| 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 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ASP1
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 141 | 145 | PF00656 | 0.434 |
| CLV_C14_Caspase3-7 | 205 | 209 | PF00656 | 0.669 |
| CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.442 |
| CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.453 |
| CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.377 |
| DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.461 |
| DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.413 |
| DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.665 |
| DOC_USP7_UBL2_3 | 241 | 245 | PF12436 | 0.467 |
| DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.735 |
| DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.533 |
| LIG_14-3-3_CanoR_1 | 188 | 196 | PF00244 | 0.735 |
| LIG_14-3-3_CanoR_1 | 91 | 97 | PF00244 | 0.390 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.550 |
| LIG_BIR_III_2 | 167 | 171 | PF00653 | 0.427 |
| LIG_FHA_1 | 56 | 62 | PF00498 | 0.378 |
| LIG_FHA_1 | 84 | 90 | PF00498 | 0.592 |
| LIG_FHA_1 | 99 | 105 | PF00498 | 0.385 |
| LIG_FHA_2 | 141 | 147 | PF00498 | 0.516 |
| LIG_FHA_2 | 169 | 175 | PF00498 | 0.584 |
| LIG_FHA_2 | 218 | 224 | PF00498 | 0.513 |
| LIG_GBD_Chelix_1 | 104 | 112 | PF00786 | 0.314 |
| LIG_LIR_Gen_1 | 131 | 140 | PF02991 | 0.391 |
| LIG_LIR_Gen_1 | 85 | 93 | PF02991 | 0.483 |
| LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.392 |
| LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.507 |
| LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.394 |
| LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.347 |
| LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.454 |
| LIG_PCNA_PIPBox_1 | 112 | 121 | PF02747 | 0.391 |
| LIG_PCNA_PIPBox_1 | 240 | 249 | PF02747 | 0.630 |
| LIG_PCNA_yPIPBox_3 | 240 | 250 | PF02747 | 0.551 |
| LIG_PTB_Apo_2 | 78 | 85 | PF02174 | 0.398 |
| LIG_SH2_CRK | 222 | 226 | PF00017 | 0.414 |
| LIG_SH2_GRB2like | 246 | 249 | PF00017 | 0.481 |
| LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.514 |
| LIG_SH2_STAT3 | 19 | 22 | PF00017 | 0.551 |
| LIG_SH2_STAT3 | 237 | 240 | PF00017 | 0.584 |
| LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.433 |
| LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.483 |
| LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.541 |
| LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.267 |
| LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.467 |
| LIG_SH3_3 | 236 | 242 | PF00018 | 0.481 |
| LIG_SH3_4 | 241 | 248 | PF00018 | 0.472 |
| LIG_TYR_ITSM | 218 | 225 | PF00017 | 0.427 |
| LIG_WRC_WIRS_1 | 169 | 174 | PF05994 | 0.445 |
| MOD_CDK_SPK_2 | 2 | 7 | PF00069 | 0.490 |
| MOD_CDK_SPxxK_3 | 181 | 188 | PF00069 | 0.552 |
| MOD_CK1_1 | 138 | 144 | PF00069 | 0.544 |
| MOD_CK1_1 | 192 | 198 | PF00069 | 0.573 |
| MOD_CK1_1 | 48 | 54 | PF00069 | 0.419 |
| MOD_CK1_1 | 5 | 11 | PF00069 | 0.524 |
| MOD_CK1_1 | 85 | 91 | PF00069 | 0.527 |
| MOD_CK2_1 | 140 | 146 | PF00069 | 0.347 |
| MOD_CK2_1 | 168 | 174 | PF00069 | 0.578 |
| MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.429 |
| MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.636 |
| MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.662 |
| MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.449 |
| MOD_GSK3_1 | 1 | 8 | PF00069 | 0.573 |
| MOD_GSK3_1 | 138 | 145 | PF00069 | 0.434 |
| MOD_GSK3_1 | 152 | 159 | PF00069 | 0.386 |
| MOD_GSK3_1 | 187 | 194 | PF00069 | 0.676 |
| MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.541 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.719 |
| MOD_NEK2_1 | 10 | 15 | PF00069 | 0.395 |
| MOD_NEK2_1 | 106 | 111 | PF00069 | 0.297 |
| MOD_NEK2_1 | 150 | 155 | PF00069 | 0.503 |
| MOD_NEK2_1 | 199 | 204 | PF00069 | 0.551 |
| MOD_NEK2_1 | 229 | 234 | PF00069 | 0.395 |
| MOD_NEK2_1 | 50 | 55 | PF00069 | 0.403 |
| MOD_NEK2_1 | 98 | 103 | PF00069 | 0.373 |
| MOD_NEK2_2 | 45 | 50 | PF00069 | 0.379 |
| MOD_NEK2_2 | 55 | 60 | PF00069 | 0.295 |
| MOD_PIKK_1 | 179 | 185 | PF00454 | 0.698 |
| MOD_PIKK_1 | 92 | 98 | PF00454 | 0.498 |
| MOD_PKA_2 | 187 | 193 | PF00069 | 0.760 |
| MOD_Plk_1 | 210 | 216 | PF00069 | 0.605 |
| MOD_Plk_4 | 210 | 216 | PF00069 | 0.521 |
| MOD_Plk_4 | 217 | 223 | PF00069 | 0.411 |
| MOD_Plk_4 | 229 | 235 | PF00069 | 0.392 |
| MOD_Plk_4 | 45 | 51 | PF00069 | 0.455 |
| MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.734 |
| MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.531 |
| MOD_SUMO_rev_2 | 204 | 212 | PF00179 | 0.612 |
| TRG_DiLeu_BaEn_2 | 145 | 151 | PF01217 | 0.320 |
| TRG_DiLeu_BaLyEn_6 | 57 | 62 | PF01217 | 0.371 |
| TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.446 |
| TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.562 |
| TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.361 |
| TRG_Pf-PMV_PEXEL_1 | 60 | 64 | PF00026 | 0.377 |
| TRG_Pf-PMV_PEXEL_1 | 91 | 96 | PF00026 | 0.495 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PDB2 | Leptomonas seymouri | 47% | 91% |
| A0A0S4JAI8 | Bodo saltans | 31% | 100% |
| A0A1X0P886 | Trypanosomatidae | 38% | 100% |
| A0A3S7XAI3 | Leishmania donovani | 85% | 100% |
| A4ICL3 | Leishmania infantum | 85% | 100% |
| D0A2U7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
| Q4Q1V5 | Leishmania major | 83% | 100% |
| V5B9R5 | Trypanosoma cruzi | 37% | 100% |