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: A4HHM9
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 | 685 | 689 | PF00656 | 0.365 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 748 | 750 | PF00675 | 0.407 |
CLV_PCSK_KEX2_1 | 547 | 549 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.216 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.216 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 675 | 679 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 684 | 688 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 722 | 726 | PF00082 | 0.327 |
DOC_CDC14_PxL_1 | 115 | 123 | PF14671 | 0.528 |
DOC_CKS1_1 | 670 | 675 | PF01111 | 0.216 |
DOC_CYCLIN_RxL_1 | 716 | 729 | PF00134 | 0.333 |
DOC_CYCLIN_yCln2_LP_2 | 163 | 169 | PF00134 | 0.574 |
DOC_CYCLIN_yCln2_LP_2 | 466 | 472 | PF00134 | 0.296 |
DOC_MAPK_FxFP_2 | 330 | 333 | PF00069 | 0.281 |
DOC_MAPK_gen_1 | 462 | 470 | PF00069 | 0.322 |
DOC_MAPK_gen_1 | 559 | 567 | PF00069 | 0.300 |
DOC_MAPK_MEF2A_6 | 462 | 470 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 559 | 567 | PF00069 | 0.233 |
DOC_PP1_RVXF_1 | 720 | 727 | PF00149 | 0.327 |
DOC_PP2B_LxvP_1 | 466 | 469 | PF13499 | 0.296 |
DOC_PP4_FxxP_1 | 330 | 333 | PF00568 | 0.281 |
DOC_PP4_FxxP_1 | 649 | 652 | PF00568 | 0.387 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.220 |
DOC_USP7_MATH_1 | 589 | 593 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.275 |
DOC_USP7_UBL2_3 | 265 | 269 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 385 | 389 | PF12436 | 0.322 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 669 | 674 | PF00397 | 0.291 |
LIG_14-3-3_CanoR_1 | 455 | 461 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 498 | 504 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 508 | 513 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 534 | 539 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 547 | 551 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 675 | 683 | PF00244 | 0.376 |
LIG_14-3-3_CterR_2 | 749 | 751 | PF00244 | 0.413 |
LIG_APCC_ABBA_1 | 26 | 31 | PF00400 | 0.216 |
LIG_APCC_ABBA_1 | 561 | 566 | PF00400 | 0.227 |
LIG_APCC_ABBAyCdc20_2 | 560 | 566 | PF00400 | 0.217 |
LIG_APCC_ABBAyCdc20_2 | 722 | 728 | PF00400 | 0.327 |
LIG_BRCT_BRCA1_1 | 278 | 282 | PF00533 | 0.495 |
LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.308 |
LIG_Clathr_ClatBox_1 | 157 | 161 | PF01394 | 0.411 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.361 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.394 |
LIG_FHA_1 | 694 | 700 | PF00498 | 0.412 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.671 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.566 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.480 |
LIG_FHA_2 | 547 | 553 | PF00498 | 0.412 |
LIG_FHA_2 | 592 | 598 | PF00498 | 0.349 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.503 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.420 |
LIG_KLC1_Yacidic_2 | 562 | 566 | PF13176 | 0.216 |
LIG_LIR_Apic_2 | 646 | 652 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 283 | 292 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 44 | 51 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 526 | 536 | PF02991 | 0.216 |
LIG_LIR_Gen_1 | 562 | 571 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 720 | 731 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 283 | 287 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 404 | 408 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 537 | 541 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 549 | 553 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 562 | 567 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 574 | 579 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 720 | 726 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.727 |
LIG_NRBOX | 405 | 411 | PF00104 | 0.387 |
LIG_Pex14_2 | 327 | 331 | PF04695 | 0.293 |
LIG_Pex14_2 | 383 | 387 | PF04695 | 0.217 |
LIG_PTB_Apo_2 | 307 | 314 | PF02174 | 0.293 |
LIG_PTB_Apo_2 | 733 | 740 | PF02174 | 0.387 |
LIG_PTB_Phospho_1 | 307 | 313 | PF10480 | 0.293 |
LIG_REV1ctd_RIR_1 | 744 | 751 | PF16727 | 0.492 |
LIG_SH2_CRK | 529 | 533 | PF00017 | 0.216 |
LIG_SH2_CRK | 576 | 580 | PF00017 | 0.216 |
LIG_SH2_CRK | 632 | 636 | PF00017 | 0.352 |
LIG_SH2_CRK | 74 | 78 | PF00017 | 0.498 |
LIG_SH2_NCK_1 | 529 | 533 | PF00017 | 0.438 |
LIG_SH2_NCK_1 | 632 | 636 | PF00017 | 0.216 |
LIG_SH2_PTP2 | 416 | 419 | PF00017 | 0.227 |
LIG_SH2_PTP2 | 564 | 567 | PF00017 | 0.438 |
LIG_SH2_SRC | 276 | 279 | PF00017 | 0.547 |
LIG_SH2_SRC | 564 | 567 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 278 | 282 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 693 | 697 | PF00017 | 0.358 |
LIG_SH2_STAT3 | 278 | 281 | PF00017 | 0.487 |
LIG_SH2_STAT3 | 745 | 748 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 647 | 650 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 745 | 748 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.726 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.475 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.506 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.394 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.312 |
LIG_SH3_3 | 562 | 568 | PF00018 | 0.327 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.308 |
LIG_SH3_3 | 602 | 608 | PF00018 | 0.406 |
LIG_SH3_3 | 677 | 683 | PF00018 | 0.398 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.604 |
LIG_SUMO_SIM_anti_2 | 613 | 619 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 488 | 493 | PF11976 | 0.216 |
LIG_SUMO_SIM_par_1 | 616 | 622 | PF11976 | 0.438 |
LIG_TRAF2_1 | 608 | 611 | PF00917 | 0.438 |
LIG_TRAF2_2 | 608 | 613 | PF00917 | 0.358 |
LIG_TYR_ITIM | 527 | 532 | PF00017 | 0.259 |
LIG_TYR_ITIM | 72 | 77 | PF00017 | 0.289 |
LIG_TYR_ITIM | 91 | 96 | PF00017 | 0.713 |
MOD_CDK_SPxK_1 | 669 | 675 | PF00069 | 0.347 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.273 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.384 |
MOD_CK1_1 | 619 | 625 | PF00069 | 0.465 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.308 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.481 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.316 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.346 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.503 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.372 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.503 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.498 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.427 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.295 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.440 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.415 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.269 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.326 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.575 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.455 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.611 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.335 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.261 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.313 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.308 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.267 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.405 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.235 |
MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.514 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.343 |
MOD_N-GLC_2 | 310 | 312 | PF02516 | 0.293 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.464 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.265 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.294 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.352 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.544 |
MOD_NEK2_2 | 24 | 29 | PF00069 | 0.428 |
MOD_OFUCOSY | 33 | 40 | PF10250 | 0.308 |
MOD_OFUCOSY | 343 | 350 | PF10250 | 0.216 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.449 |
MOD_PIKK_1 | 731 | 737 | PF00454 | 0.438 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.347 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.352 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.438 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.413 |
MOD_Plk_1 | 693 | 699 | PF00069 | 0.289 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.308 |
MOD_Plk_4 | 616 | 622 | PF00069 | 0.358 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.425 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.551 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.441 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.451 |
MOD_ProDKin_1 | 669 | 675 | PF00069 | 0.291 |
MOD_SUMO_rev_2 | 656 | 661 | PF00179 | 0.358 |
MOD_SUMO_rev_2 | 84 | 91 | PF00179 | 0.655 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 550 | 553 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 564 | 567 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.726 |
TRG_ER_diArg_1 | 455 | 458 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 497 | 500 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 546 | 548 | PF00400 | 0.341 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2C0 | Leptomonas seymouri | 72% | 100% |
A0A0S4IPD1 | Bodo saltans | 46% | 100% |
A0A1X0PA40 | Trypanosomatidae | 54% | 100% |
A0A3Q8IDW9 | Leishmania donovani | 84% | 100% |
A0A422NEJ9 | Trypanosoma rangeli | 57% | 100% |
A4I4U4 | Leishmania infantum | 84% | 100% |
C9ZLJ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E1BMF7 | Bos taurus | 29% | 87% |
E1BY77 | Gallus gallus | 28% | 87% |
E9AE92 | Leishmania major | 83% | 99% |
E9ALJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
F1QFS9 | Danio rerio | 29% | 87% |
F6V6I0 | Xenopus tropicalis | 28% | 89% |
P0C8Z3 | Bos taurus | 23% | 100% |
P38237 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 96% |
P45974 | Homo sapiens | 31% | 88% |
P54201 | Dictyostelium discoideum | 29% | 90% |
P56399 | Mus musculus | 31% | 88% |
Q11119 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 97% |
Q5BKP2 | Mus musculus | 29% | 88% |
Q5R407 | Pongo abelii | 31% | 88% |
Q8L6Y1 | Arabidopsis thaliana | 30% | 94% |
Q92995 | Homo sapiens | 28% | 87% |
V5BC27 | Trypanosoma cruzi | 56% | 100% |