| 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: 8 |
| NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9AKK5
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.627 |
| DOC_PP4_FxxP_1 | 57 | 60 | PF00568 | 0.389 |
| DOC_USP7_UBL2_3 | 36 | 40 | PF12436 | 0.513 |
| LIG_14-3-3_CanoR_1 | 50 | 58 | PF00244 | 0.453 |
| LIG_deltaCOP1_diTrp_1 | 20 | 28 | PF00928 | 0.534 |
| LIG_FHA_1 | 8 | 14 | PF00498 | 0.536 |
| LIG_FHA_2 | 76 | 82 | PF00498 | 0.530 |
| LIG_Integrin_isoDGR_2 | 15 | 17 | PF01839 | 0.611 |
| LIG_LIR_Apic_2 | 54 | 60 | PF02991 | 0.392 |
| LIG_LIR_Gen_1 | 20 | 28 | PF02991 | 0.534 |
| LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.489 |
| MOD_CK2_1 | 61 | 67 | PF00069 | 0.374 |
| MOD_CK2_1 | 75 | 81 | PF00069 | 0.542 |
| MOD_GSK3_1 | 71 | 78 | PF00069 | 0.484 |
| MOD_PIKK_1 | 80 | 86 | PF00454 | 0.558 |
| MOD_Plk_2-3 | 61 | 67 | PF00069 | 0.260 |
| TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.389 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I250 | Leptomonas seymouri | 76% | 100% |
| A0A0S4J1N5 | Bodo saltans | 60% | 94% |
| A0A3S7WP86 | Leishmania donovani | 93% | 100% |
| A4H4E4 | Leishmania braziliensis | 85% | 100% |
| A4HSM1 | Leishmania infantum | 93% | 100% |
| C9ZND0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 81% |
| Q4QJA3 | Leishmania major | 90% | 100% |