| 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: 5 |
| NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HM33
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 122 | 126 | PF00656 | 0.700 |
| CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.811 |
| CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.744 |
| CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.608 |
| CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.640 |
| CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.596 |
| CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.492 |
| CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.436 |
| CLV_PCSK_PC7_1 | 29 | 35 | PF00082 | 0.390 |
| CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.486 |
| CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.541 |
| CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.566 |
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.484 |
| DEG_SCF_FBW7_1 | 311 | 316 | PF00400 | 0.545 |
| DEG_SPOP_SBC_1 | 158 | 162 | PF00917 | 0.828 |
| DEG_SPOP_SBC_1 | 182 | 186 | PF00917 | 0.601 |
| DOC_CKS1_1 | 177 | 182 | PF01111 | 0.608 |
| DOC_MAPK_gen_1 | 167 | 177 | PF00069 | 0.543 |
| DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.831 |
| DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.578 |
| DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.532 |
| DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.817 |
| DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.755 |
| DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.787 |
| DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.475 |
| DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.427 |
| DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.453 |
| DOC_USP7_MATH_2 | 271 | 277 | PF00917 | 0.477 |
| DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.609 |
| DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.800 |
| DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.652 |
| LIG_14-3-3_CanoR_1 | 167 | 177 | PF00244 | 0.757 |
| LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.669 |
| LIG_14-3-3_CanoR_1 | 291 | 295 | PF00244 | 0.630 |
| LIG_14-3-3_CanoR_1 | 94 | 104 | PF00244 | 0.456 |
| LIG_FHA_1 | 112 | 118 | PF00498 | 0.724 |
| LIG_FHA_1 | 169 | 175 | PF00498 | 0.631 |
| LIG_FHA_1 | 177 | 183 | PF00498 | 0.593 |
| LIG_FHA_1 | 184 | 190 | PF00498 | 0.566 |
| LIG_FHA_1 | 223 | 229 | PF00498 | 0.619 |
| LIG_FHA_1 | 291 | 297 | PF00498 | 0.516 |
| LIG_FHA_1 | 314 | 320 | PF00498 | 0.719 |
| LIG_FHA_2 | 241 | 247 | PF00498 | 0.586 |
| LIG_PDZ_Class_2 | 324 | 329 | PF00595 | 0.759 |
| LIG_PTAP_UEV_1 | 303 | 308 | PF05743 | 0.562 |
| LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.436 |
| LIG_SH3_3 | 254 | 260 | PF00018 | 0.679 |
| LIG_SH3_3 | 298 | 304 | PF00018 | 0.546 |
| LIG_SH3_3 | 308 | 314 | PF00018 | 0.526 |
| LIG_SUMO_SIM_anti_2 | 171 | 179 | PF11976 | 0.544 |
| LIG_SUMO_SIM_par_1 | 171 | 179 | PF11976 | 0.544 |
| LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.402 |
| LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.663 |
| LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.694 |
| LIG_TRAF2_1 | 54 | 57 | PF00917 | 0.425 |
| LIG_UBA3_1 | 131 | 140 | PF00899 | 0.440 |
| LIG_WW_3 | 312 | 316 | PF00397 | 0.543 |
| MOD_CDK_SPxK_1 | 309 | 315 | PF00069 | 0.553 |
| MOD_CK1_1 | 162 | 168 | PF00069 | 0.815 |
| MOD_CK1_1 | 265 | 271 | PF00069 | 0.532 |
| MOD_CK1_1 | 309 | 315 | PF00069 | 0.553 |
| MOD_CK1_1 | 72 | 78 | PF00069 | 0.426 |
| MOD_CK2_1 | 182 | 188 | PF00069 | 0.715 |
| MOD_CK2_1 | 201 | 207 | PF00069 | 0.507 |
| MOD_CK2_1 | 240 | 246 | PF00069 | 0.584 |
| MOD_CK2_1 | 273 | 279 | PF00069 | 0.730 |
| MOD_CK2_1 | 95 | 101 | PF00069 | 0.446 |
| MOD_Cter_Amidation | 165 | 168 | PF01082 | 0.539 |
| MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.650 |
| MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.745 |
| MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.655 |
| MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.690 |
| MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.820 |
| MOD_GlcNHglycan | 63 | 67 | PF01048 | 0.426 |
| MOD_GSK3_1 | 153 | 160 | PF00069 | 0.769 |
| MOD_GSK3_1 | 222 | 229 | PF00069 | 0.786 |
| MOD_GSK3_1 | 302 | 309 | PF00069 | 0.672 |
| MOD_GSK3_1 | 92 | 99 | PF00069 | 0.518 |
| MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.619 |
| MOD_NEK2_1 | 23 | 28 | PF00069 | 0.666 |
| MOD_NEK2_1 | 90 | 95 | PF00069 | 0.436 |
| MOD_PKA_2 | 162 | 168 | PF00069 | 0.815 |
| MOD_PKA_2 | 2 | 8 | PF00069 | 0.471 |
| MOD_PKA_2 | 290 | 296 | PF00069 | 0.730 |
| MOD_Plk_1 | 201 | 207 | PF00069 | 0.566 |
| MOD_Plk_1 | 72 | 78 | PF00069 | 0.591 |
| MOD_Plk_2-3 | 139 | 145 | PF00069 | 0.502 |
| MOD_Plk_2-3 | 69 | 75 | PF00069 | 0.430 |
| MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.609 |
| MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.801 |
| MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.649 |
| MOD_SUMO_for_1 | 46 | 49 | PF00179 | 0.616 |
| MOD_SUMO_for_1 | 54 | 57 | PF00179 | 0.503 |
| MOD_SUMO_for_1 | 60 | 63 | PF00179 | 0.525 |
| MOD_SUMO_rev_2 | 265 | 274 | PF00179 | 0.520 |
| TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.519 |
| TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.433 |
| TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.652 |
| TRG_NLS_MonoExtC_3 | 33 | 39 | PF00514 | 0.384 |
| TRG_NLS_MonoExtN_4 | 164 | 171 | PF00514 | 0.541 |
| TRG_NLS_MonoExtN_4 | 33 | 38 | PF00514 | 0.497 |
| TRG_Pf-PMV_PEXEL_1 | 88 | 92 | PF00026 | 0.578 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A3Q8IUB2 | Leishmania donovani | 53% | 72% |
| A4I9G6 | Leishmania infantum | 53% | 72% |
| E9B4G4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 85% |
| Q4Q3L1 | Leishmania major | 54% | 100% |