Translation, Uncharacterized
| 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. | yes | yes: 18 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005840 | ribosome | 5 | 12 |
| GO:0032991 | protein-containing complex | 1 | 11 |
| GO:0043226 | organelle | 2 | 12 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
| GO:0043229 | intracellular organelle | 3 | 12 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
| GO:0110165 | cellular anatomical entity | 1 | 12 |
| GO:1990904 | ribonucleoprotein complex | 2 | 11 |
Related structures:
AlphaFold database: A0A3S5H5H3
PDB structure(s): 7ane_f
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006412 | translation | 4 | 12 |
| GO:0006518 | peptide metabolic process | 4 | 12 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
| GO:0008152 | metabolic process | 1 | 12 |
| GO:0009058 | biosynthetic process | 2 | 12 |
| GO:0009059 | macromolecule biosynthetic process | 4 | 12 |
| GO:0009987 | cellular process | 1 | 12 |
| GO:0019538 | protein metabolic process | 3 | 12 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
| GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 12 |
| GO:0043043 | peptide biosynthetic process | 5 | 12 |
| GO:0043170 | macromolecule metabolic process | 3 | 12 |
| GO:0043603 | amide metabolic process | 3 | 12 |
| GO:0043604 | amide biosynthetic process | 4 | 12 |
| GO:0044237 | cellular metabolic process | 2 | 12 |
| GO:0044238 | primary metabolic process | 2 | 12 |
| GO:0044249 | cellular biosynthetic process | 3 | 12 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
| GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 12 |
| GO:0071704 | organic substance metabolic process | 2 | 12 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
| GO:1901566 | organonitrogen compound biosynthetic process | 4 | 12 |
| GO:1901576 | organic substance biosynthetic process | 3 | 12 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003735 | structural constituent of ribosome | 2 | 12 |
| GO:0005198 | structural molecule activity | 1 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.638 |
| CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.567 |
| CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.774 |
| CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.522 |
| CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.400 |
| CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.479 |
| CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.522 |
| CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.412 |
| CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.429 |
| CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.494 |
| CLV_PCSK_PC1ET2_1 | 259 | 261 | PF00082 | 0.445 |
| CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.423 |
| CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.466 |
| CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.504 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.645 |
| DEG_SPOP_SBC_1 | 167 | 171 | PF00917 | 0.741 |
| DOC_ANK_TNKS_1 | 148 | 155 | PF00023 | 0.626 |
| DOC_CDC14_PxL_1 | 25 | 33 | PF14671 | 0.494 |
| DOC_MAPK_gen_1 | 316 | 326 | PF00069 | 0.403 |
| DOC_MAPK_MEF2A_6 | 235 | 242 | PF00069 | 0.433 |
| DOC_MAPK_MEF2A_6 | 316 | 324 | PF00069 | 0.410 |
| DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.721 |
| DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.648 |
| DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.670 |
| DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.703 |
| DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.556 |
| DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.706 |
| DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.591 |
| DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.435 |
| LIG_14-3-3_CanoR_1 | 147 | 155 | PF00244 | 0.655 |
| LIG_14-3-3_CanoR_1 | 245 | 251 | PF00244 | 0.388 |
| LIG_APCC_ABBAyCdc20_2 | 17 | 23 | PF00400 | 0.511 |
| LIG_BRCT_BRCA1_1 | 233 | 237 | PF00533 | 0.550 |
| LIG_BRCT_BRCA1_1 | 343 | 347 | PF00533 | 0.530 |
| LIG_CaM_IQ_9 | 113 | 128 | PF13499 | 0.615 |
| LIG_eIF4E_1 | 256 | 262 | PF01652 | 0.547 |
| LIG_eIF4E_1 | 41 | 47 | PF01652 | 0.514 |
| LIG_FHA_1 | 247 | 253 | PF00498 | 0.361 |
| LIG_FHA_2 | 113 | 119 | PF00498 | 0.396 |
| LIG_FHA_2 | 148 | 154 | PF00498 | 0.622 |
| LIG_FHA_2 | 73 | 79 | PF00498 | 0.660 |
| LIG_Integrin_isoDGR_2 | 331 | 333 | PF01839 | 0.400 |
| LIG_Integrin_RGD_1 | 280 | 282 | PF01839 | 0.596 |
| LIG_LIR_Gen_1 | 234 | 243 | PF02991 | 0.391 |
| LIG_LIR_LC3C_4 | 321 | 324 | PF02991 | 0.380 |
| LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.470 |
| LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.389 |
| LIG_PCNA_yPIPBox_3 | 110 | 124 | PF02747 | 0.402 |
| LIG_PCNA_yPIPBox_3 | 98 | 108 | PF02747 | 0.603 |
| LIG_Pex14_2 | 195 | 199 | PF04695 | 0.448 |
| LIG_SH2_CRK | 201 | 205 | PF00017 | 0.475 |
| LIG_SH2_CRK | 25 | 29 | PF00017 | 0.492 |
| LIG_SH2_GRB2like | 295 | 298 | PF00017 | 0.415 |
| LIG_SH2_GRB2like | 41 | 44 | PF00017 | 0.578 |
| LIG_SH2_NCK_1 | 250 | 254 | PF00017 | 0.390 |
| LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.437 |
| LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.375 |
| LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.438 |
| LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.358 |
| LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.439 |
| LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.386 |
| LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.426 |
| LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.514 |
| LIG_SH3_3 | 360 | 366 | PF00018 | 0.493 |
| LIG_SH3_3 | 94 | 100 | PF00018 | 0.617 |
| LIG_SUMO_SIM_anti_2 | 318 | 324 | PF11976 | 0.385 |
| LIG_SUMO_SIM_anti_2 | 4 | 10 | PF11976 | 0.586 |
| LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.503 |
| MOD_CK1_1 | 169 | 175 | PF00069 | 0.771 |
| MOD_CK2_1 | 108 | 114 | PF00069 | 0.519 |
| MOD_CK2_1 | 155 | 161 | PF00069 | 0.641 |
| MOD_CK2_1 | 168 | 174 | PF00069 | 0.683 |
| MOD_Cter_Amidation | 257 | 260 | PF01082 | 0.444 |
| MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.690 |
| MOD_GlcNHglycan | 210 | 214 | PF01048 | 0.555 |
| MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.601 |
| MOD_GlcNHglycan | 342 | 346 | PF01048 | 0.536 |
| MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.554 |
| MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.730 |
| MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.759 |
| MOD_GSK3_1 | 108 | 115 | PF00069 | 0.502 |
| MOD_GSK3_1 | 162 | 169 | PF00069 | 0.710 |
| MOD_GSK3_1 | 205 | 212 | PF00069 | 0.590 |
| MOD_LATS_1 | 145 | 151 | PF00433 | 0.573 |
| MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.663 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.568 |
| MOD_NEK2_1 | 108 | 113 | PF00069 | 0.600 |
| MOD_NEK2_1 | 199 | 204 | PF00069 | 0.459 |
| MOD_NEK2_1 | 46 | 51 | PF00069 | 0.483 |
| MOD_PIKK_1 | 128 | 134 | PF00454 | 0.561 |
| MOD_PKA_1 | 246 | 252 | PF00069 | 0.382 |
| MOD_PKA_2 | 246 | 252 | PF00069 | 0.382 |
| MOD_PKB_1 | 110 | 118 | PF00069 | 0.578 |
| MOD_Plk_1 | 90 | 96 | PF00069 | 0.701 |
| MOD_Plk_4 | 199 | 205 | PF00069 | 0.473 |
| MOD_Plk_4 | 2 | 8 | PF00069 | 0.624 |
| MOD_Plk_4 | 290 | 296 | PF00069 | 0.414 |
| MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.705 |
| MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.590 |
| MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.443 |
| MOD_SUMO_rev_2 | 114 | 123 | PF00179 | 0.610 |
| MOD_SUMO_rev_2 | 255 | 261 | PF00179 | 0.578 |
| TRG_AP2beta_CARGO_1 | 236 | 246 | PF09066 | 0.389 |
| TRG_DiLeu_BaEn_1 | 119 | 124 | PF01217 | 0.515 |
| TRG_DiLeu_BaEn_1 | 318 | 323 | PF01217 | 0.406 |
| TRG_DiLeu_BaLyEn_6 | 257 | 262 | PF01217 | 0.547 |
| TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.468 |
| TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.275 |
| TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.493 |
| TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.501 |
| TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.413 |
| TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.501 |
| TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.538 |
| TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.539 |
| TRG_Pf-PMV_PEXEL_1 | 183 | 187 | PF00026 | 0.568 |
| TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.465 |
| TRG_Pf-PMV_PEXEL_1 | 350 | 354 | PF00026 | 0.532 |
| TRG_Pf-PMV_PEXEL_1 | 74 | 78 | PF00026 | 0.697 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HUU3 | Leptomonas seymouri | 69% | 98% |
| A0A0S4J6I9 | Bodo saltans | 51% | 100% |
| A0A1X0P0T0 | Trypanosomatidae | 59% | 100% |
| A0A422NDL4 | Trypanosoma rangeli | 60% | 100% |
| A4H478 | Leishmania braziliensis | 82% | 97% |
| A4HSF3 | Leishmania infantum | 100% | 100% |
| D0A4H9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
| E9AKE0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
| Q4QJG8 | Leishmania major | 95% | 100% |
| V5AZT2 | Trypanosoma cruzi | 60% | 100% |