| 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: 10 | 
| NetGPI | no | yes: 0, no: 10 | 
Related structures:
AlphaFold database: A4IB80
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 | 
| GO:0006396 | RNA processing | 6 | 11 | 
| GO:0006399 | tRNA metabolic process | 7 | 11 | 
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 | 
| GO:0006807 | nitrogen compound metabolic process | 2 | 11 | 
| GO:0008033 | tRNA processing | 8 | 11 | 
| GO:0008152 | metabolic process | 1 | 11 | 
| GO:0009987 | cellular process | 1 | 11 | 
| GO:0016070 | RNA metabolic process | 5 | 11 | 
| GO:0034470 | ncRNA processing | 7 | 11 | 
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 | 
| GO:0034660 | ncRNA metabolic process | 6 | 11 | 
| GO:0043170 | macromolecule metabolic process | 3 | 11 | 
| GO:0044237 | cellular metabolic process | 2 | 11 | 
| GO:0044238 | primary metabolic process | 2 | 11 | 
| GO:0046483 | heterocycle metabolic process | 3 | 11 | 
| GO:0071704 | organic substance metabolic process | 2 | 11 | 
| GO:0090304 | nucleic acid metabolic process | 4 | 11 | 
| GO:1901360 | organic cyclic compound metabolic process | 3 | 11 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 11 | 
| GO:0016432 | tRNA-uridine aminocarboxypropyltransferase activity | 4 | 11 | 
| GO:0016740 | transferase activity | 2 | 11 | 
| GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 11 | 
| GO:0140098 | catalytic activity, acting on RNA | 3 | 11 | 
| GO:0140101 | catalytic activity, acting on a tRNA | 4 | 11 | 
| GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 228 | 232 | PF00656 | 0.706 | 
| CLV_C14_Caspase3-7 | 252 | 256 | PF00656 | 0.486 | 
| CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.562 | 
| CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.418 | 
| CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.323 | 
| CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.558 | 
| CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.567 | 
| CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.418 | 
| CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.331 | 
| CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.549 | 
| CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.347 | 
| CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.484 | 
| CLV_Separin_Metazoa | 324 | 328 | PF03568 | 0.563 | 
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.583 | 
| DEG_SPOP_SBC_1 | 250 | 254 | PF00917 | 0.406 | 
| DOC_CYCLIN_RxL_1 | 18 | 29 | PF00134 | 0.390 | 
| DOC_CYCLIN_RxL_1 | 46 | 57 | PF00134 | 0.320 | 
| DOC_CYCLIN_yCln2_LP_2 | 71 | 77 | PF00134 | 0.257 | 
| DOC_MAPK_gen_1 | 161 | 170 | PF00069 | 0.306 | 
| DOC_PP1_RVXF_1 | 139 | 146 | PF00149 | 0.238 | 
| DOC_PP1_RVXF_1 | 22 | 29 | PF00149 | 0.368 | 
| DOC_PP2B_LxvP_1 | 219 | 222 | PF13499 | 0.506 | 
| DOC_PP2B_LxvP_1 | 308 | 311 | PF13499 | 0.451 | 
| DOC_PP2B_LxvP_1 | 71 | 74 | PF13499 | 0.257 | 
| DOC_PP4_FxxP_1 | 28 | 31 | PF00568 | 0.300 | 
| DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.528 | 
| DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.744 | 
| DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.551 | 
| DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.596 | 
| DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.694 | 
| DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.238 | 
| LIG_14-3-3_CanoR_1 | 169 | 178 | PF00244 | 0.296 | 
| LIG_14-3-3_CanoR_1 | 281 | 287 | PF00244 | 0.450 | 
| LIG_APCC_ABBA_1 | 60 | 65 | PF00400 | 0.251 | 
| LIG_APCC_ABBAyCdc20_2 | 141 | 147 | PF00400 | 0.238 | 
| LIG_BRCT_BRCA1_1 | 24 | 28 | PF00533 | 0.289 | 
| LIG_eIF4E_1 | 54 | 60 | PF01652 | 0.251 | 
| LIG_FHA_1 | 117 | 123 | PF00498 | 0.238 | 
| LIG_FHA_2 | 244 | 250 | PF00498 | 0.502 | 
| LIG_FHA_2 | 301 | 307 | PF00498 | 0.448 | 
| LIG_LIR_Apic_2 | 25 | 31 | PF02991 | 0.282 | 
| LIG_LIR_Gen_1 | 303 | 313 | PF02991 | 0.392 | 
| LIG_LIR_Nem_3 | 106 | 110 | PF02991 | 0.238 | 
| LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.300 | 
| LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.268 | 
| LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.210 | 
| LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.387 | 
| LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.278 | 
| LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.400 | 
| LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.349 | 
| LIG_LYPXL_yS_3 | 107 | 110 | PF13949 | 0.238 | 
| LIG_SH2_CRK | 56 | 60 | PF00017 | 0.238 | 
| LIG_SH2_GRB2like | 271 | 274 | PF00017 | 0.283 | 
| LIG_SH2_PTP2 | 275 | 278 | PF00017 | 0.288 | 
| LIG_SH2_PTP2 | 78 | 81 | PF00017 | 0.257 | 
| LIG_SH2_STAP1 | 56 | 60 | PF00017 | 0.251 | 
| LIG_SH2_STAT3 | 201 | 204 | PF00017 | 0.293 | 
| LIG_SH2_STAT3 | 271 | 274 | PF00017 | 0.283 | 
| LIG_SH2_STAT3 | 298 | 301 | PF00017 | 0.450 | 
| LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.238 | 
| LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.238 | 
| LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.238 | 
| LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.283 | 
| LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.288 | 
| LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.403 | 
| LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.405 | 
| LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.308 | 
| LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.241 | 
| LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.257 | 
| LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.474 | 
| LIG_SH3_3 | 102 | 108 | PF00018 | 0.245 | 
| LIG_SH3_3 | 118 | 124 | PF00018 | 0.218 | 
| LIG_SH3_3 | 306 | 312 | PF00018 | 0.417 | 
| LIG_SH3_3 | 319 | 325 | PF00018 | 0.558 | 
| LIG_SH3_3 | 77 | 83 | PF00018 | 0.437 | 
| LIG_SUMO_SIM_anti_2 | 117 | 122 | PF11976 | 0.259 | 
| LIG_TYR_ITIM | 105 | 110 | PF00017 | 0.212 | 
| LIG_WW_3 | 324 | 328 | PF00397 | 0.563 | 
| MOD_CDK_SPK_2 | 240 | 245 | PF00069 | 0.558 | 
| MOD_CK1_1 | 172 | 178 | PF00069 | 0.281 | 
| MOD_CK1_1 | 229 | 235 | PF00069 | 0.736 | 
| MOD_CK1_1 | 237 | 243 | PF00069 | 0.680 | 
| MOD_CK1_1 | 316 | 322 | PF00069 | 0.670 | 
| MOD_CK1_1 | 96 | 102 | PF00069 | 0.237 | 
| MOD_CK2_1 | 243 | 249 | PF00069 | 0.505 | 
| MOD_CK2_1 | 8 | 14 | PF00069 | 0.541 | 
| MOD_Cter_Amidation | 215 | 218 | PF01082 | 0.455 | 
| MOD_GlcNHglycan | 213 | 217 | PF01048 | 0.579 | 
| MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.723 | 
| MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.567 | 
| MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.493 | 
| MOD_GSK3_1 | 146 | 153 | PF00069 | 0.254 | 
| MOD_GSK3_1 | 183 | 190 | PF00069 | 0.278 | 
| MOD_GSK3_1 | 22 | 29 | PF00069 | 0.299 | 
| MOD_GSK3_1 | 229 | 236 | PF00069 | 0.765 | 
| MOD_GSK3_1 | 250 | 257 | PF00069 | 0.513 | 
| MOD_GSK3_1 | 316 | 323 | PF00069 | 0.643 | 
| MOD_GSK3_1 | 89 | 96 | PF00069 | 0.243 | 
| MOD_LATS_1 | 167 | 173 | PF00433 | 0.316 | 
| MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.417 | 
| MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.630 | 
| MOD_NEK2_1 | 145 | 150 | PF00069 | 0.279 | 
| MOD_NEK2_1 | 22 | 27 | PF00069 | 0.338 | 
| MOD_NEK2_1 | 93 | 98 | PF00069 | 0.238 | 
| MOD_NEK2_2 | 58 | 63 | PF00069 | 0.259 | 
| MOD_PIKK_1 | 169 | 175 | PF00454 | 0.281 | 
| MOD_PIKK_1 | 200 | 206 | PF00454 | 0.293 | 
| MOD_PKA_2 | 160 | 166 | PF00069 | 0.293 | 
| MOD_PKA_2 | 280 | 286 | PF00069 | 0.453 | 
| MOD_Plk_1 | 116 | 122 | PF00069 | 0.312 | 
| MOD_Plk_1 | 125 | 131 | PF00069 | 0.355 | 
| MOD_Plk_1 | 146 | 152 | PF00069 | 0.257 | 
| MOD_Plk_1 | 254 | 260 | PF00069 | 0.369 | 
| MOD_Plk_1 | 301 | 307 | PF00069 | 0.424 | 
| MOD_Plk_4 | 116 | 122 | PF00069 | 0.238 | 
| MOD_Plk_4 | 172 | 178 | PF00069 | 0.247 | 
| MOD_Plk_4 | 183 | 189 | PF00069 | 0.305 | 
| MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.597 | 
| MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.690 | 
| MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.238 | 
| MOD_SUMO_rev_2 | 128 | 137 | PF00179 | 0.220 | 
| MOD_SUMO_rev_2 | 228 | 235 | PF00179 | 0.561 | 
| TRG_DiLeu_BaEn_1 | 263 | 268 | PF01217 | 0.307 | 
| TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.238 | 
| TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.371 | 
| TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.238 | 
| TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.293 | 
| TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.238 | 
| TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.257 | 
| TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.454 | 
| TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.369 | 
| TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.367 | 
| TRG_NLS_MonoCore_2 | 1 | 6 | PF00514 | 0.650 | 
| TRG_NLS_MonoExtN_4 | 46 | 53 | PF00514 | 0.386 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1PCD7 | Leptomonas seymouri | 76% | 100% | 
| A0A0S4IR26 | Bodo saltans | 49% | 100% | 
| A0A1X0P5T8 | Trypanosomatidae | 64% | 100% | 
| A0A3S7X980 | Leishmania donovani | 100% | 100% | 
| A4HMK1 | Leishmania braziliensis | 85% | 100% | 
| C9ZZK5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% | 
| E9AF01 | Leishmania major | 94% | 100% | 
| E9B657 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% | 
| Q5RCQ0 | Pongo abelii | 33% | 100% | 
| Q8N5C7 | Homo sapiens | 33% | 100% | 
| Q9D8U7 | Mus musculus | 34% | 100% | 
| V5B8W4 | Trypanosoma cruzi | 62% | 100% |