| 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: 9 |
| NetGPI | no | yes: 0, no: 9 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 10 |
| GO:0110165 | cellular anatomical entity | 1 | 10 |
| GO:0031974 | membrane-enclosed lumen | 2 | 1 |
| GO:0031981 | nuclear lumen | 5 | 1 |
| GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
| GO:0043233 | organelle lumen | 3 | 1 |
| GO:0070013 | intracellular organelle lumen | 4 | 1 |
| GO:0097014 | ciliary plasm | 5 | 1 |
| GO:0099568 | cytoplasmic region | 3 | 1 |
| GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9AUK4
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
| GO:0006396 | RNA processing | 6 | 10 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
| GO:0008152 | metabolic process | 1 | 10 |
| GO:0009987 | cellular process | 1 | 10 |
| GO:0016070 | RNA metabolic process | 5 | 10 |
| GO:0031123 | RNA 3'-end processing | 7 | 10 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
| GO:0043170 | macromolecule metabolic process | 3 | 10 |
| GO:0044237 | cellular metabolic process | 2 | 10 |
| GO:0044238 | primary metabolic process | 2 | 10 |
| GO:0046483 | heterocycle metabolic process | 3 | 10 |
| GO:0071076 | RNA 3' uridylation | 8 | 10 |
| GO:0071704 | organic substance metabolic process | 2 | 10 |
| GO:0090304 | nucleic acid metabolic process | 4 | 10 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 10 |
| GO:0016740 | transferase activity | 2 | 10 |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
| GO:0016779 | nucleotidyltransferase activity | 4 | 10 |
| GO:0050265 | RNA uridylyltransferase activity | 4 | 10 |
| GO:0070569 | uridylyltransferase activity | 5 | 10 |
| GO:0140098 | catalytic activity, acting on RNA | 3 | 10 |
| GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.396 |
| CLV_C14_Caspase3-7 | 83 | 87 | PF00656 | 0.490 |
| CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.237 |
| CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.337 |
| CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.399 |
| CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.289 |
| CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.357 |
| CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.431 |
| CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.228 |
| CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.237 |
| CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.337 |
| CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.417 |
| CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.289 |
| CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.357 |
| CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.343 |
| CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.371 |
| CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.351 |
| CLV_PCSK_PC1ET2_1 | 168 | 170 | PF00082 | 0.228 |
| CLV_PCSK_PC1ET2_1 | 291 | 293 | PF00082 | 0.392 |
| CLV_PCSK_PC1ET2_1 | 365 | 367 | PF00082 | 0.421 |
| CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.351 |
| CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.441 |
| CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.391 |
| CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.277 |
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.473 |
| DEG_SPOP_SBC_1 | 307 | 311 | PF00917 | 0.617 |
| DOC_ANK_TNKS_1 | 349 | 356 | PF00023 | 0.431 |
| DOC_MAPK_gen_1 | 356 | 364 | PF00069 | 0.523 |
| DOC_MAPK_HePTP_8 | 39 | 51 | PF00069 | 0.373 |
| DOC_MAPK_MEF2A_6 | 356 | 364 | PF00069 | 0.416 |
| DOC_MAPK_MEF2A_6 | 42 | 51 | PF00069 | 0.477 |
| DOC_PP2B_LxvP_1 | 211 | 214 | PF13499 | 0.391 |
| DOC_PP4_FxxP_1 | 223 | 226 | PF00568 | 0.351 |
| DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.279 |
| DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.698 |
| DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.527 |
| DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.299 |
| DOC_USP7_UBL2_3 | 164 | 168 | PF12436 | 0.295 |
| DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.348 |
| LIG_14-3-3_CanoR_1 | 20 | 28 | PF00244 | 0.334 |
| LIG_14-3-3_CanoR_1 | 270 | 276 | PF00244 | 0.363 |
| LIG_14-3-3_CanoR_1 | 306 | 316 | PF00244 | 0.551 |
| LIG_14-3-3_CanoR_1 | 331 | 339 | PF00244 | 0.300 |
| LIG_Actin_WH2_2 | 236 | 251 | PF00022 | 0.428 |
| LIG_BRCT_BRCA1_1 | 311 | 315 | PF00533 | 0.689 |
| LIG_BRCT_BRCA1_1 | 379 | 383 | PF00533 | 0.419 |
| LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.418 |
| LIG_FHA_1 | 185 | 191 | PF00498 | 0.272 |
| LIG_FHA_1 | 261 | 267 | PF00498 | 0.296 |
| LIG_FHA_1 | 333 | 339 | PF00498 | 0.453 |
| LIG_FHA_1 | 384 | 390 | PF00498 | 0.572 |
| LIG_FHA_2 | 20 | 26 | PF00498 | 0.507 |
| LIG_FHA_2 | 210 | 216 | PF00498 | 0.314 |
| LIG_FHA_2 | 60 | 66 | PF00498 | 0.390 |
| LIG_GBD_Chelix_1 | 28 | 36 | PF00786 | 0.225 |
| LIG_LIR_Apic_2 | 221 | 226 | PF02991 | 0.355 |
| LIG_LIR_Gen_1 | 252 | 259 | PF02991 | 0.381 |
| LIG_LIR_Gen_1 | 274 | 284 | PF02991 | 0.351 |
| LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.320 |
| LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.321 |
| LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.296 |
| LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.281 |
| LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.352 |
| LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.391 |
| LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.298 |
| LIG_LIR_Nem_3 | 363 | 367 | PF02991 | 0.332 |
| LIG_LIR_Nem_3 | 69 | 75 | PF02991 | 0.312 |
| LIG_PCNA_yPIPBox_3 | 372 | 383 | PF02747 | 0.277 |
| LIG_SH2_CRK | 276 | 280 | PF00017 | 0.456 |
| LIG_SH2_GRB2like | 345 | 348 | PF00017 | 0.303 |
| LIG_SH2_PTP2 | 159 | 162 | PF00017 | 0.275 |
| LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.340 |
| LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.283 |
| LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.329 |
| LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.475 |
| LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.326 |
| LIG_SH3_3 | 169 | 175 | PF00018 | 0.324 |
| LIG_SUMO_SIM_anti_2 | 189 | 195 | PF11976 | 0.411 |
| LIG_SUMO_SIM_anti_2 | 263 | 268 | PF11976 | 0.295 |
| LIG_SUMO_SIM_anti_2 | 80 | 86 | PF11976 | 0.322 |
| LIG_SUMO_SIM_par_1 | 35 | 41 | PF11976 | 0.438 |
| LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.438 |
| LIG_TRFH_1 | 223 | 227 | PF08558 | 0.384 |
| LIG_WRC_WIRS_1 | 180 | 185 | PF05994 | 0.295 |
| LIG_WRC_WIRS_1 | 402 | 407 | PF05994 | 0.456 |
| LIG_WW_1 | 226 | 229 | PF00397 | 0.363 |
| MOD_CK1_1 | 19 | 25 | PF00069 | 0.417 |
| MOD_CK1_1 | 309 | 315 | PF00069 | 0.623 |
| MOD_CK1_1 | 54 | 60 | PF00069 | 0.311 |
| MOD_CK2_1 | 204 | 210 | PF00069 | 0.388 |
| MOD_CK2_1 | 316 | 322 | PF00069 | 0.601 |
| MOD_CK2_1 | 397 | 403 | PF00069 | 0.532 |
| MOD_CK2_1 | 77 | 83 | PF00069 | 0.384 |
| MOD_Cter_Amidation | 3 | 6 | PF01082 | 0.419 |
| MOD_Cter_Amidation | 348 | 351 | PF01082 | 0.343 |
| MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.401 |
| MOD_GlcNHglycan | 294 | 298 | PF01048 | 0.419 |
| MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.370 |
| MOD_GSK3_1 | 16 | 23 | PF00069 | 0.412 |
| MOD_GSK3_1 | 179 | 186 | PF00069 | 0.302 |
| MOD_GSK3_1 | 306 | 313 | PF00069 | 0.634 |
| MOD_GSK3_1 | 316 | 323 | PF00069 | 0.467 |
| MOD_GSK3_1 | 385 | 392 | PF00069 | 0.437 |
| MOD_GSK3_1 | 397 | 404 | PF00069 | 0.613 |
| MOD_GSK3_1 | 54 | 61 | PF00069 | 0.444 |
| MOD_GSK3_1 | 73 | 80 | PF00069 | 0.390 |
| MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.397 |
| MOD_N-GLC_1 | 375 | 380 | PF02516 | 0.538 |
| MOD_N-GLC_1 | 392 | 397 | PF02516 | 0.493 |
| MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.330 |
| MOD_NEK2_1 | 179 | 184 | PF00069 | 0.409 |
| MOD_NEK2_1 | 320 | 325 | PF00069 | 0.453 |
| MOD_NEK2_1 | 383 | 388 | PF00069 | 0.622 |
| MOD_NEK2_1 | 51 | 56 | PF00069 | 0.342 |
| MOD_NEK2_1 | 68 | 73 | PF00069 | 0.222 |
| MOD_PKA_2 | 16 | 22 | PF00069 | 0.345 |
| MOD_PKA_2 | 355 | 361 | PF00069 | 0.442 |
| MOD_Plk_1 | 129 | 135 | PF00069 | 0.296 |
| MOD_Plk_1 | 209 | 215 | PF00069 | 0.355 |
| MOD_Plk_1 | 293 | 299 | PF00069 | 0.495 |
| MOD_Plk_1 | 316 | 322 | PF00069 | 0.416 |
| MOD_Plk_1 | 375 | 381 | PF00069 | 0.580 |
| MOD_Plk_1 | 66 | 72 | PF00069 | 0.288 |
| MOD_Plk_4 | 186 | 192 | PF00069 | 0.405 |
| MOD_Plk_4 | 262 | 268 | PF00069 | 0.333 |
| MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.342 |
| MOD_SUMO_rev_2 | 357 | 367 | PF00179 | 0.512 |
| TRG_DiLeu_BaEn_1 | 106 | 111 | PF01217 | 0.320 |
| TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.275 |
| TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.369 |
| TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.339 |
| TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.328 |
| TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.343 |
| TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.327 |
| TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.467 |
| TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.230 |
| TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.323 |
| TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.287 |
| TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.357 |
| TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.360 |
| TRG_Pf-PMV_PEXEL_1 | 273 | 278 | PF00026 | 0.464 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P7H1 | Leptomonas seymouri | 63% | 100% |
| A0A0S4J0S6 | Bodo saltans | 56% | 100% |
| A0A1X0NX27 | Trypanosomatidae | 55% | 100% |
| A0A3Q8IDK5 | Leishmania donovani | 89% | 100% |
| A0A422NJM7 | Trypanosoma rangeli | 53% | 88% |
| A4HYQ1 | Leishmania infantum | 89% | 100% |
| C7AJA4 | Trypanosoma brucei brucei | 52% | 100% |
| C9ZI80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
| Q4QCY0 | Leishmania major | 88% | 100% |