| 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: 9 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 10 |
| NetGPI | no | yes: 0, no: 10 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 67 | 71 | PF00656 | 0.787 |
| CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.565 |
| CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.664 |
| CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.587 |
| CLV_PCSK_FUR_1 | 176 | 180 | PF00082 | 0.501 |
| CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.565 |
| CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.664 |
| CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.587 |
| CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.589 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.581 |
| DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.613 |
| DOC_CYCLIN_yCln2_LP_2 | 159 | 165 | PF00134 | 0.511 |
| DOC_MAPK_gen_1 | 129 | 137 | PF00069 | 0.439 |
| DOC_MAPK_MEF2A_6 | 120 | 128 | PF00069 | 0.459 |
| DOC_MAPK_MEF2A_6 | 35 | 42 | PF00069 | 0.519 |
| DOC_MAPK_NFAT4_5 | 35 | 43 | PF00069 | 0.517 |
| DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.536 |
| DOC_PP4_FxxP_1 | 183 | 186 | PF00568 | 0.729 |
| DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.613 |
| DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.706 |
| DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.587 |
| DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.752 |
| DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.498 |
| LIG_14-3-3_CanoR_1 | 100 | 108 | PF00244 | 0.716 |
| LIG_14-3-3_CanoR_1 | 129 | 137 | PF00244 | 0.474 |
| LIG_14-3-3_CanoR_1 | 167 | 174 | PF00244 | 0.520 |
| LIG_14-3-3_CanoR_1 | 273 | 282 | PF00244 | 0.644 |
| LIG_14-3-3_CanoR_1 | 322 | 328 | PF00244 | 0.595 |
| LIG_FHA_1 | 111 | 117 | PF00498 | 0.578 |
| LIG_FHA_1 | 130 | 136 | PF00498 | 0.510 |
| LIG_FHA_1 | 152 | 158 | PF00498 | 0.283 |
| LIG_FHA_1 | 202 | 208 | PF00498 | 0.684 |
| LIG_FHA_1 | 221 | 227 | PF00498 | 0.323 |
| LIG_LIR_Apic_2 | 160 | 164 | PF02991 | 0.479 |
| LIG_LIR_Apic_2 | 180 | 186 | PF02991 | 0.504 |
| LIG_LIR_Gen_1 | 169 | 177 | PF02991 | 0.637 |
| LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.706 |
| LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.629 |
| LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.619 |
| LIG_RPA_C_Fungi | 262 | 274 | PF08784 | 0.439 |
| LIG_SH2_CRK | 171 | 175 | PF00017 | 0.624 |
| LIG_SH2_CRK | 51 | 55 | PF00017 | 0.675 |
| LIG_SH2_NCK_1 | 51 | 55 | PF00017 | 0.662 |
| LIG_SH2_STAT3 | 10 | 13 | PF00017 | 0.617 |
| LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.617 |
| LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.739 |
| LIG_SH3_3 | 246 | 252 | PF00018 | 0.662 |
| LIG_SH3_3 | 298 | 304 | PF00018 | 0.515 |
| LIG_SH3_3 | 9 | 15 | PF00018 | 0.523 |
| LIG_SUMO_SIM_anti_2 | 217 | 223 | PF11976 | 0.565 |
| MOD_CK1_1 | 166 | 172 | PF00069 | 0.519 |
| MOD_CK1_1 | 217 | 223 | PF00069 | 0.506 |
| MOD_CK1_1 | 233 | 239 | PF00069 | 0.588 |
| MOD_CK1_1 | 265 | 271 | PF00069 | 0.720 |
| MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.555 |
| MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.737 |
| MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.690 |
| MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.568 |
| MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.536 |
| MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.467 |
| MOD_GSK3_1 | 102 | 109 | PF00069 | 0.652 |
| MOD_GSK3_1 | 230 | 237 | PF00069 | 0.706 |
| MOD_GSK3_1 | 258 | 265 | PF00069 | 0.696 |
| MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.684 |
| MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.477 |
| MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.530 |
| MOD_NEK2_1 | 151 | 156 | PF00069 | 0.410 |
| MOD_NEK2_2 | 281 | 286 | PF00069 | 0.536 |
| MOD_PIKK_1 | 166 | 172 | PF00454 | 0.618 |
| MOD_PIKK_1 | 273 | 279 | PF00454 | 0.683 |
| MOD_PKA_1 | 321 | 327 | PF00069 | 0.581 |
| MOD_PKA_2 | 166 | 172 | PF00069 | 0.563 |
| MOD_PKA_2 | 296 | 302 | PF00069 | 0.497 |
| MOD_PKA_2 | 321 | 327 | PF00069 | 0.581 |
| MOD_Plk_1 | 102 | 108 | PF00069 | 0.718 |
| MOD_Plk_1 | 217 | 223 | PF00069 | 0.621 |
| MOD_Plk_4 | 217 | 223 | PF00069 | 0.484 |
| MOD_Plk_4 | 27 | 33 | PF00069 | 0.608 |
| MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.496 |
| MOD_SUMO_rev_2 | 311 | 318 | PF00179 | 0.562 |
| TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.622 |
| TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.634 |
| TRG_ER_diArg_1 | 128 | 131 | PF00400 | 0.454 |
| TRG_ER_diArg_1 | 135 | 138 | PF00400 | 0.433 |
| TRG_ER_diArg_1 | 176 | 179 | PF00400 | 0.496 |
| TRG_NLS_MonoExtC_3 | 320 | 325 | PF00514 | 0.589 |
| TRG_NLS_MonoExtN_4 | 321 | 326 | PF00514 | 0.583 |
| TRG_Pf-PMV_PEXEL_1 | 278 | 283 | PF00026 | 0.632 |
| TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.558 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IM80 | Leptomonas seymouri | 64% | 96% |
| A0A1X0P627 | Trypanosomatidae | 36% | 100% |
| A0A3Q8IDC8 | Leishmania donovani | 92% | 100% |
| A0A3R7NH36 | Trypanosoma rangeli | 44% | 100% |
| A4HA69 | Leishmania braziliensis | 84% | 100% |
| A4HYE1 | Leishmania infantum | 91% | 100% |
| D0A0S6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
| Q4QD92 | Leishmania major | 88% | 99% |
| V5AZ17 | Trypanosoma cruzi | 43% | 100% |