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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0000152 | nuclear ubiquitin ligase complex | 3 | 1 |
GO:0005680 | anaphase-promoting complex | 4 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HN46
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 10 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009056 | catabolic process | 2 | 10 |
GO:0009057 | macromolecule catabolic process | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044248 | cellular catabolic process | 3 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 10 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:1901575 | organic substance catabolic process | 3 | 10 |
GO:0000209 | protein polyubiquitination | 8 | 1 |
GO:0007091 | metaphase/anaphase transition of mitotic cell cycle | 5 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010965 | regulation of mitotic sister chromatid separation | 6 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0033044 | regulation of chromosome organization | 6 | 1 |
GO:0033045 | regulation of sister chromatid segregation | 5 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044770 | cell cycle phase transition | 3 | 1 |
GO:0044772 | mitotic cell cycle phase transition | 4 | 1 |
GO:0044784 | metaphase/anaphase transition of cell cycle | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0051983 | regulation of chromosome segregation | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0070979 | protein K11-linked ubiquitination | 9 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
GO:1905818 | regulation of chromosome separation | 5 | 1 |
GO:0007049 | cell cycle | 2 | 4 |
GO:0051301 | cell division | 2 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0005515 | protein binding | 2 | 10 |
GO:0019899 | enzyme binding | 3 | 10 |
GO:0031625 | ubiquitin protein ligase binding | 5 | 10 |
GO:0044389 | ubiquitin-like protein ligase binding | 4 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 204 | 208 | PF00656 | 0.677 |
CLV_C14_Caspase3-7 | 307 | 311 | PF00656 | 0.403 |
CLV_C14_Caspase3-7 | 397 | 401 | PF00656 | 0.413 |
CLV_C14_Caspase3-7 | 44 | 48 | PF00656 | 0.522 |
CLV_MEL_PAP_1 | 95 | 101 | PF00089 | 0.503 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.245 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.245 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 699 | 701 | PF00082 | 0.270 |
CLV_PCSK_PC1ET2_1 | 699 | 701 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 699 | 703 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 750 | 754 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 839 | 843 | PF00082 | 0.455 |
CLV_Separin_Metazoa | 875 | 879 | PF03568 | 0.523 |
DEG_APCC_DBOX_1 | 271 | 279 | PF00400 | 0.551 |
DEG_APCC_DBOX_1 | 371 | 379 | PF00400 | 0.262 |
DEG_APCC_DBOX_1 | 546 | 554 | PF00400 | 0.392 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.523 |
DOC_CKS1_1 | 413 | 418 | PF01111 | 0.573 |
DOC_CKS1_1 | 758 | 763 | PF01111 | 0.424 |
DOC_CYCLIN_RxL_1 | 426 | 434 | PF00134 | 0.484 |
DOC_CYCLIN_RxL_1 | 542 | 552 | PF00134 | 0.396 |
DOC_MAPK_gen_1 | 190 | 197 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 540 | 548 | PF00069 | 0.502 |
DOC_MAPK_HePTP_8 | 95 | 107 | PF00069 | 0.508 |
DOC_MAPK_JIP1_4 | 542 | 548 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 372 | 379 | PF00069 | 0.265 |
DOC_MAPK_MEF2A_6 | 442 | 451 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 542 | 550 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 784 | 793 | PF00069 | 0.621 |
DOC_MAPK_MEF2A_6 | 98 | 107 | PF00069 | 0.513 |
DOC_MAPK_NFAT4_5 | 372 | 380 | PF00069 | 0.260 |
DOC_PP1_RVXF_1 | 287 | 294 | PF00149 | 0.515 |
DOC_PP1_RVXF_1 | 704 | 710 | PF00149 | 0.371 |
DOC_PP2B_LxvP_1 | 151 | 154 | PF13499 | 0.417 |
DOC_PP2B_LxvP_1 | 238 | 241 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 505 | 508 | PF13499 | 0.622 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 628 | 632 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 648 | 652 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 683 | 687 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 823 | 827 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 855 | 859 | PF00917 | 0.459 |
DOC_USP7_UBL2_3 | 723 | 727 | PF12436 | 0.549 |
DOC_USP7_UBL2_3 | 861 | 865 | PF12436 | 0.538 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 578 | 583 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 679 | 684 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 757 | 762 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 783 | 788 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 827 | 832 | PF00397 | 0.466 |
LIG_14-3-3_CanoR_1 | 138 | 147 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 183 | 189 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 342 | 346 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 706 | 710 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 72 | 81 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 839 | 845 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 98 | 105 | PF00244 | 0.492 |
LIG_Actin_WH2_2 | 208 | 224 | PF00022 | 0.497 |
LIG_APCC_ABBA_1 | 54 | 59 | PF00400 | 0.528 |
LIG_BRCT_BRCA1_1 | 278 | 282 | PF00533 | 0.531 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.489 |
LIG_BRCT_BRCA1_1 | 467 | 471 | PF00533 | 0.399 |
LIG_BRCT_BRCA1_1 | 807 | 811 | PF00533 | 0.552 |
LIG_CaM_IQ_9 | 606 | 622 | PF13499 | 0.457 |
LIG_CSL_BTD_1 | 657 | 660 | PF09270 | 0.532 |
LIG_CtBP_PxDLS_1 | 7 | 11 | PF00389 | 0.450 |
LIG_EVH1_1 | 505 | 509 | PF00568 | 0.468 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.449 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.511 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.654 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.514 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.369 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.491 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.656 |
LIG_FHA_1 | 706 | 712 | PF00498 | 0.466 |
LIG_FHA_1 | 794 | 800 | PF00498 | 0.425 |
LIG_FHA_1 | 840 | 846 | PF00498 | 0.405 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.591 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.491 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.725 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.422 |
LIG_FHA_2 | 578 | 584 | PF00498 | 0.439 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.554 |
LIG_FHA_2 | 719 | 725 | PF00498 | 0.407 |
LIG_FHA_2 | 805 | 811 | PF00498 | 0.471 |
LIG_FHA_2 | 817 | 823 | PF00498 | 0.640 |
LIG_GBD_Chelix_1 | 156 | 164 | PF00786 | 0.509 |
LIG_LIR_Gen_1 | 389 | 399 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 808 | 816 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 389 | 395 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 656 | 661 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 696 | 701 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 808 | 814 | PF02991 | 0.565 |
LIG_MYND_3 | 127 | 131 | PF01753 | 0.532 |
LIG_MYND_3 | 402 | 406 | PF01753 | 0.496 |
LIG_NRBOX | 374 | 380 | PF00104 | 0.384 |
LIG_NRBOX | 545 | 551 | PF00104 | 0.290 |
LIG_OCRL_FandH_1 | 187 | 199 | PF00620 | 0.400 |
LIG_Pex14_2 | 457 | 461 | PF04695 | 0.474 |
LIG_Rb_pABgroove_1 | 735 | 743 | PF01858 | 0.532 |
LIG_RPA_C_Fungi | 608 | 620 | PF08784 | 0.443 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.508 |
LIG_SH2_CRK | 698 | 702 | PF00017 | 0.383 |
LIG_SH2_CRK | 894 | 898 | PF00017 | 0.460 |
LIG_SH2_NCK_1 | 894 | 898 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 141 | 145 | PF00017 | 0.370 |
LIG_SH2_STAT3 | 410 | 413 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.473 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.534 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.574 |
LIG_SH3_3 | 503 | 509 | PF00018 | 0.636 |
LIG_SH3_3 | 755 | 761 | PF00018 | 0.346 |
LIG_SH3_3 | 788 | 794 | PF00018 | 0.286 |
LIG_SH3_CIN85_PxpxPR_1 | 67 | 72 | PF14604 | 0.374 |
LIG_SUMO_SIM_anti_2 | 443 | 451 | PF11976 | 0.387 |
LIG_SUMO_SIM_anti_2 | 649 | 654 | PF11976 | 0.355 |
LIG_SUMO_SIM_par_1 | 376 | 382 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 736 | 742 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 760 | 766 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 884 | 890 | PF11976 | 0.521 |
LIG_SxIP_EBH_1 | 546 | 556 | PF03271 | 0.544 |
LIG_TRAF2_1 | 175 | 178 | PF00917 | 0.574 |
LIG_TRAF2_1 | 581 | 584 | PF00917 | 0.303 |
LIG_TRAF2_1 | 819 | 822 | PF00917 | 0.749 |
LIG_TRFH_1 | 894 | 898 | PF08558 | 0.523 |
LIG_WRC_WIRS_1 | 185 | 190 | PF05994 | 0.493 |
LIG_WRC_WIRS_1 | 877 | 882 | PF05994 | 0.503 |
MOD_CDC14_SPxK_1 | 830 | 833 | PF00782 | 0.399 |
MOD_CDK_SPK_2 | 67 | 72 | PF00069 | 0.374 |
MOD_CDK_SPxK_1 | 827 | 833 | PF00069 | 0.413 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.581 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.497 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.712 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.602 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.518 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.496 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.350 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.289 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.579 |
MOD_CK1_1 | 804 | 810 | PF00069 | 0.393 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.548 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.670 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.488 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.515 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.584 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.677 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.529 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.319 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.519 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.289 |
MOD_CK2_1 | 766 | 772 | PF00069 | 0.257 |
MOD_CK2_1 | 816 | 822 | PF00069 | 0.685 |
MOD_Cter_Amidation | 180 | 183 | PF01082 | 0.392 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.514 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.558 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.455 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.638 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.631 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.310 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.727 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.666 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.550 |
MOD_GlcNHglycan | 525 | 529 | PF01048 | 0.709 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.458 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.401 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.508 |
MOD_GlcNHglycan | 807 | 810 | PF01048 | 0.609 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.421 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.238 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.372 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.534 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.597 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.702 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.539 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.551 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.562 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.611 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.520 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.436 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.313 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.412 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.202 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.403 |
MOD_GSK3_1 | 793 | 800 | PF00069 | 0.423 |
MOD_GSK3_1 | 801 | 808 | PF00069 | 0.451 |
MOD_GSK3_1 | 823 | 830 | PF00069 | 0.705 |
MOD_GSK3_1 | 840 | 847 | PF00069 | 0.514 |
MOD_GSK3_1 | 851 | 858 | PF00069 | 0.441 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.490 |
MOD_LATS_1 | 748 | 754 | PF00433 | 0.334 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.543 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.533 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.627 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.442 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.513 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.716 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.430 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.343 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.395 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.390 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.338 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.433 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.544 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.443 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.115 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.355 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.154 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.313 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.279 |
MOD_NEK2_1 | 718 | 723 | PF00069 | 0.244 |
MOD_NEK2_1 | 741 | 746 | PF00069 | 0.298 |
MOD_NEK2_1 | 801 | 806 | PF00069 | 0.444 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.468 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.452 |
MOD_NEK2_1 | 876 | 881 | PF00069 | 0.360 |
MOD_NEK2_2 | 147 | 152 | PF00069 | 0.483 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.475 |
MOD_PIKK_1 | 355 | 361 | PF00454 | 0.647 |
MOD_PIKK_1 | 507 | 513 | PF00454 | 0.707 |
MOD_PIKK_1 | 613 | 619 | PF00454 | 0.380 |
MOD_PIKK_1 | 718 | 724 | PF00454 | 0.222 |
MOD_PKA_1 | 201 | 207 | PF00069 | 0.430 |
MOD_PKA_1 | 613 | 619 | PF00069 | 0.313 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.535 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.497 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.427 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.313 |
MOD_PKA_2 | 634 | 640 | PF00069 | 0.432 |
MOD_PKA_2 | 662 | 668 | PF00069 | 0.399 |
MOD_PKA_2 | 705 | 711 | PF00069 | 0.438 |
MOD_PKA_2 | 816 | 822 | PF00069 | 0.721 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.484 |
MOD_PKB_1 | 274 | 282 | PF00069 | 0.317 |
MOD_PKB_1 | 633 | 641 | PF00069 | 0.202 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.464 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.438 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.482 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.451 |
MOD_Plk_1 | 741 | 747 | PF00069 | 0.327 |
MOD_Plk_2-3 | 766 | 772 | PF00069 | 0.202 |
MOD_Plk_2-3 | 816 | 822 | PF00069 | 0.721 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.577 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.431 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.676 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.410 |
MOD_Plk_4 | 648 | 654 | PF00069 | 0.361 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.443 |
MOD_Plk_4 | 736 | 742 | PF00069 | 0.305 |
MOD_Plk_4 | 766 | 772 | PF00069 | 0.346 |
MOD_Plk_4 | 840 | 846 | PF00069 | 0.433 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.678 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.524 |
MOD_ProDKin_1 | 578 | 584 | PF00069 | 0.418 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.612 |
MOD_ProDKin_1 | 679 | 685 | PF00069 | 0.360 |
MOD_ProDKin_1 | 757 | 763 | PF00069 | 0.363 |
MOD_ProDKin_1 | 783 | 789 | PF00069 | 0.418 |
MOD_ProDKin_1 | 827 | 833 | PF00069 | 0.461 |
MOD_SUMO_for_1 | 420 | 423 | PF00179 | 0.544 |
MOD_SUMO_rev_2 | 256 | 262 | PF00179 | 0.415 |
TRG_DiLeu_BaEn_1 | 832 | 837 | PF01217 | 0.570 |
TRG_DiLeu_BaEn_3 | 35 | 41 | PF01217 | 0.322 |
TRG_DiLeu_BaLyEn_6 | 373 | 378 | PF01217 | 0.510 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 698 | 701 | PF00928 | 0.332 |
TRG_ER_diArg_1 | 162 | 165 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 481 | 484 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 554 | 556 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 613 | 615 | PF00400 | 0.305 |
TRG_ER_diArg_1 | 632 | 635 | PF00400 | 0.216 |
TRG_NES_CRM1_1 | 242 | 255 | PF08389 | 0.492 |
TRG_NES_CRM1_1 | 511 | 525 | PF08389 | 0.482 |
TRG_NES_CRM1_1 | 875 | 890 | PF08389 | 0.436 |
TRG_NES_CRM1_1 | 93 | 106 | PF08389 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 276 | 280 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 285 | 290 | PF00026 | 0.368 |
TRG_Pf-PMV_PEXEL_1 | 386 | 390 | PF00026 | 0.255 |
TRG_Pf-PMV_PEXEL_1 | 556 | 560 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 613 | 617 | PF00026 | 0.383 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I206 | Leptomonas seymouri | 56% | 98% |
A0A0S4J0P6 | Bodo saltans | 31% | 100% |
A0A1X0P5D0 | Trypanosomatidae | 36% | 100% |
A0A3S7X9N5 | Leishmania donovani | 81% | 100% |
A0A422MYM3 | Trypanosoma rangeli | 37% | 100% |
A4IBR4 | Leishmania infantum | 81% | 100% |
C9ZYV9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AFJ9 | Leishmania major | 80% | 100% |
Q8H1U5 | Arabidopsis thaliana | 25% | 100% |
V5BTC2 | Trypanosoma cruzi | 36% | 100% |