| 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: 9 |
| NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4Q5L2
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.460 |
| CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.403 |
| CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.588 |
| CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.701 |
| CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.432 |
| CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.460 |
| CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.444 |
| CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.372 |
| CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.355 |
| CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.401 |
| CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.475 |
| CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.344 |
| CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.369 |
| CLV_Separin_Metazoa | 286 | 290 | PF03568 | 0.480 |
| DEG_APCC_DBOX_1 | 231 | 239 | PF00400 | 0.592 |
| DOC_CYCLIN_RxL_1 | 246 | 257 | PF00134 | 0.482 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 211 | 220 | PF00134 | 0.496 |
| DOC_MAPK_gen_1 | 134 | 140 | PF00069 | 0.452 |
| DOC_MAPK_gen_1 | 79 | 87 | PF00069 | 0.367 |
| DOC_MAPK_MEF2A_6 | 79 | 87 | PF00069 | 0.252 |
| DOC_PP1_RVXF_1 | 192 | 199 | PF00149 | 0.347 |
| DOC_PP1_RVXF_1 | 247 | 254 | PF00149 | 0.463 |
| DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.392 |
| DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.566 |
| LIG_14-3-3_CanoR_1 | 155 | 165 | PF00244 | 0.484 |
| LIG_14-3-3_CanoR_1 | 239 | 245 | PF00244 | 0.483 |
| LIG_14-3-3_CanoR_1 | 60 | 69 | PF00244 | 0.444 |
| LIG_14-3-3_CanoR_1 | 79 | 84 | PF00244 | 0.444 |
| LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.444 |
| LIG_Clathr_ClatBox_1 | 164 | 168 | PF01394 | 0.386 |
| LIG_FHA_1 | 145 | 151 | PF00498 | 0.408 |
| LIG_FHA_1 | 80 | 86 | PF00498 | 0.469 |
| LIG_FHA_2 | 157 | 163 | PF00498 | 0.429 |
| LIG_LIR_Gen_1 | 182 | 191 | PF02991 | 0.364 |
| LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.341 |
| LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.412 |
| LIG_LIR_Nem_3 | 243 | 247 | PF02991 | 0.497 |
| LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.400 |
| LIG_MAD2 | 60 | 68 | PF02301 | 0.429 |
| LIG_PCNA_PIPBox_1 | 26 | 35 | PF02747 | 0.485 |
| LIG_Pex14_2 | 124 | 128 | PF04695 | 0.444 |
| LIG_Pex14_2 | 20 | 24 | PF04695 | 0.369 |
| LIG_Pex14_2 | 200 | 204 | PF04695 | 0.540 |
| LIG_SH2_CRK | 38 | 42 | PF00017 | 0.344 |
| LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.473 |
| LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.344 |
| LIG_SH3_3 | 263 | 269 | PF00018 | 0.484 |
| LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.598 |
| LIG_TYR_ITIM | 36 | 41 | PF00017 | 0.344 |
| LIG_UBA3_1 | 163 | 169 | PF00899 | 0.312 |
| LIG_WRC_WIRS_1 | 208 | 213 | PF05994 | 0.477 |
| MOD_CK1_1 | 107 | 113 | PF00069 | 0.379 |
| MOD_CK1_1 | 210 | 216 | PF00069 | 0.448 |
| MOD_CK1_1 | 281 | 287 | PF00069 | 0.578 |
| MOD_CK1_1 | 6 | 12 | PF00069 | 0.658 |
| MOD_CK2_1 | 100 | 106 | PF00069 | 0.338 |
| MOD_CK2_1 | 156 | 162 | PF00069 | 0.444 |
| MOD_CK2_1 | 251 | 257 | PF00069 | 0.531 |
| MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.430 |
| MOD_GSK3_1 | 100 | 107 | PF00069 | 0.334 |
| MOD_GSK3_1 | 185 | 192 | PF00069 | 0.358 |
| MOD_GSK3_1 | 3 | 10 | PF00069 | 0.639 |
| MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.348 |
| MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.672 |
| MOD_NEK2_1 | 216 | 221 | PF00069 | 0.468 |
| MOD_NEK2_1 | 22 | 27 | PF00069 | 0.341 |
| MOD_NEK2_1 | 251 | 256 | PF00069 | 0.484 |
| MOD_NEK2_1 | 69 | 74 | PF00069 | 0.384 |
| MOD_PIKK_1 | 122 | 128 | PF00454 | 0.485 |
| MOD_PKA_2 | 281 | 287 | PF00069 | 0.570 |
| MOD_Plk_1 | 22 | 28 | PF00069 | 0.344 |
| MOD_Plk_1 | 230 | 236 | PF00069 | 0.565 |
| MOD_Plk_1 | 262 | 268 | PF00069 | 0.345 |
| MOD_Plk_4 | 104 | 110 | PF00069 | 0.384 |
| MOD_Plk_4 | 262 | 268 | PF00069 | 0.499 |
| MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.562 |
| MOD_SUMO_rev_2 | 130 | 136 | PF00179 | 0.454 |
| TRG_DiLeu_BaEn_1 | 58 | 63 | PF01217 | 0.444 |
| TRG_DiLeu_BaEn_4 | 230 | 236 | PF01217 | 0.644 |
| TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.344 |
| TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.344 |
| TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.440 |
| TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.330 |
| TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.318 |
| TRG_ER_diArg_1 | 154 | 156 | PF00400 | 0.460 |
| TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.408 |
| TRG_ER_diArg_1 | 232 | 235 | PF00400 | 0.555 |
| TRG_Pf-PMV_PEXEL_1 | 121 | 126 | PF00026 | 0.395 |
| TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.444 |
| TRG_Pf-PMV_PEXEL_1 | 272 | 276 | PF00026 | 0.530 |
| TRG_Pf-PMV_PEXEL_1 | 34 | 39 | PF00026 | 0.384 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I881 | Leptomonas seymouri | 71% | 100% |
| A0A0S4J6L8 | Bodo saltans | 31% | 78% |
| A0A1X0NV53 | Trypanosomatidae | 44% | 100% |
| A0A3S7X590 | Leishmania donovani | 92% | 100% |
| A4HK51 | Leishmania braziliensis | 82% | 99% |
| A4I7N7 | Leishmania infantum | 92% | 100% |
| D0A9T8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
| E9B2J4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |