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: E9AH79
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_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.646 |
CLV_MEL_PAP_1 | 688 | 694 | PF00089 | 0.328 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 716 | 718 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.715 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 716 | 718 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.657 |
CLV_Separin_Metazoa | 454 | 458 | PF03568 | 0.490 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.651 |
DEG_SCF_FBW7_1 | 12 | 18 | PF00400 | 0.626 |
DEG_SPOP_SBC_1 | 560 | 564 | PF00917 | 0.525 |
DEG_SPOP_SBC_1 | 771 | 775 | PF00917 | 0.526 |
DEG_SPOP_SBC_1 | 798 | 802 | PF00917 | 0.621 |
DOC_CDC14_PxL_1 | 709 | 717 | PF14671 | 0.445 |
DOC_CKS1_1 | 12 | 17 | PF01111 | 0.606 |
DOC_CKS1_1 | 3 | 8 | PF01111 | 0.692 |
DOC_CKS1_1 | 395 | 400 | PF01111 | 0.586 |
DOC_CKS1_1 | 404 | 409 | PF01111 | 0.410 |
DOC_CYCLIN_RxL_1 | 247 | 257 | PF00134 | 0.646 |
DOC_CYCLIN_RxL_1 | 724 | 734 | PF00134 | 0.532 |
DOC_MAPK_gen_1 | 106 | 114 | PF00069 | 0.678 |
DOC_MAPK_MEF2A_6 | 378 | 387 | PF00069 | 0.575 |
DOC_PP1_RVXF_1 | 639 | 646 | PF00149 | 0.512 |
DOC_PP1_RVXF_1 | 660 | 667 | PF00149 | 0.532 |
DOC_PP4_FxxP_1 | 26 | 29 | PF00568 | 0.708 |
DOC_PP4_FxxP_1 | 3 | 6 | PF00568 | 0.687 |
DOC_PP4_FxxP_1 | 395 | 398 | PF00568 | 0.604 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 771 | 775 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 798 | 802 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 810 | 814 | PF00917 | 0.574 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 761 | 766 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 789 | 794 | PF00397 | 0.618 |
LIG_14-3-3_CanoR_1 | 154 | 162 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 166 | 172 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 173 | 181 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 185 | 190 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 352 | 358 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 393 | 398 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 457 | 465 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 51 | 60 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 518 | 523 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 614 | 622 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 665 | 671 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 769 | 778 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 86 | 91 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 93 | 99 | PF00244 | 0.627 |
LIG_Actin_WH2_2 | 186 | 204 | PF00022 | 0.561 |
LIG_BRCT_BRCA1_1 | 186 | 190 | PF00533 | 0.663 |
LIG_BRCT_BRCA1_2 | 186 | 192 | PF00533 | 0.667 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.680 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.639 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.623 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.474 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.677 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.430 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.288 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.355 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.286 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.451 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.385 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.588 |
LIG_FHA_1 | 635 | 641 | PF00498 | 0.440 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.438 |
LIG_FHA_1 | 723 | 729 | PF00498 | 0.532 |
LIG_FHA_1 | 798 | 804 | PF00498 | 0.599 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.679 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.638 |
LIG_LIR_Apic_2 | 2 | 6 | PF02991 | 0.645 |
LIG_LIR_Apic_2 | 23 | 29 | PF02991 | 0.707 |
LIG_LIR_Apic_2 | 392 | 398 | PF02991 | 0.594 |
LIG_LIR_Apic_2 | 708 | 713 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.667 |
LIG_LIR_Gen_1 | 187 | 197 | PF02991 | 0.669 |
LIG_LIR_Gen_1 | 251 | 261 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 418 | 429 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.663 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.385 |
LIG_LYPXL_yS_3 | 712 | 715 | PF13949 | 0.443 |
LIG_PCNA_yPIPBox_3 | 81 | 93 | PF02747 | 0.691 |
LIG_Pex14_2 | 751 | 755 | PF04695 | 0.568 |
LIG_PTB_Apo_2 | 437 | 444 | PF02174 | 0.418 |
LIG_PTB_Phospho_1 | 437 | 443 | PF10480 | 0.421 |
LIG_REV1ctd_RIR_1 | 629 | 639 | PF16727 | 0.532 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.666 |
LIG_SH2_CRK | 421 | 425 | PF00017 | 0.444 |
LIG_SH2_GRB2like | 421 | 424 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 244 | 248 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 702 | 705 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.693 |
LIG_SH3_1 | 401 | 407 | PF00018 | 0.487 |
LIG_SH3_2 | 404 | 409 | PF14604 | 0.494 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.658 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.616 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.647 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.487 |
LIG_SH3_3 | 644 | 650 | PF00018 | 0.532 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.652 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.627 |
LIG_SUMO_SIM_par_1 | 517 | 523 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 538 | 545 | PF11976 | 0.455 |
LIG_UBA3_1 | 630 | 635 | PF00899 | 0.517 |
MOD_CDC14_SPxK_1 | 127 | 130 | PF00782 | 0.630 |
MOD_CDC14_SPxK_1 | 293 | 296 | PF00782 | 0.651 |
MOD_CDK_SPK_2 | 161 | 166 | PF00069 | 0.653 |
MOD_CDK_SPxK_1 | 124 | 130 | PF00069 | 0.638 |
MOD_CDK_SPxK_1 | 2 | 8 | PF00069 | 0.692 |
MOD_CDK_SPxK_1 | 290 | 296 | PF00069 | 0.650 |
MOD_CDK_SPxK_1 | 403 | 409 | PF00069 | 0.488 |
MOD_CDK_SPxxK_3 | 28 | 35 | PF00069 | 0.709 |
MOD_CDK_SPxxK_3 | 394 | 401 | PF00069 | 0.573 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.624 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.666 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.585 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.690 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.695 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.708 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.600 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.430 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.545 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.448 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.588 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.485 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.442 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.552 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.574 |
MOD_CK1_1 | 770 | 776 | PF00069 | 0.645 |
MOD_CK1_1 | 779 | 785 | PF00069 | 0.563 |
MOD_CK1_1 | 797 | 803 | PF00069 | 0.497 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.654 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.591 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.680 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.605 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.712 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.667 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.517 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.558 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.587 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.628 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.615 |
MOD_GlcNHglycan | 206 | 210 | PF01048 | 0.667 |
MOD_GlcNHglycan | 218 | 222 | PF01048 | 0.566 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.558 |
MOD_GlcNHglycan | 309 | 313 | PF01048 | 0.652 |
MOD_GlcNHglycan | 426 | 430 | PF01048 | 0.413 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.339 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.385 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.419 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.487 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.392 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.348 |
MOD_GlcNHglycan | 617 | 621 | PF01048 | 0.637 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.332 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.332 |
MOD_GlcNHglycan | 741 | 744 | PF01048 | 0.279 |
MOD_GlcNHglycan | 769 | 772 | PF01048 | 0.584 |
MOD_GlcNHglycan | 796 | 799 | PF01048 | 0.646 |
MOD_GlcNHglycan | 812 | 815 | PF01048 | 0.522 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.685 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.677 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.675 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.572 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.518 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.569 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.653 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.582 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.599 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.696 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.657 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.528 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.460 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.585 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.385 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.280 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.488 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.558 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.560 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.494 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.435 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.685 |
MOD_GSK3_1 | 767 | 774 | PF00069 | 0.663 |
MOD_GSK3_1 | 776 | 783 | PF00069 | 0.559 |
MOD_GSK3_1 | 789 | 796 | PF00069 | 0.537 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.548 |
MOD_LATS_1 | 49 | 55 | PF00433 | 0.651 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.655 |
MOD_N-GLC_1 | 389 | 394 | PF02516 | 0.693 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.607 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.585 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.684 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.672 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.607 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.657 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.664 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.602 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.420 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.532 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.532 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.482 |
MOD_NEK2_1 | 760 | 765 | PF00069 | 0.635 |
MOD_NEK2_1 | 767 | 772 | PF00069 | 0.618 |
MOD_NEK2_1 | 778 | 783 | PF00069 | 0.490 |
MOD_NEK2_2 | 197 | 202 | PF00069 | 0.696 |
MOD_NEK2_2 | 21 | 26 | PF00069 | 0.629 |
MOD_NEK2_2 | 745 | 750 | PF00069 | 0.532 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.342 |
MOD_PIKK_1 | 679 | 685 | PF00454 | 0.439 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.628 |
MOD_PIKK_1 | 817 | 823 | PF00454 | 0.673 |
MOD_PK_1 | 185 | 191 | PF00069 | 0.623 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.639 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.640 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.547 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.402 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.448 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.497 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.513 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.554 |
MOD_PKA_2 | 760 | 766 | PF00069 | 0.652 |
MOD_PKA_2 | 822 | 828 | PF00069 | 0.652 |
MOD_PKB_1 | 205 | 213 | PF00069 | 0.697 |
MOD_PKB_1 | 391 | 399 | PF00069 | 0.592 |
MOD_PKB_1 | 547 | 555 | PF00069 | 0.611 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.649 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.567 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.569 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.627 |
MOD_Plk_1 | 516 | 522 | PF00069 | 0.385 |
MOD_Plk_1 | 537 | 543 | PF00069 | 0.453 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.584 |
MOD_Plk_1 | 745 | 751 | PF00069 | 0.532 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.622 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.631 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.684 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.574 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.453 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.420 |
MOD_Plk_4 | 736 | 742 | PF00069 | 0.532 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.675 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.607 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.505 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.675 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.529 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.692 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.646 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.697 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.590 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.650 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.585 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.585 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.404 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.527 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.606 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.532 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.560 |
MOD_ProDKin_1 | 761 | 767 | PF00069 | 0.662 |
MOD_ProDKin_1 | 789 | 795 | PF00069 | 0.617 |
MOD_SUMO_rev_2 | 105 | 111 | PF00179 | 0.675 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.667 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 712 | 715 | PF00928 | 0.443 |
TRG_ER_diArg_1 | 314 | 317 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 34 | 36 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 715 | 717 | PF00400 | 0.464 |
TRG_NES_CRM1_1 | 432 | 446 | PF08389 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 250 | 255 | PF00026 | 0.662 |
TRG_Pf-PMV_PEXEL_1 | 305 | 309 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 826 | 831 | PF00026 | 0.610 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IG81 | Leishmania donovani | 100% | 100% |
A4HDN2 | Leishmania braziliensis | 82% | 100% |
E9AX17 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
Q4QAF9 | Leishmania major | 94% | 100% |