| 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: 3 | 
| Silverman et al. | no | yes: 0 | 
| Pissara et al. | yes | yes: 20 | 
| 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: 11 | 
| NetGPI | no | yes: 0, no: 11 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005654 | nucleoplasm | 2 | 1 | 
| GO:0110165 | cellular anatomical entity | 1 | 1 | 
Related structures:
AlphaFold database: E9ALJ4
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006508 | proteolysis | 4 | 12 | 
| GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 12 | 
| GO:0006807 | nitrogen compound metabolic process | 2 | 12 | 
| GO:0008152 | metabolic process | 1 | 12 | 
| GO:0009056 | catabolic process | 2 | 12 | 
| GO:0009057 | macromolecule catabolic process | 4 | 12 | 
| GO:0009987 | cellular process | 1 | 12 | 
| GO:0016579 | protein deubiquitination | 6 | 12 | 
| GO:0019538 | protein metabolic process | 3 | 12 | 
| GO:0019941 | modification-dependent protein catabolic process | 6 | 12 | 
| GO:0036211 | protein modification process | 4 | 12 | 
| GO:0043170 | macromolecule metabolic process | 3 | 12 | 
| GO:0043412 | macromolecule modification | 4 | 12 | 
| GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 12 | 
| GO:0044237 | cellular metabolic process | 2 | 12 | 
| GO:0044238 | primary metabolic process | 2 | 12 | 
| GO:0044248 | cellular catabolic process | 3 | 12 | 
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 | 
| GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 12 | 
| GO:0051603 | proteolysis involved in protein catabolic process | 5 | 12 | 
| GO:0070646 | protein modification by small protein removal | 5 | 12 | 
| GO:0070647 | protein modification by small protein conjugation or removal | 5 | 12 | 
| GO:0071704 | organic substance metabolic process | 2 | 12 | 
| GO:1901564 | organonitrogen compound metabolic process | 3 | 12 | 
| GO:1901575 | organic substance catabolic process | 3 | 12 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 12 | 
| GO:0004843 | cysteine-type deubiquitinase activity | 5 | 12 | 
| GO:0005488 | binding | 1 | 12 | 
| GO:0008233 | peptidase activity | 3 | 12 | 
| GO:0008234 | cysteine-type peptidase activity | 4 | 12 | 
| GO:0008270 | zinc ion binding | 6 | 12 | 
| GO:0016787 | hydrolase activity | 2 | 12 | 
| GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 12 | 
| GO:0043167 | ion binding | 2 | 12 | 
| GO:0043169 | cation binding | 3 | 12 | 
| GO:0046872 | metal ion binding | 4 | 12 | 
| GO:0046914 | transition metal ion binding | 5 | 12 | 
| GO:0101005 | deubiquitinase activity | 5 | 12 | 
| GO:0140096 | catalytic activity, acting on a protein | 2 | 12 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 140 | 144 | PF00656 | 0.756 | 
| CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.353 | 
| CLV_NRD_NRD_1 | 745 | 747 | PF00675 | 0.469 | 
| CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.353 | 
| CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.528 | 
| CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.353 | 
| CLV_PCSK_SKI1_1 | 626 | 630 | PF00082 | 0.371 | 
| CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.454 | 
| CLV_PCSK_SKI1_1 | 719 | 723 | PF00082 | 0.387 | 
| DOC_CDC14_PxL_1 | 115 | 123 | PF14671 | 0.553 | 
| DOC_CDC14_PxL_1 | 653 | 661 | PF14671 | 0.383 | 
| DOC_CKS1_1 | 19 | 24 | PF01111 | 0.461 | 
| DOC_CYCLIN_RxL_1 | 713 | 726 | PF00134 | 0.394 | 
| DOC_CYCLIN_yCln2_LP_2 | 163 | 169 | PF00134 | 0.596 | 
| DOC_CYCLIN_yCln2_LP_2 | 466 | 472 | PF00134 | 0.354 | 
| DOC_MAPK_gen_1 | 38 | 48 | PF00069 | 0.420 | 
| DOC_MAPK_gen_1 | 554 | 562 | PF00069 | 0.354 | 
| DOC_MAPK_MEF2A_6 | 41 | 50 | PF00069 | 0.420 | 
| DOC_MAPK_MEF2A_6 | 464 | 472 | PF00069 | 0.445 | 
| DOC_PP1_RVXF_1 | 717 | 724 | PF00149 | 0.387 | 
| DOC_PP2B_LxvP_1 | 466 | 469 | PF13499 | 0.354 | 
| DOC_PP4_FxxP_1 | 644 | 647 | PF00568 | 0.438 | 
| DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.776 | 
| DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.686 | 
| DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.458 | 
| DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.379 | 
| DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.492 | 
| DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.256 | 
| DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.451 | 
| DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.495 | 
| DOC_USP7_UBL2_3 | 265 | 269 | PF12436 | 0.557 | 
| DOC_USP7_UBL2_3 | 79 | 83 | PF12436 | 0.619 | 
| DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.462 | 
| DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.566 | 
| DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.543 | 
| DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.499 | 
| DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.461 | 
| DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.345 | 
| LIG_14-3-3_CanoR_1 | 455 | 461 | PF00244 | 0.415 | 
| LIG_14-3-3_CanoR_1 | 493 | 499 | PF00244 | 0.361 | 
| LIG_14-3-3_CanoR_1 | 529 | 534 | PF00244 | 0.397 | 
| LIG_14-3-3_CanoR_1 | 542 | 546 | PF00244 | 0.379 | 
| LIG_APCC_ABBAyCdc20_2 | 719 | 725 | PF00400 | 0.387 | 
| LIG_BRCT_BRCA1_1 | 278 | 282 | PF00533 | 0.543 | 
| LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.353 | 
| LIG_BRCT_BRCA1_1 | 739 | 743 | PF00533 | 0.370 | 
| LIG_Clathr_ClatBox_1 | 157 | 161 | PF01394 | 0.460 | 
| LIG_FHA_1 | 353 | 359 | PF00498 | 0.377 | 
| LIG_FHA_1 | 373 | 379 | PF00498 | 0.410 | 
| LIG_FHA_1 | 691 | 697 | PF00498 | 0.456 | 
| LIG_FHA_2 | 171 | 177 | PF00498 | 0.581 | 
| LIG_FHA_2 | 268 | 274 | PF00498 | 0.530 | 
| LIG_FHA_2 | 301 | 307 | PF00498 | 0.422 | 
| LIG_FHA_2 | 542 | 548 | PF00498 | 0.410 | 
| LIG_IBAR_NPY_1 | 346 | 348 | PF08397 | 0.322 | 
| LIG_LIR_Apic_2 | 641 | 647 | PF02991 | 0.438 | 
| LIG_LIR_Gen_1 | 283 | 292 | PF02991 | 0.510 | 
| LIG_LIR_Gen_1 | 44 | 51 | PF02991 | 0.438 | 
| LIG_LIR_Gen_1 | 557 | 567 | PF02991 | 0.387 | 
| LIG_LIR_Gen_1 | 717 | 728 | PF02991 | 0.353 | 
| LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.413 | 
| LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.512 | 
| LIG_LIR_Nem_3 | 283 | 287 | PF02991 | 0.471 | 
| LIG_LIR_Nem_3 | 404 | 408 | PF02991 | 0.353 | 
| LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.418 | 
| LIG_LIR_Nem_3 | 532 | 536 | PF02991 | 0.285 | 
| LIG_LIR_Nem_3 | 557 | 562 | PF02991 | 0.373 | 
| LIG_LIR_Nem_3 | 717 | 723 | PF02991 | 0.353 | 
| LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.729 | 
| LIG_MLH1_MIPbox_1 | 739 | 743 | PF16413 | 0.395 | 
| LIG_NRBOX | 405 | 411 | PF00104 | 0.438 | 
| LIG_Pex14_2 | 327 | 331 | PF04695 | 0.353 | 
| LIG_PTB_Apo_2 | 307 | 314 | PF02174 | 0.353 | 
| LIG_PTB_Apo_2 | 730 | 737 | PF02174 | 0.438 | 
| LIG_PTB_Phospho_1 | 307 | 313 | PF10480 | 0.353 | 
| LIG_REV1ctd_RIR_1 | 741 | 748 | PF16727 | 0.529 | 
| LIG_SH2_CRK | 126 | 130 | PF00017 | 0.455 | 
| LIG_SH2_CRK | 627 | 631 | PF00017 | 0.410 | 
| LIG_SH2_CRK | 74 | 78 | PF00017 | 0.473 | 
| LIG_SH2_PTP2 | 559 | 562 | PF00017 | 0.473 | 
| LIG_SH2_SRC | 276 | 279 | PF00017 | 0.554 | 
| LIG_SH2_SRC | 559 | 562 | PF00017 | 0.473 | 
| LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.407 | 
| LIG_SH2_STAP1 | 278 | 282 | PF00017 | 0.543 | 
| LIG_SH2_STAP1 | 690 | 694 | PF00017 | 0.500 | 
| LIG_SH2_STAT3 | 278 | 281 | PF00017 | 0.538 | 
| LIG_SH2_STAT3 | 387 | 390 | PF00017 | 0.422 | 
| LIG_SH2_STAT3 | 742 | 745 | PF00017 | 0.505 | 
| LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.494 | 
| LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.443 | 
| LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.353 | 
| LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.371 | 
| LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.387 | 
| LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.353 | 
| LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.407 | 
| LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.322 | 
| LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.303 | 
| LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.330 | 
| LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.369 | 
| LIG_SH2_STAT5 | 667 | 670 | PF00017 | 0.208 | 
| LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.353 | 
| LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.387 | 
| LIG_SH2_STAT5 | 742 | 745 | PF00017 | 0.385 | 
| LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.731 | 
| LIG_SH3_3 | 149 | 155 | PF00018 | 0.529 | 
| LIG_SH3_3 | 166 | 172 | PF00018 | 0.380 | 
| LIG_SH3_3 | 468 | 474 | PF00018 | 0.373 | 
| LIG_SH3_3 | 557 | 563 | PF00018 | 0.387 | 
| LIG_SH3_3 | 578 | 584 | PF00018 | 0.369 | 
| LIG_SH3_3 | 598 | 604 | PF00018 | 0.169 | 
| LIG_SH3_3 | 674 | 680 | PF00018 | 0.446 | 
| LIG_SH3_3 | 93 | 99 | PF00018 | 0.600 | 
| LIG_SUMO_SIM_anti_2 | 608 | 614 | PF11976 | 0.438 | 
| LIG_SUMO_SIM_par_1 | 611 | 617 | PF11976 | 0.473 | 
| LIG_TRAF2_1 | 484 | 487 | PF00917 | 0.233 | 
| LIG_TRAF2_1 | 603 | 606 | PF00917 | 0.473 | 
| LIG_TRAF2_2 | 603 | 608 | PF00917 | 0.500 | 
| LIG_TYR_ITIM | 91 | 96 | PF00017 | 0.729 | 
| MOD_CDC14_SPxK_1 | 589 | 592 | PF00782 | 0.305 | 
| MOD_CDK_SPxK_1 | 586 | 592 | PF00069 | 0.425 | 
| MOD_CK1_1 | 421 | 427 | PF00069 | 0.439 | 
| MOD_CK1_1 | 476 | 482 | PF00069 | 0.331 | 
| MOD_CK1_1 | 586 | 592 | PF00069 | 0.423 | 
| MOD_CK1_1 | 614 | 620 | PF00069 | 0.453 | 
| MOD_CK1_1 | 702 | 708 | PF00069 | 0.369 | 
| MOD_CK1_1 | 737 | 743 | PF00069 | 0.438 | 
| MOD_CK2_1 | 267 | 273 | PF00069 | 0.538 | 
| MOD_CK2_1 | 300 | 306 | PF00069 | 0.422 | 
| MOD_CK2_1 | 482 | 488 | PF00069 | 0.377 | 
| MOD_CK2_1 | 506 | 512 | PF00069 | 0.412 | 
| MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.537 | 
| MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.520 | 
| MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.342 | 
| MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.350 | 
| MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.472 | 
| MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.474 | 
| MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.368 | 
| MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.386 | 
| MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.298 | 
| MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.445 | 
| MOD_GlcNHglycan | 677 | 680 | PF01048 | 0.515 | 
| MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.345 | 
| MOD_GSK3_1 | 14 | 21 | PF00069 | 0.576 | 
| MOD_GSK3_1 | 260 | 267 | PF00069 | 0.511 | 
| MOD_GSK3_1 | 290 | 297 | PF00069 | 0.648 | 
| MOD_GSK3_1 | 361 | 368 | PF00069 | 0.353 | 
| MOD_GSK3_1 | 418 | 425 | PF00069 | 0.464 | 
| MOD_GSK3_1 | 525 | 532 | PF00069 | 0.402 | 
| MOD_GSK3_1 | 546 | 553 | PF00069 | 0.464 | 
| MOD_GSK3_1 | 668 | 675 | PF00069 | 0.451 | 
| MOD_GSK3_1 | 686 | 693 | PF00069 | 0.279 | 
| MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.492 | 
| MOD_N-GLC_1 | 672 | 677 | PF02516 | 0.444 | 
| MOD_N-GLC_2 | 310 | 312 | PF02516 | 0.353 | 
| MOD_NEK2_1 | 191 | 196 | PF00069 | 0.500 | 
| MOD_NEK2_1 | 327 | 332 | PF00069 | 0.490 | 
| MOD_NEK2_1 | 419 | 424 | PF00069 | 0.422 | 
| MOD_NEK2_1 | 448 | 453 | PF00069 | 0.512 | 
| MOD_NEK2_1 | 546 | 551 | PF00069 | 0.474 | 
| MOD_NEK2_1 | 629 | 634 | PF00069 | 0.393 | 
| MOD_NEK2_1 | 699 | 704 | PF00069 | 0.410 | 
| MOD_NEK2_1 | 73 | 78 | PF00069 | 0.477 | 
| MOD_NEK2_2 | 24 | 29 | PF00069 | 0.444 | 
| MOD_NEK2_2 | 36 | 41 | PF00069 | 0.353 | 
| MOD_OFUCOSY | 33 | 40 | PF10250 | 0.369 | 
| MOD_PIKK_1 | 277 | 283 | PF00454 | 0.499 | 
| MOD_PIKK_1 | 3 | 9 | PF00454 | 0.530 | 
| MOD_PIKK_1 | 728 | 734 | PF00454 | 0.473 | 
| MOD_PKA_2 | 456 | 462 | PF00069 | 0.383 | 
| MOD_PKA_2 | 494 | 500 | PF00069 | 0.410 | 
| MOD_PKA_2 | 541 | 547 | PF00069 | 0.467 | 
| MOD_PKA_2 | 550 | 556 | PF00069 | 0.473 | 
| MOD_PKA_2 | 571 | 577 | PF00069 | 0.420 | 
| MOD_Plk_1 | 672 | 678 | PF00069 | 0.325 | 
| MOD_Plk_1 | 690 | 696 | PF00069 | 0.377 | 
| MOD_Plk_2-3 | 176 | 182 | PF00069 | 0.572 | 
| MOD_Plk_4 | 313 | 319 | PF00069 | 0.360 | 
| MOD_Plk_4 | 327 | 333 | PF00069 | 0.353 | 
| MOD_Plk_4 | 611 | 617 | PF00069 | 0.411 | 
| MOD_Plk_4 | 737 | 743 | PF00069 | 0.405 | 
| MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.474 | 
| MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.473 | 
| MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.538 | 
| MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.499 | 
| MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.461 | 
| MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.345 | 
| MOD_SUMO_rev_2 | 651 | 656 | PF00179 | 0.500 | 
| MOD_SUMO_rev_2 | 84 | 91 | PF00179 | 0.690 | 
| TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.419 | 
| TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.473 | 
| TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.500 | 
| TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.473 | 
| TRG_ENDOCYTIC_2 | 559 | 562 | PF00928 | 0.473 | 
| TRG_ENDOCYTIC_2 | 627 | 630 | PF00928 | 0.387 | 
| TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.387 | 
| TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.731 | 
| TRG_ER_diArg_1 | 455 | 458 | PF00400 | 0.475 | 
| TRG_ER_diArg_1 | 492 | 495 | PF00400 | 0.457 | 
| TRG_ER_diArg_1 | 541 | 543 | PF00400 | 0.353 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1I2C0 | Leptomonas seymouri | 73% | 100% | 
| A0A0S4IPD1 | Bodo saltans | 45% | 100% | 
| A0A1X0PA40 | Trypanosomatidae | 56% | 100% | 
| A0A3Q8IDW9 | Leishmania donovani | 95% | 100% | 
| A0A422NEJ9 | Trypanosoma rangeli | 55% | 100% | 
| A4HHM9 | Leishmania braziliensis | 83% | 100% | 
| A4I4U4 | Leishmania infantum | 95% | 100% | 
| C9ZLJ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% | 
| E1BMF7 | Bos taurus | 30% | 87% | 
| E1BY77 | Gallus gallus | 29% | 87% | 
| E9AE92 | Leishmania major | 94% | 100% | 
| F1QFS9 | Danio rerio | 29% | 87% | 
| F6V6I0 | Xenopus tropicalis | 28% | 88% | 
| P38237 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 96% | 
| P45974 | Homo sapiens | 30% | 87% | 
| P54201 | Dictyostelium discoideum | 27% | 89% | 
| P56399 | Mus musculus | 30% | 87% | 
| Q11119 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 97% | 
| Q5BKP2 | Mus musculus | 28% | 87% | 
| Q5R407 | Pongo abelii | 31% | 87% | 
| Q8L6Y1 | Arabidopsis thaliana | 30% | 94% | 
| Q92995 | Homo sapiens | 29% | 87% | 
| V5BC27 | Trypanosoma cruzi | 56% | 100% |