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: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: A4HP71
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 | 494 | 498 | PF00656 | 0.546 |
CLV_C14_Caspase3-7 | 605 | 609 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 723 | 727 | PF00656 | 0.611 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 647 | 649 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 733 | 735 | PF00675 | 0.678 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 647 | 649 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 733 | 735 | PF00082 | 0.634 |
CLV_PCSK_PC7_1 | 585 | 591 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 687 | 691 | PF00082 | 0.506 |
DEG_SPOP_SBC_1 | 280 | 284 | PF00917 | 0.590 |
DEG_SPOP_SBC_1 | 33 | 37 | PF00917 | 0.626 |
DEG_SPOP_SBC_1 | 519 | 523 | PF00917 | 0.647 |
DEG_SPOP_SBC_1 | 565 | 569 | PF00917 | 0.574 |
DOC_CKS1_1 | 750 | 755 | PF01111 | 0.654 |
DOC_CYCLIN_RxL_1 | 262 | 273 | PF00134 | 0.655 |
DOC_CYCLIN_RxL_1 | 684 | 693 | PF00134 | 0.363 |
DOC_CYCLIN_yCln2_LP_2 | 470 | 476 | PF00134 | 0.525 |
DOC_MAPK_MEF2A_6 | 14 | 23 | PF00069 | 0.563 |
DOC_MAPK_MEF2A_6 | 305 | 313 | PF00069 | 0.539 |
DOC_PP1_RVXF_1 | 402 | 409 | PF00149 | 0.553 |
DOC_PP2B_LxvP_1 | 331 | 334 | PF13499 | 0.571 |
DOC_PP2B_LxvP_1 | 385 | 388 | PF13499 | 0.492 |
DOC_PP2B_LxvP_1 | 470 | 473 | PF13499 | 0.613 |
DOC_PP2B_LxvP_1 | 476 | 479 | PF13499 | 0.632 |
DOC_PP4_FxxP_1 | 185 | 188 | PF00568 | 0.596 |
DOC_PP4_FxxP_1 | 230 | 233 | PF00568 | 0.516 |
DOC_PP4_MxPP_1 | 232 | 235 | PF00568 | 0.636 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.675 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.813 |
DOC_WW_Pin1_4 | 690 | 695 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 749 | 754 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 110 | 116 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 156 | 164 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 189 | 196 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 32 | 38 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 324 | 330 | PF00244 | 0.821 |
LIG_14-3-3_CanoR_1 | 348 | 353 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 358 | 363 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 390 | 396 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 46 | 52 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 515 | 519 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 82 | 88 | PF00244 | 0.803 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.670 |
LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.666 |
LIG_BRCT_BRCA1_1 | 181 | 185 | PF00533 | 0.622 |
LIG_Clathr_ClatBox_1 | 299 | 303 | PF01394 | 0.473 |
LIG_CSL_BTD_1 | 105 | 108 | PF09270 | 0.465 |
LIG_CtBP_PxDLS_1 | 473 | 477 | PF00389 | 0.529 |
LIG_eIF4E_1 | 594 | 600 | PF01652 | 0.724 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.480 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.572 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.552 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.562 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.546 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.604 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.478 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.606 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.493 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.626 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.642 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.661 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.705 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.572 |
LIG_FHA_2 | 721 | 727 | PF00498 | 0.585 |
LIG_FHA_2 | 740 | 746 | PF00498 | 0.510 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.718 |
LIG_HP1_1 | 413 | 417 | PF01393 | 0.524 |
LIG_Integrin_RGD_1 | 219 | 221 | PF01839 | 0.565 |
LIG_Integrin_RGD_1 | 247 | 249 | PF01839 | 0.507 |
LIG_Integrin_RGD_1 | 606 | 608 | PF01839 | 0.530 |
LIG_LIR_Apic_2 | 182 | 188 | PF02991 | 0.617 |
LIG_LIR_Apic_2 | 227 | 233 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 112 | 123 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 15 | 23 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 412 | 422 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 15 | 21 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 412 | 417 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 499 | 504 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 714 | 720 | PF02991 | 0.507 |
LIG_LYPXL_yS_3 | 481 | 484 | PF13949 | 0.686 |
LIG_Pex14_1 | 675 | 679 | PF04695 | 0.546 |
LIG_Pex14_2 | 717 | 721 | PF04695 | 0.526 |
LIG_PTAP_UEV_1 | 57 | 62 | PF05743 | 0.538 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.530 |
LIG_SH2_CRK | 679 | 683 | PF00017 | 0.663 |
LIG_SH2_CRK | 704 | 708 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 679 | 683 | PF00017 | 0.663 |
LIG_SH2_NCK_1 | 704 | 708 | PF00017 | 0.586 |
LIG_SH2_PTP2 | 414 | 417 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 704 | 708 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.713 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.520 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.645 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.529 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.548 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.511 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.472 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.681 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.648 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.609 |
LIG_SH3_3 | 693 | 699 | PF00018 | 0.509 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.733 |
LIG_SH3_5 | 235 | 239 | PF00018 | 0.436 |
LIG_SUMO_SIM_par_1 | 298 | 303 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 472 | 477 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 687 | 693 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 76 | 81 | PF11976 | 0.571 |
LIG_SxIP_EBH_1 | 100 | 110 | PF03271 | 0.506 |
LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.605 |
LIG_TRAF2_1 | 742 | 745 | PF00917 | 0.649 |
LIG_WRC_WIRS_1 | 392 | 397 | PF05994 | 0.498 |
LIG_WW_1 | 478 | 481 | PF00397 | 0.561 |
MOD_CDC14_SPxK_1 | 5 | 8 | PF00782 | 0.638 |
MOD_CDK_SPK_2 | 27 | 32 | PF00069 | 0.610 |
MOD_CDK_SPxK_1 | 2 | 8 | PF00069 | 0.643 |
MOD_CDK_SPxxK_3 | 508 | 515 | PF00069 | 0.549 |
MOD_CDK_SPxxK_3 | 749 | 756 | PF00069 | 0.655 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.521 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.555 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.462 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.744 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.643 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.613 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.724 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.353 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.387 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.714 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.705 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.573 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.693 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.703 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.643 |
MOD_CK1_1 | 725 | 731 | PF00069 | 0.639 |
MOD_CK1_1 | 740 | 746 | PF00069 | 0.654 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.763 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.717 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.593 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.513 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.809 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.598 |
MOD_CK2_1 | 739 | 745 | PF00069 | 0.569 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.722 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.675 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.493 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.749 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.642 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.537 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.469 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.574 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.683 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.776 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.349 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.498 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.537 |
MOD_GlcNHglycan | 431 | 435 | PF01048 | 0.514 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.269 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.741 |
MOD_GlcNHglycan | 497 | 501 | PF01048 | 0.776 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.659 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.824 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.623 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.772 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.747 |
MOD_GlcNHglycan | 739 | 742 | PF01048 | 0.670 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.628 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.254 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.574 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.703 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.710 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.606 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.453 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.682 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.505 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.565 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.716 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.712 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.546 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.546 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.478 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.510 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.505 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.660 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.717 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.741 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.511 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.693 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.525 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.710 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.717 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.714 |
MOD_GSK3_1 | 721 | 728 | PF00069 | 0.615 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.740 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.691 |
MOD_LATS_1 | 154 | 160 | PF00433 | 0.571 |
MOD_LATS_1 | 356 | 362 | PF00433 | 0.619 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.565 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.346 |
MOD_N-GLC_1 | 519 | 524 | PF02516 | 0.552 |
MOD_N-GLC_1 | 538 | 543 | PF02516 | 0.489 |
MOD_N-GLC_1 | 565 | 570 | PF02516 | 0.685 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.609 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.481 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.448 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.566 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.589 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.527 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.546 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.554 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.708 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.703 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.557 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.582 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.791 |
MOD_NEK2_2 | 220 | 225 | PF00069 | 0.383 |
MOD_OFUCOSY | 199 | 204 | PF10250 | 0.377 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.628 |
MOD_PIKK_1 | 447 | 453 | PF00454 | 0.498 |
MOD_PIKK_1 | 740 | 746 | PF00454 | 0.654 |
MOD_PK_1 | 358 | 364 | PF00069 | 0.546 |
MOD_PKA_1 | 189 | 195 | PF00069 | 0.489 |
MOD_PKA_1 | 602 | 608 | PF00069 | 0.526 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.606 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.643 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.489 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.491 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.691 |
MOD_PKA_2 | 514 | 520 | PF00069 | 0.718 |
MOD_PKA_2 | 602 | 608 | PF00069 | 0.622 |
MOD_PKA_2 | 617 | 623 | PF00069 | 0.738 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.679 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.641 |
MOD_PKB_1 | 198 | 206 | PF00069 | 0.366 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.481 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.489 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.552 |
MOD_Plk_1 | 654 | 660 | PF00069 | 0.707 |
MOD_Plk_1 | 725 | 731 | PF00069 | 0.712 |
MOD_Plk_2-3 | 626 | 632 | PF00069 | 0.815 |
MOD_Plk_2-3 | 636 | 642 | PF00069 | 0.541 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.543 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.565 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.560 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.658 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.422 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.495 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.691 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.806 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.519 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.669 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.628 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.562 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.530 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.650 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.710 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.813 |
MOD_ProDKin_1 | 690 | 696 | PF00069 | 0.502 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.713 |
MOD_ProDKin_1 | 749 | 755 | PF00069 | 0.652 |
TRG_DiLeu_BaEn_1 | 745 | 750 | PF01217 | 0.641 |
TRG_DiLeu_BaEn_2 | 200 | 206 | PF01217 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.548 |
TRG_DiLeu_BaLyEn_6 | 465 | 470 | PF01217 | 0.586 |
TRG_DiLeu_BaLyEn_6 | 685 | 690 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.686 |
TRG_ENDOCYTIC_2 | 704 | 707 | PF00928 | 0.486 |
TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 588 | 591 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 647 | 650 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 685 | 688 | PF00400 | 0.538 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZD9 | Leptomonas seymouri | 54% | 98% |
A0A3S7XAS2 | Leishmania donovani | 78% | 100% |
A4IDH6 | Leishmania infantum | 78% | 100% |
E9ASX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q1L9 | Leishmania major | 80% | 98% |