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: 5 |
NetGPI | no | yes: 0, no: 5 |
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:0031461 | cullin-RING ubiquitin ligase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 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: Q4QAF9
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:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 6 |
GO:0009894 | regulation of catabolic process | 4 | 2 |
GO:0009896 | positive regulation of catabolic process | 5 | 2 |
GO:0009987 | cellular process | 1 | 6 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 6 |
GO:0019222 | regulation of metabolic process | 3 | 6 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030162 | regulation of proteolysis | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0031145 | anaphase-promoting complex-dependent catabolic process | 7 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 2 |
GO:0031329 | regulation of cellular catabolic process | 5 | 2 |
GO:0031331 | positive regulation of cellular catabolic process | 6 | 2 |
GO:0032434 | regulation of proteasomal ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0032436 | positive regulation of proteasomal ubiquitin-dependent protein catabolic process | 8 | 2 |
GO:0042176 | regulation of protein catabolic process | 5 | 2 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 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:0045732 | positive regulation of protein catabolic process | 6 | 2 |
GO:0045862 | positive regulation of proteolysis | 7 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 6 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 6 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 6 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 6 |
GO:0051246 | regulation of protein metabolic process | 5 | 6 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 6 |
GO:0051301 | cell division | 2 | 6 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 6 |
GO:0061136 | regulation of proteasomal protein catabolic process | 6 | 2 |
GO:0065007 | biological regulation | 1 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 6 |
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:1901800 | positive regulation of proteasomal protein catabolic process | 7 | 2 |
GO:1903050 | regulation of proteolysis involved in protein catabolic process | 7 | 2 |
GO:1903052 | positive regulation of proteolysis involved in protein catabolic process | 8 | 2 |
GO:1905784 | regulation of anaphase-promoting complex-dependent catabolic process | 8 | 2 |
GO:1905786 | positive regulation of anaphase-promoting complex-dependent catabolic process | 9 | 2 |
GO:2000058 | regulation of ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:2000060 | positive regulation of ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0031396 | regulation of protein ubiquitination | 8 | 4 |
GO:0031398 | positive regulation of protein ubiquitination | 9 | 4 |
GO:0031399 | regulation of protein modification process | 6 | 4 |
GO:0031401 | positive regulation of protein modification process | 7 | 4 |
GO:0043085 | positive regulation of catalytic activity | 4 | 4 |
GO:0044093 | positive regulation of molecular function | 3 | 4 |
GO:0050790 | regulation of catalytic activity | 3 | 4 |
GO:0051338 | regulation of transferase activity | 4 | 4 |
GO:0051347 | positive regulation of transferase activity | 5 | 4 |
GO:0051438 | regulation of ubiquitin-protein transferase activity | 5 | 4 |
GO:0051443 | positive regulation of ubiquitin-protein transferase activity | 6 | 4 |
GO:0065009 | regulation of molecular function | 2 | 4 |
GO:1903320 | regulation of protein modification by small protein conjugation or removal | 7 | 4 |
GO:1903322 | positive regulation of protein modification by small protein conjugation or removal | 8 | 4 |
GO:1904666 | regulation of ubiquitin protein ligase activity | 6 | 4 |
GO:1904668 | positive regulation of ubiquitin protein ligase activity | 7 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0008047 | enzyme activator activity | 3 | 6 |
GO:0010997 | anaphase-promoting complex binding | 3 | 6 |
GO:0030234 | enzyme regulator activity | 2 | 6 |
GO:0044877 | protein-containing complex binding | 2 | 6 |
GO:0055106 | ubiquitin-protein transferase regulator activity | 3 | 6 |
GO:0097027 | ubiquitin-protein transferase activator activity | 4 | 6 |
GO:0098772 | molecular function regulator activity | 1 | 6 |
GO:0140677 | molecular function activator activity | 2 | 6 |
GO:1990757 | ubiquitin ligase activator activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.717 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.828 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.856 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.770 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 718 | 720 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.856 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 718 | 720 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.728 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.815 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.819 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.792 |
CLV_Separin_Metazoa | 456 | 460 | PF03568 | 0.647 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.792 |
DEG_SPOP_SBC_1 | 800 | 804 | PF00917 | 0.730 |
DOC_CDC14_PxL_1 | 711 | 719 | PF14671 | 0.600 |
DOC_CKS1_1 | 3 | 8 | PF01111 | 0.849 |
DOC_CKS1_1 | 397 | 402 | PF01111 | 0.758 |
DOC_CKS1_1 | 406 | 411 | PF01111 | 0.502 |
DOC_CYCLIN_RxL_1 | 249 | 259 | PF00134 | 0.817 |
DOC_CYCLIN_RxL_1 | 726 | 736 | PF00134 | 0.636 |
DOC_MAPK_gen_1 | 106 | 114 | PF00069 | 0.823 |
DOC_MAPK_MEF2A_6 | 380 | 389 | PF00069 | 0.783 |
DOC_PP1_RVXF_1 | 641 | 648 | PF00149 | 0.600 |
DOC_PP1_RVXF_1 | 662 | 669 | PF00149 | 0.636 |
DOC_PP2B_LxvP_1 | 73 | 76 | PF13499 | 0.646 |
DOC_PP4_FxxP_1 | 26 | 29 | PF00568 | 0.850 |
DOC_PP4_FxxP_1 | 3 | 6 | PF00568 | 0.848 |
DOC_PP4_FxxP_1 | 397 | 400 | PF00568 | 0.764 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 800 | 804 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 812 | 816 | PF00917 | 0.764 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.821 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.835 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.810 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.847 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.848 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.810 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 763 | 768 | PF00397 | 0.796 |
DOC_WW_Pin1_4 | 791 | 796 | PF00397 | 0.750 |
LIG_14-3-3_CanoR_1 | 156 | 164 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 168 | 174 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 175 | 183 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 187 | 192 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 354 | 360 | PF00244 | 0.802 |
LIG_14-3-3_CanoR_1 | 395 | 400 | PF00244 | 0.765 |
LIG_14-3-3_CanoR_1 | 520 | 525 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 65 | 75 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 667 | 673 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 771 | 775 | PF00244 | 0.770 |
LIG_14-3-3_CanoR_1 | 817 | 822 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 825 | 831 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 86 | 91 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 93 | 102 | PF00244 | 0.652 |
LIG_BRCT_BRCA1_1 | 188 | 192 | PF00533 | 0.679 |
LIG_BRCT_BRCA1_1 | 212 | 216 | PF00533 | 0.608 |
LIG_BRCT_BRCA1_1 | 562 | 566 | PF00533 | 0.518 |
LIG_BRCT_BRCA1_2 | 188 | 194 | PF00533 | 0.819 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.810 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.731 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.737 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.833 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.831 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.575 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.295 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.371 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.530 |
LIG_FHA_1 | 540 | 546 | PF00498 | 0.446 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.530 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.472 |
LIG_FHA_1 | 694 | 700 | PF00498 | 0.587 |
LIG_FHA_1 | 725 | 731 | PF00498 | 0.582 |
LIG_FHA_1 | 775 | 781 | PF00498 | 0.573 |
LIG_FHA_1 | 800 | 806 | PF00498 | 0.693 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.663 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.763 |
LIG_LIR_Apic_2 | 2 | 6 | PF02991 | 0.773 |
LIG_LIR_Apic_2 | 23 | 29 | PF02991 | 0.849 |
LIG_LIR_Apic_2 | 394 | 400 | PF02991 | 0.764 |
LIG_LIR_Apic_2 | 710 | 715 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 143 | 154 | PF02991 | 0.810 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.819 |
LIG_LIR_Gen_1 | 253 | 263 | PF02991 | 0.822 |
LIG_LIR_Gen_1 | 420 | 431 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.808 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 253 | 258 | PF02991 | 0.815 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 523 | 529 | PF02991 | 0.400 |
LIG_LYPXL_yS_3 | 714 | 717 | PF13949 | 0.600 |
LIG_PCNA_yPIPBox_3 | 81 | 93 | PF02747 | 0.839 |
LIG_Pex14_2 | 753 | 757 | PF04695 | 0.671 |
LIG_PTB_Apo_2 | 439 | 446 | PF02174 | 0.566 |
LIG_PTB_Phospho_1 | 439 | 445 | PF10480 | 0.569 |
LIG_REV1ctd_RIR_1 | 631 | 641 | PF16727 | 0.636 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.805 |
LIG_SH2_CRK | 423 | 427 | PF00017 | 0.572 |
LIG_SH2_GRB2like | 423 | 426 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.738 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.737 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 704 | 707 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.840 |
LIG_SH3_1 | 403 | 409 | PF00018 | 0.651 |
LIG_SH3_2 | 406 | 411 | PF14604 | 0.490 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.659 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.849 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.762 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.495 |
LIG_SH3_3 | 556 | 562 | PF00018 | 0.562 |
LIG_SH3_3 | 646 | 652 | PF00018 | 0.636 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.764 |
LIG_SUMO_SIM_par_1 | 519 | 525 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 540 | 547 | PF11976 | 0.600 |
LIG_UBA3_1 | 632 | 637 | PF00899 | 0.608 |
LIG_WW_3 | 5 | 9 | PF00397 | 0.688 |
MOD_CDC14_SPxK_1 | 129 | 132 | PF00782 | 0.756 |
MOD_CDC14_SPxK_1 | 295 | 298 | PF00782 | 0.757 |
MOD_CDK_SPK_2 | 163 | 168 | PF00069 | 0.767 |
MOD_CDK_SPxK_1 | 126 | 132 | PF00069 | 0.766 |
MOD_CDK_SPxK_1 | 2 | 8 | PF00069 | 0.851 |
MOD_CDK_SPxK_1 | 292 | 298 | PF00069 | 0.762 |
MOD_CDK_SPxK_1 | 405 | 411 | PF00069 | 0.644 |
MOD_CDK_SPxxK_3 | 28 | 35 | PF00069 | 0.843 |
MOD_CDK_SPxxK_3 | 396 | 403 | PF00069 | 0.629 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.734 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.750 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.843 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.785 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.839 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.575 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.854 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.472 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.680 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.458 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.494 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.575 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.597 |
MOD_CK1_1 | 773 | 779 | PF00069 | 0.796 |
MOD_CK1_1 | 781 | 787 | PF00069 | 0.663 |
MOD_CK1_1 | 799 | 805 | PF00069 | 0.513 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.770 |
MOD_CK1_1 | 819 | 825 | PF00069 | 0.627 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.672 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.824 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.706 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.846 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.776 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.816 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.776 |
MOD_GlcNHglycan | 208 | 212 | PF01048 | 0.790 |
MOD_GlcNHglycan | 220 | 224 | PF01048 | 0.620 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.766 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.798 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.764 |
MOD_GlcNHglycan | 428 | 432 | PF01048 | 0.542 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.483 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.530 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.561 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.462 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.415 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.435 |
MOD_GlcNHglycan | 619 | 623 | PF01048 | 0.649 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.406 |
MOD_GlcNHglycan | 735 | 738 | PF01048 | 0.435 |
MOD_GlcNHglycan | 743 | 746 | PF01048 | 0.341 |
MOD_GlcNHglycan | 777 | 780 | PF01048 | 0.675 |
MOD_GlcNHglycan | 798 | 801 | PF01048 | 0.791 |
MOD_GlcNHglycan | 814 | 817 | PF01048 | 0.768 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.735 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.688 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.684 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.688 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.552 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.765 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.759 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.790 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.650 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.849 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.807 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.767 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.718 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.605 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.781 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.530 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.490 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.627 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.594 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.717 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.574 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.567 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.577 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.770 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.816 |
MOD_GSK3_1 | 778 | 785 | PF00069 | 0.657 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.607 |
MOD_GSK3_1 | 812 | 819 | PF00069 | 0.571 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.572 |
MOD_LATS_1 | 49 | 55 | PF00433 | 0.791 |
MOD_N-GLC_1 | 266 | 271 | PF02516 | 0.836 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.737 |
MOD_N-GLC_1 | 391 | 396 | PF02516 | 0.768 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.825 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.829 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.709 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.677 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.660 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.784 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.564 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.636 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.615 |
MOD_NEK2_1 | 668 | 673 | PF00069 | 0.505 |
MOD_NEK2_1 | 762 | 767 | PF00069 | 0.770 |
MOD_NEK2_1 | 769 | 774 | PF00069 | 0.727 |
MOD_NEK2_1 | 782 | 787 | PF00069 | 0.505 |
MOD_NEK2_2 | 199 | 204 | PF00069 | 0.718 |
MOD_NEK2_2 | 747 | 752 | PF00069 | 0.636 |
MOD_PIKK_1 | 504 | 510 | PF00454 | 0.452 |
MOD_PIKK_1 | 647 | 653 | PF00454 | 0.525 |
MOD_PIKK_1 | 681 | 687 | PF00454 | 0.586 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.724 |
MOD_PIKK_1 | 819 | 825 | PF00454 | 0.814 |
MOD_PK_1 | 187 | 193 | PF00069 | 0.743 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.747 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.773 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.555 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.460 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.540 |
MOD_PKA_2 | 607 | 613 | PF00069 | 0.628 |
MOD_PKA_2 | 762 | 768 | PF00069 | 0.673 |
MOD_PKA_2 | 770 | 776 | PF00069 | 0.743 |
MOD_PKA_2 | 816 | 822 | PF00069 | 0.716 |
MOD_PKA_2 | 824 | 830 | PF00069 | 0.786 |
MOD_PKB_1 | 207 | 215 | PF00069 | 0.844 |
MOD_PKB_1 | 393 | 401 | PF00069 | 0.764 |
MOD_PKB_1 | 549 | 557 | PF00069 | 0.741 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.785 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.831 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.781 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.741 |
MOD_Plk_1 | 518 | 524 | PF00069 | 0.530 |
MOD_Plk_1 | 539 | 545 | PF00069 | 0.600 |
MOD_Plk_1 | 747 | 753 | PF00069 | 0.636 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.730 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.660 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.746 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.833 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.507 |
MOD_Plk_4 | 707 | 713 | PF00069 | 0.572 |
MOD_Plk_4 | 738 | 744 | PF00069 | 0.636 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.823 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.835 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.530 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.810 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.494 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.851 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.765 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.849 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.638 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.762 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.642 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.642 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.437 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.808 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.672 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.636 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.584 |
MOD_ProDKin_1 | 763 | 769 | PF00069 | 0.799 |
MOD_ProDKin_1 | 791 | 797 | PF00069 | 0.750 |
MOD_SUMO_rev_2 | 105 | 111 | PF00179 | 0.823 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.806 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.575 |
TRG_ENDOCYTIC_2 | 714 | 717 | PF00928 | 0.600 |
TRG_ER_diArg_1 | 316 | 319 | PF00400 | 0.750 |
TRG_ER_diArg_1 | 34 | 36 | PF00400 | 0.843 |
TRG_ER_diArg_1 | 352 | 354 | PF00400 | 0.692 |
TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 717 | 719 | PF00400 | 0.610 |
TRG_NES_CRM1_1 | 434 | 448 | PF08389 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 252 | 257 | PF00026 | 0.815 |
TRG_Pf-PMV_PEXEL_1 | 828 | 833 | PF00026 | 0.708 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IG81 | Leishmania donovani | 94% | 100% |
A4HDN2 | Leishmania braziliensis | 81% | 100% |
E9AH79 | Leishmania infantum | 94% | 100% |
E9AX17 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |