| 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: A4HV52
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.456 |
| CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.456 |
| CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.456 |
| CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.456 |
| CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.534 |
| CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.453 |
| DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.456 |
| DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.663 |
| DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.486 |
| DOC_PP4_FxxP_1 | 60 | 63 | PF00568 | 0.479 |
| DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.550 |
| DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.485 |
| DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.588 |
| DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.453 |
| DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.450 |
| LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.474 |
| LIG_14-3-3_CanoR_1 | 160 | 164 | PF00244 | 0.617 |
| LIG_14-3-3_CanoR_1 | 179 | 188 | PF00244 | 0.459 |
| LIG_14-3-3_CanoR_1 | 201 | 206 | PF00244 | 0.599 |
| LIG_deltaCOP1_diTrp_1 | 144 | 154 | PF00928 | 0.510 |
| LIG_FHA_1 | 140 | 146 | PF00498 | 0.600 |
| LIG_FHA_1 | 194 | 200 | PF00498 | 0.466 |
| LIG_FHA_2 | 146 | 152 | PF00498 | 0.505 |
| LIG_FHA_2 | 160 | 166 | PF00498 | 0.467 |
| LIG_LIR_Gen_1 | 105 | 116 | PF02991 | 0.705 |
| LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.711 |
| LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.399 |
| LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.441 |
| LIG_Pex14_2 | 33 | 37 | PF04695 | 0.440 |
| LIG_SH2_CRK | 225 | 229 | PF00017 | 0.496 |
| LIG_SH2_GRB2like | 108 | 111 | PF00017 | 0.628 |
| LIG_SH2_PTP2 | 108 | 111 | PF00017 | 0.711 |
| LIG_SH2_SRC | 108 | 111 | PF00017 | 0.698 |
| LIG_SH2_STAT3 | 178 | 181 | PF00017 | 0.634 |
| LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.711 |
| LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.556 |
| LIG_SH3_3 | 108 | 114 | PF00018 | 0.649 |
| LIG_SUMO_SIM_anti_2 | 263 | 271 | PF11976 | 0.608 |
| LIG_SUMO_SIM_par_1 | 87 | 92 | PF11976 | 0.477 |
| LIG_UBA3_1 | 245 | 249 | PF00899 | 0.569 |
| LIG_UBA3_1 | 269 | 276 | PF00899 | 0.581 |
| MOD_CK1_1 | 139 | 145 | PF00069 | 0.632 |
| MOD_CK1_1 | 17 | 23 | PF00069 | 0.471 |
| MOD_CK2_1 | 143 | 149 | PF00069 | 0.539 |
| MOD_CK2_1 | 159 | 165 | PF00069 | 0.501 |
| MOD_CK2_1 | 235 | 241 | PF00069 | 0.472 |
| MOD_Cter_Amidation | 11 | 14 | PF01082 | 0.479 |
| MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.629 |
| MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.620 |
| MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.486 |
| MOD_GSK3_1 | 139 | 146 | PF00069 | 0.593 |
| MOD_GSK3_1 | 268 | 275 | PF00069 | 0.540 |
| MOD_GSK3_1 | 42 | 49 | PF00069 | 0.453 |
| MOD_GSK3_1 | 8 | 15 | PF00069 | 0.472 |
| MOD_GSK3_1 | 98 | 105 | PF00069 | 0.626 |
| MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.546 |
| MOD_NEK2_1 | 235 | 240 | PF00069 | 0.468 |
| MOD_NEK2_1 | 47 | 52 | PF00069 | 0.463 |
| MOD_NEK2_1 | 8 | 13 | PF00069 | 0.468 |
| MOD_PIKK_1 | 203 | 209 | PF00454 | 0.608 |
| MOD_PKA_1 | 13 | 19 | PF00069 | 0.476 |
| MOD_PKA_2 | 13 | 19 | PF00069 | 0.644 |
| MOD_PKA_2 | 159 | 165 | PF00069 | 0.540 |
| MOD_PKA_2 | 63 | 69 | PF00069 | 0.479 |
| MOD_Plk_1 | 143 | 149 | PF00069 | 0.567 |
| MOD_Plk_1 | 184 | 190 | PF00069 | 0.472 |
| MOD_Plk_1 | 235 | 241 | PF00069 | 0.472 |
| MOD_Plk_4 | 268 | 274 | PF00069 | 0.484 |
| MOD_Plk_4 | 28 | 34 | PF00069 | 0.443 |
| MOD_Plk_4 | 74 | 80 | PF00069 | 0.471 |
| MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.588 |
| MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.452 |
| MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.452 |
| TRG_DiLeu_BaEn_1 | 166 | 171 | PF01217 | 0.470 |
| TRG_DiLeu_BaEn_1 | 92 | 97 | PF01217 | 0.690 |
| TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.711 |
| TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.495 |
| TRG_ER_diArg_1 | 218 | 221 | PF00400 | 0.533 |
| TRG_NES_CRM1_1 | 222 | 236 | PF08389 | 0.486 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PBR7 | Leptomonas seymouri | 88% | 100% |
| A0A0S4JQ09 | Bodo saltans | 45% | 100% |
| A0A1X0NM53 | Trypanosomatidae | 73% | 100% |
| A0A3S7WRW2 | Leishmania donovani | 100% | 100% |
| A0A422N6G0 | Trypanosoma rangeli | 70% | 100% |
| A4H6S4 | Leishmania braziliensis | 92% | 100% |
| C9ZQD3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
| E9ANT5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
| Q4QGT5 | Leishmania major | 98% | 100% |