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 | 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: Q4QJG1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0007088 | regulation of mitotic nuclear division | 6 | 2 |
GO:0007091 | metaphase/anaphase transition of mitotic cell cycle | 5 | 2 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0010564 | regulation of cell cycle process | 5 | 2 |
GO:0010638 | positive regulation of organelle organization | 6 | 2 |
GO:0010965 | regulation of mitotic sister chromatid separation | 6 | 2 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0030071 | regulation of mitotic metaphase/anaphase transition | 7 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0031145 | anaphase-promoting complex-dependent catabolic process | 7 | 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:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
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:0045787 | positive regulation of cell cycle | 5 | 2 |
GO:0045840 | positive regulation of mitotic nuclear division | 7 | 2 |
GO:0045842 | positive regulation of mitotic metaphase/anaphase transition | 8 | 2 |
GO:0045931 | positive regulation of mitotic cell cycle | 6 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048522 | positive regulation of cellular process | 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:0051130 | positive regulation of cellular component organization | 5 | 2 |
GO:0051301 | cell division | 2 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0051726 | regulation of cell cycle | 4 | 2 |
GO:0051783 | regulation of nuclear division | 6 | 2 |
GO:0051785 | positive regulation of nuclear division | 7 | 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:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090068 | positive regulation of cell cycle process | 6 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1901970 | positive regulation of mitotic sister chromatid separation | 7 | 2 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 2 |
GO:1901989 | positive regulation of cell cycle phase transition | 7 | 2 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 2 |
GO:1901992 | positive regulation of mitotic cell cycle phase transition | 7 | 2 |
GO:1902099 | regulation of metaphase/anaphase transition of cell cycle | 6 | 2 |
GO:1902101 | positive regulation of metaphase/anaphase transition of cell cycle | 7 | 2 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
GO:1905818 | regulation of chromosome separation | 5 | 2 |
GO:1905820 | positive regulation of chromosome separation | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 645 | 649 | PF00656 | 0.447 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.816 |
CLV_NRD_NRD_1 | 839 | 841 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 884 | 886 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 902 | 904 | PF00675 | 0.338 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.816 |
CLV_PCSK_KEX2_1 | 721 | 723 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 839 | 841 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 884 | 886 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 902 | 904 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 721 | 723 | PF00082 | 0.376 |
CLV_PCSK_PC7_1 | 453 | 459 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 538 | 542 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 714 | 718 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 755 | 759 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 803 | 807 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 819 | 823 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 860 | 864 | PF00082 | 0.423 |
DEG_APCC_DBOX_1 | 321 | 329 | PF00400 | 0.476 |
DEG_APCC_DBOX_1 | 713 | 721 | PF00400 | 0.371 |
DEG_SPOP_SBC_1 | 314 | 318 | PF00917 | 0.358 |
DEG_SPOP_SBC_1 | 597 | 601 | PF00917 | 0.571 |
DEG_SPOP_SBC_1 | 621 | 625 | PF00917 | 0.437 |
DOC_CKS1_1 | 104 | 109 | PF01111 | 0.650 |
DOC_CYCLIN_yCln2_LP_2 | 661 | 667 | PF00134 | 0.439 |
DOC_CYCLIN_yCln2_LP_2 | 849 | 855 | PF00134 | 0.303 |
DOC_MAPK_gen_1 | 457 | 467 | PF00069 | 0.649 |
DOC_MAPK_gen_1 | 711 | 720 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 839 | 849 | PF00069 | 0.304 |
DOC_MAPK_MEF2A_6 | 460 | 469 | PF00069 | 0.644 |
DOC_MAPK_MEF2A_6 | 840 | 849 | PF00069 | 0.304 |
DOC_MAPK_RevD_3 | 870 | 885 | PF00069 | 0.354 |
DOC_MIT_MIM_1 | 149 | 157 | PF04212 | 0.491 |
DOC_PP2B_LxvP_1 | 520 | 523 | PF13499 | 0.580 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.623 |
DOC_USP7_UBL2_3 | 789 | 793 | PF12436 | 0.304 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 623 | 628 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 794 | 799 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.700 |
LIG_14-3-3_CanoR_1 | 225 | 234 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 302 | 310 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 354 | 360 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 370 | 378 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 479 | 487 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 598 | 608 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 688 | 695 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 71 | 76 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 803 | 809 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 810 | 816 | PF00244 | 0.428 |
LIG_APCC_ABBA_1 | 822 | 827 | PF00400 | 0.304 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.611 |
LIG_BIR_III_2 | 691 | 695 | PF00653 | 0.426 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.608 |
LIG_Clathr_ClatBox_1 | 154 | 158 | PF01394 | 0.434 |
LIG_Clathr_ClatBox_1 | 846 | 850 | PF01394 | 0.304 |
LIG_eIF4E_1 | 161 | 167 | PF01652 | 0.422 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.483 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.541 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.490 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.401 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.487 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.474 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.621 |
LIG_FHA_1 | 697 | 703 | PF00498 | 0.338 |
LIG_FHA_1 | 795 | 801 | PF00498 | 0.371 |
LIG_FHA_1 | 824 | 830 | PF00498 | 0.455 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.705 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.618 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.609 |
LIG_FHA_2 | 688 | 694 | PF00498 | 0.411 |
LIG_FHA_2 | 873 | 879 | PF00498 | 0.338 |
LIG_LIR_Apic_2 | 549 | 553 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 158 | 168 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 269 | 277 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 411 | 418 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 648 | 658 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 179 | 184 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 648 | 653 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 74 | 78 | PF02991 | 0.719 |
LIG_LIR_Nem_3 | 763 | 768 | PF02991 | 0.304 |
LIG_LYPXL_yS_3 | 188 | 191 | PF13949 | 0.667 |
LIG_NRBOX | 303 | 309 | PF00104 | 0.414 |
LIG_NRBOX | 558 | 564 | PF00104 | 0.452 |
LIG_NRBOX | 858 | 864 | PF00104 | 0.384 |
LIG_PCNA_PIPBox_1 | 136 | 145 | PF02747 | 0.521 |
LIG_PCNA_yPIPBox_3 | 902 | 915 | PF02747 | 0.404 |
LIG_Pex14_1 | 228 | 232 | PF04695 | 0.645 |
LIG_Pex14_1 | 281 | 285 | PF04695 | 0.357 |
LIG_PROFILIN_1 | 5 | 11 | PF00235 | 0.548 |
LIG_RPA_C_Fungi | 835 | 847 | PF08784 | 0.369 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.397 |
LIG_SH2_CRK | 707 | 711 | PF00017 | 0.377 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.711 |
LIG_SH2_CRK | 768 | 772 | PF00017 | 0.304 |
LIG_SH2_NCK_1 | 272 | 276 | PF00017 | 0.499 |
LIG_SH2_PTP2 | 412 | 415 | PF00017 | 0.482 |
LIG_SH2_PTP2 | 873 | 876 | PF00017 | 0.402 |
LIG_SH2_SRC | 297 | 300 | PF00017 | 0.406 |
LIG_SH2_SRC | 732 | 735 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 669 | 673 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 732 | 736 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 825 | 829 | PF00017 | 0.304 |
LIG_SH2_STAT3 | 292 | 295 | PF00017 | 0.410 |
LIG_SH2_STAT3 | 808 | 811 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 765 | 768 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 825 | 828 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 873 | 876 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 906 | 909 | PF00017 | 0.395 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.654 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.573 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.596 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.562 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.679 |
LIG_SH3_3 | 861 | 867 | PF00018 | 0.372 |
LIG_SUMO_SIM_anti_2 | 516 | 522 | PF11976 | 0.513 |
LIG_SUMO_SIM_par_1 | 273 | 279 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 425 | 432 | PF11976 | 0.512 |
LIG_TRAF2_1 | 134 | 137 | PF00917 | 0.515 |
LIG_TRAF2_1 | 341 | 344 | PF00917 | 0.607 |
LIG_TRAF2_1 | 408 | 411 | PF00917 | 0.463 |
LIG_TRAF2_1 | 855 | 858 | PF00917 | 0.304 |
LIG_TYR_ITIM | 270 | 275 | PF00017 | 0.583 |
LIG_TYR_ITIM | 766 | 771 | PF00017 | 0.304 |
LIG_TYR_ITIM | 871 | 876 | PF00017 | 0.402 |
LIG_Vh1_VBS_1 | 349 | 367 | PF01044 | 0.452 |
LIG_WW_2 | 107 | 110 | PF00397 | 0.648 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.665 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.461 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.624 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.403 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.626 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.697 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.589 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.533 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.588 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.699 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.583 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.615 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.647 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.612 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.438 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.342 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.636 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.520 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.620 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.566 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.601 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.522 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.413 |
MOD_CK2_1 | 743 | 749 | PF00069 | 0.325 |
MOD_CK2_1 | 872 | 878 | PF00069 | 0.338 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.797 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.647 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.503 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.418 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.673 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.524 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.622 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.610 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.589 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.608 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.701 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.600 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.542 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.578 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.564 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.599 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.534 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.619 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.573 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.387 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.446 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.294 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.640 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.697 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.632 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.534 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.552 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.607 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.650 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.606 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.527 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.609 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.510 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.534 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.662 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.535 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.735 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.559 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.452 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.623 |
MOD_LATS_1 | 675 | 681 | PF00433 | 0.455 |
MOD_N-GLC_1 | 13 | 18 | PF02516 | 0.654 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.496 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.593 |
MOD_N-GLC_1 | 834 | 839 | PF02516 | 0.304 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.472 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.427 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.564 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.600 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.558 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.493 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.649 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.562 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.432 |
MOD_NEK2_1 | 668 | 673 | PF00069 | 0.298 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.429 |
MOD_NEK2_1 | 804 | 809 | PF00069 | 0.359 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.548 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.518 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.321 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.411 |
MOD_PIKK_1 | 369 | 375 | PF00454 | 0.422 |
MOD_PIKK_1 | 505 | 511 | PF00454 | 0.790 |
MOD_PKA_1 | 902 | 908 | PF00069 | 0.422 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.599 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.576 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.335 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.570 |
MOD_PKA_2 | 597 | 603 | PF00069 | 0.620 |
MOD_PKA_2 | 687 | 693 | PF00069 | 0.413 |
MOD_PKA_2 | 902 | 908 | PF00069 | 0.422 |
MOD_PKB_1 | 458 | 466 | PF00069 | 0.647 |
MOD_PKB_1 | 69 | 77 | PF00069 | 0.636 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.498 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.415 |
MOD_Plk_1 | 760 | 766 | PF00069 | 0.284 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.518 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.557 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.537 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.627 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.366 |
MOD_Plk_4 | 760 | 766 | PF00069 | 0.304 |
MOD_Plk_4 | 902 | 908 | PF00069 | 0.422 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.605 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.605 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.692 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.631 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.643 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.501 |
MOD_ProDKin_1 | 623 | 629 | PF00069 | 0.431 |
MOD_ProDKin_1 | 794 | 800 | PF00069 | 0.377 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.699 |
MOD_SUMO_for_1 | 676 | 679 | PF00179 | 0.390 |
MOD_SUMO_rev_2 | 740 | 748 | PF00179 | 0.369 |
MOD_SUMO_rev_2 | 749 | 757 | PF00179 | 0.285 |
MOD_SUMO_rev_2 | 814 | 821 | PF00179 | 0.399 |
MOD_SUMO_rev_2 | 857 | 862 | PF00179 | 0.398 |
TRG_DiLeu_BaEn_1 | 858 | 863 | PF01217 | 0.376 |
TRG_DiLeu_BaLyEn_6 | 179 | 184 | PF01217 | 0.388 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 739 | 742 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.712 |
TRG_ENDOCYTIC_2 | 768 | 771 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 873 | 876 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 321 | 324 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 395 | 397 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 457 | 460 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 69 | 72 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 839 | 842 | PF00400 | 0.304 |
TRG_ER_diArg_1 | 883 | 885 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 901 | 903 | PF00400 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 302 | 306 | PF00026 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 323 | 327 | PF00026 | 0.529 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU62 | Leptomonas seymouri | 56% | 99% |
A0A3S5H5H6 | Leishmania donovani | 93% | 100% |
A4H487 | Leishmania braziliensis | 81% | 100% |
A4HSG3 | Leishmania infantum | 93% | 100% |
E9AKE7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |