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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 3 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 3 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0140535 | intracellular protein-containing complex | 2 | 3 |
GO:1902494 | catalytic complex | 2 | 3 |
GO:1990234 | transferase complex | 3 | 3 |
Related structures:
AlphaFold database: Q4Q854
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 14 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 14 |
GO:0006807 | nitrogen compound metabolic process | 2 | 14 |
GO:0008152 | metabolic process | 1 | 14 |
GO:0009056 | catabolic process | 2 | 14 |
GO:0009057 | macromolecule catabolic process | 4 | 14 |
GO:0009987 | cellular process | 1 | 14 |
GO:0016567 | protein ubiquitination | 7 | 3 |
GO:0019538 | protein metabolic process | 3 | 14 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 14 |
GO:0032446 | protein modification by small protein conjugation | 6 | 3 |
GO:0036211 | protein modification process | 4 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 14 |
GO:0043412 | macromolecule modification | 4 | 3 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 14 |
GO:0044237 | cellular metabolic process | 2 | 14 |
GO:0044238 | primary metabolic process | 2 | 14 |
GO:0044248 | cellular catabolic process | 3 | 14 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 14 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 14 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 14 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 14 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 14 |
GO:1901575 | organic substance catabolic process | 3 | 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 14 |
GO:0005515 | protein binding | 2 | 14 |
GO:0019899 | enzyme binding | 3 | 14 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 3 |
GO:0031625 | ubiquitin protein ligase binding | 5 | 14 |
GO:0044389 | ubiquitin-like protein ligase binding | 4 | 14 |
GO:0060090 | molecular adaptor activity | 1 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.521 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 738 | 740 | PF00675 | 0.544 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.250 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 636 | 638 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 738 | 740 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 146 | 148 | PF00082 | 0.283 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.250 |
CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 418 | 420 | PF00082 | 0.258 |
CLV_PCSK_PC1ET2_1 | 518 | 520 | PF00082 | 0.238 |
CLV_PCSK_PC1ET2_1 | 636 | 638 | PF00082 | 0.258 |
CLV_PCSK_PC7_1 | 514 | 520 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.146 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 710 | 714 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 739 | 743 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.288 |
DOC_CYCLIN_yCln2_LP_2 | 527 | 533 | PF00134 | 0.521 |
DOC_MAPK_DCC_7 | 710 | 720 | PF00069 | 0.394 |
DOC_MAPK_gen_1 | 205 | 211 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 437 | 445 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 518 | 528 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 695 | 704 | PF00069 | 0.614 |
DOC_MAPK_gen_1 | 710 | 720 | PF00069 | 0.235 |
DOC_MAPK_MEF2A_6 | 549 | 556 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 713 | 722 | PF00069 | 0.490 |
DOC_PIKK_1 | 331 | 338 | PF02985 | 0.456 |
DOC_PP1_RVXF_1 | 572 | 579 | PF00149 | 0.453 |
DOC_PP1_SILK_1 | 361 | 366 | PF00149 | 0.458 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 664 | 668 | PF00917 | 0.613 |
DOC_USP7_MATH_2 | 553 | 559 | PF00917 | 0.427 |
DOC_USP7_UBL2_3 | 259 | 263 | PF12436 | 0.571 |
DOC_USP7_UBL2_3 | 40 | 44 | PF12436 | 0.537 |
DOC_USP7_UBL2_3 | 418 | 422 | PF12436 | 0.458 |
DOC_USP7_UBL2_3 | 743 | 747 | PF12436 | 0.506 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 637 | 642 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 206 | 210 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 218 | 222 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 274 | 278 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 549 | 553 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 586 | 592 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 629 | 633 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 7 | 13 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 72 | 78 | PF00244 | 0.553 |
LIG_Actin_WH2_2 | 162 | 178 | PF00022 | 0.521 |
LIG_Actin_WH2_2 | 336 | 354 | PF00022 | 0.521 |
LIG_Actin_WH2_2 | 424 | 439 | PF00022 | 0.427 |
LIG_Actin_WH2_2 | 557 | 573 | PF00022 | 0.372 |
LIG_APCC_ABBA_1 | 287 | 292 | PF00400 | 0.521 |
LIG_APCC_ABBAyCdc20_2 | 286 | 292 | PF00400 | 0.521 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.651 |
LIG_BRCT_BRCA1_1 | 378 | 382 | PF00533 | 0.458 |
LIG_DLG_GKlike_1 | 484 | 492 | PF00625 | 0.506 |
LIG_eIF4E_1 | 94 | 100 | PF01652 | 0.396 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.454 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.454 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.554 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.448 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.440 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.474 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.600 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.521 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.288 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.498 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.455 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.525 |
LIG_GBD_Chelix_1 | 132 | 140 | PF00786 | 0.258 |
LIG_GBD_Chelix_1 | 91 | 99 | PF00786 | 0.343 |
LIG_Integrin_isoDGR_2 | 572 | 574 | PF01839 | 0.258 |
LIG_LIR_Apic_2 | 292 | 298 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 220 | 230 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 25 | 34 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 275 | 285 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 320 | 330 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 41 | 49 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 439 | 449 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 459 | 468 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 496 | 506 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 597 | 605 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 6 | 15 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 759 | 766 | PF02991 | 0.504 |
LIG_LIR_LC3C_4 | 87 | 92 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 41 | 45 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 459 | 463 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 496 | 502 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 565 | 570 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 597 | 601 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 65 | 70 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 674 | 680 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 759 | 765 | PF02991 | 0.413 |
LIG_LYPXL_yS_3 | 67 | 70 | PF13949 | 0.523 |
LIG_NRBOX | 321 | 327 | PF00104 | 0.458 |
LIG_NRBOX | 488 | 494 | PF00104 | 0.521 |
LIG_NRBOX | 600 | 606 | PF00104 | 0.518 |
LIG_NRBOX | 95 | 101 | PF00104 | 0.490 |
LIG_Pex14_2 | 12 | 16 | PF04695 | 0.351 |
LIG_Pex14_2 | 499 | 503 | PF04695 | 0.521 |
LIG_PTB_Apo_2 | 21 | 28 | PF02174 | 0.469 |
LIG_Rb_pABgroove_1 | 317 | 325 | PF01858 | 0.458 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.458 |
LIG_SH2_CRK | 393 | 397 | PF00017 | 0.575 |
LIG_SH2_CRK | 42 | 46 | PF00017 | 0.440 |
LIG_SH2_CRK | 567 | 571 | PF00017 | 0.490 |
LIG_SH2_GRB2like | 253 | 256 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 277 | 281 | PF00017 | 0.521 |
LIG_SH2_PTP2 | 677 | 680 | PF00017 | 0.449 |
LIG_SH2_SRC | 119 | 122 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 222 | 226 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 460 | 464 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 673 | 677 | PF00017 | 0.534 |
LIG_SH2_STAT3 | 253 | 256 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 677 | 680 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 753 | 756 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.283 |
LIG_SUMO_SIM_anti_2 | 597 | 603 | PF11976 | 0.419 |
LIG_SUMO_SIM_anti_2 | 719 | 724 | PF11976 | 0.340 |
LIG_SUMO_SIM_anti_2 | 85 | 93 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 550 | 558 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 597 | 603 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 699 | 705 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 716 | 721 | PF11976 | 0.410 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.520 |
LIG_TRAF2_1 | 424 | 427 | PF00917 | 0.540 |
LIG_TRAF2_1 | 631 | 634 | PF00917 | 0.443 |
LIG_TRAF2_1 | 667 | 670 | PF00917 | 0.468 |
LIG_TRFH_1 | 656 | 660 | PF08558 | 0.432 |
LIG_TYR_ITIM | 675 | 680 | PF00017 | 0.433 |
LIG_TYR_ITIM | 91 | 96 | PF00017 | 0.311 |
LIG_UBA3_1 | 116 | 125 | PF00899 | 0.308 |
LIG_UBA3_1 | 363 | 369 | PF00899 | 0.396 |
LIG_UBA3_1 | 468 | 477 | PF00899 | 0.308 |
LIG_UBA3_1 | 488 | 497 | PF00899 | 0.133 |
LIG_UBA3_1 | 610 | 615 | PF00899 | 0.451 |
LIG_UBA3_1 | 95 | 102 | PF00899 | 0.343 |
LIG_WRC_WIRS_1 | 234 | 239 | PF05994 | 0.375 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.351 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.384 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.362 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.396 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.338 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.404 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.359 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.357 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.288 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.426 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.570 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.565 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.392 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.338 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.367 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.308 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.396 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.441 |
MOD_CK2_1 | 617 | 623 | PF00069 | 0.418 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.387 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.480 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.589 |
MOD_Cter_Amidation | 572 | 575 | PF01082 | 0.396 |
MOD_DYRK1A_RPxSP_1 | 637 | 641 | PF00069 | 0.242 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.345 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.402 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.451 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.435 |
MOD_GlcNHglycan | 581 | 585 | PF01048 | 0.347 |
MOD_GlcNHglycan | 618 | 622 | PF01048 | 0.405 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.592 |
MOD_GlcNHglycan | 727 | 730 | PF01048 | 0.480 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.435 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.352 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.337 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.279 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.435 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.418 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.462 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.308 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.372 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.301 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.378 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.358 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.616 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.524 |
MOD_N-GLC_1 | 514 | 519 | PF02516 | 0.361 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.543 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.438 |
MOD_N-GLC_2 | 255 | 257 | PF02516 | 0.389 |
MOD_N-GLC_2 | 37 | 39 | PF02516 | 0.612 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.372 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.316 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.335 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.317 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.370 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.406 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.451 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.329 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.468 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.462 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.416 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.323 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.394 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.545 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.589 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.393 |
MOD_PIKK_1 | 623 | 629 | PF00454 | 0.343 |
MOD_PIKK_1 | 679 | 685 | PF00454 | 0.625 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.352 |
MOD_PKA_1 | 205 | 211 | PF00069 | 0.396 |
MOD_PKA_1 | 32 | 38 | PF00069 | 0.573 |
MOD_PKA_1 | 352 | 358 | PF00069 | 0.265 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.329 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.262 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.329 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.534 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.232 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.430 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.408 |
MOD_PKA_2 | 587 | 593 | PF00069 | 0.314 |
MOD_PKA_2 | 628 | 634 | PF00069 | 0.265 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.509 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.396 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.402 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.357 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.409 |
MOD_Plk_1 | 484 | 490 | PF00069 | 0.386 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.480 |
MOD_Plk_1 | 696 | 702 | PF00069 | 0.578 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.464 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.328 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.389 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.342 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.279 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.220 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.360 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.349 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.319 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.396 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.399 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.388 |
MOD_Plk_4 | 688 | 694 | PF00069 | 0.617 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.390 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.316 |
MOD_ProDKin_1 | 637 | 643 | PF00069 | 0.361 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.575 |
MOD_SUMO_for_1 | 261 | 264 | PF00179 | 0.387 |
MOD_SUMO_rev_2 | 168 | 178 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 344 | 354 | PF00179 | 0.308 |
MOD_SUMO_rev_2 | 426 | 431 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 511 | 520 | PF00179 | 0.414 |
MOD_SUMO_rev_2 | 631 | 638 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 667 | 672 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 735 | 744 | PF00179 | 0.543 |
TRG_DiLeu_BaEn_1 | 292 | 297 | PF01217 | 0.308 |
TRG_DiLeu_BaEn_1 | 51 | 56 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 384 | 389 | PF01217 | 0.308 |
TRG_DiLeu_BaLyEn_6 | 464 | 469 | PF01217 | 0.306 |
TRG_DiLeu_BaLyEn_6 | 707 | 712 | PF01217 | 0.329 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 567 | 570 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 609 | 612 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 677 | 680 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.317 |
TRG_ER_diArg_1 | 436 | 438 | PF00400 | 0.265 |
TRG_ER_diArg_1 | 586 | 589 | PF00400 | 0.412 |
TRG_NLS_MonoExtN_4 | 29 | 35 | PF00514 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 147 | 152 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 286 | 291 | PF00026 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 462 | 466 | PF00026 | 0.295 |
TRG_Pf-PMV_PEXEL_1 | 507 | 511 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 710 | 714 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILK0 | Leptomonas seymouri | 22% | 99% |
A0A0N1PDU6 | Leptomonas seymouri | 61% | 100% |
A0A0S4J5R6 | Bodo saltans | 23% | 93% |
A0A1X0NS98 | Trypanosomatidae | 25% | 95% |
A0A3Q8II83 | Leishmania donovani | 22% | 100% |
A0A3R7K7T8 | Trypanosoma rangeli | 24% | 95% |
A0A3S7X1Q2 | Leishmania donovani | 97% | 100% |
A2A432 | Mus musculus | 22% | 79% |
A4HGR5 | Leishmania braziliensis | 90% | 100% |
A4HGR6 | Leishmania braziliensis | 22% | 100% |
A4I3U0 | Leishmania infantum | 97% | 100% |
A4I3U1 | Leishmania infantum | 22% | 100% |
D0A911 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 95% |
E9B032 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9B033 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
O13790 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 20% | 100% |
Q13617 | Homo sapiens | 21% | 100% |
Q13619 | Homo sapiens | 22% | 100% |
Q24311 | Drosophila melanogaster | 21% | 99% |
Q4Q853 | Leishmania major | 22% | 95% |
Q54XF7 | Dictyostelium discoideum | 21% | 100% |
Q5RCF3 | Pongo abelii | 21% | 100% |
Q9C9L0 | Arabidopsis thaliana | 21% | 100% |
Q9D4H8 | Mus musculus | 22% | 100% |
Q9JJ31 | Rattus norvegicus | 21% | 98% |
Q9XZJ3 | Dictyostelium discoideum | 21% | 99% |
Q9ZVH4 | Arabidopsis thaliana | 21% | 100% |