| 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: A4H512
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.734 |
| CLV_MEL_PAP_1 | 116 | 122 | PF00089 | 0.506 |
| CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.524 |
| CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.629 |
| CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.790 |
| CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.524 |
| CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.629 |
| CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.774 |
| DEG_SPOP_SBC_1 | 132 | 136 | PF00917 | 0.740 |
| DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.696 |
| DOC_MAPK_JIP1_4 | 2 | 8 | PF00069 | 0.728 |
| DOC_PP1_RVXF_1 | 188 | 194 | PF00149 | 0.591 |
| DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.753 |
| DOC_PP4_FxxP_1 | 8 | 11 | PF00568 | 0.577 |
| DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.768 |
| DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.606 |
| DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.617 |
| DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.792 |
| DOC_USP7_UBL2_3 | 69 | 73 | PF12436 | 0.552 |
| DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.599 |
| LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.621 |
| LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.553 |
| LIG_FHA_1 | 123 | 129 | PF00498 | 0.610 |
| LIG_FHA_1 | 142 | 148 | PF00498 | 0.707 |
| LIG_FHA_1 | 31 | 37 | PF00498 | 0.634 |
| LIG_FHA_1 | 42 | 48 | PF00498 | 0.545 |
| LIG_FHA_2 | 182 | 188 | PF00498 | 0.662 |
| LIG_IRF3_LxIS_1 | 43 | 48 | PF10401 | 0.502 |
| LIG_LIR_Apic_2 | 7 | 11 | PF02991 | 0.549 |
| LIG_LIR_Gen_1 | 174 | 182 | PF02991 | 0.606 |
| LIG_LIR_Gen_1 | 192 | 201 | PF02991 | 0.554 |
| LIG_LIR_LC3C_4 | 33 | 36 | PF02991 | 0.510 |
| LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.601 |
| LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.577 |
| LIG_Pex14_2 | 173 | 177 | PF04695 | 0.667 |
| LIG_PTAP_UEV_1 | 147 | 152 | PF05743 | 0.497 |
| LIG_PTB_Apo_2 | 37 | 44 | PF02174 | 0.497 |
| LIG_SH2_STAP1 | 152 | 156 | PF00017 | 0.634 |
| LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.647 |
| LIG_SH3_3 | 142 | 148 | PF00018 | 0.610 |
| LIG_SH3_3 | 165 | 171 | PF00018 | 0.578 |
| LIG_SH3_3 | 33 | 39 | PF00018 | 0.633 |
| LIG_SH3_4 | 69 | 76 | PF00018 | 0.551 |
| LIG_SUMO_SIM_anti_2 | 242 | 248 | PF11976 | 0.662 |
| LIG_SUMO_SIM_par_1 | 143 | 149 | PF11976 | 0.512 |
| LIG_SUMO_SIM_par_1 | 2 | 7 | PF11976 | 0.475 |
| LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.476 |
| MOD_CK1_1 | 136 | 142 | PF00069 | 0.630 |
| MOD_CK1_1 | 60 | 66 | PF00069 | 0.770 |
| MOD_CK1_1 | 82 | 88 | PF00069 | 0.750 |
| MOD_CK2_1 | 181 | 187 | PF00069 | 0.654 |
| MOD_Cter_Amidation | 216 | 219 | PF01082 | 0.693 |
| MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.777 |
| MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.658 |
| MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.655 |
| MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.680 |
| MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.653 |
| MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.662 |
| MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.787 |
| MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.697 |
| MOD_GSK3_1 | 122 | 129 | PF00069 | 0.588 |
| MOD_GSK3_1 | 132 | 139 | PF00069 | 0.627 |
| MOD_GSK3_1 | 241 | 248 | PF00069 | 0.573 |
| MOD_GSK3_1 | 41 | 48 | PF00069 | 0.595 |
| MOD_GSK3_1 | 56 | 63 | PF00069 | 0.626 |
| MOD_GSK3_1 | 79 | 86 | PF00069 | 0.746 |
| MOD_NEK2_1 | 120 | 125 | PF00069 | 0.730 |
| MOD_NEK2_1 | 191 | 196 | PF00069 | 0.635 |
| MOD_NEK2_1 | 45 | 50 | PF00069 | 0.602 |
| MOD_PIKK_1 | 181 | 187 | PF00454 | 0.654 |
| MOD_PKA_1 | 22 | 28 | PF00069 | 0.649 |
| MOD_PKA_2 | 189 | 195 | PF00069 | 0.626 |
| MOD_PKA_2 | 21 | 27 | PF00069 | 0.662 |
| MOD_Plk_1 | 241 | 247 | PF00069 | 0.608 |
| MOD_Plk_4 | 241 | 247 | PF00069 | 0.634 |
| MOD_Plk_4 | 30 | 36 | PF00069 | 0.629 |
| MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.605 |
| TRG_ER_diArg_1 | 188 | 191 | PF00400 | 0.674 |
| TRG_Pf-PMV_PEXEL_1 | 218 | 222 | PF00026 | 0.793 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P403 | Leptomonas seymouri | 46% | 97% |
| A0A3S5H5Y8 | Leishmania donovani | 66% | 100% |
| A4HT86 | Leishmania infantum | 67% | 100% |
| C9ZUN8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
| E9AL74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 99% |
| Q4QIN0 | Leishmania major | 66% | 100% |