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: 6 |
NetGPI | no | yes: 0, no: 6 |
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: E9AKE7
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007088 | regulation of mitotic nuclear division | 6 | 1 |
GO:0007091 | metaphase/anaphase transition of mitotic cell cycle | 5 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010638 | positive regulation of organelle organization | 6 | 1 |
GO:0010965 | regulation of mitotic sister chromatid separation | 6 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0030071 | regulation of mitotic metaphase/anaphase transition | 7 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031145 | anaphase-promoting complex-dependent catabolic process | 7 | 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:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 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:0045787 | positive regulation of cell cycle | 5 | 1 |
GO:0045840 | positive regulation of mitotic nuclear division | 7 | 1 |
GO:0045842 | positive regulation of mitotic metaphase/anaphase transition | 8 | 1 |
GO:0045931 | positive regulation of mitotic cell cycle | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 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:0051130 | positive regulation of cellular component organization | 5 | 1 |
GO:0051301 | cell division | 2 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0051783 | regulation of nuclear division | 6 | 1 |
GO:0051785 | positive regulation of nuclear division | 7 | 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:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090068 | positive regulation of cell cycle process | 6 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901970 | positive regulation of mitotic sister chromatid separation | 7 | 1 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901989 | positive regulation of cell cycle phase transition | 7 | 1 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 1 |
GO:1901992 | positive regulation of mitotic cell cycle phase transition | 7 | 1 |
GO:1902099 | regulation of metaphase/anaphase transition of cell cycle | 6 | 1 |
GO:1902101 | positive regulation of metaphase/anaphase transition of cell cycle | 7 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
GO:1905818 | regulation of chromosome separation | 5 | 1 |
GO:1905820 | positive regulation of chromosome separation | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 638 | 642 | PF00656 | 0.474 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 832 | 834 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 877 | 879 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 895 | 897 | PF00675 | 0.337 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 714 | 716 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 832 | 834 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 877 | 879 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 895 | 897 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 714 | 716 | PF00082 | 0.377 |
CLV_PCSK_PC7_1 | 446 | 452 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 707 | 711 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 748 | 752 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 796 | 800 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 812 | 816 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 853 | 857 | PF00082 | 0.341 |
DEG_APCC_DBOX_1 | 313 | 321 | PF00400 | 0.464 |
DEG_APCC_DBOX_1 | 706 | 714 | PF00400 | 0.376 |
DEG_SPOP_SBC_1 | 573 | 577 | PF00917 | 0.520 |
DEG_SPOP_SBC_1 | 593 | 597 | PF00917 | 0.609 |
DOC_CKS1_1 | 97 | 102 | PF01111 | 0.647 |
DOC_CYCLIN_yCln2_LP_2 | 654 | 660 | PF00134 | 0.444 |
DOC_MAPK_gen_1 | 321 | 330 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 450 | 460 | PF00069 | 0.665 |
DOC_MAPK_gen_1 | 704 | 713 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 832 | 842 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 453 | 462 | PF00069 | 0.661 |
DOC_MAPK_MEF2A_6 | 833 | 842 | PF00069 | 0.312 |
DOC_MAPK_RevD_3 | 863 | 878 | PF00069 | 0.362 |
DOC_MIT_MIM_1 | 142 | 150 | PF04212 | 0.472 |
DOC_PP2B_LxvP_1 | 513 | 516 | PF13499 | 0.604 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.807 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 613 | 617 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 674 | 678 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.651 |
DOC_USP7_UBL2_3 | 782 | 786 | PF12436 | 0.312 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 616 | 621 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 787 | 792 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 217 | 226 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 347 | 353 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 363 | 371 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 472 | 480 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 591 | 601 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 64 | 69 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 681 | 688 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 796 | 802 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 803 | 809 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 92 | 101 | PF00244 | 0.644 |
LIG_APCC_ABBA_1 | 815 | 820 | PF00400 | 0.312 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.648 |
LIG_BIR_III_2 | 684 | 688 | PF00653 | 0.425 |
LIG_BRCT_BRCA1_1 | 9 | 13 | PF00533 | 0.538 |
LIG_Clathr_ClatBox_1 | 147 | 151 | PF01394 | 0.412 |
LIG_Clathr_ClatBox_1 | 839 | 843 | PF01394 | 0.312 |
LIG_eIF4E_1 | 154 | 160 | PF01652 | 0.380 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.502 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.471 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.601 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.665 |
LIG_FHA_1 | 609 | 615 | PF00498 | 0.593 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.342 |
LIG_FHA_1 | 788 | 794 | PF00498 | 0.371 |
LIG_FHA_1 | 817 | 823 | PF00498 | 0.461 |
LIG_FHA_1 | 844 | 850 | PF00498 | 0.225 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.714 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.629 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.626 |
LIG_FHA_2 | 681 | 687 | PF00498 | 0.412 |
LIG_FHA_2 | 866 | 872 | PF00498 | 0.346 |
LIG_LIR_Apic_2 | 542 | 546 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 151 | 161 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 404 | 411 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 172 | 177 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 641 | 646 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 67 | 71 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 756 | 761 | PF02991 | 0.312 |
LIG_LYPXL_yS_3 | 181 | 184 | PF13949 | 0.549 |
LIG_NRBOX | 295 | 301 | PF00104 | 0.394 |
LIG_NRBOX | 551 | 557 | PF00104 | 0.448 |
LIG_NRBOX | 851 | 857 | PF00104 | 0.312 |
LIG_PCNA_PIPBox_1 | 129 | 138 | PF02747 | 0.508 |
LIG_PCNA_yPIPBox_3 | 895 | 908 | PF02747 | 0.411 |
LIG_Pex14_1 | 220 | 224 | PF04695 | 0.668 |
LIG_Pex14_1 | 273 | 277 | PF04695 | 0.364 |
LIG_RPA_C_Fungi | 828 | 840 | PF08784 | 0.388 |
LIG_SH2_CRK | 174 | 178 | PF00017 | 0.370 |
LIG_SH2_CRK | 356 | 360 | PF00017 | 0.340 |
LIG_SH2_CRK | 68 | 72 | PF00017 | 0.651 |
LIG_SH2_CRK | 700 | 704 | PF00017 | 0.382 |
LIG_SH2_CRK | 761 | 765 | PF00017 | 0.312 |
LIG_SH2_PTP2 | 405 | 408 | PF00017 | 0.468 |
LIG_SH2_PTP2 | 866 | 869 | PF00017 | 0.420 |
LIG_SH2_SRC | 135 | 138 | PF00017 | 0.376 |
LIG_SH2_SRC | 16 | 19 | PF00017 | 0.530 |
LIG_SH2_SRC | 289 | 292 | PF00017 | 0.394 |
LIG_SH2_SRC | 725 | 728 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 662 | 666 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 725 | 729 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 818 | 822 | PF00017 | 0.312 |
LIG_SH2_STAT3 | 284 | 287 | PF00017 | 0.404 |
LIG_SH2_STAT3 | 801 | 804 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 758 | 761 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 818 | 821 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 866 | 869 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 899 | 902 | PF00017 | 0.402 |
LIG_SH3_1 | 36 | 42 | PF00018 | 0.531 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.556 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.672 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.531 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.511 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.678 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.532 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.636 |
LIG_SH3_3 | 854 | 860 | PF00018 | 0.291 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.655 |
LIG_SUMO_SIM_par_1 | 265 | 271 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 418 | 425 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 492 | 497 | PF11976 | 0.525 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.488 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.622 |
LIG_TRAF2_1 | 401 | 404 | PF00917 | 0.433 |
LIG_TRAF2_1 | 848 | 851 | PF00917 | 0.312 |
LIG_TYR_ITIM | 262 | 267 | PF00017 | 0.552 |
LIG_TYR_ITIM | 759 | 764 | PF00017 | 0.312 |
LIG_TYR_ITIM | 864 | 869 | PF00017 | 0.422 |
LIG_WW_2 | 100 | 103 | PF00397 | 0.639 |
MOD_CDK_SPxxK_3 | 85 | 92 | PF00069 | 0.533 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.617 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.451 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.320 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.384 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.622 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.713 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.605 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.422 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.632 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.823 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.596 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.645 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.560 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.427 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.348 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.491 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.640 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.577 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.618 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.500 |
MOD_CK2_1 | 680 | 686 | PF00069 | 0.414 |
MOD_CK2_1 | 736 | 742 | PF00069 | 0.340 |
MOD_CK2_1 | 865 | 871 | PF00069 | 0.346 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.753 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.657 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.371 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.458 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.439 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.723 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.533 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.600 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.697 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.612 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.744 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.624 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.614 |
MOD_GlcNHglycan | 571 | 574 | PF01048 | 0.580 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.553 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.645 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.595 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.401 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.465 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.296 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.699 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.527 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.319 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.576 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.595 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.577 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.614 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.515 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.514 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.431 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.819 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.611 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.745 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.591 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.471 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.626 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.578 |
MOD_LATS_1 | 668 | 674 | PF00433 | 0.474 |
MOD_N-GLC_1 | 489 | 494 | PF02516 | 0.665 |
MOD_N-GLC_1 | 827 | 832 | PF02516 | 0.312 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.432 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.426 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.587 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.627 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.617 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.611 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.490 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.675 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.564 |
MOD_NEK2_1 | 646 | 651 | PF00069 | 0.424 |
MOD_NEK2_1 | 661 | 666 | PF00069 | 0.303 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.446 |
MOD_NEK2_1 | 797 | 802 | PF00069 | 0.361 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.540 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.542 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.302 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.391 |
MOD_PIKK_1 | 362 | 368 | PF00454 | 0.395 |
MOD_PIKK_1 | 498 | 504 | PF00454 | 0.703 |
MOD_PIKK_1 | 600 | 606 | PF00454 | 0.510 |
MOD_PIKK_1 | 843 | 849 | PF00454 | 0.207 |
MOD_PKA_1 | 895 | 901 | PF00069 | 0.429 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.577 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.617 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.560 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.303 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.553 |
MOD_PKA_2 | 680 | 686 | PF00069 | 0.414 |
MOD_PKA_2 | 895 | 901 | PF00069 | 0.429 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.642 |
MOD_PKB_1 | 451 | 459 | PF00069 | 0.663 |
MOD_PKB_1 | 62 | 70 | PF00069 | 0.666 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.452 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.515 |
MOD_Plk_1 | 753 | 759 | PF00069 | 0.291 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.565 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.448 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.538 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.515 |
MOD_Plk_4 | 698 | 704 | PF00069 | 0.371 |
MOD_Plk_4 | 753 | 759 | PF00069 | 0.312 |
MOD_Plk_4 | 895 | 901 | PF00069 | 0.429 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.675 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.697 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.568 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.635 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.651 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.520 |
MOD_ProDKin_1 | 616 | 622 | PF00069 | 0.416 |
MOD_ProDKin_1 | 787 | 793 | PF00069 | 0.377 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.658 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.639 |
MOD_SUMO_for_1 | 669 | 672 | PF00179 | 0.398 |
MOD_SUMO_rev_2 | 733 | 741 | PF00179 | 0.388 |
MOD_SUMO_rev_2 | 807 | 814 | PF00179 | 0.312 |
MOD_SUMO_rev_2 | 850 | 855 | PF00179 | 0.326 |
TRG_DiLeu_BaEn_1 | 851 | 856 | PF01217 | 0.312 |
TRG_DiLeu_BaLyEn_6 | 172 | 177 | PF01217 | 0.356 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.229 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.652 |
TRG_ENDOCYTIC_2 | 700 | 703 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 732 | 735 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 761 | 764 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 866 | 869 | PF00928 | 0.345 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 450 | 453 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 62 | 65 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 832 | 835 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 876 | 878 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 894 | 896 | PF00400 | 0.340 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.520 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU62 | Leptomonas seymouri | 55% | 99% |
A0A3S5H5H6 | Leishmania donovani | 90% | 99% |
A4H487 | Leishmania braziliensis | 80% | 98% |
A4HSG3 | Leishmania infantum | 90% | 99% |
Q4QJG1 | Leishmania major | 91% | 100% |