| 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: 7 |
| NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9AT62
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.447 |
| DOC_USP7_UBL2_3 | 55 | 59 | PF12436 | 0.680 |
| LIG_14-3-3_CanoR_1 | 61 | 67 | PF00244 | 0.461 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.553 |
| LIG_FHA_1 | 41 | 47 | PF00498 | 0.553 |
| LIG_FHA_1 | 71 | 77 | PF00498 | 0.609 |
| LIG_FHA_2 | 1 | 7 | PF00498 | 0.539 |
| LIG_TRAF2_1 | 47 | 50 | PF00917 | 0.353 |
| MOD_CK1_1 | 62 | 68 | PF00069 | 0.620 |
| MOD_CK1_1 | 70 | 76 | PF00069 | 0.637 |
| MOD_CK2_1 | 44 | 50 | PF00069 | 0.350 |
| MOD_CK2_1 | 65 | 71 | PF00069 | 0.450 |
| MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.594 |
| MOD_GSK3_1 | 40 | 47 | PF00069 | 0.370 |
| MOD_GSK3_1 | 62 | 69 | PF00069 | 0.589 |
| MOD_PKA_2 | 60 | 66 | PF00069 | 0.739 |
| TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.552 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I666 | Leptomonas seymouri | 49% | 98% |
| A0A3Q8IG76 | Leishmania donovani | 88% | 100% |
| A4HPF1 | Leishmania braziliensis | 77% | 100% |
| A4ICJ2 | Leishmania infantum | 88% | 100% |
| D0A3G0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 97% |
| Q4Q1D5 | Leishmania major | 90% | 100% |