| 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: A4I6H0
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 232 | 236 | PF00656 | 0.485 |
| CLV_MEL_PAP_1 | 214 | 220 | PF00089 | 0.529 |
| CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.546 |
| CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.576 |
| CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.517 |
| CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.682 |
| CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.546 |
| CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.525 |
| CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.682 |
| CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.555 |
| CLV_PCSK_PC7_1 | 172 | 178 | PF00082 | 0.486 |
| CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.602 |
| CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.567 |
| DEG_APCC_DBOX_1 | 134 | 142 | PF00400 | 0.451 |
| DOC_MAPK_gen_1 | 15 | 25 | PF00069 | 0.537 |
| DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.518 |
| DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.527 |
| DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.766 |
| DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.478 |
| DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.530 |
| DOC_USP7_UBL2_3 | 165 | 169 | PF12436 | 0.624 |
| DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.567 |
| DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.535 |
| LIG_14-3-3_CanoR_1 | 154 | 163 | PF00244 | 0.519 |
| LIG_14-3-3_CanoR_1 | 243 | 249 | PF00244 | 0.669 |
| LIG_APCC_ABBA_1 | 139 | 144 | PF00400 | 0.466 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.687 |
| LIG_BRCT_BRCA1_1 | 200 | 204 | PF00533 | 0.534 |
| LIG_FHA_1 | 113 | 119 | PF00498 | 0.522 |
| LIG_FHA_1 | 237 | 243 | PF00498 | 0.654 |
| LIG_FHA_2 | 230 | 236 | PF00498 | 0.669 |
| LIG_FHA_2 | 46 | 52 | PF00498 | 0.517 |
| LIG_IRF3_LxIS_1 | 87 | 94 | PF10401 | 0.447 |
| LIG_LIR_Gen_1 | 70 | 78 | PF02991 | 0.613 |
| LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.589 |
| LIG_LIR_Nem_3 | 59 | 63 | PF02991 | 0.524 |
| LIG_LIR_Nem_3 | 70 | 74 | PF02991 | 0.458 |
| LIG_MLH1_MIPbox_1 | 200 | 204 | PF16413 | 0.534 |
| LIG_REV1ctd_RIR_1 | 201 | 209 | PF16727 | 0.531 |
| LIG_SH2_STAP1 | 290 | 294 | PF00017 | 0.642 |
| LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.430 |
| LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.412 |
| LIG_SUMO_SIM_par_1 | 195 | 201 | PF11976 | 0.507 |
| LIG_UBA3_1 | 138 | 145 | PF00899 | 0.461 |
| LIG_WRC_WIRS_1 | 265 | 270 | PF05994 | 0.654 |
| MOD_CDC14_SPxK_1 | 219 | 222 | PF00782 | 0.579 |
| MOD_CDK_SPxK_1 | 216 | 222 | PF00069 | 0.569 |
| MOD_CK1_1 | 122 | 128 | PF00069 | 0.540 |
| MOD_CK1_1 | 198 | 204 | PF00069 | 0.535 |
| MOD_CK1_1 | 247 | 253 | PF00069 | 0.670 |
| MOD_CK2_1 | 45 | 51 | PF00069 | 0.518 |
| MOD_GlcNHglycan | 144 | 148 | PF01048 | 0.522 |
| MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.668 |
| MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.690 |
| MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.530 |
| MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.441 |
| MOD_GSK3_1 | 119 | 126 | PF00069 | 0.522 |
| MOD_GSK3_1 | 247 | 254 | PF00069 | 0.661 |
| MOD_GSK3_1 | 264 | 271 | PF00069 | 0.616 |
| MOD_N-GLC_2 | 86 | 88 | PF02516 | 0.433 |
| MOD_NEK2_1 | 10 | 15 | PF00069 | 0.545 |
| MOD_NEK2_1 | 148 | 153 | PF00069 | 0.487 |
| MOD_NEK2_1 | 197 | 202 | PF00069 | 0.472 |
| MOD_NEK2_1 | 32 | 37 | PF00069 | 0.454 |
| MOD_NEK2_1 | 91 | 96 | PF00069 | 0.442 |
| MOD_PIKK_1 | 112 | 118 | PF00454 | 0.568 |
| MOD_PIKK_1 | 198 | 204 | PF00454 | 0.473 |
| MOD_PK_1 | 244 | 250 | PF00069 | 0.667 |
| MOD_PKA_1 | 154 | 160 | PF00069 | 0.560 |
| MOD_PKA_2 | 275 | 281 | PF00069 | 0.669 |
| MOD_Plk_1 | 143 | 149 | PF00069 | 0.542 |
| MOD_Plk_1 | 250 | 256 | PF00069 | 0.674 |
| MOD_Plk_4 | 67 | 73 | PF00069 | 0.587 |
| MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.538 |
| MOD_SUMO_rev_2 | 77 | 87 | PF00179 | 0.562 |
| TRG_DiLeu_BaEn_1 | 144 | 149 | PF01217 | 0.504 |
| TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.687 |
| TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.523 |
| TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.659 |
| TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.511 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P3D2 | Leptomonas seymouri | 25% | 100% |
| A0A0N1HUM2 | Leptomonas seymouri | 26% | 100% |
| A0A3Q8IF80 | Leishmania donovani | 99% | 100% |
| E9B1M7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
| E9B1M9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
| Q4Q6I7 | Leishmania major | 92% | 100% |