| 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: 11 | 
| NetGPI | no | yes: 0, no: 11 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016604 | nuclear body | 2 | 12 | 
| GO:0016605 | PML body | 3 | 12 | 
| GO:0110165 | cellular anatomical entity | 1 | 12 | 
| GO:0005634 | nucleus | 5 | 1 | 
| GO:0031974 | membrane-enclosed lumen | 2 | 1 | 
| GO:0031981 | nuclear lumen | 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:0043233 | organelle lumen | 3 | 1 | 
| GO:0070013 | intracellular organelle lumen | 4 | 1 | 
| GO:0016020 | membrane | 2 | 1 | 
Related structures:
AlphaFold database: E9AML5
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006807 | nitrogen compound metabolic process | 2 | 12 | 
| GO:0008152 | metabolic process | 1 | 12 | 
| GO:0016567 | protein ubiquitination | 7 | 12 | 
| GO:0019538 | protein metabolic process | 3 | 12 | 
| GO:0032446 | protein modification by small protein conjugation | 6 | 12 | 
| GO:0036211 | protein modification process | 4 | 12 | 
| GO:0043170 | macromolecule metabolic process | 3 | 12 | 
| GO:0043412 | macromolecule modification | 4 | 12 | 
| GO:0044238 | primary metabolic process | 2 | 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:0006508 | proteolysis | 4 | 1 | 
| GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 | 
| GO:0009056 | catabolic process | 2 | 1 | 
| GO:0009057 | macromolecule catabolic process | 4 | 1 | 
| GO:0009987 | cellular process | 1 | 1 | 
| GO:0019941 | modification-dependent protein catabolic process | 6 | 1 | 
| GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 | 
| GO:0044237 | cellular 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:1901575 | organic substance catabolic process | 3 | 1 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005488 | binding | 1 | 12 | 
| GO:0043167 | ion binding | 2 | 12 | 
| GO:0043169 | cation binding | 3 | 12 | 
| GO:0046872 | metal ion binding | 4 | 12 | 
| GO:0003824 | catalytic activity | 1 | 1 | 
| GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 | 
| GO:0016740 | transferase activity | 2 | 1 | 
| GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 | 
| GO:0140096 | catalytic activity, acting on a protein | 2 | 1 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.580 | 
| CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.341 | 
| CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.595 | 
| CLV_NRD_NRD_1 | 461 | 463 | PF00675 | 0.439 | 
| CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.246 | 
| CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.468 | 
| CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.376 | 
| CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.504 | 
| CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.558 | 
| CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.439 | 
| CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.241 | 
| CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.257 | 
| CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.460 | 
| CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.523 | 
| CLV_PCSK_PC1ET2_1 | 490 | 492 | PF00082 | 0.321 | 
| CLV_PCSK_PC1ET2_1 | 521 | 523 | PF00082 | 0.460 | 
| CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.289 | 
| CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.161 | 
| CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.477 | 
| DEG_APCC_DBOX_1 | 99 | 107 | PF00400 | 0.392 | 
| DEG_SCF_TRCP1_1 | 295 | 300 | PF00400 | 0.475 | 
| DOC_CDC14_PxL_1 | 50 | 58 | PF14671 | 0.505 | 
| DOC_CYCLIN_yCln2_LP_2 | 38 | 44 | PF00134 | 0.534 | 
| DOC_MAPK_gen_1 | 117 | 126 | PF00069 | 0.246 | 
| DOC_MAPK_gen_1 | 302 | 311 | PF00069 | 0.544 | 
| DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.562 | 
| DOC_PP4_FxxP_1 | 190 | 193 | PF00568 | 0.343 | 
| DOC_PP4_FxxP_1 | 334 | 337 | PF00568 | 0.309 | 
| DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.568 | 
| DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.614 | 
| DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.368 | 
| DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.315 | 
| DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.611 | 
| DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.676 | 
| DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.708 | 
| DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.392 | 
| DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.343 | 
| LIG_14-3-3_CanoR_1 | 174 | 184 | PF00244 | 0.332 | 
| LIG_14-3-3_CanoR_1 | 192 | 197 | PF00244 | 0.284 | 
| LIG_14-3-3_CanoR_1 | 235 | 245 | PF00244 | 0.571 | 
| LIG_14-3-3_CanoR_1 | 344 | 352 | PF00244 | 0.392 | 
| LIG_14-3-3_CanoR_1 | 462 | 468 | PF00244 | 0.458 | 
| LIG_14-3-3_CanoR_1 | 477 | 485 | PF00244 | 0.481 | 
| LIG_APCC_ABBA_1 | 388 | 393 | PF00400 | 0.330 | 
| LIG_APCC_ABBA_1 | 56 | 61 | PF00400 | 0.338 | 
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.646 | 
| LIG_deltaCOP1_diTrp_1 | 428 | 437 | PF00928 | 0.217 | 
| LIG_EVH1_2 | 401 | 405 | PF00568 | 0.343 | 
| LIG_FHA_1 | 180 | 186 | PF00498 | 0.278 | 
| LIG_FHA_1 | 231 | 237 | PF00498 | 0.398 | 
| LIG_FHA_1 | 312 | 318 | PF00498 | 0.428 | 
| LIG_FHA_1 | 53 | 59 | PF00498 | 0.436 | 
| LIG_FHA_1 | 96 | 102 | PF00498 | 0.313 | 
| LIG_FHA_2 | 117 | 123 | PF00498 | 0.288 | 
| LIG_Integrin_isoDGR_2 | 158 | 160 | PF01839 | 0.526 | 
| LIG_LIR_Apic_2 | 188 | 193 | PF02991 | 0.395 | 
| LIG_LIR_Apic_2 | 332 | 337 | PF02991 | 0.264 | 
| LIG_LIR_Gen_1 | 395 | 405 | PF02991 | 0.280 | 
| LIG_LIR_LC3C_4 | 91 | 94 | PF02991 | 0.142 | 
| LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.375 | 
| LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.218 | 
| LIG_LIR_Nem_3 | 466 | 471 | PF02991 | 0.312 | 
| LIG_PCNA_PIPBox_1 | 412 | 421 | PF02747 | 0.249 | 
| LIG_PTB_Apo_2 | 184 | 191 | PF02174 | 0.142 | 
| LIG_PTB_Apo_2 | 365 | 372 | PF02174 | 0.216 | 
| LIG_SH2_CRK | 50 | 54 | PF00017 | 0.529 | 
| LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.430 | 
| LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.249 | 
| LIG_SH3_3 | 396 | 402 | PF00018 | 0.441 | 
| LIG_SH3_3 | 452 | 458 | PF00018 | 0.187 | 
| LIG_SH3_3 | 90 | 96 | PF00018 | 0.142 | 
| LIG_UBA3_1 | 164 | 169 | PF00899 | 0.471 | 
| MOD_CDK_SPK_2 | 3 | 8 | PF00069 | 0.616 | 
| MOD_CDK_SPxxK_3 | 11 | 18 | PF00069 | 0.642 | 
| MOD_CDK_SPxxK_3 | 454 | 461 | PF00069 | 0.280 | 
| MOD_CK1_1 | 3 | 9 | PF00069 | 0.632 | 
| MOD_CK1_1 | 406 | 412 | PF00069 | 0.347 | 
| MOD_CK2_1 | 116 | 122 | PF00069 | 0.182 | 
| MOD_Cter_Amidation | 273 | 276 | PF01082 | 0.625 | 
| MOD_DYRK1A_RPxSP_1 | 454 | 458 | PF00069 | 0.280 | 
| MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.607 | 
| MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.567 | 
| MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.601 | 
| MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.396 | 
| MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.455 | 
| MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.532 | 
| MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.330 | 
| MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.441 | 
| MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.372 | 
| MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.498 | 
| MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.290 | 
| MOD_GSK3_1 | 104 | 111 | PF00069 | 0.285 | 
| MOD_GSK3_1 | 175 | 182 | PF00069 | 0.555 | 
| MOD_GSK3_1 | 291 | 298 | PF00069 | 0.538 | 
| MOD_GSK3_1 | 3 | 10 | PF00069 | 0.642 | 
| MOD_GSK3_1 | 343 | 350 | PF00069 | 0.280 | 
| MOD_GSK3_1 | 380 | 387 | PF00069 | 0.376 | 
| MOD_GSK3_1 | 79 | 86 | PF00069 | 0.448 | 
| MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.249 | 
| MOD_NEK2_1 | 236 | 241 | PF00069 | 0.398 | 
| MOD_NEK2_1 | 311 | 316 | PF00069 | 0.634 | 
| MOD_NEK2_1 | 343 | 348 | PF00069 | 0.351 | 
| MOD_NEK2_2 | 262 | 267 | PF00069 | 0.275 | 
| MOD_NEK2_2 | 297 | 302 | PF00069 | 0.551 | 
| MOD_NEK2_2 | 347 | 352 | PF00069 | 0.280 | 
| MOD_NEK2_2 | 463 | 468 | PF00069 | 0.343 | 
| MOD_OFUCOSY | 345 | 351 | PF10250 | 0.280 | 
| MOD_PK_1 | 192 | 198 | PF00069 | 0.343 | 
| MOD_PKA_2 | 116 | 122 | PF00069 | 0.430 | 
| MOD_PKA_2 | 175 | 181 | PF00069 | 0.471 | 
| MOD_PKA_2 | 223 | 229 | PF00069 | 0.461 | 
| MOD_PKA_2 | 230 | 236 | PF00069 | 0.327 | 
| MOD_PKA_2 | 343 | 349 | PF00069 | 0.330 | 
| MOD_PKA_2 | 7 | 13 | PF00069 | 0.677 | 
| MOD_Plk_4 | 108 | 114 | PF00069 | 0.249 | 
| MOD_Plk_4 | 185 | 191 | PF00069 | 0.304 | 
| MOD_Plk_4 | 192 | 198 | PF00069 | 0.266 | 
| MOD_Plk_4 | 420 | 426 | PF00069 | 0.304 | 
| MOD_Plk_4 | 463 | 469 | PF00069 | 0.305 | 
| MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.676 | 
| MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.708 | 
| MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.392 | 
| MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.343 | 
| MOD_SUMO_for_1 | 168 | 171 | PF00179 | 0.486 | 
| MOD_SUMO_for_1 | 435 | 438 | PF00179 | 0.369 | 
| TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.515 | 
| TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.435 | 
| TRG_ER_diArg_1 | 165 | 167 | PF00400 | 0.461 | 
| TRG_ER_diArg_1 | 174 | 177 | PF00400 | 0.563 | 
| TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.581 | 
| TRG_ER_diArg_1 | 475 | 477 | PF00400 | 0.302 | 
| TRG_NLS_MonoExtC_3 | 274 | 280 | PF00514 | 0.520 | 
| TRG_Pf-PMV_PEXEL_1 | 166 | 170 | PF00026 | 0.376 | 
| TRG_Pf-PMV_PEXEL_1 | 477 | 482 | PF00026 | 0.456 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P377 | Leptomonas seymouri | 63% | 98% | 
| A0A0S4JT63 | Bodo saltans | 41% | 100% | 
| A0A1X0NPC5 | Trypanosomatidae | 43% | 99% | 
| A0A3R7MDE3 | Trypanosoma rangeli | 44% | 96% | 
| A0A3S5H6B1 | Leishmania donovani | 91% | 100% | 
| A4H5J1 | Leishmania braziliensis | 75% | 99% | 
| A4HTT2 | Leishmania infantum | 91% | 100% | 
| A5WW08 | Danio rerio | 30% | 82% | 
| D0A993 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 94% | 
| Q4QI21 | Leishmania major | 90% | 100% | 
| Q5FWP4 | Xenopus laevis | 29% | 84% | 
| Q5RF77 | Pongo abelii | 28% | 92% | 
| Q6P256 | Xenopus tropicalis | 29% | 84% | 
| Q810L3 | Mus musculus | 30% | 79% | 
| Q96EP1 | Homo sapiens | 30% | 79% | 
| V5DJC2 | Trypanosoma cruzi | 43% | 84% |