| 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: 6 |
| NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q550
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.548 |
| CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.431 |
| CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.449 |
| CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.494 |
| CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.453 |
| CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.521 |
| CLV_PCSK_PC1ET2_1 | 277 | 279 | PF00082 | 0.453 |
| CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.368 |
| CLV_PCSK_PC7_1 | 238 | 244 | PF00082 | 0.472 |
| CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.365 |
| CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.500 |
| DEG_SCF_FBW7_1 | 59 | 66 | PF00400 | 0.511 |
| DEG_SPOP_SBC_1 | 194 | 198 | PF00917 | 0.586 |
| DOC_CYCLIN_RxL_1 | 313 | 324 | PF00134 | 0.402 |
| DOC_MAPK_gen_1 | 242 | 251 | PF00069 | 0.556 |
| DOC_MAPK_MEF2A_6 | 242 | 250 | PF00069 | 0.409 |
| DOC_PP1_RVXF_1 | 108 | 114 | PF00149 | 0.284 |
| DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.599 |
| DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.620 |
| DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.651 |
| DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.559 |
| LIG_14-3-3_CanoR_1 | 149 | 157 | PF00244 | 0.409 |
| LIG_14-3-3_CanoR_1 | 216 | 224 | PF00244 | 0.617 |
| LIG_BRCT_BRCA1_1 | 232 | 236 | PF00533 | 0.478 |
| LIG_FHA_1 | 10 | 16 | PF00498 | 0.794 |
| LIG_FHA_1 | 135 | 141 | PF00498 | 0.376 |
| LIG_FHA_1 | 179 | 185 | PF00498 | 0.720 |
| LIG_FHA_1 | 200 | 206 | PF00498 | 0.677 |
| LIG_FHA_1 | 227 | 233 | PF00498 | 0.538 |
| LIG_FHA_1 | 261 | 267 | PF00498 | 0.404 |
| LIG_FHA_1 | 28 | 34 | PF00498 | 0.531 |
| LIG_FHA_1 | 326 | 332 | PF00498 | 0.462 |
| LIG_FHA_2 | 115 | 121 | PF00498 | 0.367 |
| LIG_FHA_2 | 196 | 202 | PF00498 | 0.660 |
| LIG_FHA_2 | 210 | 216 | PF00498 | 0.654 |
| LIG_PTAP_UEV_1 | 288 | 293 | PF05743 | 0.570 |
| LIG_SH2_GRB2like | 129 | 132 | PF00017 | 0.438 |
| LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.458 |
| LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.332 |
| LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.397 |
| LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.677 |
| LIG_SH3_3 | 169 | 175 | PF00018 | 0.618 |
| LIG_SH3_3 | 286 | 292 | PF00018 | 0.566 |
| LIG_SH3_3 | 299 | 305 | PF00018 | 0.507 |
| LIG_SUMO_SIM_anti_2 | 122 | 129 | PF11976 | 0.415 |
| LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.515 |
| LIG_UBA3_1 | 248 | 254 | PF00899 | 0.407 |
| LIG_WW_3 | 305 | 309 | PF00397 | 0.478 |
| MOD_CK1_1 | 10 | 16 | PF00069 | 0.583 |
| MOD_CK1_1 | 179 | 185 | PF00069 | 0.593 |
| MOD_CK1_1 | 196 | 202 | PF00069 | 0.658 |
| MOD_CK1_1 | 226 | 232 | PF00069 | 0.697 |
| MOD_CK1_1 | 3 | 9 | PF00069 | 0.659 |
| MOD_CK1_1 | 31 | 37 | PF00069 | 0.666 |
| MOD_CK1_1 | 40 | 46 | PF00069 | 0.574 |
| MOD_CK1_1 | 57 | 63 | PF00069 | 0.530 |
| MOD_CK2_1 | 114 | 120 | PF00069 | 0.441 |
| MOD_CK2_1 | 26 | 32 | PF00069 | 0.658 |
| MOD_CK2_1 | 276 | 282 | PF00069 | 0.514 |
| MOD_GlcNHglycan | 168 | 172 | PF01048 | 0.625 |
| MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.512 |
| MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.583 |
| MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.640 |
| MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.527 |
| MOD_GSK3_1 | 149 | 156 | PF00069 | 0.452 |
| MOD_GSK3_1 | 167 | 174 | PF00069 | 0.504 |
| MOD_GSK3_1 | 179 | 186 | PF00069 | 0.771 |
| MOD_GSK3_1 | 189 | 196 | PF00069 | 0.654 |
| MOD_GSK3_1 | 226 | 233 | PF00069 | 0.638 |
| MOD_GSK3_1 | 27 | 34 | PF00069 | 0.597 |
| MOD_GSK3_1 | 292 | 299 | PF00069 | 0.557 |
| MOD_GSK3_1 | 3 | 10 | PF00069 | 0.615 |
| MOD_GSK3_1 | 36 | 43 | PF00069 | 0.638 |
| MOD_GSK3_1 | 55 | 62 | PF00069 | 0.470 |
| MOD_GSK3_1 | 73 | 80 | PF00069 | 0.583 |
| MOD_GSK3_1 | 92 | 99 | PF00069 | 0.294 |
| MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.520 |
| MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.656 |
| MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.734 |
| MOD_NEK2_1 | 112 | 117 | PF00069 | 0.398 |
| MOD_NEK2_1 | 325 | 330 | PF00069 | 0.390 |
| MOD_NEK2_2 | 77 | 82 | PF00069 | 0.523 |
| MOD_PKA_2 | 148 | 154 | PF00069 | 0.379 |
| MOD_PKA_2 | 215 | 221 | PF00069 | 0.593 |
| MOD_Plk_1 | 167 | 173 | PF00069 | 0.559 |
| MOD_Plk_1 | 209 | 215 | PF00069 | 0.583 |
| MOD_Plk_1 | 40 | 46 | PF00069 | 0.793 |
| MOD_Plk_1 | 96 | 102 | PF00069 | 0.353 |
| MOD_Plk_2-3 | 209 | 215 | PF00069 | 0.673 |
| MOD_Plk_2-3 | 276 | 282 | PF00069 | 0.514 |
| MOD_Plk_4 | 296 | 302 | PF00069 | 0.535 |
| MOD_Plk_4 | 325 | 331 | PF00069 | 0.386 |
| MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.600 |
| MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.620 |
| MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.650 |
| MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.556 |
| TRG_DiLeu_BaEn_4 | 275 | 281 | PF01217 | 0.379 |
| TRG_DiLeu_BaLyEn_6 | 86 | 91 | PF01217 | 0.461 |
| TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.444 |
| TRG_Pf-PMV_PEXEL_1 | 278 | 282 | PF00026 | 0.474 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I1Y8 | Leptomonas seymouri | 46% | 99% |
| A0A3S7X5S5 | Leishmania donovani | 93% | 100% |
| A4HKL6 | Leishmania braziliensis | 64% | 100% |
| A4I848 | Leishmania infantum | 93% | 100% |
| E9B306 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |