| 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: E9AU03
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.454 |
| CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.621 |
| CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.502 |
| CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.641 |
| CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.367 |
| CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.574 |
| CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.641 |
| CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.367 |
| CLV_PCSK_PC1ET2_1 | 281 | 283 | PF00082 | 0.527 |
| CLV_PCSK_PC7_1 | 211 | 217 | PF00082 | 0.398 |
| CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.345 |
| CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.551 |
| CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.497 |
| CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.535 |
| DEG_APCC_DBOX_1 | 38 | 46 | PF00400 | 0.724 |
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.645 |
| DOC_CYCLIN_RxL_1 | 137 | 150 | PF00134 | 0.357 |
| DOC_MAPK_MEF2A_6 | 118 | 125 | PF00069 | 0.515 |
| DOC_PP2B_LxvP_1 | 246 | 249 | PF13499 | 0.553 |
| DOC_PP2B_LxvP_1 | 309 | 312 | PF13499 | 0.570 |
| DOC_PP4_FxxP_1 | 286 | 289 | PF00568 | 0.557 |
| DOC_PP4_FxxP_1 | 295 | 298 | PF00568 | 0.600 |
| DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.616 |
| DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.568 |
| DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.550 |
| DOC_USP7_UBL2_3 | 143 | 147 | PF12436 | 0.478 |
| DOC_USP7_UBL2_3 | 293 | 297 | PF12436 | 0.543 |
| DOC_USP7_UBL2_3 | 54 | 58 | PF12436 | 0.497 |
| LIG_14-3-3_CanoR_1 | 232 | 240 | PF00244 | 0.612 |
| LIG_14-3-3_CanoR_1 | 52 | 57 | PF00244 | 0.495 |
| LIG_APCC_ABBA_1 | 161 | 166 | PF00400 | 0.531 |
| LIG_FHA_1 | 105 | 111 | PF00498 | 0.506 |
| LIG_FHA_1 | 241 | 247 | PF00498 | 0.483 |
| LIG_FHA_1 | 278 | 284 | PF00498 | 0.402 |
| LIG_LIR_Apic_2 | 284 | 289 | PF02991 | 0.560 |
| LIG_LIR_Gen_1 | 150 | 157 | PF02991 | 0.355 |
| LIG_LIR_Gen_1 | 88 | 97 | PF02991 | 0.620 |
| LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.431 |
| LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.505 |
| LIG_Pex14_2 | 63 | 67 | PF04695 | 0.494 |
| LIG_SH2_CRK | 53 | 57 | PF00017 | 0.625 |
| LIG_SH2_NCK_1 | 75 | 79 | PF00017 | 0.612 |
| LIG_SH2_SRC | 178 | 181 | PF00017 | 0.342 |
| LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.568 |
| LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.398 |
| LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.481 |
| LIG_SH3_3 | 273 | 279 | PF00018 | 0.452 |
| LIG_SH3_3 | 309 | 315 | PF00018 | 0.515 |
| LIG_SH3_4 | 297 | 304 | PF00018 | 0.377 |
| LIG_SUMO_SIM_par_1 | 121 | 128 | PF11976 | 0.455 |
| MOD_CK1_1 | 21 | 27 | PF00069 | 0.603 |
| MOD_CK2_1 | 247 | 253 | PF00069 | 0.500 |
| MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.422 |
| MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.586 |
| MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.322 |
| MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.411 |
| MOD_GSK3_1 | 18 | 25 | PF00069 | 0.608 |
| MOD_GSK3_1 | 249 | 256 | PF00069 | 0.591 |
| MOD_GSK3_1 | 26 | 33 | PF00069 | 0.593 |
| MOD_GSK3_1 | 3 | 10 | PF00069 | 0.520 |
| MOD_LATS_1 | 50 | 56 | PF00433 | 0.580 |
| MOD_LATS_1 | 83 | 89 | PF00433 | 0.497 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.529 |
| MOD_NEK2_1 | 155 | 160 | PF00069 | 0.410 |
| MOD_NEK2_1 | 240 | 245 | PF00069 | 0.414 |
| MOD_PK_1 | 247 | 253 | PF00069 | 0.380 |
| MOD_PKA_2 | 155 | 161 | PF00069 | 0.429 |
| MOD_Plk_1 | 217 | 223 | PF00069 | 0.436 |
| MOD_Plk_4 | 171 | 177 | PF00069 | 0.395 |
| MOD_Plk_4 | 23 | 29 | PF00069 | 0.601 |
| MOD_Plk_4 | 31 | 37 | PF00069 | 0.534 |
| MOD_Plk_4 | 52 | 58 | PF00069 | 0.498 |
| TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.627 |
| TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.522 |
| TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.543 |
| TRG_Pf-PMV_PEXEL_1 | 264 | 268 | PF00026 | 0.536 |
| TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.536 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PGJ4 | Leptomonas seymouri | 78% | 99% |
| A0A0S4IS55 | Bodo saltans | 45% | 100% |
| A0A1X0P0I2 | Trypanosomatidae | 58% | 100% |
| A0A3R7M3K5 | Trypanosoma rangeli | 59% | 100% |
| A0A3S7XBV5 | Leishmania donovani | 94% | 100% |
| A4HQ85 | Leishmania braziliensis | 84% | 100% |
| A4IDY3 | Leishmania infantum | 94% | 100% |
| D0A426 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
| Q4Q0J2 | Leishmania major | 93% | 100% |