| 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: A0A3Q8IAW9
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.510 | 
| CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.697 | 
| CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.727 | 
| CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.581 | 
| CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.580 | 
| CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.411 | 
| CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.547 | 
| CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.538 | 
| CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.725 | 
| CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.587 | 
| CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.577 | 
| CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.641 | 
| CLV_PCSK_PC7_1 | 134 | 140 | PF00082 | 0.544 | 
| CLV_PCSK_PC7_1 | 19 | 25 | PF00082 | 0.627 | 
| CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.603 | 
| CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.624 | 
| CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.593 | 
| CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.627 | 
| CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.549 | 
| CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.540 | 
| DEG_SCF_TRCP1_1 | 35 | 41 | PF00400 | 0.524 | 
| DEG_SPOP_SBC_1 | 58 | 62 | PF00917 | 0.478 | 
| DOC_MAPK_gen_1 | 138 | 146 | PF00069 | 0.562 | 
| DOC_MAPK_gen_1 | 201 | 210 | PF00069 | 0.558 | 
| DOC_MAPK_MEF2A_6 | 204 | 212 | PF00069 | 0.612 | 
| DOC_PP1_RVXF_1 | 110 | 116 | PF00149 | 0.451 | 
| DOC_PP1_RVXF_1 | 169 | 175 | PF00149 | 0.518 | 
| DOC_PP4_FxxP_1 | 72 | 75 | PF00568 | 0.422 | 
| DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.681 | 
| DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.596 | 
| DOC_USP7_UBL2_3 | 138 | 142 | PF12436 | 0.574 | 
| DOC_USP7_UBL2_3 | 201 | 205 | PF12436 | 0.628 | 
| DOC_USP7_UBL2_3 | 272 | 276 | PF12436 | 0.549 | 
| DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.782 | 
| DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.586 | 
| LIG_14-3-3_CanoR_1 | 57 | 66 | PF00244 | 0.606 | 
| LIG_Actin_WH2_2 | 77 | 95 | PF00022 | 0.435 | 
| LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.543 | 
| LIG_FHA_1 | 58 | 64 | PF00498 | 0.522 | 
| LIG_FHA_2 | 131 | 137 | PF00498 | 0.574 | 
| LIG_FHA_2 | 182 | 188 | PF00498 | 0.557 | 
| LIG_FHA_2 | 192 | 198 | PF00498 | 0.512 | 
| LIG_FHA_2 | 256 | 262 | PF00498 | 0.560 | 
| LIG_LIR_Apic_2 | 123 | 129 | PF02991 | 0.609 | 
| LIG_LIR_Apic_2 | 48 | 54 | PF02991 | 0.643 | 
| LIG_LIR_Gen_1 | 280 | 289 | PF02991 | 0.609 | 
| LIG_LIR_Nem_3 | 148 | 152 | PF02991 | 0.454 | 
| LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.629 | 
| LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.584 | 
| LIG_Pex14_1 | 141 | 145 | PF04695 | 0.445 | 
| LIG_SH2_GRB2like | 105 | 108 | PF00017 | 0.454 | 
| LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.678 | 
| LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.524 | 
| LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.615 | 
| LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.577 | 
| MOD_CK1_1 | 221 | 227 | PF00069 | 0.610 | 
| MOD_CK1_1 | 36 | 42 | PF00069 | 0.606 | 
| MOD_CK2_1 | 130 | 136 | PF00069 | 0.514 | 
| MOD_CK2_1 | 181 | 187 | PF00069 | 0.538 | 
| MOD_CK2_1 | 191 | 197 | PF00069 | 0.485 | 
| MOD_Cter_Amidation | 136 | 139 | PF01082 | 0.492 | 
| MOD_Cter_Amidation | 14 | 17 | PF01082 | 0.656 | 
| MOD_Cter_Amidation | 21 | 24 | PF01082 | 0.606 | 
| MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.722 | 
| MOD_GSK3_1 | 253 | 260 | PF00069 | 0.571 | 
| MOD_GSK3_1 | 277 | 284 | PF00069 | 0.612 | 
| MOD_GSK3_1 | 35 | 42 | PF00069 | 0.668 | 
| MOD_GSK3_1 | 92 | 99 | PF00069 | 0.462 | 
| MOD_LATS_1 | 275 | 281 | PF00433 | 0.612 | 
| MOD_NEK2_1 | 59 | 64 | PF00069 | 0.511 | 
| MOD_NEK2_1 | 92 | 97 | PF00069 | 0.444 | 
| MOD_PIKK_1 | 36 | 42 | PF00454 | 0.604 | 
| MOD_PKA_2 | 281 | 287 | PF00069 | 0.728 | 
| MOD_PKA_2 | 82 | 88 | PF00069 | 0.475 | 
| MOD_Plk_1 | 191 | 197 | PF00069 | 0.610 | 
| MOD_Plk_2-3 | 118 | 124 | PF00069 | 0.475 | 
| MOD_Plk_4 | 127 | 133 | PF00069 | 0.671 | 
| MOD_Plk_4 | 59 | 65 | PF00069 | 0.539 | 
| MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.783 | 
| MOD_SUMO_for_1 | 234 | 237 | PF00179 | 0.528 | 
| MOD_SUMO_rev_2 | 117 | 127 | PF00179 | 0.592 | 
| TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.523 | 
| TRG_NLS_Bipartite_1 | 124 | 143 | PF00514 | 0.524 | 
| TRG_NLS_MonoExtC_3 | 137 | 142 | PF00514 | 0.494 | 
| TRG_NLS_MonoExtC_3 | 15 | 20 | PF00514 | 0.633 | 
| TRG_NLS_MonoExtC_3 | 203 | 209 | PF00514 | 0.627 | 
| TRG_NLS_MonoExtN_4 | 13 | 20 | PF00514 | 0.632 | 
| TRG_NLS_MonoExtN_4 | 138 | 143 | PF00514 | 0.475 | 
| TRG_NLS_MonoExtN_4 | 201 | 208 | PF00514 | 0.638 | 
| TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.575 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P555 | Leptomonas seymouri | 60% | 84% | 
| A0A0S4IRA8 | Bodo saltans | 26% | 93% | 
| A0A1X0NX54 | Trypanosomatidae | 38% | 100% | 
| A0A422NW66 | Trypanosoma rangeli | 40% | 100% | 
| A4HCP9 | Leishmania braziliensis | 73% | 100% | 
| A4I075 | Leishmania infantum | 100% | 100% | 
| C9ZUZ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% | 
| E9AW38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% | 
| Q4QBD9 | Leishmania major | 94% | 100% |