| 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: E9B402
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.508 |
| CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.521 |
| CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.508 |
| CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.513 |
| CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.521 |
| CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.417 |
| CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.441 |
| CLV_Separin_Metazoa | 153 | 157 | PF03568 | 0.290 |
| DOC_MAPK_FxFP_2 | 3 | 6 | PF00069 | 0.377 |
| DOC_MAPK_gen_1 | 253 | 262 | PF00069 | 0.457 |
| DOC_MAPK_gen_1 | 31 | 40 | PF00069 | 0.495 |
| DOC_MAPK_MEF2A_6 | 230 | 237 | PF00069 | 0.457 |
| DOC_PP4_FxxP_1 | 3 | 6 | PF00568 | 0.342 |
| DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.515 |
| DOC_USP7_UBL2_3 | 226 | 230 | PF12436 | 0.427 |
| DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.326 |
| LIG_14-3-3_CanoR_1 | 171 | 180 | PF00244 | 0.454 |
| LIG_14-3-3_CanoR_1 | 210 | 217 | PF00244 | 0.394 |
| LIG_14-3-3_CanoR_1 | 253 | 262 | PF00244 | 0.347 |
| LIG_14-3-3_CanoR_1 | 34 | 38 | PF00244 | 0.382 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.461 |
| LIG_Clathr_ClatBox_1 | 18 | 22 | PF01394 | 0.331 |
| LIG_Clathr_ClatBox_1 | 244 | 248 | PF01394 | 0.369 |
| LIG_FHA_1 | 182 | 188 | PF00498 | 0.474 |
| LIG_FHA_1 | 255 | 261 | PF00498 | 0.379 |
| LIG_FHA_1 | 40 | 46 | PF00498 | 0.447 |
| LIG_FHA_1 | 81 | 87 | PF00498 | 0.463 |
| LIG_FHA_1 | 94 | 100 | PF00498 | 0.289 |
| LIG_FHA_2 | 142 | 148 | PF00498 | 0.500 |
| LIG_FHA_2 | 174 | 180 | PF00498 | 0.501 |
| LIG_FHA_2 | 49 | 55 | PF00498 | 0.417 |
| LIG_GBD_Chelix_1 | 99 | 107 | PF00786 | 0.489 |
| LIG_LIR_Gen_1 | 10 | 19 | PF02991 | 0.411 |
| LIG_LIR_Gen_1 | 216 | 224 | PF02991 | 0.447 |
| LIG_LIR_Gen_1 | 49 | 56 | PF02991 | 0.332 |
| LIG_LIR_Nem_3 | 10 | 14 | PF02991 | 0.408 |
| LIG_LIR_Nem_3 | 216 | 220 | PF02991 | 0.384 |
| LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.326 |
| LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.419 |
| LIG_NRBOX | 190 | 196 | PF00104 | 0.484 |
| LIG_Pex14_2 | 245 | 249 | PF04695 | 0.305 |
| LIG_SH2_CRK | 217 | 221 | PF00017 | 0.372 |
| LIG_SH2_NCK_1 | 143 | 147 | PF00017 | 0.406 |
| LIG_SH2_NCK_1 | 50 | 54 | PF00017 | 0.457 |
| LIG_SH2_STAT3 | 17 | 20 | PF00017 | 0.439 |
| LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.452 |
| LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.306 |
| LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.441 |
| LIG_SH3_3 | 40 | 46 | PF00018 | 0.423 |
| LIG_SUMO_SIM_par_1 | 93 | 98 | PF11976 | 0.409 |
| MOD_CK1_1 | 185 | 191 | PF00069 | 0.416 |
| MOD_CK1_1 | 49 | 55 | PF00069 | 0.521 |
| MOD_CK1_1 | 84 | 90 | PF00069 | 0.534 |
| MOD_CK1_1 | 93 | 99 | PF00069 | 0.442 |
| MOD_CK2_1 | 171 | 177 | PF00069 | 0.400 |
| MOD_Cter_Amidation | 32 | 35 | PF01082 | 0.432 |
| MOD_GlcNHglycan | 206 | 210 | PF01048 | 0.438 |
| MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.406 |
| MOD_GSK3_1 | 181 | 188 | PF00069 | 0.393 |
| MOD_GSK3_1 | 205 | 212 | PF00069 | 0.540 |
| MOD_GSK3_1 | 248 | 255 | PF00069 | 0.374 |
| MOD_GSK3_1 | 80 | 87 | PF00069 | 0.469 |
| MOD_NEK2_1 | 182 | 187 | PF00069 | 0.384 |
| MOD_NEK2_1 | 205 | 210 | PF00069 | 0.439 |
| MOD_NEK2_1 | 21 | 26 | PF00069 | 0.337 |
| MOD_NEK2_1 | 38 | 43 | PF00069 | 0.259 |
| MOD_NEK2_1 | 48 | 53 | PF00069 | 0.374 |
| MOD_NEK2_1 | 81 | 86 | PF00069 | 0.348 |
| MOD_PKA_1 | 171 | 177 | PF00069 | 0.509 |
| MOD_PKA_2 | 171 | 177 | PF00069 | 0.545 |
| MOD_PKA_2 | 209 | 215 | PF00069 | 0.444 |
| MOD_PKA_2 | 222 | 228 | PF00069 | 0.300 |
| MOD_PKA_2 | 252 | 258 | PF00069 | 0.363 |
| MOD_PKA_2 | 33 | 39 | PF00069 | 0.396 |
| MOD_Plk_1 | 21 | 27 | PF00069 | 0.392 |
| MOD_Plk_1 | 228 | 234 | PF00069 | 0.409 |
| MOD_Plk_4 | 229 | 235 | PF00069 | 0.392 |
| MOD_Plk_4 | 81 | 87 | PF00069 | 0.482 |
| MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.322 |
| TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.397 |
| TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.362 |
| TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.483 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I7K0 | Leptomonas seymouri | 61% | 100% |
| A0A1X0P1S9 | Trypanosomatidae | 29% | 100% |
| A0A3Q8IGM7 | Leishmania donovani | 97% | 100% |
| A0A3R7MBB6 | Trypanosoma rangeli | 31% | 98% |
| A4HLM6 | Leishmania braziliensis | 84% | 100% |
| A4I937 | Leishmania infantum | 96% | 100% |
| C9ZIV4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 98% |
| Q4Q422 | Leishmania major | 95% | 100% |
| V5AXA5 | Trypanosoma cruzi | 29% | 98% |