| 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: E9AS73
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 234 | 238 | PF00656 | 0.506 |
| CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.603 |
| CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.543 |
| CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.603 |
| CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.592 |
| CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.569 |
| CLV_PCSK_FUR_1 | 260 | 264 | PF00082 | 0.579 |
| CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.557 |
| CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.592 |
| CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.590 |
| CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.572 |
| CLV_PCSK_PC7_1 | 256 | 262 | PF00082 | 0.666 |
| CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.600 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.662 |
| DEG_SCF_FBW7_1 | 168 | 173 | PF00400 | 0.552 |
| DOC_ANK_TNKS_1 | 208 | 215 | PF00023 | 0.573 |
| DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.439 |
| DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.503 |
| DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.788 |
| DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.540 |
| DOC_USP7_UBL2_3 | 270 | 274 | PF12436 | 0.575 |
| DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.576 |
| DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.673 |
| DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.709 |
| LIG_14-3-3_CanoR_1 | 232 | 236 | PF00244 | 0.719 |
| LIG_14-3-3_CanoR_1 | 41 | 50 | PF00244 | 0.551 |
| LIG_14-3-3_CanoR_1 | 54 | 59 | PF00244 | 0.443 |
| LIG_BRCT_BRCA1_1 | 172 | 176 | PF00533 | 0.470 |
| LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.452 |
| LIG_FHA_1 | 31 | 37 | PF00498 | 0.643 |
| LIG_FHA_1 | 88 | 94 | PF00498 | 0.543 |
| LIG_FHA_2 | 185 | 191 | PF00498 | 0.289 |
| LIG_FHA_2 | 232 | 238 | PF00498 | 0.741 |
| LIG_Integrin_RGD_1 | 106 | 108 | PF01839 | 0.494 |
| LIG_LIR_Apic_2 | 286 | 292 | PF02991 | 0.734 |
| LIG_LIR_Gen_1 | 57 | 64 | PF02991 | 0.530 |
| LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.565 |
| LIG_LIR_Nem_3 | 57 | 61 | PF02991 | 0.425 |
| LIG_NRBOX | 92 | 98 | PF00104 | 0.388 |
| LIG_SH2_CRK | 192 | 196 | PF00017 | 0.458 |
| LIG_SH2_SRC | 92 | 95 | PF00017 | 0.508 |
| LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.442 |
| LIG_SH2_STAT3 | 118 | 121 | PF00017 | 0.572 |
| LIG_SH2_STAT3 | 273 | 276 | PF00017 | 0.571 |
| LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.463 |
| LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.276 |
| LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.499 |
| LIG_SH3_3 | 11 | 17 | PF00018 | 0.636 |
| MOD_CDK_SPxxK_3 | 277 | 284 | PF00069 | 0.662 |
| MOD_CK1_1 | 128 | 134 | PF00069 | 0.521 |
| MOD_CK1_1 | 162 | 168 | PF00069 | 0.595 |
| MOD_CK1_1 | 280 | 286 | PF00069 | 0.749 |
| MOD_CK1_1 | 30 | 36 | PF00069 | 0.651 |
| MOD_CK1_1 | 39 | 45 | PF00069 | 0.696 |
| MOD_CK2_1 | 184 | 190 | PF00069 | 0.287 |
| MOD_CK2_1 | 280 | 286 | PF00069 | 0.703 |
| MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.502 |
| MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.587 |
| MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.411 |
| MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.704 |
| MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.655 |
| MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.681 |
| MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.668 |
| MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.474 |
| MOD_GSK3_1 | 162 | 169 | PF00069 | 0.542 |
| MOD_GSK3_1 | 170 | 177 | PF00069 | 0.470 |
| MOD_GSK3_1 | 219 | 226 | PF00069 | 0.673 |
| MOD_GSK3_1 | 26 | 33 | PF00069 | 0.615 |
| MOD_GSK3_1 | 280 | 287 | PF00069 | 0.699 |
| MOD_GSK3_1 | 36 | 43 | PF00069 | 0.588 |
| MOD_GSK3_1 | 44 | 51 | PF00069 | 0.514 |
| MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.667 |
| MOD_NEK2_1 | 135 | 140 | PF00069 | 0.380 |
| MOD_NEK2_1 | 40 | 45 | PF00069 | 0.625 |
| MOD_NEK2_1 | 99 | 104 | PF00069 | 0.403 |
| MOD_PKA_1 | 86 | 92 | PF00069 | 0.567 |
| MOD_PKA_2 | 208 | 214 | PF00069 | 0.701 |
| MOD_PKA_2 | 219 | 225 | PF00069 | 0.708 |
| MOD_PKA_2 | 228 | 234 | PF00069 | 0.611 |
| MOD_PKA_2 | 40 | 46 | PF00069 | 0.585 |
| MOD_Plk_1 | 159 | 165 | PF00069 | 0.646 |
| MOD_Plk_1 | 87 | 93 | PF00069 | 0.543 |
| MOD_Plk_4 | 128 | 134 | PF00069 | 0.423 |
| MOD_Plk_4 | 170 | 176 | PF00069 | 0.479 |
| MOD_Plk_4 | 92 | 98 | PF00069 | 0.432 |
| MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.567 |
| MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.677 |
| MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.707 |
| MOD_SUMO_rev_2 | 79 | 89 | PF00179 | 0.541 |
| TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.444 |
| TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.415 |
| TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.587 |
| TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.566 |
| TRG_NLS_MonoExtC_3 | 182 | 188 | PF00514 | 0.580 |
| TRG_NLS_MonoExtN_4 | 180 | 187 | PF00514 | 0.590 |
| TRG_Pf-PMV_PEXEL_1 | 72 | 76 | PF00026 | 0.615 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PDU4 | Leptomonas seymouri | 60% | 100% |
| A0A1X0P732 | Trypanosomatidae | 49% | 99% |
| A0A3R7K6K4 | Trypanosoma rangeli | 46% | 100% |
| A0A3S7WVI0 | Leishmania donovani | 95% | 100% |
| A4HA59 | Leishmania braziliensis | 80% | 100% |
| A4HYE0 | Leishmania infantum | 95% | 100% |
| D0A0S5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
| Q4QD93 | Leishmania major | 93% | 100% |
| V5BNH1 | Trypanosoma cruzi | 43% | 100% |