| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 2 |
| Forrest at al. (procyclic) | no | yes: 2 |
| 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: 6 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | no | yes: 6 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000502 | proteasome complex | 3 | 12 |
| GO:0032991 | protein-containing complex | 1 | 12 |
| GO:0140535 | intracellular protein-containing complex | 2 | 12 |
| GO:1902494 | catalytic complex | 2 | 12 |
| GO:1905368 | peptidase complex | 3 | 12 |
| GO:1905369 | endopeptidase complex | 4 | 12 |
Related structures:
AlphaFold database: E9B361
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006508 | proteolysis | 4 | 1 |
| GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009056 | catabolic process | 2 | 1 |
| GO:0009057 | macromolecule catabolic process | 4 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
| GO:0019538 | protein metabolic process | 3 | 1 |
| GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
| GO:0030163 | protein catabolic process | 4 | 1 |
| GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0044248 | cellular catabolic process | 3 | 1 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
| GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
| GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
| GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
| GO:1901575 | organic substance catabolic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0030234 | enzyme regulator activity | 2 | 12 |
| GO:0098772 | molecular function regulator activity | 1 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.431 |
| CLV_C14_Caspase3-7 | 367 | 371 | PF00656 | 0.515 |
| CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.212 |
| CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.317 |
| CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.295 |
| CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.230 |
| CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.518 |
| CLV_PCSK_PC1ET2_1 | 259 | 261 | PF00082 | 0.509 |
| CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.290 |
| CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.255 |
| CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.182 |
| CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.353 |
| DEG_SPOP_SBC_1 | 49 | 53 | PF00917 | 0.604 |
| DOC_MAPK_gen_1 | 166 | 173 | PF00069 | 0.515 |
| DOC_MAPK_gen_1 | 197 | 203 | PF00069 | 0.412 |
| DOC_MAPK_gen_1 | 387 | 396 | PF00069 | 0.374 |
| DOC_MAPK_MEF2A_6 | 166 | 173 | PF00069 | 0.423 |
| DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.553 |
| DOC_MAPK_MEF2A_6 | 69 | 78 | PF00069 | 0.565 |
| DOC_PP1_RVXF_1 | 317 | 324 | PF00149 | 0.412 |
| DOC_PP2B_LxvP_1 | 83 | 86 | PF13499 | 0.568 |
| DOC_PP4_FxxP_1 | 342 | 345 | PF00568 | 0.412 |
| DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.515 |
| DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.509 |
| DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.604 |
| DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.354 |
| DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.515 |
| DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.593 |
| LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.417 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.691 |
| LIG_BRCT_BRCA1_1 | 311 | 315 | PF00533 | 0.535 |
| LIG_FAT_LD_1 | 349 | 357 | PF03623 | 0.423 |
| LIG_FHA_1 | 322 | 328 | PF00498 | 0.437 |
| LIG_FHA_2 | 143 | 149 | PF00498 | 0.515 |
| LIG_FHA_2 | 234 | 240 | PF00498 | 0.509 |
| LIG_FHA_2 | 268 | 274 | PF00498 | 0.440 |
| LIG_FHA_2 | 379 | 385 | PF00498 | 0.385 |
| LIG_Integrin_RGD_1 | 377 | 379 | PF01839 | 0.428 |
| LIG_LIR_Apic_2 | 340 | 345 | PF02991 | 0.343 |
| LIG_LIR_Gen_1 | 131 | 141 | PF02991 | 0.452 |
| LIG_LIR_Gen_1 | 161 | 172 | PF02991 | 0.412 |
| LIG_LIR_Gen_1 | 205 | 215 | PF02991 | 0.456 |
| LIG_LIR_Gen_1 | 236 | 245 | PF02991 | 0.441 |
| LIG_LIR_Gen_1 | 284 | 294 | PF02991 | 0.466 |
| LIG_LIR_Gen_1 | 328 | 338 | PF02991 | 0.412 |
| LIG_LIR_Gen_1 | 384 | 389 | PF02991 | 0.355 |
| LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.456 |
| LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.412 |
| LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.413 |
| LIG_LIR_Nem_3 | 236 | 240 | PF02991 | 0.433 |
| LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.445 |
| LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.412 |
| LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.359 |
| LIG_MLH1_MIPbox_1 | 311 | 315 | PF16413 | 0.535 |
| LIG_Pex14_2 | 211 | 215 | PF04695 | 0.423 |
| LIG_PTB_Apo_2 | 277 | 284 | PF02174 | 0.431 |
| LIG_PTB_Phospho_1 | 277 | 283 | PF10480 | 0.431 |
| LIG_REV1ctd_RIR_1 | 312 | 320 | PF16727 | 0.418 |
| LIG_SH2_CRK | 133 | 137 | PF00017 | 0.479 |
| LIG_SH2_CRK | 287 | 291 | PF00017 | 0.515 |
| LIG_SH2_CRK | 330 | 334 | PF00017 | 0.412 |
| LIG_SH2_CRK | 385 | 389 | PF00017 | 0.357 |
| LIG_SH2_NCK_1 | 133 | 137 | PF00017 | 0.479 |
| LIG_SH2_NCK_1 | 287 | 291 | PF00017 | 0.515 |
| LIG_SH2_NCK_1 | 330 | 334 | PF00017 | 0.412 |
| LIG_SH2_PTP2 | 75 | 78 | PF00017 | 0.457 |
| LIG_SH2_STAP1 | 283 | 287 | PF00017 | 0.479 |
| LIG_SH2_STAT3 | 283 | 286 | PF00017 | 0.536 |
| LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.515 |
| LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.429 |
| LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.407 |
| LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.403 |
| LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.404 |
| LIG_SH3_3 | 1 | 7 | PF00018 | 0.758 |
| LIG_SH3_3 | 259 | 265 | PF00018 | 0.420 |
| LIG_SH3_3 | 29 | 35 | PF00018 | 0.497 |
| LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.515 |
| LIG_TRAF2_1 | 52 | 55 | PF00917 | 0.550 |
| LIG_UBA3_1 | 395 | 401 | PF00899 | 0.336 |
| LIG_UBA3_1 | 63 | 69 | PF00899 | 0.490 |
| LIG_WRC_WIRS_1 | 226 | 231 | PF05994 | 0.412 |
| LIG_WRC_WIRS_1 | 234 | 239 | PF05994 | 0.412 |
| LIG_WW_3 | 5 | 9 | PF00397 | 0.604 |
| MOD_CK1_1 | 225 | 231 | PF00069 | 0.412 |
| MOD_CK1_1 | 329 | 335 | PF00069 | 0.412 |
| MOD_CK1_1 | 337 | 343 | PF00069 | 0.412 |
| MOD_CK1_1 | 372 | 378 | PF00069 | 0.491 |
| MOD_CK1_1 | 48 | 54 | PF00069 | 0.534 |
| MOD_CK2_1 | 142 | 148 | PF00069 | 0.479 |
| MOD_CK2_1 | 250 | 256 | PF00069 | 0.423 |
| MOD_CK2_1 | 48 | 54 | PF00069 | 0.524 |
| MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.299 |
| MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.147 |
| MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.499 |
| MOD_GSK3_1 | 241 | 248 | PF00069 | 0.512 |
| MOD_GSK3_1 | 305 | 312 | PF00069 | 0.515 |
| MOD_GSK3_1 | 348 | 355 | PF00069 | 0.479 |
| MOD_GSK3_1 | 44 | 51 | PF00069 | 0.487 |
| MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.434 |
| MOD_NEK2_1 | 222 | 227 | PF00069 | 0.426 |
| MOD_NEK2_1 | 278 | 283 | PF00069 | 0.479 |
| MOD_NEK2_1 | 321 | 326 | PF00069 | 0.431 |
| MOD_NEK2_1 | 352 | 357 | PF00069 | 0.442 |
| MOD_NEK2_1 | 87 | 92 | PF00069 | 0.359 |
| MOD_PIKK_1 | 321 | 327 | PF00454 | 0.463 |
| MOD_PKA_2 | 216 | 222 | PF00069 | 0.468 |
| MOD_PKA_2 | 42 | 48 | PF00069 | 0.424 |
| MOD_PKA_2 | 55 | 61 | PF00069 | 0.485 |
| MOD_Plk_2-3 | 233 | 239 | PF00069 | 0.515 |
| MOD_Plk_4 | 278 | 284 | PF00069 | 0.479 |
| MOD_Plk_4 | 309 | 315 | PF00069 | 0.515 |
| MOD_Plk_4 | 348 | 354 | PF00069 | 0.418 |
| MOD_Plk_4 | 35 | 41 | PF00069 | 0.515 |
| MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.352 |
| MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.515 |
| MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.590 |
| MOD_SUMO_rev_2 | 88 | 93 | PF00179 | 0.455 |
| TRG_DiLeu_BaEn_1 | 317 | 322 | PF01217 | 0.423 |
| TRG_DiLeu_BaLyEn_6 | 32 | 37 | PF01217 | 0.401 |
| TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.479 |
| TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.412 |
| TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.412 |
| TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.429 |
| TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.412 |
| TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.362 |
| TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.389 |
| TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.479 |
| TRG_ER_diArg_1 | 197 | 200 | PF00400 | 0.413 |
| TRG_ER_diArg_1 | 257 | 260 | PF00400 | 0.515 |
| TRG_NLS_MonoExtN_4 | 255 | 262 | PF00514 | 0.472 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P8Z9 | Leptomonas seymouri | 88% | 100% |
| A0A0S4IM85 | Bodo saltans | 61% | 100% |
| A0A1X0NRP1 | Trypanosomatidae | 68% | 100% |
| A0A3Q8IJI2 | Leishmania donovani | 98% | 100% |
| A0A3R7NSJ6 | Trypanosoma rangeli | 68% | 100% |
| A4HKS3 | Leishmania braziliensis | 96% | 100% |
| A4I8A3 | Leishmania infantum | 99% | 100% |
| D0AAH5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
| P97834 | Rattus norvegicus | 21% | 87% |
| Q06103 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 95% |
| Q10335 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
| Q15008 | Homo sapiens | 38% | 100% |
| Q20585 | Caenorhabditis elegans | 36% | 100% |
| Q3T0B2 | Bos taurus | 37% | 100% |
| Q4Q4Z3 | Leishmania major | 99% | 100% |
| Q54QX3 | Dictyostelium discoideum | 22% | 89% |
| Q55C75 | Dictyostelium discoideum | 36% | 100% |
| Q8W425 | Oryza sativa subsp. japonica | 36% | 100% |
| Q93Y35 | Arabidopsis thaliana | 37% | 100% |
| Q99JI4 | Mus musculus | 37% | 100% |
| Q99LD4 | Mus musculus | 21% | 87% |
| Q9V3G7 | Drosophila melanogaster | 38% | 100% |
| V5AXY2 | Trypanosoma cruzi | 68% | 100% |