| 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:0005634 | nucleus | 5 | 1 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AXK7
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006508 | proteolysis | 4 | 7 |
| GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 7 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
| GO:0008152 | metabolic process | 1 | 7 |
| GO:0009056 | catabolic process | 2 | 7 |
| GO:0009057 | macromolecule catabolic process | 4 | 7 |
| GO:0009987 | cellular process | 1 | 7 |
| GO:0019538 | protein metabolic process | 3 | 7 |
| GO:0019941 | modification-dependent protein catabolic process | 6 | 7 |
| GO:0043170 | macromolecule metabolic process | 3 | 7 |
| GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 7 |
| GO:0044237 | cellular metabolic process | 2 | 7 |
| GO:0044238 | primary metabolic process | 2 | 7 |
| GO:0044248 | cellular catabolic process | 3 | 7 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
| GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 7 |
| GO:0051603 | proteolysis involved in protein catabolic process | 5 | 7 |
| GO:0071704 | organic substance metabolic process | 2 | 7 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
| GO:1901575 | organic substance catabolic process | 3 | 7 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005488 | binding | 1 | 1 |
| GO:0005515 | protein binding | 2 | 1 |
| GO:0019899 | enzyme binding | 3 | 1 |
| GO:0031625 | ubiquitin protein ligase binding | 5 | 1 |
| GO:0032182 | ubiquitin-like protein binding | 3 | 1 |
| GO:0043130 | ubiquitin binding | 4 | 1 |
| GO:0044389 | ubiquitin-like protein ligase binding | 4 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 206 | 210 | PF00656 | 0.642 |
| CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.503 |
| CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.482 |
| CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.438 |
| CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.533 |
| CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.558 |
| CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.312 |
| CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.312 |
| CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.503 |
| CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.552 |
| CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.482 |
| CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.492 |
| CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.312 |
| CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.287 |
| CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.586 |
| CLV_PCSK_PC1ET2_1 | 572 | 574 | PF00082 | 0.312 |
| CLV_PCSK_PC7_1 | 215 | 221 | PF00082 | 0.558 |
| CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.399 |
| CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.322 |
| CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.313 |
| CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.246 |
| CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.287 |
| CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.385 |
| DEG_APCC_DBOX_1 | 294 | 302 | PF00400 | 0.481 |
| DEG_SPOP_SBC_1 | 274 | 278 | PF00917 | 0.616 |
| DOC_CYCLIN_yCln2_LP_2 | 37 | 40 | PF00134 | 0.435 |
| DOC_MAPK_DCC_7 | 100 | 109 | PF00069 | 0.465 |
| DOC_MAPK_gen_1 | 3 | 14 | PF00069 | 0.443 |
| DOC_MAPK_gen_1 | 364 | 374 | PF00069 | 0.599 |
| DOC_MAPK_gen_1 | 569 | 578 | PF00069 | 0.545 |
| DOC_MAPK_gen_1 | 98 | 106 | PF00069 | 0.512 |
| DOC_MAPK_MEF2A_6 | 100 | 109 | PF00069 | 0.465 |
| DOC_MAPK_MEF2A_6 | 30 | 37 | PF00069 | 0.446 |
| DOC_MAPK_MEF2A_6 | 386 | 395 | PF00069 | 0.533 |
| DOC_MAPK_RevD_3 | 360 | 376 | PF00069 | 0.533 |
| DOC_PP1_RVXF_1 | 286 | 292 | PF00149 | 0.470 |
| DOC_PP2B_LxvP_1 | 22 | 25 | PF13499 | 0.433 |
| DOC_PP2B_LxvP_1 | 37 | 40 | PF13499 | 0.400 |
| DOC_PP2B_PxIxI_1 | 104 | 110 | PF00149 | 0.441 |
| DOC_PP2B_PxIxI_1 | 451 | 457 | PF00149 | 0.533 |
| DOC_PP4_FxxP_1 | 539 | 542 | PF00568 | 0.550 |
| DOC_PP4_MxPP_1 | 556 | 559 | PF00568 | 0.512 |
| DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.439 |
| DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.444 |
| DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.547 |
| DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.550 |
| DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.366 |
| DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.527 |
| DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.497 |
| DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.502 |
| DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.642 |
| DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.452 |
| DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.527 |
| DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.545 |
| DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.512 |
| DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.550 |
| LIG_14-3-3_CanoR_1 | 20 | 25 | PF00244 | 0.437 |
| LIG_14-3-3_CanoR_1 | 515 | 521 | PF00244 | 0.471 |
| LIG_14-3-3_CanoR_1 | 528 | 534 | PF00244 | 0.496 |
| LIG_14-3-3_CanoR_1 | 573 | 579 | PF00244 | 0.479 |
| LIG_14-3-3_CanoR_1 | 603 | 609 | PF00244 | 0.550 |
| LIG_14-3-3_CanoR_1 | 87 | 93 | PF00244 | 0.513 |
| LIG_Actin_WH2_2 | 361 | 377 | PF00022 | 0.550 |
| LIG_BRCT_BRCA1_1 | 114 | 118 | PF00533 | 0.467 |
| LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.660 |
| LIG_BRCT_BRCA1_1 | 22 | 26 | PF00533 | 0.458 |
| LIG_BRCT_BRCA1_1 | 252 | 256 | PF00533 | 0.553 |
| LIG_BRCT_BRCA1_1 | 574 | 578 | PF00533 | 0.533 |
| LIG_Clathr_ClatBox_1 | 298 | 302 | PF01394 | 0.410 |
| LIG_eIF4E_1 | 57 | 63 | PF01652 | 0.442 |
| LIG_FHA_1 | 133 | 139 | PF00498 | 0.527 |
| LIG_FHA_1 | 229 | 235 | PF00498 | 0.638 |
| LIG_FHA_1 | 269 | 275 | PF00498 | 0.546 |
| LIG_FHA_1 | 294 | 300 | PF00498 | 0.438 |
| LIG_FHA_1 | 332 | 338 | PF00498 | 0.518 |
| LIG_FHA_1 | 451 | 457 | PF00498 | 0.599 |
| LIG_FHA_1 | 496 | 502 | PF00498 | 0.515 |
| LIG_FHA_1 | 529 | 535 | PF00498 | 0.502 |
| LIG_FHA_2 | 504 | 510 | PF00498 | 0.550 |
| LIG_FHA_2 | 521 | 527 | PF00498 | 0.550 |
| LIG_FHA_2 | 579 | 585 | PF00498 | 0.604 |
| LIG_FHA_2 | 595 | 601 | PF00498 | 0.454 |
| LIG_LIR_Gen_1 | 253 | 264 | PF02991 | 0.536 |
| LIG_LIR_Gen_1 | 531 | 539 | PF02991 | 0.512 |
| LIG_LIR_Gen_1 | 584 | 592 | PF02991 | 0.506 |
| LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.451 |
| LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.421 |
| LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.516 |
| LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.612 |
| LIG_LIR_Nem_3 | 527 | 533 | PF02991 | 0.490 |
| LIG_LIR_Nem_3 | 55 | 60 | PF02991 | 0.439 |
| LIG_LIR_Nem_3 | 584 | 588 | PF02991 | 0.506 |
| LIG_LYPXL_L_2 | 56 | 65 | PF13949 | 0.445 |
| LIG_LYPXL_S_1 | 56 | 60 | PF13949 | 0.437 |
| LIG_MYND_1 | 36 | 40 | PF01753 | 0.436 |
| LIG_NRBOX | 587 | 593 | PF00104 | 0.599 |
| LIG_Pex14_1 | 529 | 533 | PF04695 | 0.512 |
| LIG_Pex14_2 | 71 | 75 | PF04695 | 0.451 |
| LIG_Rb_pABgroove_1 | 324 | 332 | PF01858 | 0.599 |
| LIG_SH2_CRK | 19 | 23 | PF00017 | 0.446 |
| LIG_SH2_CRK | 323 | 327 | PF00017 | 0.550 |
| LIG_SH2_CRK | 621 | 625 | PF00017 | 0.560 |
| LIG_SH2_NCK_1 | 330 | 334 | PF00017 | 0.512 |
| LIG_SH2_PTP2 | 533 | 536 | PF00017 | 0.512 |
| LIG_SH2_SRC | 330 | 333 | PF00017 | 0.599 |
| LIG_SH2_SRC | 46 | 49 | PF00017 | 0.477 |
| LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.518 |
| LIG_SH2_STAP1 | 323 | 327 | PF00017 | 0.599 |
| LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.558 |
| LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.512 |
| LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.491 |
| LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.550 |
| LIG_SH3_3 | 148 | 154 | PF00018 | 0.463 |
| LIG_SH3_3 | 30 | 36 | PF00018 | 0.444 |
| LIG_SH3_3 | 339 | 345 | PF00018 | 0.497 |
| LIG_SH3_3 | 37 | 43 | PF00018 | 0.422 |
| LIG_SH3_3 | 53 | 59 | PF00018 | 0.429 |
| LIG_SH3_3 | 551 | 557 | PF00018 | 0.550 |
| LIG_SUMO_SIM_par_1 | 451 | 457 | PF11976 | 0.599 |
| LIG_TYR_ITSM | 529 | 536 | PF00017 | 0.370 |
| LIG_UBA3_1 | 187 | 191 | PF00899 | 0.569 |
| LIG_UBA3_1 | 255 | 263 | PF00899 | 0.576 |
| LIG_WRC_WIRS_1 | 309 | 314 | PF05994 | 0.409 |
| LIG_WW_1 | 43 | 46 | PF00397 | 0.449 |
| LIG_WW_2 | 40 | 43 | PF00397 | 0.429 |
| MOD_CDK_SPxxK_3 | 228 | 235 | PF00069 | 0.638 |
| MOD_CDK_SPxxK_3 | 538 | 545 | PF00069 | 0.424 |
| MOD_CK1_1 | 168 | 174 | PF00069 | 0.596 |
| MOD_CK1_1 | 268 | 274 | PF00069 | 0.556 |
| MOD_CK1_1 | 350 | 356 | PF00069 | 0.399 |
| MOD_CK1_1 | 424 | 430 | PF00069 | 0.353 |
| MOD_CK1_1 | 446 | 452 | PF00069 | 0.468 |
| MOD_CK1_1 | 86 | 92 | PF00069 | 0.507 |
| MOD_CK2_1 | 574 | 580 | PF00069 | 0.399 |
| MOD_CK2_1 | 595 | 601 | PF00069 | 0.427 |
| MOD_Cter_Amidation | 1 | 4 | PF01082 | 0.444 |
| MOD_Cter_Amidation | 179 | 182 | PF01082 | 0.475 |
| MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.446 |
| MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.563 |
| MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.439 |
| MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.450 |
| MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.463 |
| MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.277 |
| MOD_GlcNHglycan | 509 | 513 | PF01048 | 0.393 |
| MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.482 |
| MOD_GSK3_1 | 108 | 115 | PF00069 | 0.444 |
| MOD_GSK3_1 | 128 | 135 | PF00069 | 0.423 |
| MOD_GSK3_1 | 154 | 161 | PF00069 | 0.559 |
| MOD_GSK3_1 | 164 | 171 | PF00069 | 0.571 |
| MOD_GSK3_1 | 191 | 198 | PF00069 | 0.607 |
| MOD_GSK3_1 | 203 | 210 | PF00069 | 0.581 |
| MOD_GSK3_1 | 265 | 272 | PF00069 | 0.475 |
| MOD_GSK3_1 | 424 | 431 | PF00069 | 0.405 |
| MOD_GSK3_1 | 446 | 453 | PF00069 | 0.399 |
| MOD_GSK3_1 | 48 | 55 | PF00069 | 0.734 |
| MOD_GSK3_1 | 515 | 522 | PF00069 | 0.368 |
| MOD_GSK3_1 | 524 | 531 | PF00069 | 0.335 |
| MOD_GSK3_1 | 574 | 581 | PF00069 | 0.401 |
| MOD_GSK3_1 | 590 | 597 | PF00069 | 0.391 |
| MOD_GSK3_1 | 604 | 611 | PF00069 | 0.314 |
| MOD_GSK3_1 | 81 | 88 | PF00069 | 0.492 |
| MOD_LATS_1 | 513 | 519 | PF00433 | 0.424 |
| MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.543 |
| MOD_N-GLC_2 | 248 | 250 | PF02516 | 0.524 |
| MOD_NEK2_1 | 516 | 521 | PF00069 | 0.213 |
| MOD_NEK2_1 | 549 | 554 | PF00069 | 0.384 |
| MOD_NEK2_1 | 578 | 583 | PF00069 | 0.399 |
| MOD_NEK2_2 | 105 | 110 | PF00069 | 0.436 |
| MOD_NEK2_2 | 154 | 159 | PF00069 | 0.544 |
| MOD_NEK2_2 | 165 | 170 | PF00069 | 0.699 |
| MOD_NEK2_2 | 66 | 71 | PF00069 | 0.476 |
| MOD_OFUCOSY | 11 | 18 | PF10250 | 0.452 |
| MOD_OFUCOSY | 153 | 158 | PF10250 | 0.448 |
| MOD_PIKK_1 | 126 | 132 | PF00454 | 0.503 |
| MOD_PIKK_1 | 293 | 299 | PF00454 | 0.498 |
| MOD_PIKK_1 | 590 | 596 | PF00454 | 0.424 |
| MOD_PKA_1 | 572 | 578 | PF00069 | 0.399 |
| MOD_PKA_2 | 138 | 144 | PF00069 | 0.552 |
| MOD_PKA_2 | 165 | 171 | PF00069 | 0.749 |
| MOD_PKA_2 | 549 | 555 | PF00069 | 0.370 |
| MOD_PKA_2 | 572 | 578 | PF00069 | 0.403 |
| MOD_PKA_2 | 81 | 87 | PF00069 | 0.485 |
| MOD_PKB_1 | 110 | 118 | PF00069 | 0.435 |
| MOD_Plk_1 | 284 | 290 | PF00069 | 0.476 |
| MOD_Plk_1 | 403 | 409 | PF00069 | 0.360 |
| MOD_Plk_4 | 165 | 171 | PF00069 | 0.646 |
| MOD_Plk_4 | 265 | 271 | PF00069 | 0.480 |
| MOD_Plk_4 | 308 | 314 | PF00069 | 0.411 |
| MOD_Plk_4 | 450 | 456 | PF00069 | 0.427 |
| MOD_Plk_4 | 529 | 535 | PF00069 | 0.356 |
| MOD_Plk_4 | 66 | 72 | PF00069 | 0.476 |
| MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.495 |
| MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.501 |
| MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.638 |
| MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.452 |
| MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.392 |
| MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.416 |
| MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.370 |
| MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.424 |
| MOD_SUMO_rev_2 | 258 | 264 | PF00179 | 0.475 |
| TRG_DiLeu_BaEn_3 | 101 | 107 | PF01217 | 0.478 |
| TRG_DiLeu_BaLyEn_6 | 183 | 188 | PF01217 | 0.602 |
| TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.458 |
| TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.450 |
| TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.424 |
| TRG_ENDOCYTIC_2 | 533 | 536 | PF00928 | 0.370 |
| TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.435 |
| TRG_ENDOCYTIC_2 | 621 | 624 | PF00928 | 0.483 |
| TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.417 |
| TRG_ER_diArg_1 | 118 | 120 | PF00400 | 0.468 |
| TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.482 |
| TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.517 |
| TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.370 |
| TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.449 |
| TRG_NES_CRM1_1 | 389 | 404 | PF08389 | 0.399 |
| TRG_NES_CRM1_1 | 580 | 594 | PF08389 | 0.424 |
| TRG_NLS_MonoExtN_4 | 569 | 576 | PF00514 | 0.427 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I4H2 | Leptomonas seymouri | 72% | 100% |
| A0A3S7WZ51 | Leishmania donovani | 94% | 100% |
| A4HE71 | Leishmania braziliensis | 87% | 100% |
| C9ZK00 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
| Q4Q9W4 | Leishmania major | 82% | 100% |