| 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: 18 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | yes | yes: 8, no: 3 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 3 |
| GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: E9AUG4
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 117 | 121 | PF00656 | 0.420 |
| CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.556 |
| CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.719 |
| CLV_PCSK_PC1ET2_1 | 217 | 219 | PF00082 | 0.700 |
| CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.584 |
| CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.487 |
| DEG_ODPH_VHL_1 | 132 | 145 | PF01847 | 0.267 |
| DOC_CDC14_PxL_1 | 130 | 138 | PF14671 | 0.262 |
| DOC_CKS1_1 | 106 | 111 | PF01111 | 0.409 |
| DOC_CYCLIN_yCln2_LP_2 | 182 | 188 | PF00134 | 0.549 |
| DOC_CYCLIN_yCln2_LP_2 | 247 | 253 | PF00134 | 0.416 |
| DOC_MAPK_DCC_7 | 179 | 188 | PF00069 | 0.501 |
| DOC_MAPK_MEF2A_6 | 169 | 176 | PF00069 | 0.441 |
| DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.426 |
| DOC_MAPK_MEF2A_6 | 6 | 14 | PF00069 | 0.522 |
| DOC_MAPK_NFAT4_5 | 242 | 250 | PF00069 | 0.486 |
| DOC_PP2B_LxvP_1 | 247 | 250 | PF13499 | 0.417 |
| DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.316 |
| DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.567 |
| DOC_USP7_MATH_2 | 233 | 239 | PF00917 | 0.504 |
| DOC_USP7_UBL2_3 | 187 | 191 | PF12436 | 0.656 |
| DOC_USP7_UBL2_3 | 208 | 212 | PF12436 | 0.448 |
| DOC_USP7_UBL2_3 | 96 | 100 | PF12436 | 0.508 |
| DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.347 |
| LIG_14-3-3_CanoR_1 | 52 | 61 | PF00244 | 0.443 |
| LIG_Actin_WH2_2 | 173 | 189 | PF00022 | 0.576 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.591 |
| LIG_deltaCOP1_diTrp_1 | 39 | 48 | PF00928 | 0.453 |
| LIG_FHA_1 | 101 | 107 | PF00498 | 0.524 |
| LIG_FHA_1 | 121 | 127 | PF00498 | 0.223 |
| LIG_FHA_1 | 171 | 177 | PF00498 | 0.486 |
| LIG_FHA_1 | 187 | 193 | PF00498 | 0.537 |
| LIG_FHA_1 | 5 | 11 | PF00498 | 0.475 |
| LIG_FHA_2 | 199 | 205 | PF00498 | 0.607 |
| LIG_LIR_Gen_1 | 39 | 50 | PF02991 | 0.410 |
| LIG_LIR_Nem_3 | 3 | 8 | PF02991 | 0.541 |
| LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.385 |
| LIG_REV1ctd_RIR_1 | 149 | 159 | PF16727 | 0.581 |
| LIG_SH2_STAT3 | 90 | 93 | PF00017 | 0.517 |
| LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.472 |
| LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.347 |
| LIG_SH3_3 | 103 | 109 | PF00018 | 0.430 |
| LIG_SH3_4 | 96 | 103 | PF00018 | 0.497 |
| LIG_SUMO_SIM_anti_2 | 7 | 13 | PF11976 | 0.536 |
| LIG_SUMO_SIM_par_1 | 102 | 108 | PF11976 | 0.496 |
| LIG_SUMO_SIM_par_1 | 120 | 128 | PF11976 | 0.252 |
| LIG_TRAF2_1 | 233 | 236 | PF00917 | 0.647 |
| LIG_TRAF2_1 | 72 | 75 | PF00917 | 0.599 |
| LIG_TRAF2_1 | 91 | 94 | PF00917 | 0.461 |
| LIG_TYR_ITIM | 192 | 197 | PF00017 | 0.594 |
| LIG_WRC_WIRS_1 | 45 | 50 | PF05994 | 0.378 |
| MOD_CK1_1 | 146 | 152 | PF00069 | 0.508 |
| MOD_CK1_1 | 51 | 57 | PF00069 | 0.409 |
| MOD_CK2_1 | 198 | 204 | PF00069 | 0.617 |
| MOD_CK2_1 | 35 | 41 | PF00069 | 0.505 |
| MOD_CK2_1 | 69 | 75 | PF00069 | 0.503 |
| MOD_GSK3_1 | 101 | 108 | PF00069 | 0.397 |
| MOD_GSK3_1 | 40 | 47 | PF00069 | 0.400 |
| MOD_GSK3_1 | 48 | 55 | PF00069 | 0.352 |
| MOD_GSK3_1 | 6 | 13 | PF00069 | 0.483 |
| MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.402 |
| MOD_NEK2_1 | 10 | 15 | PF00069 | 0.450 |
| MOD_NEK2_1 | 136 | 141 | PF00069 | 0.359 |
| MOD_NEK2_1 | 186 | 191 | PF00069 | 0.543 |
| MOD_NEK2_1 | 26 | 31 | PF00069 | 0.343 |
| MOD_NEK2_1 | 4 | 9 | PF00069 | 0.485 |
| MOD_NEK2_1 | 48 | 53 | PF00069 | 0.362 |
| MOD_PIKK_1 | 24 | 30 | PF00454 | 0.437 |
| MOD_PIKK_1 | 52 | 58 | PF00454 | 0.578 |
| MOD_PIKK_1 | 60 | 66 | PF00454 | 0.389 |
| MOD_PKA_2 | 51 | 57 | PF00069 | 0.427 |
| MOD_PKA_2 | 59 | 65 | PF00069 | 0.428 |
| MOD_Plk_1 | 136 | 142 | PF00069 | 0.365 |
| MOD_Plk_1 | 162 | 168 | PF00069 | 0.375 |
| MOD_Plk_1 | 235 | 241 | PF00069 | 0.478 |
| MOD_Plk_1 | 40 | 46 | PF00069 | 0.480 |
| MOD_Plk_1 | 67 | 73 | PF00069 | 0.485 |
| MOD_Plk_4 | 101 | 107 | PF00069 | 0.398 |
| MOD_Plk_4 | 108 | 114 | PF00069 | 0.316 |
| MOD_Plk_4 | 120 | 126 | PF00069 | 0.266 |
| MOD_Plk_4 | 136 | 142 | PF00069 | 0.329 |
| MOD_Plk_4 | 251 | 257 | PF00069 | 0.425 |
| MOD_Plk_4 | 26 | 32 | PF00069 | 0.237 |
| MOD_Plk_4 | 6 | 12 | PF00069 | 0.465 |
| MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.350 |
| MOD_SUMO_rev_2 | 117 | 124 | PF00179 | 0.447 |
| MOD_SUMO_rev_2 | 202 | 209 | PF00179 | 0.524 |
| TRG_DiLeu_BaEn_2 | 234 | 240 | PF01217 | 0.495 |
| TRG_DiLeu_BaEn_4 | 235 | 241 | PF01217 | 0.491 |
| TRG_DiLeu_BaEn_4 | 74 | 80 | PF01217 | 0.378 |
| TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.463 |
| TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.448 |
| TRG_NLS_Bipartite_1 | 190 | 211 | PF00514 | 0.427 |
| TRG_NLS_MonoExtC_3 | 189 | 195 | PF00514 | 0.544 |
| TRG_NLS_MonoExtN_4 | 187 | 194 | PF00514 | 0.551 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PCK3 | Leptomonas seymouri | 68% | 100% |
| A0A0S4J8Z8 | Bodo saltans | 31% | 100% |
| A0A1X0NWH6 | Trypanosomatidae | 44% | 96% |
| A0A3R7KYG2 | Trypanosoma rangeli | 38% | 93% |
| A0A3S7WVR1 | Leishmania donovani | 93% | 100% |
| A4HYL5 | Leishmania infantum | 93% | 100% |
| C9ZHW3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 97% |
| E9AI78 | Leishmania braziliensis | 78% | 100% |
| Q4QD20 | Leishmania major | 95% | 100% |
| V5BQW5 | Trypanosoma cruzi | 38% | 94% |