| 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. | yes | yes: 9 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 10 | 
| NetGPI | no | yes: 0, no: 10 | 
Related structures:
AlphaFold database: A0A3Q8IB20
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.336 | 
| CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.267 | 
| CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.472 | 
| CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.267 | 
| CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.492 | 
| CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.459 | 
| CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.442 | 
| CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.153 | 
| CLV_PCSK_PC1ET2_1 | 250 | 252 | PF00082 | 0.613 | 
| CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.450 | 
| CLV_PCSK_PC7_1 | 251 | 257 | PF00082 | 0.462 | 
| CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.360 | 
| CLV_Separin_Metazoa | 129 | 133 | PF03568 | 0.423 | 
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.524 | 
| DOC_MAPK_gen_1 | 73 | 81 | PF00069 | 0.296 | 
| DOC_MAPK_MEF2A_6 | 132 | 140 | PF00069 | 0.565 | 
| DOC_MAPK_MEF2A_6 | 74 | 83 | PF00069 | 0.267 | 
| DOC_PP1_RVXF_1 | 42 | 49 | PF00149 | 0.408 | 
| DOC_PP1_RVXF_1 | 90 | 97 | PF00149 | 0.267 | 
| DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.471 | 
| LIG_14-3-3_CanoR_1 | 106 | 112 | PF00244 | 0.256 | 
| LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.439 | 
| LIG_14-3-3_CanoR_1 | 189 | 195 | PF00244 | 0.383 | 
| LIG_14-3-3_CanoR_1 | 217 | 225 | PF00244 | 0.316 | 
| LIG_14-3-3_CanoR_1 | 62 | 67 | PF00244 | 0.376 | 
| LIG_14-3-3_CterR_2 | 256 | 260 | PF00244 | 0.451 | 
| LIG_FHA_1 | 133 | 139 | PF00498 | 0.580 | 
| LIG_FHA_1 | 220 | 226 | PF00498 | 0.344 | 
| LIG_FHA_1 | 3 | 9 | PF00498 | 0.462 | 
| LIG_HP1_1 | 136 | 140 | PF01393 | 0.426 | 
| LIG_LIR_Gen_1 | 17 | 26 | PF02991 | 0.389 | 
| LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.410 | 
| LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.385 | 
| LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.418 | 
| LIG_Pex14_1 | 96 | 100 | PF04695 | 0.282 | 
| LIG_Pex14_2 | 169 | 173 | PF04695 | 0.267 | 
| LIG_SH2_CRK | 63 | 67 | PF00017 | 0.360 | 
| LIG_SH2_GRB2like | 32 | 35 | PF00017 | 0.443 | 
| LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.487 | 
| LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.355 | 
| LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.472 | 
| LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.422 | 
| LIG_SH3_3 | 196 | 202 | PF00018 | 0.301 | 
| LIG_SUMO_SIM_par_1 | 135 | 142 | PF11976 | 0.457 | 
| LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.425 | 
| LIG_UBA3_1 | 147 | 156 | PF00899 | 0.360 | 
| MOD_CK1_1 | 110 | 116 | PF00069 | 0.276 | 
| MOD_CK1_1 | 164 | 170 | PF00069 | 0.412 | 
| MOD_CK1_1 | 17 | 23 | PF00069 | 0.395 | 
| MOD_CK2_1 | 236 | 242 | PF00069 | 0.495 | 
| MOD_CK2_1 | 62 | 68 | PF00069 | 0.445 | 
| MOD_Cter_Amidation | 248 | 251 | PF01082 | 0.617 | 
| MOD_GlcNHglycan | 206 | 210 | PF01048 | 0.291 | 
| MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.512 | 
| MOD_GSK3_1 | 14 | 21 | PF00069 | 0.434 | 
| MOD_GSK3_1 | 159 | 166 | PF00069 | 0.268 | 
| MOD_GSK3_1 | 50 | 57 | PF00069 | 0.438 | 
| MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.410 | 
| MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.429 | 
| MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.442 | 
| MOD_N-GLC_2 | 120 | 122 | PF02516 | 0.282 | 
| MOD_NEK2_1 | 100 | 105 | PF00069 | 0.304 | 
| MOD_NEK2_1 | 163 | 168 | PF00069 | 0.267 | 
| MOD_NEK2_1 | 236 | 241 | PF00069 | 0.497 | 
| MOD_NEK2_1 | 33 | 38 | PF00069 | 0.367 | 
| MOD_NEK2_2 | 182 | 187 | PF00069 | 0.278 | 
| MOD_PK_1 | 107 | 113 | PF00069 | 0.301 | 
| MOD_PK_1 | 18 | 24 | PF00069 | 0.435 | 
| MOD_PK_1 | 62 | 68 | PF00069 | 0.410 | 
| MOD_PKA_2 | 17 | 23 | PF00069 | 0.395 | 
| MOD_PKA_2 | 182 | 188 | PF00069 | 0.278 | 
| MOD_PKA_2 | 2 | 8 | PF00069 | 0.510 | 
| MOD_PKA_2 | 202 | 208 | PF00069 | 0.432 | 
| MOD_PKA_2 | 50 | 56 | PF00069 | 0.350 | 
| MOD_PKA_2 | 61 | 67 | PF00069 | 0.462 | 
| MOD_Plk_1 | 107 | 113 | PF00069 | 0.419 | 
| MOD_Plk_1 | 218 | 224 | PF00069 | 0.508 | 
| MOD_Plk_1 | 236 | 242 | PF00069 | 0.499 | 
| MOD_Plk_1 | 33 | 39 | PF00069 | 0.472 | 
| MOD_Plk_4 | 18 | 24 | PF00069 | 0.435 | 
| MOD_Plk_4 | 62 | 68 | PF00069 | 0.426 | 
| MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.470 | 
| TRG_DiLeu_BaEn_4 | 229 | 235 | PF01217 | 0.453 | 
| TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.472 | 
| TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.428 | 
| TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.361 | 
| TRG_ER_diArg_1 | 186 | 189 | PF00400 | 0.324 | 
| TRG_ER_diArg_1 | 253 | 256 | PF00400 | 0.466 | 
| TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.304 | 
| TRG_Pf-PMV_PEXEL_1 | 149 | 153 | PF00026 | 0.326 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1IIG6 | Leptomonas seymouri | 73% | 100% | 
| A0A0S4JHH1 | Bodo saltans | 51% | 100% | 
| A0A1X0P874 | Trypanosomatidae | 68% | 100% | 
| A0A422NWN7 | Trypanosoma rangeli | 72% | 100% | 
| A4H9D6 | Leishmania braziliensis | 90% | 100% | 
| D0A038 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 100% | 
| E9AGQ2 | Leishmania infantum | 100% | 100% | 
| E9ARG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% | 
| V5B6F4 | Trypanosoma cruzi | 68% | 100% |