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 | 2 |
GO:0000152 | nuclear ubiquitin ligase complex | 3 | 2 |
GO:0005680 | anaphase-promoting complex | 4 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0051286 | cell tip | 3 | 2 |
GO:0060187 | cell pole | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: E9AFJ9
Term | Name | Level | Count |
---|---|---|---|
GO:0000209 | protein polyubiquitination | 8 | 2 |
GO:0006508 | proteolysis | 4 | 10 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0007091 | metaphase/anaphase transition of mitotic cell cycle | 5 | 2 |
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:0010564 | regulation of cell cycle process | 5 | 2 |
GO:0010965 | regulation of mitotic sister chromatid separation | 6 | 2 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 10 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0033043 | regulation of organelle organization | 5 | 2 |
GO:0033044 | regulation of chromosome organization | 6 | 2 |
GO:0033045 | regulation of sister chromatid segregation | 5 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 2 |
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:0044770 | cell cycle phase transition | 3 | 2 |
GO:0044772 | mitotic cell cycle phase transition | 4 | 2 |
GO:0044784 | metaphase/anaphase transition of cell cycle | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051128 | regulation of cellular component organization | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 10 |
GO:0051726 | regulation of cell cycle | 4 | 2 |
GO:0051983 | regulation of chromosome segregation | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0070979 | protein K11-linked ubiquitination | 9 | 2 |
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:1903047 | mitotic cell cycle process | 3 | 2 |
GO:1905818 | regulation of chromosome separation | 5 | 2 |
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 | 186 | 190 | PF00656 | 0.748 |
CLV_C14_Caspase3-7 | 19 | 23 | PF00656 | 0.549 |
CLV_C14_Caspase3-7 | 198 | 202 | PF00656 | 0.748 |
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.447 |
CLV_C14_Caspase3-7 | 665 | 669 | PF00656 | 0.511 |
CLV_MEL_PAP_1 | 70 | 76 | PF00089 | 0.536 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.270 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 675 | 677 | PF00082 | 0.295 |
CLV_PCSK_PC1ET2_1 | 675 | 677 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 675 | 679 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 815 | 819 | PF00082 | 0.490 |
CLV_Separin_Metazoa | 851 | 855 | PF03568 | 0.548 |
DEG_APCC_DBOX_1 | 246 | 254 | PF00400 | 0.582 |
DEG_APCC_DBOX_1 | 522 | 530 | PF00400 | 0.415 |
DEG_SCF_TRCP1_1 | 189 | 195 | PF00400 | 0.561 |
DEG_SCF_TRCP1_1 | 647 | 652 | PF00400 | 0.402 |
DEG_SPOP_SBC_1 | 311 | 315 | PF00917 | 0.773 |
DEG_SPOP_SBC_1 | 826 | 830 | PF00917 | 0.490 |
DOC_CDC14_PxL_1 | 683 | 691 | PF14671 | 0.546 |
DOC_CKS1_1 | 126 | 131 | PF01111 | 0.469 |
DOC_CKS1_1 | 389 | 394 | PF01111 | 0.604 |
DOC_CKS1_1 | 734 | 739 | PF01111 | 0.449 |
DOC_CYCLIN_RxL_1 | 402 | 410 | PF00134 | 0.509 |
DOC_CYCLIN_RxL_1 | 518 | 528 | PF00134 | 0.440 |
DOC_MAPK_gen_1 | 516 | 524 | PF00069 | 0.557 |
DOC_MAPK_HePTP_8 | 70 | 82 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 418 | 427 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 518 | 526 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 73 | 82 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 760 | 767 | PF00069 | 0.550 |
DOC_PP1_RVXF_1 | 262 | 269 | PF00149 | 0.544 |
DOC_PP4_FxxP_1 | 734 | 737 | PF00568 | 0.388 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 638 | 642 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 826 | 830 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 831 | 835 | PF00917 | 0.530 |
DOC_USP7_UBL2_3 | 699 | 703 | PF12436 | 0.574 |
DOC_USP7_UBL2_3 | 837 | 841 | PF12436 | 0.579 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 618 | 623 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 733 | 738 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 759 | 764 | PF00397 | 0.563 |
LIG_14-3-3_CanoR_1 | 113 | 122 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 249 | 257 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 682 | 686 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 73 | 80 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 731 | 737 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 815 | 821 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 824 | 832 | PF00244 | 0.556 |
LIG_Actin_WH2_2 | 127 | 142 | PF00022 | 0.462 |
LIG_APCC_ABBA_1 | 29 | 34 | PF00400 | 0.566 |
LIG_BIR_III_2 | 329 | 333 | PF00653 | 0.752 |
LIG_BRCT_BRCA1_1 | 253 | 257 | PF00533 | 0.568 |
LIG_BRCT_BRCA1_1 | 443 | 447 | PF00533 | 0.417 |
LIG_BRCT_BRCA1_1 | 783 | 787 | PF00533 | 0.580 |
LIG_CaM_IQ_9 | 582 | 598 | PF13499 | 0.481 |
LIG_CSL_BTD_1 | 633 | 636 | PF09270 | 0.556 |
LIG_CSL_BTD_1 | 684 | 687 | PF09270 | 0.546 |
LIG_EVH1_1 | 634 | 638 | PF00568 | 0.418 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.421 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.484 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.530 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.543 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.541 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.396 |
LIG_FHA_1 | 770 | 776 | PF00498 | 0.448 |
LIG_FHA_1 | 816 | 822 | PF00498 | 0.447 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.627 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.764 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.591 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.448 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.470 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.574 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.458 |
LIG_FHA_2 | 793 | 799 | PF00498 | 0.683 |
LIG_GBD_Chelix_1 | 131 | 139 | PF00786 | 0.538 |
LIG_LIR_Gen_1 | 365 | 375 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 536 | 546 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 784 | 794 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 632 | 637 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 672 | 677 | PF02991 | 0.527 |
LIG_MYND_1 | 608 | 612 | PF01753 | 0.511 |
LIG_MYND_3 | 102 | 106 | PF01753 | 0.563 |
LIG_MYND_3 | 378 | 382 | PF01753 | 0.536 |
LIG_NRBOX | 350 | 356 | PF00104 | 0.407 |
LIG_OCRL_FandH_1 | 162 | 174 | PF00620 | 0.411 |
LIG_PCNA_yPIPBox_3 | 841 | 853 | PF02747 | 0.486 |
LIG_Pex14_2 | 161 | 165 | PF04695 | 0.313 |
LIG_Pex14_2 | 433 | 437 | PF04695 | 0.507 |
LIG_Pex14_2 | 717 | 721 | PF04695 | 0.511 |
LIG_PTB_Apo_2 | 493 | 500 | PF02174 | 0.536 |
LIG_Rb_pABgroove_1 | 711 | 719 | PF01858 | 0.556 |
LIG_RPA_C_Fungi | 584 | 596 | PF08784 | 0.467 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.539 |
LIG_SH2_CRK | 674 | 678 | PF00017 | 0.408 |
LIG_SH2_CRK | 870 | 874 | PF00017 | 0.494 |
LIG_SH2_NCK_1 | 870 | 874 | PF00017 | 0.555 |
LIG_SH2_SRC | 4 | 7 | PF00017 | 0.617 |
LIG_SH2_STAT3 | 386 | 389 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.507 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.607 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.653 |
LIG_SH3_3 | 632 | 638 | PF00018 | 0.365 |
LIG_SH3_3 | 705 | 711 | PF00018 | 0.380 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.559 |
LIG_SH3_4 | 549 | 556 | PF00018 | 0.380 |
LIG_SUMO_SIM_anti_2 | 419 | 427 | PF11976 | 0.414 |
LIG_SUMO_SIM_anti_2 | 50 | 59 | PF11976 | 0.487 |
LIG_SUMO_SIM_anti_2 | 625 | 630 | PF11976 | 0.365 |
LIG_SUMO_SIM_anti_2 | 742 | 748 | PF11976 | 0.358 |
LIG_SUMO_SIM_anti_2 | 848 | 855 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 352 | 358 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 712 | 718 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 860 | 866 | PF11976 | 0.554 |
LIG_SxIP_EBH_1 | 522 | 532 | PF03271 | 0.577 |
LIG_TRAF2_1 | 150 | 153 | PF00917 | 0.610 |
LIG_TRAF2_1 | 557 | 560 | PF00917 | 0.338 |
LIG_TRAF2_1 | 662 | 665 | PF00917 | 0.380 |
LIG_TRAF2_1 | 795 | 798 | PF00917 | 0.783 |
LIG_TRFH_1 | 870 | 874 | PF08558 | 0.558 |
LIG_WRC_WIRS_1 | 160 | 165 | PF05994 | 0.507 |
LIG_WRC_WIRS_1 | 853 | 858 | PF05994 | 0.528 |
LIG_WW_2 | 635 | 638 | PF00397 | 0.435 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.530 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.515 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.760 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.640 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.605 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.547 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.343 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.584 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.771 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.521 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.545 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.392 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.769 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.561 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.599 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.322 |
MOD_CK2_1 | 598 | 604 | PF00069 | 0.310 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.439 |
MOD_CK2_1 | 792 | 798 | PF00069 | 0.727 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.519 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.694 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.621 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.609 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.341 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.774 |
MOD_GlcNHglycan | 300 | 305 | PF01048 | 0.667 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.594 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.545 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.467 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.540 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.462 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.470 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.365 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.400 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.337 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.267 |
MOD_GlcNHglycan | 783 | 786 | PF01048 | 0.636 |
MOD_GlcNHglycan | 796 | 801 | PF01048 | 0.754 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.540 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.580 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.553 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.568 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.707 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.572 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.586 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.552 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.609 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.463 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.687 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.332 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.447 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.340 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.439 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.521 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.464 |
MOD_GSK3_1 | 792 | 799 | PF00069 | 0.674 |
MOD_GSK3_1 | 816 | 823 | PF00069 | 0.548 |
MOD_GSK3_1 | 827 | 834 | PF00069 | 0.548 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.398 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.569 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.576 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.410 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.474 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.544 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.750 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.581 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.368 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.421 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.416 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.362 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.479 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.507 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.460 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.246 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.298 |
MOD_NEK2_1 | 717 | 722 | PF00069 | 0.365 |
MOD_NEK2_1 | 816 | 821 | PF00069 | 0.490 |
MOD_NEK2_1 | 842 | 847 | PF00069 | 0.520 |
MOD_NEK2_1 | 852 | 857 | PF00069 | 0.403 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.557 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.695 |
MOD_PIKK_1 | 483 | 489 | PF00454 | 0.737 |
MOD_PIKK_1 | 589 | 595 | PF00454 | 0.404 |
MOD_PKA_1 | 589 | 595 | PF00069 | 0.338 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.501 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.687 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.338 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.457 |
MOD_PKA_2 | 638 | 644 | PF00069 | 0.421 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.462 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.516 |
MOD_PKA_2 | 792 | 798 | PF00069 | 0.760 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.512 |
MOD_Plk_1 | 440 | 446 | PF00069 | 0.453 |
MOD_Plk_1 | 717 | 723 | PF00069 | 0.400 |
MOD_Plk_2-3 | 792 | 798 | PF00069 | 0.763 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.600 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.461 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.430 |
MOD_Plk_4 | 624 | 630 | PF00069 | 0.408 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.435 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.469 |
MOD_Plk_4 | 712 | 718 | PF00069 | 0.316 |
MOD_Plk_4 | 816 | 822 | PF00069 | 0.479 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.467 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.739 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.557 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.638 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.422 |
MOD_ProDKin_1 | 618 | 624 | PF00069 | 0.448 |
MOD_ProDKin_1 | 733 | 739 | PF00069 | 0.549 |
MOD_ProDKin_1 | 759 | 765 | PF00069 | 0.557 |
MOD_SUMO_for_1 | 396 | 399 | PF00179 | 0.585 |
MOD_SUMO_rev_2 | 231 | 237 | PF00179 | 0.441 |
TRG_DiLeu_BaEn_1 | 808 | 813 | PF01217 | 0.599 |
TRG_DiLeu_BaEn_4 | 665 | 671 | PF01217 | 0.380 |
TRG_DiLeu_BaLyEn_6 | 349 | 354 | PF01217 | 0.534 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 674 | 677 | PF00928 | 0.357 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 457 | 460 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 516 | 519 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 530 | 532 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 589 | 591 | PF00400 | 0.330 |
TRG_NES_CRM1_1 | 68 | 83 | PF08389 | 0.542 |
TRG_NES_CRM1_1 | 712 | 727 | PF08389 | 0.427 |
TRG_NES_CRM1_1 | 851 | 866 | PF08389 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 15 | 19 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 532 | 536 | PF00026 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 589 | 593 | PF00026 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I206 | Leptomonas seymouri | 54% | 95% |
A0A0S4J0P6 | Bodo saltans | 30% | 100% |
A0A1X0P5D0 | Trypanosomatidae | 36% | 100% |
A0A3S7X9N5 | Leishmania donovani | 94% | 100% |
A0A422MYM3 | Trypanosoma rangeli | 37% | 100% |
A4HN46 | Leishmania braziliensis | 80% | 97% |
A4IBR4 | Leishmania infantum | 94% | 100% |
C9ZYV9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
V5BTC2 | Trypanosoma cruzi | 37% | 100% |