| 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: Q4QJ25
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.596 |
| CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.586 |
| CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.478 |
| CLV_PCSK_PC1ET2_1 | 96 | 98 | PF00082 | 0.478 |
| CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.683 |
| CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.433 |
| CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.539 |
| DEG_APCC_DBOX_1 | 30 | 38 | PF00400 | 0.433 |
| DOC_CKS1_1 | 234 | 239 | PF01111 | 0.422 |
| DOC_CYCLIN_RxL_1 | 240 | 249 | PF00134 | 0.484 |
| DOC_PP1_RVXF_1 | 241 | 248 | PF00149 | 0.389 |
| DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.539 |
| DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.440 |
| DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.699 |
| DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.764 |
| DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.657 |
| DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.708 |
| DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.694 |
| DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.599 |
| DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.718 |
| DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.722 |
| DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.421 |
| DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.676 |
| LIG_14-3-3_CanoR_1 | 159 | 168 | PF00244 | 0.666 |
| LIG_14-3-3_CanoR_1 | 172 | 178 | PF00244 | 0.484 |
| LIG_14-3-3_CanoR_1 | 289 | 294 | PF00244 | 0.575 |
| LIG_14-3-3_CanoR_1 | 83 | 91 | PF00244 | 0.603 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.681 |
| LIG_BRCT_BRCA1_1 | 291 | 295 | PF00533 | 0.635 |
| LIG_CSL_BTD_1 | 221 | 224 | PF09270 | 0.398 |
| LIG_CSL_BTD_1 | 234 | 237 | PF09270 | 0.395 |
| LIG_deltaCOP1_diTrp_1 | 238 | 247 | PF00928 | 0.399 |
| LIG_FHA_1 | 17 | 23 | PF00498 | 0.697 |
| LIG_FHA_1 | 171 | 177 | PF00498 | 0.610 |
| LIG_FHA_1 | 234 | 240 | PF00498 | 0.423 |
| LIG_FHA_1 | 28 | 34 | PF00498 | 0.539 |
| LIG_HCF-1_HBM_1 | 249 | 252 | PF13415 | 0.460 |
| LIG_LIR_Gen_1 | 249 | 259 | PF02991 | 0.377 |
| LIG_LIR_Nem_3 | 213 | 217 | PF02991 | 0.629 |
| LIG_LIR_Nem_3 | 249 | 255 | PF02991 | 0.385 |
| LIG_REV1ctd_RIR_1 | 88 | 97 | PF16727 | 0.494 |
| LIG_SH2_CRK | 252 | 256 | PF00017 | 0.431 |
| LIG_SH2_NCK_1 | 69 | 73 | PF00017 | 0.455 |
| LIG_SH2_SRC | 273 | 276 | PF00017 | 0.423 |
| LIG_SH2_SRC | 69 | 72 | PF00017 | 0.516 |
| LIG_SH2_STAP1 | 273 | 277 | PF00017 | 0.407 |
| LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.414 |
| LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.676 |
| LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.547 |
| LIG_SH3_3 | 194 | 200 | PF00018 | 0.674 |
| LIG_SH3_3 | 41 | 47 | PF00018 | 0.692 |
| LIG_SUMO_SIM_anti_2 | 230 | 236 | PF11976 | 0.539 |
| LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.442 |
| LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.645 |
| LIG_UBA3_1 | 33 | 39 | PF00899 | 0.563 |
| MOD_CAAXbox | 293 | 296 | PF01239 | 0.651 |
| MOD_CDK_SPK_2 | 161 | 166 | PF00069 | 0.595 |
| MOD_CK1_1 | 130 | 136 | PF00069 | 0.740 |
| MOD_CK1_1 | 15 | 21 | PF00069 | 0.599 |
| MOD_CK1_1 | 189 | 195 | PF00069 | 0.705 |
| MOD_CK1_1 | 43 | 49 | PF00069 | 0.560 |
| MOD_CK1_1 | 7 | 13 | PF00069 | 0.633 |
| MOD_CK2_1 | 139 | 145 | PF00069 | 0.663 |
| MOD_CMANNOS | 222 | 225 | PF00535 | 0.511 |
| MOD_GlcNHglycan | 128 | 132 | PF01048 | 0.755 |
| MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.607 |
| MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.661 |
| MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.572 |
| MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.659 |
| MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.667 |
| MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.617 |
| MOD_GSK3_1 | 111 | 118 | PF00069 | 0.627 |
| MOD_GSK3_1 | 12 | 19 | PF00069 | 0.611 |
| MOD_GSK3_1 | 127 | 134 | PF00069 | 0.660 |
| MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.746 |
| MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.602 |
| MOD_NEK2_1 | 255 | 260 | PF00069 | 0.419 |
| MOD_NEK2_2 | 264 | 269 | PF00069 | 0.318 |
| MOD_PIKK_1 | 159 | 165 | PF00454 | 0.653 |
| MOD_PIKK_1 | 179 | 185 | PF00454 | 0.423 |
| MOD_PKA_2 | 158 | 164 | PF00069 | 0.600 |
| MOD_PKA_2 | 171 | 177 | PF00069 | 0.490 |
| MOD_PKA_2 | 255 | 261 | PF00069 | 0.420 |
| MOD_PKA_2 | 283 | 289 | PF00069 | 0.666 |
| MOD_PKB_1 | 287 | 295 | PF00069 | 0.635 |
| MOD_Plk_4 | 201 | 207 | PF00069 | 0.534 |
| MOD_Plk_4 | 210 | 216 | PF00069 | 0.497 |
| MOD_Plk_4 | 227 | 233 | PF00069 | 0.493 |
| MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.712 |
| MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.722 |
| MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.421 |
| MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.668 |
| MOD_SUMO_for_1 | 168 | 171 | PF00179 | 0.679 |
| MOD_SUMO_rev_2 | 189 | 197 | PF00179 | 0.491 |
| TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.373 |
| TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.601 |
| TRG_Pf-PMV_PEXEL_1 | 97 | 102 | PF00026 | 0.594 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I6B6 | Leptomonas seymouri | 67% | 97% |
| A0A1X0NKM4 | Trypanosomatidae | 42% | 98% |
| A0A3S7WPG5 | Leishmania donovani | 92% | 100% |
| A0A422NGX7 | Trypanosoma rangeli | 41% | 100% |
| A4H4L9 | Leishmania braziliensis | 78% | 95% |
| A4HSU5 | Leishmania infantum | 92% | 100% |
| C9ZTF5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
| E9AKT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
| V5B7V6 | Trypanosoma cruzi | 44% | 100% |