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 | 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:0032991 | protein-containing complex | 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: A4HDN2
Term | Name | Level | Count |
---|---|---|---|
GO:0009893 | positive regulation of metabolic process | 4 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 6 |
GO:0019222 | regulation of metabolic process | 3 | 6 |
GO:0031396 | regulation of protein ubiquitination | 8 | 5 |
GO:0031398 | positive regulation of protein ubiquitination | 9 | 5 |
GO:0031399 | regulation of protein modification process | 6 | 5 |
GO:0031401 | positive regulation of protein modification process | 7 | 5 |
GO:0043085 | positive regulation of catalytic activity | 4 | 5 |
GO:0044093 | positive regulation of molecular function | 3 | 5 |
GO:0048518 | positive regulation of biological process | 3 | 6 |
GO:0050789 | regulation of biological process | 2 | 6 |
GO:0050790 | regulation of catalytic activity | 3 | 5 |
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:0051338 | regulation of transferase activity | 4 | 5 |
GO:0051347 | positive regulation of transferase activity | 5 | 5 |
GO:0051438 | regulation of ubiquitin-protein transferase activity | 5 | 5 |
GO:0051443 | positive regulation of ubiquitin-protein transferase activity | 6 | 5 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 6 |
GO:0065007 | biological regulation | 1 | 6 |
GO:0065009 | regulation of molecular function | 2 | 5 |
GO:0080090 | regulation of primary metabolic process | 4 | 6 |
GO:1903320 | regulation of protein modification by small protein conjugation or removal | 7 | 5 |
GO:1903322 | positive regulation of protein modification by small protein conjugation or removal | 8 | 5 |
GO:1904666 | regulation of ubiquitin protein ligase activity | 6 | 5 |
GO:1904668 | positive regulation of ubiquitin protein ligase activity | 7 | 5 |
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: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 | 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 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.822 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.851 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 717 | 719 | PF00675 | 0.615 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.851 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.768 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 717 | 719 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.745 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.775 |
CLV_PCSK_SKI1_1 | 629 | 633 | PF00082 | 0.373 |
CLV_Separin_Metazoa | 455 | 459 | PF03568 | 0.645 |
DEG_SCF_FBW7_1 | 12 | 18 | PF00400 | 0.721 |
DEG_SCF_FBW7_1 | 179 | 185 | PF00400 | 0.562 |
DEG_SCF_FBW7_1 | 73 | 80 | PF00400 | 0.585 |
DEG_SPOP_SBC_1 | 15 | 19 | PF00917 | 0.583 |
DEG_SPOP_SBC_1 | 173 | 177 | PF00917 | 0.590 |
DOC_ANK_TNKS_1 | 487 | 494 | PF00023 | 0.277 |
DOC_CDC14_PxL_1 | 710 | 718 | PF14671 | 0.598 |
DOC_CKS1_1 | 12 | 17 | PF01111 | 0.689 |
DOC_CKS1_1 | 179 | 184 | PF01111 | 0.602 |
DOC_CKS1_1 | 3 | 8 | PF01111 | 0.831 |
DOC_CKS1_1 | 396 | 401 | PF01111 | 0.767 |
DOC_CKS1_1 | 405 | 410 | PF01111 | 0.502 |
DOC_CYCLIN_RxL_1 | 248 | 258 | PF00134 | 0.818 |
DOC_CYCLIN_RxL_1 | 725 | 735 | PF00134 | 0.636 |
DOC_MAPK_gen_1 | 106 | 114 | PF00069 | 0.826 |
DOC_MAPK_MEF2A_6 | 379 | 388 | PF00069 | 0.789 |
DOC_PP1_RVXF_1 | 627 | 634 | PF00149 | 0.467 |
DOC_PP1_RVXF_1 | 640 | 647 | PF00149 | 0.600 |
DOC_PP1_RVXF_1 | 661 | 668 | PF00149 | 0.636 |
DOC_PP4_FxxP_1 | 26 | 29 | PF00568 | 0.827 |
DOC_PP4_FxxP_1 | 3 | 6 | PF00568 | 0.834 |
DOC_PP4_FxxP_1 | 396 | 399 | PF00568 | 0.731 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 761 | 765 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.828 |
DOC_USP7_MATH_1 | 811 | 815 | PF00917 | 0.647 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.823 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.811 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.828 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.839 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 762 | 767 | PF00397 | 0.798 |
DOC_WW_Pin1_4 | 772 | 777 | PF00397 | 0.627 |
LIG_14-3-3_CanoR_1 | 174 | 180 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 208 | 218 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 353 | 359 | PF00244 | 0.802 |
LIG_14-3-3_CanoR_1 | 371 | 380 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 394 | 399 | PF00244 | 0.773 |
LIG_14-3-3_CanoR_1 | 458 | 466 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 508 | 514 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 519 | 524 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 666 | 672 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 770 | 776 | PF00244 | 0.797 |
LIG_14-3-3_CanoR_1 | 827 | 831 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 93 | 102 | PF00244 | 0.734 |
LIG_BIR_III_2 | 39 | 43 | PF00653 | 0.623 |
LIG_BRCT_BRCA1_1 | 187 | 191 | PF00533 | 0.809 |
LIG_BRCT_BRCA1_1 | 305 | 309 | PF00533 | 0.626 |
LIG_BRCT_BRCA1_1 | 46 | 50 | PF00533 | 0.579 |
LIG_BRCT_BRCA1_1 | 777 | 781 | PF00533 | 0.556 |
LIG_BRCT_BRCA1_2 | 187 | 193 | PF00533 | 0.809 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.828 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.602 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.814 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.484 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.454 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.353 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.450 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.530 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.690 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.636 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.589 |
LIG_FHA_1 | 724 | 730 | PF00498 | 0.552 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.823 |
LIG_FHA_2 | 691 | 697 | PF00498 | 0.509 |
LIG_LIR_Apic_2 | 23 | 29 | PF02991 | 0.831 |
LIG_LIR_Apic_2 | 393 | 399 | PF02991 | 0.733 |
LIG_LIR_Apic_2 | 709 | 714 | PF02991 | 0.582 |
LIG_LIR_Apic_2 | 771 | 776 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 142 | 153 | PF02991 | 0.810 |
LIG_LIR_Gen_1 | 188 | 198 | PF02991 | 0.699 |
LIG_LIR_Gen_1 | 252 | 262 | PF02991 | 0.821 |
LIG_LIR_Gen_1 | 419 | 430 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 561 | 569 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 142 | 148 | PF02991 | 0.801 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.717 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 522 | 528 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 561 | 566 | PF02991 | 0.542 |
LIG_LYPXL_yS_3 | 713 | 716 | PF13949 | 0.599 |
LIG_PCNA_yPIPBox_3 | 81 | 93 | PF02747 | 0.829 |
LIG_Pex14_2 | 752 | 756 | PF04695 | 0.679 |
LIG_PTB_Apo_2 | 438 | 445 | PF02174 | 0.567 |
LIG_PTB_Phospho_1 | 438 | 444 | PF10480 | 0.569 |
LIG_REV1ctd_RIR_1 | 630 | 640 | PF16727 | 0.530 |
LIG_SH2_CRK | 145 | 149 | PF00017 | 0.806 |
LIG_SH2_CRK | 422 | 426 | PF00017 | 0.573 |
LIG_SH2_CRK | 773 | 777 | PF00017 | 0.549 |
LIG_SH2_GRB2like | 422 | 425 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 773 | 777 | PF00017 | 0.674 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 703 | 706 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.830 |
LIG_SH3_1 | 402 | 408 | PF00018 | 0.653 |
LIG_SH3_2 | 405 | 410 | PF14604 | 0.650 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.624 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.663 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.653 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.636 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.726 |
LIG_SUMO_SIM_par_1 | 298 | 306 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 518 | 524 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 539 | 546 | PF11976 | 0.600 |
LIG_TRAF2_1 | 286 | 289 | PF00917 | 0.593 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.630 |
LIG_UBA3_1 | 631 | 636 | PF00899 | 0.491 |
LIG_WW_3 | 5 | 9 | PF00397 | 0.673 |
MOD_CDC14_SPxK_1 | 156 | 159 | PF00782 | 0.566 |
MOD_CDK_SPxK_1 | 153 | 159 | PF00069 | 0.569 |
MOD_CDK_SPxK_1 | 2 | 8 | PF00069 | 0.832 |
MOD_CDK_SPxK_1 | 404 | 410 | PF00069 | 0.644 |
MOD_CDK_SPxxK_3 | 28 | 35 | PF00069 | 0.828 |
MOD_CDK_SPxxK_3 | 395 | 402 | PF00069 | 0.755 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.593 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.731 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.653 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.698 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.812 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.823 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.573 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.708 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.578 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.570 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.572 |
MOD_CK1_1 | 537 | 543 | PF00069 | 0.592 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.648 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.792 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.544 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.621 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.550 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.609 |
MOD_CK1_1 | 771 | 777 | PF00069 | 0.789 |
MOD_CK1_1 | 780 | 786 | PF00069 | 0.668 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.762 |
MOD_CK1_1 | 800 | 806 | PF00069 | 0.470 |
MOD_CK1_1 | 826 | 832 | PF00069 | 0.636 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.665 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.561 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.825 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.842 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.602 |
MOD_CK2_1 | 690 | 696 | PF00069 | 0.510 |
MOD_CK2_1 | 826 | 832 | PF00069 | 0.578 |
MOD_GlcNHglycan | 197 | 201 | PF01048 | 0.603 |
MOD_GlcNHglycan | 207 | 211 | PF01048 | 0.779 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.580 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.780 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.782 |
MOD_GlcNHglycan | 427 | 431 | PF01048 | 0.545 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.700 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.483 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.530 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.455 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.717 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.704 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.463 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.435 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.767 |
MOD_GlcNHglycan | 619 | 622 | PF01048 | 0.765 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.435 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.435 |
MOD_GlcNHglycan | 742 | 745 | PF01048 | 0.341 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.623 |
MOD_GlcNHglycan | 799 | 802 | PF01048 | 0.745 |
MOD_GlcNHglycan | 813 | 816 | PF01048 | 0.546 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.821 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.819 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.824 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.644 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.695 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.726 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.670 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.644 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.840 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.588 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.622 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.778 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.519 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.610 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.648 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.530 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.299 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.737 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.623 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.615 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.525 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.636 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.546 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.799 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.671 |
MOD_GSK3_1 | 777 | 784 | PF00069 | 0.617 |
MOD_GSK3_1 | 795 | 802 | PF00069 | 0.513 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.588 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.834 |
MOD_N-GLC_1 | 390 | 395 | PF02516 | 0.778 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.828 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.822 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.700 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.591 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.489 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.819 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.585 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.652 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.735 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.584 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.790 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.452 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.636 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.552 |
MOD_NEK2_1 | 667 | 672 | PF00069 | 0.468 |
MOD_NEK2_1 | 768 | 773 | PF00069 | 0.720 |
MOD_NEK2_1 | 779 | 784 | PF00069 | 0.541 |
MOD_NEK2_2 | 122 | 127 | PF00069 | 0.592 |
MOD_NEK2_2 | 198 | 203 | PF00069 | 0.830 |
MOD_NEK2_2 | 21 | 26 | PF00069 | 0.700 |
MOD_NEK2_2 | 746 | 751 | PF00069 | 0.636 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.614 |
MOD_PIKK_1 | 646 | 652 | PF00454 | 0.525 |
MOD_PIKK_1 | 680 | 686 | PF00454 | 0.587 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.718 |
MOD_PIKK_1 | 818 | 824 | PF00454 | 0.803 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.598 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.348 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.592 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.448 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.671 |
MOD_PKA_2 | 761 | 767 | PF00069 | 0.791 |
MOD_PKA_2 | 769 | 775 | PF00069 | 0.673 |
MOD_PKA_2 | 823 | 829 | PF00069 | 0.779 |
MOD_PKB_1 | 206 | 214 | PF00069 | 0.830 |
MOD_PKB_1 | 392 | 400 | PF00069 | 0.775 |
MOD_PKB_1 | 548 | 556 | PF00069 | 0.743 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.744 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.828 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.582 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.584 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.787 |
MOD_Plk_1 | 517 | 523 | PF00069 | 0.530 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.599 |
MOD_Plk_1 | 746 | 752 | PF00069 | 0.636 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.714 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.728 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.796 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.586 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.671 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.580 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.584 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.599 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.272 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.570 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.547 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.825 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.690 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.519 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.708 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.813 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.553 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.832 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.840 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.620 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.618 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.768 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.496 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.590 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.557 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.600 |
MOD_ProDKin_1 | 762 | 768 | PF00069 | 0.800 |
MOD_ProDKin_1 | 772 | 778 | PF00069 | 0.630 |
MOD_SUMO_rev_2 | 105 | 111 | PF00179 | 0.819 |
TRG_DiLeu_BaEn_1 | 291 | 296 | PF01217 | 0.581 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.806 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.576 |
TRG_ENDOCYTIC_2 | 713 | 716 | PF00928 | 0.599 |
TRG_ER_diArg_1 | 34 | 36 | PF00400 | 0.842 |
TRG_ER_diArg_1 | 716 | 718 | PF00400 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 251 | 256 | PF00026 | 0.671 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IG81 | Leishmania donovani | 82% | 100% |
E9AH79 | Leishmania infantum | 82% | 100% |
E9AX17 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QAF9 | Leishmania major | 81% | 100% |