| 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:0005840 | ribosome | 5 | 5 |
| GO:0032991 | protein-containing complex | 1 | 5 |
| GO:0043226 | organelle | 2 | 5 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 5 |
| GO:0043229 | intracellular organelle | 3 | 5 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 5 |
| GO:0110165 | cellular anatomical entity | 1 | 5 |
| GO:1990904 | ribonucleoprotein complex | 2 | 5 |
| GO:0000151 | ubiquitin ligase complex | 3 | 1 |
| GO:0000152 | nuclear ubiquitin ligase complex | 3 | 1 |
| GO:0005680 | anaphase-promoting complex | 4 | 1 |
| GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 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: A4I8Q1
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0009893 | positive regulation of metabolic process | 4 | 7 |
| GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 7 |
| GO:0019222 | regulation of metabolic process | 3 | 7 |
| GO:0031396 | regulation of protein ubiquitination | 8 | 6 |
| GO:0031398 | positive regulation of protein ubiquitination | 9 | 6 |
| GO:0031399 | regulation of protein modification process | 6 | 6 |
| GO:0031401 | positive regulation of protein modification process | 7 | 6 |
| GO:0043085 | positive regulation of catalytic activity | 4 | 6 |
| GO:0044093 | positive regulation of molecular function | 3 | 6 |
| GO:0048518 | positive regulation of biological process | 3 | 7 |
| GO:0050789 | regulation of biological process | 2 | 7 |
| GO:0050790 | regulation of catalytic activity | 3 | 6 |
| GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 7 |
| GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 7 |
| GO:0051246 | regulation of protein metabolic process | 5 | 7 |
| GO:0051247 | positive regulation of protein metabolic process | 6 | 7 |
| GO:0051338 | regulation of transferase activity | 4 | 6 |
| GO:0051347 | positive regulation of transferase activity | 5 | 6 |
| GO:0051438 | regulation of ubiquitin-protein transferase activity | 5 | 6 |
| GO:0051443 | positive regulation of ubiquitin-protein transferase activity | 6 | 6 |
| GO:0060255 | regulation of macromolecule metabolic process | 4 | 7 |
| GO:0065007 | biological regulation | 1 | 7 |
| GO:0065009 | regulation of molecular function | 2 | 6 |
| GO:0080090 | regulation of primary metabolic process | 4 | 7 |
| GO:1903320 | regulation of protein modification by small protein conjugation or removal | 7 | 6 |
| GO:1903322 | positive regulation of protein modification by small protein conjugation or removal | 8 | 6 |
| GO:1904666 | regulation of ubiquitin protein ligase activity | 6 | 6 |
| GO:1904668 | positive regulation of ubiquitin protein ligase activity | 7 | 6 |
| GO:0006508 | proteolysis | 4 | 1 |
| GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009056 | catabolic process | 2 | 1 |
| GO:0009057 | macromolecule catabolic process | 4 | 1 |
| GO:0009894 | regulation of catabolic process | 4 | 1 |
| GO:0009896 | positive regulation of catabolic process | 5 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
| GO:0019538 | protein metabolic process | 3 | 1 |
| GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
| GO:0030162 | regulation of proteolysis | 6 | 1 |
| GO:0030163 | protein catabolic process | 4 | 1 |
| GO:0031145 | anaphase-promoting complex-dependent catabolic process | 7 | 1 |
| GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
| GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
| GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
| GO:0031331 | positive regulation of cellular catabolic process | 6 | 1 |
| GO:0032434 | regulation of proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
| GO:0032436 | positive regulation of proteasomal ubiquitin-dependent protein catabolic process | 8 | 1 |
| GO:0042176 | regulation of protein catabolic process | 5 | 1 |
| GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 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:0045732 | positive regulation of protein catabolic process | 6 | 1 |
| GO:0045862 | positive regulation of proteolysis | 7 | 1 |
| GO:0048522 | positive regulation of cellular process | 4 | 1 |
| GO:0050794 | regulation of cellular process | 3 | 1 |
| GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
| GO:0061136 | regulation of proteasomal protein catabolic process | 6 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 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:1901800 | positive regulation of proteasomal protein catabolic process | 7 | 1 |
| GO:1903050 | regulation of proteolysis involved in protein catabolic process | 7 | 1 |
| GO:1903052 | positive regulation of proteolysis involved in protein catabolic process | 8 | 1 |
| GO:1905784 | regulation of anaphase-promoting complex-dependent catabolic process | 8 | 1 |
| GO:1905786 | positive regulation of anaphase-promoting complex-dependent catabolic process | 9 | 1 |
| GO:2000058 | regulation of ubiquitin-dependent protein catabolic process | 6 | 1 |
| GO:2000060 | positive regulation of ubiquitin-dependent protein catabolic process | 7 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005488 | binding | 1 | 7 |
| GO:0008047 | enzyme activator activity | 3 | 7 |
| GO:0010997 | anaphase-promoting complex binding | 3 | 7 |
| GO:0030234 | enzyme regulator activity | 2 | 7 |
| GO:0044877 | protein-containing complex binding | 2 | 7 |
| GO:0055106 | ubiquitin-protein transferase regulator activity | 3 | 7 |
| GO:0097027 | ubiquitin-protein transferase activator activity | 4 | 7 |
| GO:0098772 | molecular function regulator activity | 1 | 7 |
| GO:0140677 | molecular function activator activity | 2 | 7 |
| GO:1990757 | ubiquitin ligase activator activity | 5 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 436 | 440 | PF00656 | 0.567 |
| CLV_MEL_PAP_1 | 85 | 91 | PF00089 | 0.729 |
| CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.799 |
| CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.734 |
| CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.734 |
| CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.521 |
| CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.488 |
| CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.818 |
| CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.761 |
| CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.799 |
| CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.734 |
| CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.734 |
| CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.521 |
| CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.527 |
| CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.640 |
| CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.653 |
| CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.761 |
| CLV_PCSK_PC1ET2_1 | 561 | 563 | PF00082 | 0.527 |
| CLV_PCSK_PC1ET2_1 | 583 | 585 | PF00082 | 0.640 |
| CLV_PCSK_PC7_1 | 41 | 47 | PF00082 | 0.731 |
| CLV_PCSK_PC7_1 | 702 | 708 | PF00082 | 0.639 |
| CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.814 |
| CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.659 |
| CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.655 |
| CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.711 |
| CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.829 |
| CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.511 |
| CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.500 |
| CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.466 |
| CLV_Separin_Metazoa | 279 | 283 | PF03568 | 0.773 |
| DEG_Kelch_Keap1_1 | 403 | 408 | PF01344 | 0.613 |
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.701 |
| DEG_SCF_FBW7_1 | 165 | 170 | PF00400 | 0.708 |
| DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.681 |
| DOC_ANK_TNKS_1 | 261 | 268 | PF00023 | 0.679 |
| DOC_CKS1_1 | 227 | 232 | PF01111 | 0.706 |
| DOC_CKS1_1 | 57 | 62 | PF01111 | 0.744 |
| DOC_MAPK_gen_1 | 454 | 464 | PF00069 | 0.483 |
| DOC_MAPK_gen_1 | 637 | 644 | PF00069 | 0.498 |
| DOC_PP1_RVXF_1 | 420 | 427 | PF00149 | 0.423 |
| DOC_PP2B_LxvP_1 | 370 | 373 | PF13499 | 0.507 |
| DOC_PP4_FxxP_1 | 656 | 659 | PF00568 | 0.517 |
| DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.763 |
| DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.738 |
| DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.627 |
| DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.685 |
| DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.629 |
| DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.454 |
| DOC_USP7_MATH_2 | 301 | 307 | PF00917 | 0.728 |
| DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.754 |
| DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.813 |
| DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.711 |
| DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.712 |
| DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.592 |
| DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.676 |
| DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.498 |
| DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.527 |
| DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.736 |
| DOC_WW_Pin1_4 | 710 | 715 | PF00397 | 0.738 |
| DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.713 |
| LIG_14-3-3_CanoR_1 | 225 | 230 | PF00244 | 0.686 |
| LIG_14-3-3_CanoR_1 | 262 | 269 | PF00244 | 0.604 |
| LIG_14-3-3_CanoR_1 | 308 | 313 | PF00244 | 0.709 |
| LIG_14-3-3_CanoR_1 | 360 | 366 | PF00244 | 0.508 |
| LIG_14-3-3_CanoR_1 | 448 | 453 | PF00244 | 0.465 |
| LIG_14-3-3_CanoR_1 | 535 | 540 | PF00244 | 0.632 |
| LIG_14-3-3_CanoR_1 | 612 | 620 | PF00244 | 0.486 |
| LIG_14-3-3_CanoR_1 | 645 | 651 | PF00244 | 0.505 |
| LIG_14-3-3_CanoR_1 | 74 | 78 | PF00244 | 0.838 |
| LIG_Actin_WH2_2 | 292 | 310 | PF00022 | 0.683 |
| LIG_BRCT_BRCA1_1 | 562 | 566 | PF00533 | 0.492 |
| LIG_EH1_1 | 617 | 625 | PF00400 | 0.587 |
| LIG_FHA_1 | 316 | 322 | PF00498 | 0.686 |
| LIG_FHA_1 | 378 | 384 | PF00498 | 0.483 |
| LIG_FHA_1 | 439 | 445 | PF00498 | 0.403 |
| LIG_FHA_1 | 52 | 58 | PF00498 | 0.696 |
| LIG_FHA_1 | 609 | 615 | PF00498 | 0.505 |
| LIG_FHA_1 | 647 | 653 | PF00498 | 0.444 |
| LIG_FHA_2 | 285 | 291 | PF00498 | 0.699 |
| LIG_FHA_2 | 362 | 368 | PF00498 | 0.503 |
| LIG_FHA_2 | 38 | 44 | PF00498 | 0.832 |
| LIG_FHA_2 | 565 | 571 | PF00498 | 0.466 |
| LIG_FHA_2 | 588 | 594 | PF00498 | 0.784 |
| LIG_IBAR_NPY_1 | 129 | 131 | PF08397 | 0.792 |
| LIG_LIR_Apic_2 | 655 | 659 | PF02991 | 0.499 |
| LIG_LIR_Gen_1 | 188 | 199 | PF02991 | 0.604 |
| LIG_LIR_Gen_1 | 449 | 459 | PF02991 | 0.593 |
| LIG_LIR_Gen_1 | 648 | 658 | PF02991 | 0.494 |
| LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.695 |
| LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.599 |
| LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.597 |
| LIG_LIR_Nem_3 | 648 | 653 | PF02991 | 0.512 |
| LIG_LIR_Nem_3 | 685 | 691 | PF02991 | 0.466 |
| LIG_MAD2 | 368 | 376 | PF02301 | 0.458 |
| LIG_MAD2 | 707 | 715 | PF02301 | 0.598 |
| LIG_PCNA_yPIPBox_3 | 612 | 624 | PF02747 | 0.595 |
| LIG_Pex14_2 | 688 | 692 | PF04695 | 0.474 |
| LIG_PTB_Apo_2 | 506 | 513 | PF02174 | 0.559 |
| LIG_PTB_Phospho_1 | 506 | 512 | PF10480 | 0.559 |
| LIG_RPA_C_Fungi | 443 | 455 | PF08784 | 0.523 |
| LIG_SH2_STAP1 | 159 | 163 | PF00017 | 0.819 |
| LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.812 |
| LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.630 |
| LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.411 |
| LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.411 |
| LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.479 |
| LIG_SH3_2 | 373 | 378 | PF14604 | 0.644 |
| LIG_SH3_3 | 162 | 168 | PF00018 | 0.621 |
| LIG_SH3_3 | 246 | 252 | PF00018 | 0.596 |
| LIG_SH3_3 | 295 | 301 | PF00018 | 0.732 |
| LIG_SH3_3 | 370 | 376 | PF00018 | 0.516 |
| LIG_SH3_3 | 453 | 459 | PF00018 | 0.492 |
| LIG_SH3_3 | 466 | 472 | PF00018 | 0.472 |
| LIG_SH3_3 | 50 | 56 | PF00018 | 0.821 |
| LIG_SUMO_SIM_par_1 | 410 | 416 | PF11976 | 0.445 |
| LIG_SUMO_SIM_par_1 | 472 | 478 | PF11976 | 0.494 |
| LIG_TRAF2_1 | 592 | 595 | PF00917 | 0.682 |
| LIG_TRAF2_1 | 672 | 675 | PF00917 | 0.571 |
| LIG_WRC_WIRS_1 | 172 | 177 | PF05994 | 0.716 |
| LIG_WRC_WIRS_1 | 653 | 658 | PF05994 | 0.471 |
| LIG_WRC_WIRS_1 | 95 | 100 | PF05994 | 0.697 |
| LIG_WW_3 | 291 | 295 | PF00397 | 0.524 |
| MOD_CDC14_SPxK_1 | 114 | 117 | PF00782 | 0.727 |
| MOD_CDK_SPK_2 | 536 | 541 | PF00069 | 0.527 |
| MOD_CDK_SPxK_1 | 111 | 117 | PF00069 | 0.721 |
| MOD_CDK_SPxK_1 | 362 | 368 | PF00069 | 0.503 |
| MOD_CDK_SPxK_1 | 56 | 62 | PF00069 | 0.739 |
| MOD_CK1_1 | 111 | 117 | PF00069 | 0.799 |
| MOD_CK1_1 | 12 | 18 | PF00069 | 0.723 |
| MOD_CK1_1 | 170 | 176 | PF00069 | 0.754 |
| MOD_CK1_1 | 178 | 184 | PF00069 | 0.758 |
| MOD_CK1_1 | 185 | 191 | PF00069 | 0.633 |
| MOD_CK1_1 | 20 | 26 | PF00069 | 0.720 |
| MOD_CK1_1 | 349 | 355 | PF00069 | 0.533 |
| MOD_CK1_1 | 377 | 383 | PF00069 | 0.515 |
| MOD_CK1_1 | 39 | 45 | PF00069 | 0.519 |
| MOD_CK1_1 | 398 | 404 | PF00069 | 0.462 |
| MOD_CK1_1 | 447 | 453 | PF00069 | 0.543 |
| MOD_CK1_1 | 525 | 531 | PF00069 | 0.471 |
| MOD_CK1_1 | 666 | 672 | PF00069 | 0.536 |
| MOD_CK2_1 | 171 | 177 | PF00069 | 0.716 |
| MOD_CK2_1 | 232 | 238 | PF00069 | 0.760 |
| MOD_CK2_1 | 284 | 290 | PF00069 | 0.734 |
| MOD_CK2_1 | 297 | 303 | PF00069 | 0.657 |
| MOD_CK2_1 | 361 | 367 | PF00069 | 0.457 |
| MOD_CK2_1 | 37 | 43 | PF00069 | 0.832 |
| MOD_CK2_1 | 457 | 463 | PF00069 | 0.533 |
| MOD_CK2_1 | 564 | 570 | PF00069 | 0.469 |
| MOD_CK2_1 | 588 | 594 | PF00069 | 0.660 |
| MOD_Cter_Amidation | 72 | 75 | PF01082 | 0.762 |
| MOD_DYRK1A_RPxSP_1 | 536 | 540 | PF00069 | 0.527 |
| MOD_GlcNHglycan | 14 | 18 | PF01048 | 0.807 |
| MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.727 |
| MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.830 |
| MOD_GlcNHglycan | 216 | 220 | PF01048 | 0.753 |
| MOD_GlcNHglycan | 238 | 242 | PF01048 | 0.793 |
| MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.755 |
| MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.714 |
| MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.642 |
| MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.719 |
| MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.764 |
| MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.540 |
| MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.521 |
| MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.452 |
| MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.641 |
| MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.290 |
| MOD_GlcNHglycan | 693 | 697 | PF01048 | 0.596 |
| MOD_GlcNHglycan | 701 | 705 | PF01048 | 0.688 |
| MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.739 |
| MOD_GSK3_1 | 107 | 114 | PF00069 | 0.699 |
| MOD_GSK3_1 | 147 | 154 | PF00069 | 0.711 |
| MOD_GSK3_1 | 159 | 166 | PF00069 | 0.726 |
| MOD_GSK3_1 | 167 | 174 | PF00069 | 0.741 |
| MOD_GSK3_1 | 178 | 185 | PF00069 | 0.596 |
| MOD_GSK3_1 | 207 | 214 | PF00069 | 0.685 |
| MOD_GSK3_1 | 232 | 239 | PF00069 | 0.811 |
| MOD_GSK3_1 | 299 | 306 | PF00069 | 0.686 |
| MOD_GSK3_1 | 32 | 39 | PF00069 | 0.772 |
| MOD_GSK3_1 | 321 | 328 | PF00069 | 0.650 |
| MOD_GSK3_1 | 342 | 349 | PF00069 | 0.642 |
| MOD_GSK3_1 | 444 | 451 | PF00069 | 0.524 |
| MOD_GSK3_1 | 51 | 58 | PF00069 | 0.576 |
| MOD_GSK3_1 | 560 | 567 | PF00069 | 0.503 |
| MOD_GSK3_1 | 9 | 16 | PF00069 | 0.717 |
| MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.544 |
| MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.706 |
| MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.607 |
| MOD_N-GLC_1 | 362 | 367 | PF02516 | 0.498 |
| MOD_N-GLC_2 | 388 | 390 | PF02516 | 0.570 |
| MOD_NEK2_1 | 100 | 105 | PF00069 | 0.695 |
| MOD_NEK2_1 | 175 | 180 | PF00069 | 0.706 |
| MOD_NEK2_1 | 207 | 212 | PF00069 | 0.756 |
| MOD_NEK2_1 | 268 | 273 | PF00069 | 0.740 |
| MOD_NEK2_1 | 395 | 400 | PF00069 | 0.457 |
| MOD_NEK2_1 | 462 | 467 | PF00069 | 0.502 |
| MOD_NEK2_1 | 576 | 581 | PF00069 | 0.488 |
| MOD_NEK2_1 | 652 | 657 | PF00069 | 0.515 |
| MOD_NEK2_1 | 692 | 697 | PF00069 | 0.553 |
| MOD_NEK2_1 | 93 | 98 | PF00069 | 0.697 |
| MOD_NEK2_2 | 186 | 191 | PF00069 | 0.630 |
| MOD_NEK2_2 | 682 | 687 | PF00069 | 0.481 |
| MOD_OFUCOSY | 661 | 667 | PF10250 | 0.486 |
| MOD_PIKK_1 | 377 | 383 | PF00454 | 0.497 |
| MOD_PIKK_1 | 613 | 619 | PF00454 | 0.564 |
| MOD_PKA_1 | 37 | 43 | PF00069 | 0.832 |
| MOD_PKA_1 | 45 | 51 | PF00069 | 0.684 |
| MOD_PKA_1 | 535 | 541 | PF00069 | 0.632 |
| MOD_PKA_1 | 645 | 651 | PF00069 | 0.505 |
| MOD_PKA_2 | 17 | 23 | PF00069 | 0.755 |
| MOD_PKA_2 | 261 | 267 | PF00069 | 0.772 |
| MOD_PKA_2 | 36 | 42 | PF00069 | 0.728 |
| MOD_PKA_2 | 447 | 453 | PF00069 | 0.504 |
| MOD_PKA_2 | 45 | 51 | PF00069 | 0.713 |
| MOD_PKA_2 | 535 | 541 | PF00069 | 0.632 |
| MOD_PKA_2 | 73 | 79 | PF00069 | 0.765 |
| MOD_PKB_1 | 340 | 348 | PF00069 | 0.739 |
| MOD_PKB_1 | 562 | 570 | PF00069 | 0.480 |
| MOD_Plk_1 | 181 | 187 | PF00069 | 0.660 |
| MOD_Plk_1 | 232 | 238 | PF00069 | 0.710 |
| MOD_Plk_1 | 302 | 308 | PF00069 | 0.748 |
| MOD_Plk_1 | 661 | 667 | PF00069 | 0.586 |
| MOD_Plk_1 | 682 | 688 | PF00069 | 0.443 |
| MOD_Plk_1 | 91 | 97 | PF00069 | 0.697 |
| MOD_Plk_4 | 167 | 173 | PF00069 | 0.735 |
| MOD_Plk_4 | 175 | 181 | PF00069 | 0.671 |
| MOD_Plk_4 | 182 | 188 | PF00069 | 0.604 |
| MOD_Plk_4 | 395 | 401 | PF00069 | 0.457 |
| MOD_Plk_4 | 448 | 454 | PF00069 | 0.486 |
| MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.757 |
| MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.814 |
| MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.711 |
| MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.709 |
| MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.592 |
| MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.674 |
| MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.503 |
| MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.521 |
| MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.739 |
| MOD_ProDKin_1 | 710 | 716 | PF00069 | 0.735 |
| MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.712 |
| MOD_SUMO_for_1 | 29 | 32 | PF00179 | 0.650 |
| TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.614 |
| TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.675 |
| TRG_ER_diArg_1 | 419 | 422 | PF00400 | 0.495 |
| TRG_ER_diArg_1 | 534 | 536 | PF00400 | 0.557 |
| TRG_ER_diArg_1 | 562 | 565 | PF00400 | 0.501 |
| TRG_ER_diArg_1 | 706 | 708 | PF00400 | 0.685 |
| TRG_NLS_MonoExtN_4 | 559 | 565 | PF00514 | 0.523 |
| TRG_Pf-PMV_PEXEL_1 | 274 | 279 | PF00026 | 0.688 |
| TRG_Pf-PMV_PEXEL_1 | 83 | 87 | PF00026 | 0.724 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P6N4 | Leptomonas seymouri | 61% | 98% |
| A0A3Q8ILY5 | Leishmania donovani | 99% | 100% |
| A4HL72 | Leishmania braziliensis | 82% | 100% |
| E9B3L5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
| Q4Q4H0 | Leishmania major | 93% | 100% |