| 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: 18 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 6 |
| NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AXS1
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0009987 | cellular process | 1 | 7 |
| GO:0016043 | cellular component organization | 3 | 7 |
| GO:0022607 | cellular component assembly | 4 | 7 |
| GO:0043248 | proteasome assembly | 6 | 7 |
| GO:0043933 | protein-containing complex organization | 4 | 7 |
| GO:0065003 | protein-containing complex assembly | 5 | 7 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.411 |
| CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.510 |
| CLV_PCSK_FUR_1 | 169 | 173 | PF00082 | 0.411 |
| CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.411 |
| CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.510 |
| CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.411 |
| CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.509 |
| CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.466 |
| CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.521 |
| CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.558 |
| DEG_APCC_DBOX_1 | 176 | 184 | PF00400 | 0.411 |
| DOC_CYCLIN_RxL_1 | 195 | 203 | PF00134 | 0.584 |
| DOC_MAPK_MEF2A_6 | 177 | 185 | PF00069 | 0.411 |
| DOC_MAPK_MEF2A_6 | 94 | 101 | PF00069 | 0.545 |
| DOC_MAPK_NFAT4_5 | 94 | 102 | PF00069 | 0.552 |
| DOC_PP1_RVXF_1 | 58 | 65 | PF00149 | 0.593 |
| DOC_PP4_FxxP_1 | 66 | 69 | PF00568 | 0.624 |
| DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.790 |
| DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.485 |
| DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.730 |
| DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.794 |
| DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.704 |
| DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.655 |
| LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.686 |
| LIG_14-3-3_CanoR_1 | 60 | 65 | PF00244 | 0.503 |
| LIG_BRCT_BRCA1_1 | 143 | 147 | PF00533 | 0.411 |
| LIG_eIF4E_1 | 204 | 210 | PF01652 | 0.330 |
| LIG_FHA_1 | 140 | 146 | PF00498 | 0.485 |
| LIG_FHA_1 | 157 | 163 | PF00498 | 0.411 |
| LIG_FHA_1 | 174 | 180 | PF00498 | 0.411 |
| LIG_FHA_1 | 9 | 15 | PF00498 | 0.711 |
| LIG_LIR_Apic_2 | 63 | 69 | PF02991 | 0.599 |
| LIG_LIR_Gen_1 | 106 | 112 | PF02991 | 0.452 |
| LIG_LIR_Gen_1 | 144 | 153 | PF02991 | 0.411 |
| LIG_LIR_Nem_3 | 106 | 110 | PF02991 | 0.408 |
| LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.411 |
| LIG_SH2_CRK | 126 | 130 | PF00017 | 0.523 |
| LIG_SH2_NCK_1 | 126 | 130 | PF00017 | 0.624 |
| LIG_SH2_PTP2 | 107 | 110 | PF00017 | 0.427 |
| LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.444 |
| LIG_SH3_3 | 213 | 219 | PF00018 | 0.574 |
| LIG_SH3_3 | 43 | 49 | PF00018 | 0.647 |
| LIG_TYR_ITIM | 105 | 110 | PF00017 | 0.463 |
| LIG_UBA3_1 | 1 | 9 | PF00899 | 0.636 |
| MOD_CDC14_SPxK_1 | 218 | 221 | PF00782 | 0.715 |
| MOD_CDK_SPxK_1 | 215 | 221 | PF00069 | 0.684 |
| MOD_CK1_1 | 70 | 76 | PF00069 | 0.651 |
| MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.450 |
| MOD_GSK3_1 | 110 | 117 | PF00069 | 0.503 |
| MOD_GSK3_1 | 181 | 188 | PF00069 | 0.411 |
| MOD_GSK3_1 | 22 | 29 | PF00069 | 0.714 |
| MOD_GSK3_1 | 32 | 39 | PF00069 | 0.654 |
| MOD_GSK3_1 | 67 | 74 | PF00069 | 0.621 |
| MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.470 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.637 |
| MOD_NEK2_1 | 161 | 166 | PF00069 | 0.494 |
| MOD_NEK2_1 | 181 | 186 | PF00069 | 0.183 |
| MOD_NEK2_1 | 192 | 197 | PF00069 | 0.497 |
| MOD_NEK2_1 | 97 | 102 | PF00069 | 0.410 |
| MOD_PKA_1 | 22 | 28 | PF00069 | 0.517 |
| MOD_PKA_2 | 21 | 27 | PF00069 | 0.637 |
| MOD_PKB_1 | 58 | 66 | PF00069 | 0.531 |
| MOD_Plk_2-3 | 141 | 147 | PF00069 | 0.411 |
| MOD_Plk_4 | 181 | 187 | PF00069 | 0.411 |
| MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.485 |
| MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.684 |
| MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.793 |
| MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.700 |
| MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.659 |
| TRG_DiLeu_LyEn_5 | 175 | 180 | PF01217 | 0.411 |
| TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.444 |
| TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.411 |
| TRG_ER_diArg_1 | 57 | 60 | PF00400 | 0.509 |
| TRG_Pf-PMV_PEXEL_1 | 3 | 8 | PF00026 | 0.468 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P8W5 | Leptomonas seymouri | 64% | 100% |
| A0A3Q8IGP4 | Leishmania donovani | 91% | 100% |
| A4HE91 | Leishmania braziliensis | 76% | 100% |
| A4I1N7 | Leishmania infantum | 91% | 100% |
| Q4Q9Q0 | Leishmania major | 90% | 100% |