| 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: A0A3S7X392
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 4 |
| GO:0016740 | transferase activity | 2 | 4 |
| GO:0016407 | acetyltransferase activity | 5 | 2 |
| GO:0016746 | acyltransferase activity | 3 | 2 |
| GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 251 | 255 | PF00656 | 0.625 |
| CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.700 |
| CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.503 |
| CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.556 |
| CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.649 |
| CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.690 |
| CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.489 |
| CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.522 |
| CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.700 |
| CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.505 |
| CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.556 |
| CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.579 |
| CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.627 |
| CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.690 |
| CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.489 |
| CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.522 |
| CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.647 |
| CLV_PCSK_PC7_1 | 272 | 278 | PF00082 | 0.780 |
| CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.690 |
| CLV_TASPASE1 | 65 | 71 | PF01112 | 0.647 |
| DEG_APCC_DBOX_1 | 261 | 269 | PF00400 | 0.581 |
| DEG_APCC_DBOX_1 | 81 | 89 | PF00400 | 0.496 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.642 |
| DOC_ANK_TNKS_1 | 207 | 214 | PF00023 | 0.516 |
| DOC_ANK_TNKS_1 | 304 | 311 | PF00023 | 0.547 |
| DOC_CYCLIN_RxL_1 | 320 | 329 | PF00134 | 0.483 |
| DOC_CYCLIN_yCln2_LP_2 | 53 | 59 | PF00134 | 0.677 |
| DOC_MAPK_gen_1 | 79 | 88 | PF00069 | 0.479 |
| DOC_PP1_RVXF_1 | 321 | 328 | PF00149 | 0.479 |
| DOC_PP2B_LxvP_1 | 53 | 56 | PF13499 | 0.654 |
| DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.543 |
| DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.662 |
| DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.654 |
| DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.681 |
| DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.823 |
| DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.551 |
| DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.393 |
| DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.664 |
| DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.648 |
| DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.587 |
| DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.494 |
| LIG_14-3-3_CanoR_1 | 170 | 176 | PF00244 | 0.717 |
| LIG_14-3-3_CanoR_1 | 227 | 233 | PF00244 | 0.470 |
| LIG_14-3-3_CanoR_1 | 96 | 104 | PF00244 | 0.622 |
| LIG_deltaCOP1_diTrp_1 | 102 | 108 | PF00928 | 0.581 |
| LIG_deltaCOP1_diTrp_1 | 69 | 74 | PF00928 | 0.564 |
| LIG_FHA_1 | 176 | 182 | PF00498 | 0.670 |
| LIG_FHA_1 | 233 | 239 | PF00498 | 0.572 |
| LIG_FHA_1 | 9 | 15 | PF00498 | 0.572 |
| LIG_Integrin_RGD_1 | 279 | 281 | PF01839 | 0.583 |
| LIG_LIR_Gen_1 | 177 | 187 | PF02991 | 0.615 |
| LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.484 |
| LIG_LIR_Gen_1 | 58 | 66 | PF02991 | 0.610 |
| LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.609 |
| LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.481 |
| LIG_LIR_Nem_3 | 58 | 62 | PF02991 | 0.510 |
| LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.549 |
| LIG_Rb_LxCxE_1 | 235 | 254 | PF01857 | 0.584 |
| LIG_RPA_C_Fungi | 248 | 260 | PF08784 | 0.465 |
| LIG_SH2_CRK | 179 | 183 | PF00017 | 0.621 |
| LIG_SH2_CRK | 322 | 326 | PF00017 | 0.483 |
| LIG_SH2_NCK_1 | 179 | 183 | PF00017 | 0.621 |
| LIG_SH2_PTP2 | 214 | 217 | PF00017 | 0.592 |
| LIG_SH2_SRC | 59 | 62 | PF00017 | 0.609 |
| LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.521 |
| LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.490 |
| LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.619 |
| LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.609 |
| LIG_SH3_3 | 103 | 109 | PF00018 | 0.719 |
| LIG_SH3_3 | 216 | 222 | PF00018 | 0.516 |
| LIG_SUMO_SIM_anti_2 | 342 | 348 | PF11976 | 0.458 |
| LIG_SUMO_SIM_anti_2 | 58 | 64 | PF11976 | 0.613 |
| LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.708 |
| LIG_TYR_ITIM | 57 | 62 | PF00017 | 0.509 |
| MOD_CDK_SPK_2 | 133 | 138 | PF00069 | 0.634 |
| MOD_CK1_1 | 121 | 127 | PF00069 | 0.729 |
| MOD_CK1_1 | 148 | 154 | PF00069 | 0.672 |
| MOD_CK1_1 | 172 | 178 | PF00069 | 0.746 |
| MOD_CK1_1 | 193 | 199 | PF00069 | 0.757 |
| MOD_CK1_1 | 42 | 48 | PF00069 | 0.807 |
| MOD_CK2_1 | 126 | 132 | PF00069 | 0.716 |
| MOD_CK2_1 | 303 | 309 | PF00069 | 0.684 |
| MOD_GlcNHglycan | 122 | 126 | PF01048 | 0.702 |
| MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.664 |
| MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.655 |
| MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.609 |
| MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.469 |
| MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.799 |
| MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.815 |
| MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.606 |
| MOD_GSK3_1 | 100 | 107 | PF00069 | 0.696 |
| MOD_GSK3_1 | 109 | 116 | PF00069 | 0.609 |
| MOD_GSK3_1 | 198 | 205 | PF00069 | 0.649 |
| MOD_GSK3_1 | 228 | 235 | PF00069 | 0.494 |
| MOD_GSK3_1 | 264 | 271 | PF00069 | 0.508 |
| MOD_GSK3_1 | 39 | 46 | PF00069 | 0.817 |
| MOD_GSK3_1 | 6 | 13 | PF00069 | 0.612 |
| MOD_NEK2_1 | 268 | 273 | PF00069 | 0.595 |
| MOD_NEK2_2 | 16 | 21 | PF00069 | 0.576 |
| MOD_OFUCOSY | 147 | 152 | PF10250 | 0.685 |
| MOD_PIKK_1 | 232 | 238 | PF00454 | 0.479 |
| MOD_PKA_2 | 169 | 175 | PF00069 | 0.638 |
| MOD_PKA_2 | 207 | 213 | PF00069 | 0.593 |
| MOD_PKA_2 | 303 | 309 | PF00069 | 0.635 |
| MOD_PKA_2 | 39 | 45 | PF00069 | 0.606 |
| MOD_PKA_2 | 78 | 84 | PF00069 | 0.547 |
| MOD_PKA_2 | 95 | 101 | PF00069 | 0.425 |
| MOD_Plk_1 | 281 | 287 | PF00069 | 0.697 |
| MOD_Plk_1 | 70 | 76 | PF00069 | 0.560 |
| MOD_Plk_4 | 177 | 183 | PF00069 | 0.788 |
| MOD_Plk_4 | 228 | 234 | PF00069 | 0.408 |
| MOD_Plk_4 | 55 | 61 | PF00069 | 0.645 |
| MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.661 |
| MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.653 |
| MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.588 |
| MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.492 |
| TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.616 |
| TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.490 |
| TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.438 |
| TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.507 |
| TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.487 |
| TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.483 |
| TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.525 |
| TRG_NES_CRM1_1 | 52 | 65 | PF08389 | 0.581 |
| TRG_NLS_MonoExtC_3 | 275 | 281 | PF00514 | 0.613 |
| TRG_NLS_MonoExtN_4 | 273 | 280 | PF00514 | 0.573 |
| TRG_Pf-PMV_PEXEL_1 | 138 | 142 | PF00026 | 0.665 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P8W0 | Leptomonas seymouri | 45% | 100% |
| A4HI78 | Leishmania braziliensis | 69% | 100% |
| A4I5F7 | Leishmania infantum | 99% | 100% |
| E9B0Q5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
| Q4Q7H8 | Leishmania major | 90% | 100% |