Uncharacterized Protein, Uncharacterized
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: A0A3S5H5H6
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 | 645 | 649 | PF00656 | 0.591 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.749 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.785 |
CLV_NRD_NRD_1 | 839 | 841 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 884 | 886 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 902 | 904 | PF00675 | 0.375 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.785 |
CLV_PCSK_KEX2_1 | 721 | 723 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 839 | 841 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 884 | 886 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 902 | 904 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 721 | 723 | PF00082 | 0.468 |
CLV_PCSK_PC7_1 | 451 | 457 | PF00082 | 0.753 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.759 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.724 |
CLV_PCSK_SKI1_1 | 714 | 718 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 755 | 759 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 803 | 807 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 819 | 823 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 860 | 864 | PF00082 | 0.460 |
DEG_APCC_DBOX_1 | 318 | 326 | PF00400 | 0.568 |
DEG_APCC_DBOX_1 | 713 | 721 | PF00400 | 0.474 |
DEG_SPOP_SBC_1 | 580 | 584 | PF00917 | 0.579 |
DOC_CKS1_1 | 101 | 106 | PF01111 | 0.765 |
DOC_CYCLIN_yCln2_LP_2 | 661 | 667 | PF00134 | 0.566 |
DOC_CYCLIN_yCln2_LP_2 | 849 | 855 | PF00134 | 0.476 |
DOC_MAPK_gen_1 | 455 | 465 | PF00069 | 0.761 |
DOC_MAPK_gen_1 | 711 | 720 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 839 | 849 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 458 | 467 | PF00069 | 0.757 |
DOC_MAPK_MEF2A_6 | 840 | 849 | PF00069 | 0.483 |
DOC_MAPK_RevD_3 | 870 | 885 | PF00069 | 0.460 |
DOC_MIT_MIM_1 | 146 | 154 | PF04212 | 0.595 |
DOC_PP2B_LxvP_1 | 518 | 521 | PF13499 | 0.697 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.830 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.756 |
DOC_USP7_UBL2_3 | 789 | 793 | PF12436 | 0.411 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 623 | 628 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 660 | 665 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 794 | 799 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.835 |
LIG_14-3-3_CanoR_1 | 222 | 231 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 352 | 358 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 36 | 41 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 368 | 376 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 477 | 485 | PF00244 | 0.828 |
LIG_14-3-3_CanoR_1 | 598 | 608 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 68 | 73 | PF00244 | 0.758 |
LIG_14-3-3_CanoR_1 | 688 | 695 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 803 | 809 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 810 | 816 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 91 | 95 | PF00244 | 0.663 |
LIG_APCC_ABBA_1 | 822 | 827 | PF00400 | 0.492 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.739 |
LIG_BIR_III_2 | 691 | 695 | PF00653 | 0.523 |
LIG_BRCT_BRCA1_1 | 261 | 265 | PF00533 | 0.683 |
LIG_Clathr_ClatBox_1 | 151 | 155 | PF01394 | 0.512 |
LIG_Clathr_ClatBox_1 | 846 | 850 | PF01394 | 0.495 |
LIG_eIF4E_1 | 158 | 164 | PF01652 | 0.479 |
LIG_EVH1_2 | 115 | 119 | PF00568 | 0.564 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.566 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.599 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.620 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.723 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.691 |
LIG_FHA_1 | 697 | 703 | PF00498 | 0.444 |
LIG_FHA_1 | 795 | 801 | PF00498 | 0.469 |
LIG_FHA_1 | 824 | 830 | PF00498 | 0.589 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.845 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.697 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.761 |
LIG_FHA_2 | 688 | 694 | PF00498 | 0.511 |
LIG_FHA_2 | 873 | 879 | PF00498 | 0.444 |
LIG_LIR_Apic_2 | 547 | 551 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 155 | 165 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 266 | 274 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 409 | 416 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 648 | 658 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 155 | 161 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 648 | 653 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.754 |
LIG_LIR_Nem_3 | 763 | 768 | PF02991 | 0.411 |
LIG_LYPXL_yS_3 | 185 | 188 | PF13949 | 0.666 |
LIG_NRBOX | 300 | 306 | PF00104 | 0.508 |
LIG_NRBOX | 556 | 562 | PF00104 | 0.552 |
LIG_NRBOX | 858 | 864 | PF00104 | 0.487 |
LIG_PCNA_PIPBox_1 | 133 | 142 | PF02747 | 0.641 |
LIG_PCNA_yPIPBox_3 | 902 | 915 | PF02747 | 0.510 |
LIG_Pex14_1 | 225 | 229 | PF04695 | 0.796 |
LIG_Pex14_1 | 278 | 282 | PF04695 | 0.469 |
LIG_RPA_C_Fungi | 835 | 847 | PF08784 | 0.595 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.470 |
LIG_SH2_CRK | 707 | 711 | PF00017 | 0.423 |
LIG_SH2_CRK | 72 | 76 | PF00017 | 0.753 |
LIG_SH2_CRK | 768 | 772 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 269 | 273 | PF00017 | 0.607 |
LIG_SH2_PTP2 | 410 | 413 | PF00017 | 0.593 |
LIG_SH2_PTP2 | 873 | 876 | PF00017 | 0.544 |
LIG_SH2_SRC | 294 | 297 | PF00017 | 0.508 |
LIG_SH2_SRC | 40 | 43 | PF00017 | 0.620 |
LIG_SH2_SRC | 732 | 735 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 141 | 145 | PF00017 | 0.623 |
LIG_SH2_STAP1 | 669 | 673 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 732 | 736 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 825 | 829 | PF00017 | 0.484 |
LIG_SH2_STAT3 | 289 | 292 | PF00017 | 0.512 |
LIG_SH2_STAT3 | 808 | 811 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.665 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.717 |
LIG_SH2_STAT5 | 765 | 768 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 825 | 828 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 873 | 876 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 906 | 909 | PF00017 | 0.500 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.634 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.712 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.583 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.696 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.775 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.713 |
LIG_SH3_3 | 861 | 867 | PF00018 | 0.448 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.764 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.608 |
LIG_SUMO_SIM_par_1 | 423 | 430 | PF11976 | 0.614 |
LIG_TRAF2_1 | 131 | 134 | PF00917 | 0.627 |
LIG_TRAF2_1 | 339 | 342 | PF00917 | 0.758 |
LIG_TRAF2_1 | 855 | 858 | PF00917 | 0.470 |
LIG_TYR_ITIM | 267 | 272 | PF00017 | 0.632 |
LIG_TYR_ITIM | 766 | 771 | PF00017 | 0.411 |
LIG_TYR_ITIM | 871 | 876 | PF00017 | 0.545 |
LIG_Vh1_VBS_1 | 347 | 365 | PF01044 | 0.543 |
LIG_WW_2 | 104 | 107 | PF00397 | 0.761 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.726 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.756 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.551 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.730 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.681 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.771 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.726 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.607 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.697 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.842 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.708 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.810 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.685 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.733 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.618 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.499 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.450 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.741 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.630 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.727 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.614 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.743 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.618 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.461 |
MOD_CK2_1 | 743 | 749 | PF00069 | 0.436 |
MOD_CK2_1 | 872 | 878 | PF00069 | 0.444 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.824 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.603 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.549 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.515 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.802 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.566 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.759 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.665 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.812 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.832 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.637 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.536 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.702 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.662 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.584 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.671 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.614 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.445 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.590 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.290 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.745 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.780 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.604 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.350 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.651 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.675 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.682 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.709 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.715 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.602 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.692 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.643 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.548 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.735 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.580 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.661 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.779 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.639 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.723 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.597 |
MOD_LATS_1 | 675 | 681 | PF00433 | 0.599 |
MOD_N-GLC_1 | 10 | 15 | PF02516 | 0.752 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.591 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.663 |
MOD_N-GLC_1 | 494 | 499 | PF02516 | 0.654 |
MOD_N-GLC_1 | 834 | 839 | PF02516 | 0.527 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.545 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.528 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.664 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.752 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.688 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.598 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.741 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.647 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.515 |
MOD_NEK2_1 | 668 | 673 | PF00069 | 0.399 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.573 |
MOD_NEK2_1 | 804 | 809 | PF00069 | 0.460 |
MOD_NEK2_2 | 553 | 558 | PF00069 | 0.421 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.595 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.388 |
MOD_PIKK_1 | 299 | 305 | PF00454 | 0.506 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.518 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.826 |
MOD_PKA_1 | 902 | 908 | PF00069 | 0.528 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.682 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.720 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.768 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.632 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.385 |
MOD_PKA_2 | 597 | 603 | PF00069 | 0.636 |
MOD_PKA_2 | 687 | 693 | PF00069 | 0.513 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.665 |
MOD_PKA_2 | 902 | 908 | PF00069 | 0.528 |
MOD_PKB_1 | 456 | 464 | PF00069 | 0.761 |
MOD_PKB_1 | 66 | 74 | PF00069 | 0.760 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.591 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.520 |
MOD_Plk_1 | 760 | 766 | PF00069 | 0.389 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.657 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.560 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.695 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.609 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.412 |
MOD_Plk_4 | 760 | 766 | PF00069 | 0.364 |
MOD_Plk_4 | 902 | 908 | PF00069 | 0.528 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.728 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.494 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.776 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.725 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.745 |
MOD_ProDKin_1 | 623 | 629 | PF00069 | 0.462 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.433 |
MOD_ProDKin_1 | 794 | 800 | PF00069 | 0.460 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.835 |
MOD_SUMO_for_1 | 676 | 679 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 740 | 748 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 814 | 821 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 857 | 862 | PF00179 | 0.498 |
TRG_DiLeu_BaEn_1 | 858 | 863 | PF01217 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 176 | 181 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.233 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.628 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.754 |
TRG_ENDOCYTIC_2 | 739 | 742 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 768 | 771 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 873 | 876 | PF00928 | 0.442 |
TRG_ER_diArg_1 | 318 | 321 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 449 | 452 | PF00400 | 0.756 |
TRG_ER_diArg_1 | 455 | 458 | PF00400 | 0.755 |
TRG_ER_diArg_1 | 839 | 842 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 883 | 885 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 901 | 903 | PF00400 | 0.377 |
TRG_NES_CRM1_1 | 854 | 865 | PF08389 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 320 | 324 | PF00026 | 0.653 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU62 | Leptomonas seymouri | 55% | 99% |
A4H487 | Leishmania braziliensis | 79% | 98% |
A4HSG3 | Leishmania infantum | 100% | 100% |
E9AKE7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
Q4QJG1 | Leishmania major | 93% | 100% |