| 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: 6 |
| NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AYR0
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 213 | 217 | PF00656 | 0.433 |
| CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.392 |
| CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.514 |
| CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.496 |
| CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.556 |
| CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.658 |
| CLV_PCSK_FUR_1 | 180 | 184 | PF00082 | 0.419 |
| CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.362 |
| CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.542 |
| CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.447 |
| CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.546 |
| CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.622 |
| CLV_PCSK_PC1ET2_1 | 232 | 234 | PF00082 | 0.596 |
| CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.383 |
| CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.485 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.468 |
| DOC_MAPK_MEF2A_6 | 34 | 42 | PF00069 | 0.431 |
| DOC_PP1_RVXF_1 | 181 | 188 | PF00149 | 0.347 |
| DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.615 |
| DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.369 |
| DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.455 |
| DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.650 |
| DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.435 |
| DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.610 |
| DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.711 |
| LIG_14-3-3_CanoR_1 | 188 | 196 | PF00244 | 0.483 |
| LIG_14-3-3_CanoR_1 | 268 | 272 | PF00244 | 0.530 |
| LIG_Clathr_ClatBox_1 | 137 | 141 | PF01394 | 0.343 |
| LIG_eIF4E_1 | 151 | 157 | PF01652 | 0.371 |
| LIG_FHA_1 | 108 | 114 | PF00498 | 0.573 |
| LIG_FHA_1 | 166 | 172 | PF00498 | 0.446 |
| LIG_FHA_1 | 54 | 60 | PF00498 | 0.508 |
| LIG_FHA_1 | 66 | 72 | PF00498 | 0.412 |
| LIG_FHA_1 | 73 | 79 | PF00498 | 0.465 |
| LIG_IBAR_NPY_1 | 239 | 241 | PF08397 | 0.573 |
| LIG_LIR_Apic_2 | 127 | 132 | PF02991 | 0.471 |
| LIG_LIR_Gen_1 | 55 | 63 | PF02991 | 0.493 |
| LIG_LIR_LC3C_4 | 168 | 172 | PF02991 | 0.286 |
| LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.441 |
| LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.470 |
| LIG_PTB_Apo_2 | 256 | 263 | PF02174 | 0.482 |
| LIG_SH2_CRK | 129 | 133 | PF00017 | 0.435 |
| LIG_SH2_NCK_1 | 302 | 306 | PF00017 | 0.551 |
| LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.528 |
| LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.472 |
| LIG_SH3_3 | 168 | 174 | PF00018 | 0.360 |
| LIG_SH3_3 | 27 | 33 | PF00018 | 0.614 |
| LIG_SH3_3 | 37 | 43 | PF00018 | 0.395 |
| LIG_SH3_3 | 73 | 79 | PF00018 | 0.527 |
| LIG_SUMO_SIM_anti_2 | 136 | 141 | PF11976 | 0.389 |
| LIG_SUMO_SIM_anti_2 | 168 | 173 | PF11976 | 0.346 |
| LIG_SUMO_SIM_par_1 | 166 | 173 | PF11976 | 0.442 |
| LIG_SUMO_SIM_par_1 | 78 | 84 | PF11976 | 0.403 |
| LIG_WRC_WIRS_1 | 97 | 102 | PF05994 | 0.429 |
| MOD_CDK_SPK_2 | 29 | 34 | PF00069 | 0.562 |
| MOD_CK1_1 | 72 | 78 | PF00069 | 0.468 |
| MOD_CK2_1 | 121 | 127 | PF00069 | 0.518 |
| MOD_CK2_1 | 158 | 164 | PF00069 | 0.449 |
| MOD_Cter_Amidation | 230 | 233 | PF01082 | 0.605 |
| MOD_DYRK1A_RPxSP_1 | 65 | 69 | PF00069 | 0.500 |
| MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.582 |
| MOD_GSK3_1 | 118 | 125 | PF00069 | 0.580 |
| MOD_GSK3_1 | 25 | 32 | PF00069 | 0.600 |
| MOD_GSK3_1 | 59 | 66 | PF00069 | 0.664 |
| MOD_NEK2_1 | 189 | 194 | PF00069 | 0.336 |
| MOD_NEK2_1 | 214 | 219 | PF00069 | 0.441 |
| MOD_NEK2_1 | 249 | 254 | PF00069 | 0.601 |
| MOD_NEK2_1 | 300 | 305 | PF00069 | 0.467 |
| MOD_PIKK_1 | 25 | 31 | PF00454 | 0.611 |
| MOD_PIKK_1 | 53 | 59 | PF00454 | 0.509 |
| MOD_PIKK_1 | 63 | 69 | PF00454 | 0.466 |
| MOD_PKA_1 | 9 | 15 | PF00069 | 0.481 |
| MOD_PKA_2 | 267 | 273 | PF00069 | 0.489 |
| MOD_PKA_2 | 9 | 15 | PF00069 | 0.481 |
| MOD_PKB_1 | 94 | 102 | PF00069 | 0.606 |
| MOD_Plk_1 | 118 | 124 | PF00069 | 0.550 |
| MOD_Plk_4 | 158 | 164 | PF00069 | 0.460 |
| MOD_Plk_4 | 165 | 171 | PF00069 | 0.386 |
| MOD_Plk_4 | 78 | 84 | PF00069 | 0.428 |
| MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.651 |
| MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.440 |
| MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.601 |
| MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.548 |
| TRG_AP2beta_CARGO_1 | 55 | 65 | PF09066 | 0.384 |
| TRG_DiLeu_BaEn_2 | 244 | 250 | PF01217 | 0.497 |
| TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.424 |
| TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.494 |
| TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.509 |
| TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.578 |
| TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.499 |
| TRG_NLS_Bipartite_1 | 220 | 236 | PF00514 | 0.657 |
| TRG_NLS_MonoExtC_3 | 231 | 236 | PF00514 | 0.454 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HUP8 | Leptomonas seymouri | 49% | 89% |
| A0A1X0NLR8 | Trypanosomatidae | 28% | 80% |
| A0A422N4S9 | Trypanosoma rangeli | 26% | 80% |
| A4HFC7 | Leishmania braziliensis | 72% | 100% |
| C9ZKU5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 81% |