| 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: 21 |
| NetGPI | no | yes: 0, no: 21 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 22 |
| GO:0110165 | cellular anatomical entity | 1 | 22 |
Related structures:
AlphaFold database: A4H3Q4
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 22 |
| GO:0008104 | protein localization | 4 | 22 |
| GO:0009987 | cellular process | 1 | 22 |
| GO:0015031 | protein transport | 4 | 22 |
| GO:0016192 | vesicle-mediated transport | 4 | 22 |
| GO:0033036 | macromolecule localization | 2 | 22 |
| GO:0045184 | establishment of protein localization | 3 | 22 |
| GO:0051179 | localization | 1 | 22 |
| GO:0051234 | establishment of localization | 2 | 22 |
| GO:0051641 | cellular localization | 2 | 22 |
| GO:0070727 | cellular macromolecule localization | 3 | 22 |
| GO:0071702 | organic substance transport | 4 | 22 |
| GO:0071705 | nitrogen compound transport | 4 | 22 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.616 |
| CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.279 |
| CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.499 |
| DOC_CYCLIN_RxL_1 | 30 | 41 | PF00134 | 0.563 |
| DOC_MAPK_MEF2A_6 | 184 | 191 | PF00069 | 0.688 |
| LIG_14-3-3_CanoR_1 | 184 | 188 | PF00244 | 0.651 |
| LIG_Actin_WH2_2 | 173 | 190 | PF00022 | 0.559 |
| LIG_BRCT_BRCA1_1 | 114 | 118 | PF00533 | 0.282 |
| LIG_eIF4E_1 | 32 | 38 | PF01652 | 0.560 |
| LIG_FHA_1 | 184 | 190 | PF00498 | 0.591 |
| LIG_FHA_1 | 44 | 50 | PF00498 | 0.762 |
| LIG_FHA_1 | 69 | 75 | PF00498 | 0.627 |
| LIG_FHA_2 | 126 | 132 | PF00498 | 0.583 |
| LIG_GBD_Chelix_1 | 169 | 177 | PF00786 | 0.260 |
| LIG_LIR_Gen_1 | 144 | 153 | PF02991 | 0.311 |
| LIG_LIR_Gen_1 | 192 | 201 | PF02991 | 0.500 |
| LIG_LIR_Gen_1 | 75 | 86 | PF02991 | 0.337 |
| LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.320 |
| LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.319 |
| LIG_LIR_Nem_3 | 178 | 182 | PF02991 | 0.349 |
| LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.604 |
| LIG_NRBOX | 85 | 91 | PF00104 | 0.260 |
| LIG_PCNA_PIPBox_1 | 147 | 156 | PF02747 | 0.249 |
| LIG_Pex14_1 | 97 | 101 | PF04695 | 0.342 |
| LIG_SH2_CRK | 193 | 197 | PF00017 | 0.634 |
| LIG_SH2_CRK | 32 | 36 | PF00017 | 0.627 |
| LIG_SH2_SRC | 141 | 144 | PF00017 | 0.260 |
| LIG_SH2_STAP1 | 175 | 179 | PF00017 | 0.276 |
| LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.574 |
| LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.596 |
| LIG_SH2_STAT3 | 182 | 185 | PF00017 | 0.661 |
| LIG_SH2_STAT3 | 26 | 29 | PF00017 | 0.641 |
| LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.390 |
| LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.660 |
| LIG_SxIP_EBH_1 | 173 | 184 | PF03271 | 0.387 |
| LIG_TYR_ITIM | 191 | 196 | PF00017 | 0.626 |
| LIG_TYR_ITIM | 30 | 35 | PF00017 | 0.498 |
| MOD_CK1_1 | 192 | 198 | PF00069 | 0.554 |
| MOD_CK1_1 | 63 | 69 | PF00069 | 0.624 |
| MOD_CK2_1 | 125 | 131 | PF00069 | 0.433 |
| MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.379 |
| MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.506 |
| MOD_GSK3_1 | 141 | 148 | PF00069 | 0.327 |
| MOD_GSK3_1 | 43 | 50 | PF00069 | 0.688 |
| MOD_GSK3_1 | 68 | 75 | PF00069 | 0.630 |
| MOD_GSK3_1 | 99 | 106 | PF00069 | 0.262 |
| MOD_NEK2_1 | 103 | 108 | PF00069 | 0.339 |
| MOD_NEK2_1 | 68 | 73 | PF00069 | 0.587 |
| MOD_NEK2_2 | 141 | 146 | PF00069 | 0.344 |
| MOD_NEK2_2 | 183 | 188 | PF00069 | 0.646 |
| MOD_PIKK_1 | 25 | 31 | PF00454 | 0.653 |
| MOD_PIKK_1 | 68 | 74 | PF00454 | 0.649 |
| MOD_PKA_1 | 99 | 105 | PF00069 | 0.329 |
| MOD_PKA_2 | 183 | 189 | PF00069 | 0.638 |
| MOD_PKA_2 | 72 | 78 | PF00069 | 0.527 |
| MOD_Plk_1 | 66 | 72 | PF00069 | 0.607 |
| MOD_Plk_4 | 112 | 118 | PF00069 | 0.344 |
| MOD_Plk_4 | 145 | 151 | PF00069 | 0.315 |
| MOD_Plk_4 | 168 | 174 | PF00069 | 0.370 |
| MOD_Plk_4 | 175 | 181 | PF00069 | 0.382 |
| MOD_Plk_4 | 192 | 198 | PF00069 | 0.645 |
| MOD_Plk_4 | 88 | 94 | PF00069 | 0.373 |
| MOD_SUMO_rev_2 | 17 | 23 | PF00179 | 0.559 |
| TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.182 |
| TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.625 |
| TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.617 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P5I1 | Leptomonas seymouri | 71% | 99% |
| A0A0N1I3M5 | Leptomonas seymouri | 28% | 100% |
| A0A0S4JF33 | Bodo saltans | 31% | 100% |
| A0A1X0P7F6 | Trypanosomatidae | 28% | 100% |
| A0A1X0P987 | Trypanosomatidae | 42% | 100% |
| A0A3Q8IBK0 | Leishmania donovani | 38% | 100% |
| A0A3S5H567 | Leishmania donovani | 86% | 100% |
| A0A3S5H5K3 | Leishmania donovani | 41% | 100% |
| A0A422N175 | Trypanosoma rangeli | 45% | 100% |
| A4HDV3 | Leishmania braziliensis | 38% | 100% |
| A4HRX8 | Leishmania infantum | 86% | 100% |
| A4HSK3 | Leishmania infantum | 41% | 100% |
| A4I148 | Leishmania infantum | 38% | 100% |
| C9ZKI8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 78% |
| E9ACN7 | Leishmania major | 88% | 100% |
| E9AJX6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
| E9AKI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
| E9AX82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
| Q4QA90 | Leishmania major | 38% | 100% |
| Q4QJC1 | Leishmania major | 41% | 100% |