| 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: 4 | 
| NetGPI | no | yes: 0, no: 4 | 
Related structures:
AlphaFold database: A4IBF1
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006508 | proteolysis | 4 | 5 | 
| GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 5 | 
| GO:0006807 | nitrogen compound metabolic process | 2 | 5 | 
| GO:0008152 | metabolic process | 1 | 5 | 
| GO:0009056 | catabolic process | 2 | 5 | 
| GO:0009057 | macromolecule catabolic process | 4 | 5 | 
| GO:0009987 | cellular process | 1 | 5 | 
| GO:0016579 | protein deubiquitination | 6 | 5 | 
| GO:0019538 | protein metabolic process | 3 | 5 | 
| GO:0019941 | modification-dependent protein catabolic process | 6 | 5 | 
| GO:0036211 | protein modification process | 4 | 5 | 
| GO:0043170 | macromolecule metabolic process | 3 | 5 | 
| GO:0043412 | macromolecule modification | 4 | 5 | 
| GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 5 | 
| GO:0044237 | cellular metabolic process | 2 | 5 | 
| GO:0044238 | primary metabolic process | 2 | 5 | 
| GO:0044248 | cellular catabolic process | 3 | 5 | 
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 5 | 
| GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 5 | 
| GO:0051603 | proteolysis involved in protein catabolic process | 5 | 5 | 
| GO:0070646 | protein modification by small protein removal | 5 | 5 | 
| GO:0070647 | protein modification by small protein conjugation or removal | 5 | 5 | 
| GO:0071704 | organic substance metabolic process | 2 | 5 | 
| GO:1901564 | organonitrogen compound metabolic process | 3 | 5 | 
| GO:1901575 | organic substance catabolic process | 3 | 5 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 5 | 
| GO:0004843 | cysteine-type deubiquitinase activity | 5 | 5 | 
| GO:0008233 | peptidase activity | 3 | 5 | 
| GO:0008234 | cysteine-type peptidase activity | 4 | 5 | 
| GO:0016787 | hydrolase activity | 2 | 5 | 
| GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 5 | 
| GO:0101005 | deubiquitinase activity | 5 | 5 | 
| GO:0140096 | catalytic activity, acting on a protein | 2 | 5 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 11 | 15 | PF00656 | 0.597 | 
| CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.435 | 
| CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.365 | 
| CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.235 | 
| CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.517 | 
| CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.528 | 
| CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.365 | 
| CLV_PCSK_FUR_1 | 338 | 342 | PF00082 | 0.259 | 
| CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.435 | 
| CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.350 | 
| CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.217 | 
| CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.329 | 
| CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.203 | 
| CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.528 | 
| CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.365 | 
| CLV_PCSK_PC1ET2_1 | 126 | 128 | PF00082 | 0.248 | 
| CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.319 | 
| CLV_PCSK_PC1ET2_1 | 358 | 360 | PF00082 | 0.203 | 
| CLV_PCSK_PC7_1 | 122 | 128 | PF00082 | 0.365 | 
| CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.515 | 
| CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.248 | 
| CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.248 | 
| CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.474 | 
| CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.344 | 
| CLV_Separin_Metazoa | 309 | 313 | PF03568 | 0.248 | 
| DEG_SPOP_SBC_1 | 143 | 147 | PF00917 | 0.248 | 
| DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.698 | 
| DOC_CKS1_1 | 97 | 102 | PF01111 | 0.248 | 
| DOC_CYCLIN_yCln2_LP_2 | 323 | 329 | PF00134 | 0.248 | 
| DOC_MAPK_gen_1 | 448 | 457 | PF00069 | 0.508 | 
| DOC_MAPK_MEF2A_6 | 264 | 273 | PF00069 | 0.248 | 
| DOC_MAPK_RevD_3 | 520 | 536 | PF00069 | 0.300 | 
| DOC_PP1_RVXF_1 | 226 | 233 | PF00149 | 0.248 | 
| DOC_PP4_FxxP_1 | 430 | 433 | PF00568 | 0.471 | 
| DOC_SPAK_OSR1_1 | 264 | 268 | PF12202 | 0.248 | 
| DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.295 | 
| DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.555 | 
| DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.673 | 
| DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.528 | 
| DOC_USP7_UBL2_3 | 298 | 302 | PF12436 | 0.248 | 
| DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.548 | 
| DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.558 | 
| DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.308 | 
| LIG_14-3-3_CanoR_1 | 228 | 233 | PF00244 | 0.248 | 
| LIG_14-3-3_CanoR_1 | 341 | 347 | PF00244 | 0.248 | 
| LIG_14-3-3_CanoR_1 | 394 | 402 | PF00244 | 0.350 | 
| LIG_14-3-3_CanoR_1 | 474 | 480 | PF00244 | 0.566 | 
| LIG_14-3-3_CanoR_1 | 55 | 65 | PF00244 | 0.581 | 
| LIG_BRCT_BRCA1_1 | 261 | 265 | PF00533 | 0.203 | 
| LIG_deltaCOP1_diTrp_1 | 116 | 123 | PF00928 | 0.248 | 
| LIG_eIF4E_1 | 263 | 269 | PF01652 | 0.248 | 
| LIG_eIF4E_1 | 348 | 354 | PF01652 | 0.391 | 
| LIG_FHA_1 | 143 | 149 | PF00498 | 0.235 | 
| LIG_FHA_1 | 367 | 373 | PF00498 | 0.411 | 
| LIG_FHA_1 | 8 | 14 | PF00498 | 0.564 | 
| LIG_FHA_1 | 84 | 90 | PF00498 | 0.235 | 
| LIG_FHA_1 | 97 | 103 | PF00498 | 0.235 | 
| LIG_FHA_2 | 1 | 7 | PF00498 | 0.598 | 
| LIG_FHA_2 | 211 | 217 | PF00498 | 0.408 | 
| LIG_FHA_2 | 238 | 244 | PF00498 | 0.248 | 
| LIG_FHA_2 | 436 | 442 | PF00498 | 0.521 | 
| LIG_Integrin_isoDGR_2 | 485 | 487 | PF01839 | 0.569 | 
| LIG_IRF3_LxIS_1 | 265 | 272 | PF10401 | 0.248 | 
| LIG_LIR_Apic_2 | 345 | 351 | PF02991 | 0.248 | 
| LIG_LIR_Apic_2 | 428 | 433 | PF02991 | 0.464 | 
| LIG_LIR_Gen_1 | 239 | 248 | PF02991 | 0.227 | 
| LIG_LIR_Gen_1 | 262 | 273 | PF02991 | 0.213 | 
| LIG_LIR_Gen_1 | 403 | 412 | PF02991 | 0.295 | 
| LIG_LIR_Gen_1 | 528 | 537 | PF02991 | 0.239 | 
| LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.431 | 
| LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.251 | 
| LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.225 | 
| LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.248 | 
| LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.235 | 
| LIG_LIR_Nem_3 | 528 | 533 | PF02991 | 0.234 | 
| LIG_NRBOX | 191 | 197 | PF00104 | 0.235 | 
| LIG_PCNA_yPIPBox_3 | 90 | 104 | PF02747 | 0.248 | 
| LIG_Pex14_2 | 373 | 377 | PF04695 | 0.295 | 
| LIG_REV1ctd_RIR_1 | 313 | 323 | PF16727 | 0.248 | 
| LIG_SH2_CRK | 405 | 409 | PF00017 | 0.416 | 
| LIG_SH2_GRB2like | 88 | 91 | PF00017 | 0.203 | 
| LIG_SH2_SRC | 88 | 91 | PF00017 | 0.235 | 
| LIG_SH2_STAP1 | 226 | 230 | PF00017 | 0.248 | 
| LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.248 | 
| LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.248 | 
| LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.230 | 
| LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.203 | 
| LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.351 | 
| LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.269 | 
| LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.330 | 
| LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.235 | 
| LIG_SH3_1 | 28 | 34 | PF00018 | 0.681 | 
| LIG_SH3_3 | 28 | 34 | PF00018 | 0.693 | 
| LIG_SH3_3 | 368 | 374 | PF00018 | 0.208 | 
| LIG_SH3_3 | 514 | 520 | PF00018 | 0.341 | 
| LIG_SH3_4 | 207 | 214 | PF00018 | 0.248 | 
| LIG_SUMO_SIM_par_1 | 145 | 153 | PF11976 | 0.248 | 
| LIG_TYR_ITIM | 532 | 537 | PF00017 | 0.328 | 
| LIG_TYR_ITSM | 401 | 408 | PF00017 | 0.235 | 
| LIG_UBA3_1 | 165 | 170 | PF00899 | 0.295 | 
| LIG_UBA3_1 | 192 | 201 | PF00899 | 0.248 | 
| LIG_UBA3_1 | 352 | 358 | PF00899 | 0.235 | 
| LIG_WRC_WIRS_1 | 13 | 18 | PF05994 | 0.531 | 
| MOD_CDC14_SPxK_1 | 445 | 448 | PF00782 | 0.439 | 
| MOD_CDK_SPxK_1 | 442 | 448 | PF00069 | 0.445 | 
| MOD_CDK_SPxK_1 | 49 | 55 | PF00069 | 0.601 | 
| MOD_CK1_1 | 276 | 282 | PF00069 | 0.399 | 
| MOD_CK1_1 | 48 | 54 | PF00069 | 0.554 | 
| MOD_CK1_1 | 56 | 62 | PF00069 | 0.488 | 
| MOD_CK1_1 | 66 | 72 | PF00069 | 0.527 | 
| MOD_CK1_1 | 9 | 15 | PF00069 | 0.591 | 
| MOD_CK2_1 | 133 | 139 | PF00069 | 0.258 | 
| MOD_CK2_1 | 253 | 259 | PF00069 | 0.248 | 
| MOD_CMANNOS | 229 | 232 | PF00535 | 0.248 | 
| MOD_Cter_Amidation | 118 | 121 | PF01082 | 0.248 | 
| MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.708 | 
| MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.298 | 
| MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.672 | 
| MOD_GlcNHglycan | 516 | 520 | PF01048 | 0.494 | 
| MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.701 | 
| MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.450 | 
| MOD_GSK3_1 | 249 | 256 | PF00069 | 0.211 | 
| MOD_GSK3_1 | 269 | 276 | PF00069 | 0.435 | 
| MOD_GSK3_1 | 32 | 39 | PF00069 | 0.625 | 
| MOD_GSK3_1 | 396 | 403 | PF00069 | 0.251 | 
| MOD_GSK3_1 | 42 | 49 | PF00069 | 0.614 | 
| MOD_GSK3_1 | 431 | 438 | PF00069 | 0.507 | 
| MOD_GSK3_1 | 474 | 481 | PF00069 | 0.675 | 
| MOD_GSK3_1 | 493 | 500 | PF00069 | 0.724 | 
| MOD_GSK3_1 | 53 | 60 | PF00069 | 0.637 | 
| MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.248 | 
| MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.411 | 
| MOD_N-GLC_1 | 512 | 517 | PF02516 | 0.339 | 
| MOD_NEK2_1 | 102 | 107 | PF00069 | 0.394 | 
| MOD_NEK2_1 | 165 | 170 | PF00069 | 0.248 | 
| MOD_NEK2_1 | 191 | 196 | PF00069 | 0.259 | 
| MOD_NEK2_1 | 21 | 26 | PF00069 | 0.657 | 
| MOD_NEK2_1 | 269 | 274 | PF00069 | 0.203 | 
| MOD_NEK2_1 | 36 | 41 | PF00069 | 0.565 | 
| MOD_NEK2_1 | 435 | 440 | PF00069 | 0.506 | 
| MOD_NEK2_1 | 83 | 88 | PF00069 | 0.250 | 
| MOD_NEK2_2 | 58 | 63 | PF00069 | 0.510 | 
| MOD_OFUCOSY | 251 | 258 | PF10250 | 0.304 | 
| MOD_OFUCOSY | 391 | 397 | PF10250 | 0.248 | 
| MOD_PIKK_1 | 278 | 284 | PF00454 | 0.313 | 
| MOD_PIKK_1 | 435 | 441 | PF00454 | 0.510 | 
| MOD_PKA_1 | 7 | 13 | PF00069 | 0.541 | 
| MOD_PKA_2 | 133 | 139 | PF00069 | 0.435 | 
| MOD_PKA_2 | 393 | 399 | PF00069 | 0.350 | 
| MOD_PKA_2 | 473 | 479 | PF00069 | 0.743 | 
| MOD_PKA_2 | 54 | 60 | PF00069 | 0.641 | 
| MOD_Plk_1 | 236 | 242 | PF00069 | 0.225 | 
| MOD_Plk_1 | 258 | 264 | PF00069 | 0.319 | 
| MOD_Plk_1 | 366 | 372 | PF00069 | 0.384 | 
| MOD_Plk_4 | 144 | 150 | PF00069 | 0.299 | 
| MOD_Plk_4 | 228 | 234 | PF00069 | 0.279 | 
| MOD_Plk_4 | 237 | 243 | PF00069 | 0.193 | 
| MOD_Plk_4 | 403 | 409 | PF00069 | 0.243 | 
| MOD_Plk_4 | 88 | 94 | PF00069 | 0.221 | 
| MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.545 | 
| MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.561 | 
| MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.308 | 
| MOD_SUMO_for_1 | 365 | 368 | PF00179 | 0.295 | 
| MOD_SUMO_rev_2 | 136 | 143 | PF00179 | 0.248 | 
| MOD_SUMO_rev_2 | 216 | 223 | PF00179 | 0.272 | 
| MOD_SUMO_rev_2 | 294 | 299 | PF00179 | 0.238 | 
| MOD_SUMO_rev_2 | 410 | 416 | PF00179 | 0.453 | 
| TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.221 | 
| TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.342 | 
| TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.257 | 
| TRG_ENDOCYTIC_2 | 534 | 537 | PF00928 | 0.274 | 
| TRG_ER_diArg_1 | 110 | 113 | PF00400 | 0.248 | 
| TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.422 | 
| TRG_ER_diArg_1 | 277 | 280 | PF00400 | 0.248 | 
| TRG_ER_diArg_1 | 450 | 452 | PF00400 | 0.531 | 
| TRG_ER_diArg_1 | 534 | 536 | PF00400 | 0.351 | 
| TRG_NLS_MonoExtC_3 | 417 | 422 | PF00514 | 0.489 | 
| TRG_Pf-PMV_PEXEL_1 | 104 | 109 | PF00026 | 0.248 | 
| TRG_Pf-PMV_PEXEL_1 | 25 | 30 | PF00026 | 0.524 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0S4KKZ6 | Bodo saltans | 29% | 100% | 
| A0A3Q8IB18 | Leishmania donovani | 24% | 76% | 
| A0A3Q8IGB5 | Leishmania donovani | 25% | 95% | 
| A0A3R7NR99 | Trypanosoma rangeli | 34% | 100% | 
| A4HZ39 | Leishmania infantum | 24% | 76% | 
| A4I2S8 | Leishmania infantum | 25% | 95% | 
| C9ZZB5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% | 
| E9ADA6 | Leishmania major | 25% | 95% | 
| Q2KHV7 | Bos taurus | 27% | 90% | 
| Q4QCH5 | Leishmania major | 24% | 82% | 
| Q9QZL6 | Mus musculus | 28% | 96% |