA_2 | 165 | 171 | PF00498 | 0.525 |
| LIG_FHA_2 | 196 | 202 | PF00498 | 0.509 |
| LIG_FHA_2 | 29 | 35 | PF00498 | 0.637 |
| LIG_FHA_2 | 582 | 588 | PF00498 | 0.391 |
| LIG_FHA_2 | 62 | 68 | PF00498 | 0.627 |
| LIG_LIR_Apic_2 | 531 | 535 | PF02991 | 0.491 |
| LIG_LIR_Gen_1 | 142 | 153 | PF02991 | 0.582 |
| LIG_LIR_Gen_1 | 165 | 176 | PF02991 | 0.630 |
| LIG_LIR_Gen_1 | 390 | 400 | PF02991 | 0.504 |
| LIG_LIR_Gen_1 | 714 | 724 | PF02991 | 0.472 |
| LIG_LIR_Gen_1 | 757 | 765 | PF02991 | 0.513 |
| LIG_LIR_Gen_1 | 819 | 829 | PF02991 | 0.439 |
| LIG_LIR_Gen_1 | 86 | 96 | PF02991 | 0.703 |
| LIG_LIR_LC3C_4 | 822 | 826 | PF02991 | 0.440 |
| LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.633 |
| LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.502 |
| LIG_LIR_Nem_3 | 566 | 571 | PF02991 | 0.403 |
| LIG_LIR_Nem_3 | 714 | 719 | PF02991 | 0.405 |
| LIG_LIR_Nem_3 | 757 | 761 | PF02991 | 0.493 |
| LIG_LIR_Nem_3 | 807 | 813 | PF02991 | 0.342 |
| LIG_LIR_Nem_3 | 819 | 824 | PF02991 | 0.363 |
| LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.737 |
| LIG_MLH1_MIPbox_1 | 392 | 396 | PF16413 | 0.385 |
| LIG_MLH1_MIPbox_1 | 806 | 810 | PF16413 | 0.390 |
| LIG_NRBOX | 363 | 369 | PF00104 | 0.450 |
| LIG_PCNA_yPIPBox_3 | 710 | 718 | PF02747 | 0.362 |
| LIG_Pex14_2 | 392 | 396 | PF04695 | 0.351 |
| LIG_REV1ctd_RIR_1 | 393 | 399 | PF16727 | 0.491 |
| LIG_SH2_CRK | 481 | 485 | PF00017 | 0.374 |
| LIG_SH2_GRB2like | 532 | 535 | PF00017 | 0.491 |
| LIG_SH2_PTP2 | 716 | 719 | PF00017 | 0.347 |
| LIG_SH2_SRC | 231 | 234 | PF00017 | 0.511 |
| LIG_SH2_STAT3 | 533 | 536 | PF00017 | 0.511 |
| LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.612 |
| LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.464 |
| LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.469 |
| LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.382 |
| LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.450 |
| LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.432 |
| LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.347 |
| LIG_SH2_STAT5 | 823 | 826 | PF00017 | 0.362 |
| LIG_SH2_STAT5 | 926 | 929 | PF00017 | 0.440 |
| LIG_SH3_3 | 121 | 127 | PF00018 | 0.655 |
| LIG_SH3_3 | 298 | 304 | PF00018 | 0.536 |
| LIG_SH3_3 | 443 | 449 | PF00018 | 0.475 |
| LIG_SH3_3 | 649 | 655 | PF00018 | 0.442 |
| LIG_SH3_3 | 822 | 828 | PF00018 | 0.473 |
| LIG_SH3_3 | 93 | 99 | PF00018 | 0.712 |
| LIG_SH3_5 | 419 | 423 | PF00018 | 0.410 |
| LIG_Sin3_3 | 128 | 135 | PF02671 | 0.506 |
| LIG_SUMO_SIM_par_1 | 211 | 218 | PF11976 | 0.442 |
| LIG_SUMO_SIM_par_1 | 678 | 684 | PF11976 | 0.475 |
| LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.488 |
| LIG_TRFH_1 | 235 | 239 | PF08558 | 0.536 |
| LIG_TRFH_1 | 651 | 655 | PF08558 | 0.511 |
| LIG_UBA3_1 | 629 | 636 | PF00899 | 0.454 |
| LIG_WRC_WIRS_1 | 755 | 760 | PF05994 | 0.470 |
| MOD_CK1_1 | 220 | 226 | PF00069 | 0.450 |
| MOD_CK1_1 | 358 | 364 | PF00069 | 0.459 |
| MOD_CK1_1 | 405 | 411 | PF00069 | 0.524 |
| MOD_CK1_1 | 427 | 433 | PF00069 | 0.444 |
| MOD_CK1_1 | 548 | 554 | PF00069 | 0.448 |
| MOD_CK1_1 | 618 | 624 | PF00069 | 0.419 |
| MOD_CK1_1 | 770 | 776 | PF00069 | 0.574 |
| MOD_CK1_1 | 832 | 838 | PF00069 | 0.746 |
| MOD_CK1_1 | 873 | 879 | PF00069 | 0.659 |
| MOD_CK2_1 | 146 | 152 | PF00069 | 0.570 |
| MOD_CK2_1 | 164 | 170 | PF00069 | 0.433 |
| MOD_CK2_1 | 195 | 201 | PF00069 | 0.331 |
| MOD_CK2_1 | 28 | 34 | PF00069 | 0.598 |
| MOD_CK2_1 | 289 | 295 | PF00069 | 0.450 |
| MOD_CK2_1 | 45 | 51 | PF00069 | 0.349 |
| MOD_CK2_1 | 581 | 587 | PF00069 | 0.398 |
| MOD_CK2_1 | 61 | 67 | PF00069 | 0.512 |
| MOD_CK2_1 | 697 | 703 | PF00069 | 0.577 |
| MOD_CK2_1 | 846 | 852 | PF00069 | 0.514 |
| MOD_Cter_Amidation | 644 | 647 | PF01082 | 0.275 |
| MOD_Cter_Amidation | 862 | 865 | PF01082 | 0.619 |
| MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.712 |
| MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.704 |
| MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.641 |
| MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.241 |
| MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.250 |
| MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.567 |
| MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.423 |
| MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.250 |
| MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.588 |
| MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.458 |
| MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.443 |
| MOD_GlcNHglycan | 789 | 792 | PF01048 | 0.628 |
| MOD_GlcNHglycan | 806 | 809 | PF01048 | 0.238 |
| MOD_GlcNHglycan | 841 | 844 | PF01048 | 0.668 |
| MOD_GlcNHglycan | 913 | 916 | PF01048 | 0.477 |
| MOD_GlcNHglycan | 920 | 923 | PF01048 | 0.439 |
| MOD_GSK3_1 | 122 | 129 | PF00069 | 0.709 |
| MOD_GSK3_1 | 134 | 141 | PF00069 | 0.681 |
| MOD_GSK3_1 | 217 | 224 | PF00069 | 0.450 |
| MOD_GSK3_1 | 316 | 323 | PF00069 | 0.462 |
| MOD_GSK3_1 | 493 | 500 | PF00069 | 0.521 |
| MOD_GSK3_1 | 544 | 551 | PF00069 | 0.487 |
| MOD_GSK3_1 | 767 | 774 | PF00069 | 0.653 |
| MOD_GSK3_1 | 828 | 835 | PF00069 | 0.655 |
| MOD_GSK3_1 | 868 | 875 | PF00069 | 0.606 |
| MOD_GSK3_1 | 907 | 914 | PF00069 | 0.395 |
| MOD_GSK3_1 | 94 | 101 | PF00069 | 0.727 |
| MOD_LATS_1 | 355 | 361 | PF00433 | 0.555 |
| MOD_NEK2_1 | 133 | 138 | PF00069 | 0.652 |
| MOD_NEK2_1 | 280 | 285 | PF00069 | 0.447 |
| MOD_NEK2_1 | 402 | 407 | PF00069 | 0.473 |
| MOD_NEK2_1 | 434 | 439 | PF00069 | 0.396 |
| MOD_NEK2_1 | 589 | 594 | PF00069 | 0.392 |
| MOD_NEK2_1 | 641 | 646 | PF00069 | 0.450 |
| MOD_NEK2_1 | 829 | 834 | PF00069 | 0.618 |
| MOD_NEK2_1 | 898 | 903 | PF00069 | 0.471 |
| MOD_PIKK_1 | 106 | 112 | PF00454 | 0.509 |
| MOD_PIKK_1 | 221 | 227 | PF00454 | 0.450 |
| MOD_PIKK_1 | 280 | 286 | PF00454 | 0.464 |
| MOD_PIKK_1 | 545 | 551 | PF00454 | 0.471 |
| MOD_PIKK_1 | 559 | 565 | PF00454 | 0.378 |
| MOD_PK_1 | 870 | 876 | PF00069 | 0.595 |
| MOD_PKA_1 | 373 | 379 | PF00069 | 0.389 |
| MOD_PKA_1 | 899 | 905 | PF00069 | 0.539 |
| MOD_PKA_2 | 189 | 195 | PF00069 | 0.401 |
| MOD_PKA_2 | 373 | 379 | PF00069 | 0.500 |
| MOD_PKA_2 | 589 | 595 | PF00069 | 0.374 |
| MOD_PKA_2 | 639 | 645 | PF00069 | 0.462 |
| MOD_PKA_2 | 837 | 843 | PF00069 | 0.505 |
| MOD_PKA_2 | 86 | 92 | PF00069 | 0.716 |
| MOD_PKA_2 | 863 | 869 | PF00069 | 0.667 |
| MOD_PKA_2 | 898 | 904 | PF00069 | 0.437 |
| MOD_PKB_1 | 242 | 250 | PF00069 | 0.500 |
| MOD_Plk_1 | 106 | 112 | PF00069 | 0.565 |
| MOD_Plk_1 | 164 | 170 | PF00069 | 0.604 |
| MOD_Plk_1 | 341 | 347 | PF00069 | 0.501 |
| MOD_Plk_1 | 355 | 361 | PF00069 | 0.387 |
| MOD_Plk_1 | 510 | 516 | PF00069 | 0.419 |
| MOD_Plk_1 | 829 | 835 | PF00069 | 0.570 |
| MOD_Plk_1 | 846 | 852 | PF00069 | 0.545 |
| MOD_Plk_4 | 28 | 34 | PF00069 | 0.626 |
| MOD_Plk_4 | 304 | 310 | PF00069 | 0.491 |
| MOD_Plk_4 | 427 | 433 | PF00069 | 0.459 |
| MOD_Plk_4 | 460 | 466 | PF00069 | 0.555 |
| MOD_Plk_4 | 681 | 687 | PF00069 | 0.451 |
| MOD_Plk_4 | 854 | 860 | PF00069 | 0.392 |
| MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.526 |
| MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.452 |
| MOD_ProDKin_1 | 868 | 874 | PF00069 | 0.732 |
| MOD_SUMO_for_1 | 814 | 817 | PF00179 | 0.511 |
| MOD_SUMO_rev_2 | 770 | 779 | PF00179 | 0.709 |
| TRG_AP2beta_CARGO_1 | 165 | 175 | PF09066 | 0.637 |
| TRG_DiLeu_BaEn_1 | 201 | 206 | PF01217 | 0.498 |
| TRG_DiLeu_BaEn_1 | 51 | 56 | PF01217 | 0.606 |
| TRG_DiLeu_BaEn_1 | 888 | 893 | PF01217 | 0.380 |
| TRG_DiLeu_BaEn_4 | 232 | 238 | PF01217 | 0.536 |
| TRG_DiLeu_BaEn_4 | 273 | 279 | PF01217 | 0.446 |
| TRG_DiLeu_BaLyEn_6 | 241 | 246 | PF01217 | 0.500 |
| TRG_DiLeu_BaLyEn_6 | 276 | 281 | PF01217 | 0.425 |
| TRG_DiLeu_BaLyEn_6 | 471 | 476 | PF01217 | 0.491 |
| TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.619 |
| TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.441 |
| TRG_ENDOCYTIC_2 | 568 | 571 | PF00928 | 0.438 |
| TRG_ENDOCYTIC_2 | 716 | 719 | PF00928 | 0.347 |
| TRG_ENDOCYTIC_2 | 823 | 826 | PF00928 | 0.396 |
| TRG_ER_diArg_1 | 239 | 242 | PF00400 | 0.460 |
| TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.462 |
| TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.464 |
| TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.647 |
| TRG_ER_diArg_1 | 646 | 648 | PF00400 | 0.475 |
| TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.647 |
| TRG_ER_diArg_1 | 745 | 748 | PF00400 | 0.394 |
| TRG_ER_diArg_1 | 898 | 900 | PF00400 | 0.558 |
| TRG_ER_diArg_1 | 936 | 939 | PF00400 | 0.625 |
| TRG_NES_CRM1_1 | 587 | 599 | PF08389 | 0.370 |
| TRG_NLS_MonoExtC_3 | 936 | 941 | PF00514 | 0.636 |
| TRG_NLS_MonoExtN_4 | 239 | 246 | PF00514 | 0.522 |
| TRG_NLS_MonoExtN_4 | 937 | 942 | PF00514 | 0.684 |
| TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.189 |
| TRG_Pf-PMV_PEXEL_1 | 357 | 362 | PF00026 | 0.262 |
| TRG_Pf-PMV_PEXEL_1 | 38 | 42 | PF00026 | 0.655 |
| TRG_Pf-PMV_PEXEL_1 | 777 | 781 | PF00026 | 0.486 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P5V0 | Leptomonas seymouri | 36% | 100% |
| A0A0N0P8Y1 | Leptomonas seymouri | 36% | 100% |
| A0A0N0P9D2 | Leptomonas seymouri | 36% | 100% |
| A0A0N1I0Z0 | Leptomonas seymouri | 35% | 87% |
| A0A0N1PEU4 | Leptomonas seymouri | 74% | 99% |
| A0A0S4IQ76 | Bodo saltans | 34% | 100% |
| A0A0S4IR78 | Bodo saltans | 49% | 100% |
| A0A0S4IS51 | Bodo saltans | 35% | 100% |
| A0A0S4ITR4 | Bodo saltans | 36% | 88% |
| A0A0S4IWU8 | Bodo saltans | 50% | 100% |
| A0A0S4J157 | Bodo saltans | 37% | 100% |
| A0A0S4JCY8 | Bodo saltans | 36% | 92% |
| A0A1X0NJ46 | Trypanosomatidae | 36% | 100% |
| A0A1X0NKY7 | Trypanosomatidae | 35% | 88% |
| A0A1X0NUZ7 | Trypanosomatidae | 31% | 72% |
| A0A1X0NVG5 | Trypanosomatidae | 38% | 88% |
| A0A1X0P0D7 | Trypanosomatidae | 36% | 100% |
| A0A1X0P872 | Trypanosomatidae | 60% | 100% |
| A0A1X0P9K6 | Trypanosomatidae | 36% | 100% |
| A0A3Q8II71 | Leishmania donovani | 36% | 100% |
| A0A3Q8IJ24 | Leishmania donovani | 95% | 100% |
| A0A3Q8IWG4 | Leishmania donovani | 35% | 100% |
| A0A3R7MA90 | Trypanosoma rangeli | 36% | 100% |
| A0A3R7MLF0 | Trypanosoma rangeli | 29% | 67% |
| A0A3R7NT42 | Trypanosoma rangeli | 36% | 100% |
| A0A3S7WYA1 | Leishmania donovani | 34% | 87% |
| A0A3S7X8Z5 | Leishmania donovani | 36% | 100% |
| A0A3S7XB01 | Leishmania donovani | 35% | 87% |
| A0A422MXB1 | Trypanosoma rangeli | 37% | 89% |
| A0A422N8L3 | Trypanosoma rangeli | 34% | 93% |
| A1Z9L3 | Drosophila melanogaster | 39% | 76% |
| A2A4P0 | Mus musculus | 39% | 76% |
| A4HAT8 | Leishmania braziliensis | 36% | 100% |
| A4HME2 | Leishmania braziliensis | 37% | 100% |
| A4HNU7 | Leishmania braziliensis | 85% | 100% |
| A4HPE9 | Leishmania braziliensis | 34% | 87% |
| A4HQ83 | Leishmania braziliensis | 35% | 100% |
| A4I0U7 | Leishmania infantum | 34% | 87% |
| A4IA06 | Leishmania infantum | 36% | 100% |
| A4IB14 | Leishmania infantum | 36% | 100% |
| A4ICJ0 | Leishmania infantum | 35% | 87% |
| A4ICP7 | Leishmania infantum | 95% | 100% |
| A4IDY1 | Leishmania infantum | 35% | 100% |
| B0XDC4 | Culex quinquefasciatus | 29% | 67% |
| B8A4F4 | Danio rerio | 30% | 70% |
| C9ZMN0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
| C9ZNP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
| D0A2R5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
| D0A3F8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 89% |
| D0A429 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
| D0A778 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 90% |
| E9AEU3 | Leishmania major | 36% | 93% |
| E9ASK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
| E9AT60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 87% |
| E9AU01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
| E9B512 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
| E9B5Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
| F4IE66 | Arabidopsis thaliana | 34% | 100% |
| F4IJV4 | Arabidopsis thaliana | 41% | 90% |
| F4JMJ3 | Arabidopsis thaliana | 37% | 100% |
| F4JRJ6 | Arabidopsis thaliana | 36% | 100% |
| F4K2E9 | Arabidopsis thaliana | 34% | 75% |
| O22899 | Arabidopsis thaliana | 36% | 100% |
| O35286 | Mus musculus | 36% | 100% |
| O42643 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 81% |
| O42945 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 100% |
| O43143 | Homo sapiens | 36% | 100% |
| O45244 | Caenorhabditis elegans | 39% | 93% |
| O60231 | Homo sapiens | 41% | 90% |
| O70133 | Mus musculus | 28% | 68% |
| P15938 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 36% | 88% |
| P20095 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 36% | 100% |
| P24384 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 82% |
| P34498 | Caenorhabditis elegans | 37% | 83% |
| P36009 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 100% |
| P43329 | Escherichia coli (strain K12) | 32% | 72% |
| P45018 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 32% | 72% |
| P53131 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 40% | 100% |
| Q03319 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 100% |
| Q09530 | Caenorhabditis elegans | 39% | 78% |
| Q10752 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 89% |
| Q14562 | Homo sapiens | 39% | 77% |
| Q14BI7 | Mus musculus | 28% | 68% |
| Q17R09 | Bos taurus | 36% | 77% |
| Q20875 | Caenorhabditis elegans | 35% | 100% |
| Q2NKY8 | Bos taurus | 31% | 77% |
| Q38953 | Arabidopsis thaliana | 39% | 81% |
| Q3ZBE0 | Bos taurus | 30% | 100% |
| Q4Q0J4 | Leishmania major | 35% | 91% |
| Q4Q1D7 | Leishmania major | 35% | 100% |
| Q4Q2X4 | Leishmania major | 36% | 100% |
| Q54F05 | Dictyostelium discoideum | 38% | 81% |
| Q54MH3 | Dictyostelium discoideum | 40% | 85% |
| Q54NJ4 | Dictyostelium discoideum | 39% | 100% |
| Q5BJS0 | Rattus norvegicus | 32% | 79% |
| Q5R607 | Pongo abelii | 32% | 79% |
| Q5R864 | Pongo abelii | 36% | 100% |
| Q5RAZ4 | Pongo abelii | 36% | 100% |
| Q5RBD4 | Pongo abelii | 37% | 100% |
| Q5XH12 | Xenopus laevis | 27% | 100% |
| Q5XI69 | Rattus norvegicus | 35% | 100% |
| Q68FK8 | Xenopus laevis | 30% | 75% |
| Q6PE54 | Mus musculus | 36% | 100% |
| Q767K6 | Sus scrofa | 41% | 90% |
| Q7K3M5 | Drosophila melanogaster | 36% | 100% |
| Q7L2E3 | Homo sapiens | 32% | 79% |
| Q7L7V1 | Homo sapiens | 25% | 100% |
| Q7YR39 | Pan troglodytes | 41% | 90% |
| Q80VY9 | Mus musculus | 34% | 100% |
| Q8BZS9 | Mus musculus | 26% | 100% |
| Q8IX18 | Homo sapiens | 36% | 100% |
| Q8TE96 | Homo sapiens | 29% | 100% |
| Q8VY00 | Arabidopsis thaliana | 40% | 90% |
| Q924H9 | Mus musculus | 29% | 100% |
| Q92620 | Homo sapiens | 36% | 77% |
| Q99PU8 | Mus musculus | 32% | 77% |
| Q9BKQ8 | Caenorhabditis elegans | 38% | 100% |
| Q9C6G0 | Arabidopsis thaliana | 31% | 66% |
| Q9H5Z1 | Homo sapiens | 37% | 100% |
| Q9H6R0 | Homo sapiens | 34% | 100% |
| Q9HDY4 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 80% |
| Q9HE06 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
| Q9LZQ9 | Arabidopsis thaliana | 40% | 100% |
| V5B3L7 | Trypanosoma cruzi | 35% | 100% |
| V5B7H6 | Trypanosoma cruzi | 32% | 86% |
| V5BKH2 | Trypanosoma cruzi | 38% | 100% |
| V5BND8 | Trypanosoma cruzi | 29% | 67% |
| V5BPV3 | Trypanosoma cruzi | 37% | 89% |
| V5BV22 | Trypanosoma cruzi | 57% | 100% |
| V5C0I9 | Trypanosoma cruzi | 35% | 100% |
| V5D886 | Trypanosoma cruzi | 36% | 100% |