| 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: E9B277
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 304 | 308 | PF00656 | 0.594 | 
| CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.666 | 
| CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.792 | 
| CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.706 | 
| CLV_PCSK_FUR_1 | 133 | 137 | PF00082 | 0.607 | 
| CLV_PCSK_FUR_1 | 177 | 181 | PF00082 | 0.657 | 
| CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.660 | 
| CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.793 | 
| CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.467 | 
| CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.487 | 
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.521 | 
| DEG_SPOP_SBC_1 | 25 | 29 | PF00917 | 0.456 | 
| DOC_CYCLIN_yCln2_LP_2 | 34 | 37 | PF00134 | 0.457 | 
| DOC_MAPK_MEF2A_6 | 40 | 47 | PF00069 | 0.483 | 
| DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.457 | 
| DOC_PP2B_LxvP_1 | 68 | 71 | PF13499 | 0.473 | 
| DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.591 | 
| DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.616 | 
| DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.646 | 
| DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.481 | 
| DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.615 | 
| DOC_USP7_UBL2_3 | 315 | 319 | PF12436 | 0.592 | 
| DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.670 | 
| DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.668 | 
| DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.500 | 
| LIG_14-3-3_CanoR_1 | 162 | 170 | PF00244 | 0.637 | 
| LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.722 | 
| LIG_14-3-3_CanoR_1 | 187 | 195 | PF00244 | 0.604 | 
| LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.542 | 
| LIG_Actin_WH2_2 | 34 | 50 | PF00022 | 0.477 | 
| LIG_APCC_ABBA_1 | 80 | 85 | PF00400 | 0.469 | 
| LIG_APCC_ABBAyCdc20_2 | 79 | 85 | PF00400 | 0.468 | 
| LIG_BIR_III_2 | 307 | 311 | PF00653 | 0.586 | 
| LIG_BRCT_BRCA1_1 | 238 | 242 | PF00533 | 0.535 | 
| LIG_BRCT_BRCA1_1 | 265 | 269 | PF00533 | 0.528 | 
| LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.459 | 
| LIG_Clathr_ClatBox_1 | 38 | 42 | PF01394 | 0.467 | 
| LIG_FHA_1 | 209 | 215 | PF00498 | 0.536 | 
| LIG_FHA_1 | 252 | 258 | PF00498 | 0.562 | 
| LIG_FHA_1 | 55 | 61 | PF00498 | 0.525 | 
| LIG_FHA_1 | 75 | 81 | PF00498 | 0.447 | 
| LIG_FHA_2 | 191 | 197 | PF00498 | 0.666 | 
| LIG_FHA_2 | 257 | 263 | PF00498 | 0.573 | 
| LIG_FHA_2 | 311 | 317 | PF00498 | 0.573 | 
| LIG_Integrin_isoDGR_2 | 94 | 96 | PF01839 | 0.494 | 
| LIG_LIR_Gen_1 | 28 | 39 | PF02991 | 0.459 | 
| LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.497 | 
| LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.519 | 
| LIG_LYPXL_yS_3 | 309 | 312 | PF13949 | 0.517 | 
| LIG_RPA_C_Fungi | 175 | 187 | PF08784 | 0.567 | 
| LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.485 | 
| LIG_SH3_3 | 123 | 129 | PF00018 | 0.650 | 
| LIG_SH3_3 | 167 | 173 | PF00018 | 0.647 | 
| LIG_SH3_3 | 20 | 26 | PF00018 | 0.455 | 
| LIG_SH3_3 | 228 | 234 | PF00018 | 0.642 | 
| LIG_SH3_3 | 250 | 256 | PF00018 | 0.676 | 
| LIG_SH3_3 | 3 | 9 | PF00018 | 0.502 | 
| LIG_SH3_3 | 43 | 49 | PF00018 | 0.494 | 
| LIG_SH3_3 | 61 | 67 | PF00018 | 0.476 | 
| LIG_SUMO_SIM_anti_2 | 42 | 47 | PF11976 | 0.489 | 
| LIG_SUMO_SIM_par_1 | 85 | 92 | PF11976 | 0.474 | 
| LIG_SUMO_SIM_par_1 | 96 | 102 | PF11976 | 0.474 | 
| LIG_TRAF2_1 | 243 | 246 | PF00917 | 0.668 | 
| LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.637 | 
| LIG_TYR_ITIM | 70 | 75 | PF00017 | 0.480 | 
| MOD_CAAXbox | 323 | 326 | PF01239 | 0.637 | 
| MOD_CDK_SPK_2 | 205 | 210 | PF00069 | 0.589 | 
| MOD_CK1_1 | 138 | 144 | PF00069 | 0.668 | 
| MOD_CK1_1 | 148 | 154 | PF00069 | 0.586 | 
| MOD_CK1_1 | 19 | 25 | PF00069 | 0.476 | 
| MOD_CK1_1 | 205 | 211 | PF00069 | 0.670 | 
| MOD_CK1_1 | 29 | 35 | PF00069 | 0.450 | 
| MOD_CK1_1 | 54 | 60 | PF00069 | 0.523 | 
| MOD_CK2_1 | 152 | 158 | PF00069 | 0.705 | 
| MOD_CK2_1 | 190 | 196 | PF00069 | 0.644 | 
| MOD_CK2_1 | 271 | 277 | PF00069 | 0.645 | 
| MOD_CK2_1 | 284 | 290 | PF00069 | 0.607 | 
| MOD_CK2_1 | 310 | 316 | PF00069 | 0.633 | 
| MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.630 | 
| MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.467 | 
| MOD_GlcNHglycan | 264 | 268 | PF01048 | 0.596 | 
| MOD_GSK3_1 | 101 | 108 | PF00069 | 0.629 | 
| MOD_GSK3_1 | 135 | 142 | PF00069 | 0.687 | 
| MOD_GSK3_1 | 148 | 155 | PF00069 | 0.680 | 
| MOD_GSK3_1 | 15 | 22 | PF00069 | 0.482 | 
| MOD_GSK3_1 | 186 | 193 | PF00069 | 0.688 | 
| MOD_GSK3_1 | 201 | 208 | PF00069 | 0.631 | 
| MOD_GSK3_1 | 25 | 32 | PF00069 | 0.449 | 
| MOD_GSK3_1 | 280 | 287 | PF00069 | 0.669 | 
| MOD_GSK3_1 | 71 | 78 | PF00069 | 0.519 | 
| MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.709 | 
| MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.582 | 
| MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.532 | 
| MOD_N-GLC_2 | 13 | 15 | PF02516 | 0.483 | 
| MOD_NEK2_1 | 21 | 26 | PF00069 | 0.471 | 
| MOD_NEK2_1 | 269 | 274 | PF00069 | 0.549 | 
| MOD_NEK2_1 | 280 | 285 | PF00069 | 0.658 | 
| MOD_NEK2_1 | 75 | 80 | PF00069 | 0.495 | 
| MOD_NEK2_2 | 71 | 76 | PF00069 | 0.622 | 
| MOD_OFUCOSY | 15 | 20 | PF10250 | 0.482 | 
| MOD_PIKK_1 | 101 | 107 | PF00454 | 0.539 | 
| MOD_PIKK_1 | 139 | 145 | PF00454 | 0.670 | 
| MOD_PIKK_1 | 89 | 95 | PF00454 | 0.508 | 
| MOD_PKA_1 | 135 | 141 | PF00069 | 0.611 | 
| MOD_PKA_1 | 178 | 184 | PF00069 | 0.665 | 
| MOD_PKA_2 | 135 | 141 | PF00069 | 0.666 | 
| MOD_PKA_2 | 161 | 167 | PF00069 | 0.558 | 
| MOD_PKA_2 | 178 | 184 | PF00069 | 0.781 | 
| MOD_PKA_2 | 186 | 192 | PF00069 | 0.690 | 
| MOD_PKB_1 | 133 | 141 | PF00069 | 0.653 | 
| MOD_PKB_1 | 178 | 186 | PF00069 | 0.668 | 
| MOD_Plk_1 | 109 | 115 | PF00069 | 0.517 | 
| MOD_Plk_1 | 41 | 47 | PF00069 | 0.484 | 
| MOD_Plk_1 | 84 | 90 | PF00069 | 0.480 | 
| MOD_Plk_4 | 284 | 290 | PF00069 | 0.673 | 
| MOD_Plk_4 | 71 | 77 | PF00069 | 0.477 | 
| MOD_Plk_4 | 84 | 90 | PF00069 | 0.457 | 
| MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.669 | 
| MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.669 | 
| MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.505 | 
| TRG_DiLeu_BaLyEn_6 | 210 | 215 | PF01217 | 0.538 | 
| TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.517 | 
| TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.614 | 
| TRG_ER_diArg_1 | 135 | 137 | PF00400 | 0.609 | 
| TRG_ER_diArg_1 | 176 | 179 | PF00400 | 0.790 | 
| TRG_Pf-PMV_PEXEL_1 | 180 | 185 | PF00026 | 0.671 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A3S7X508 | Leishmania donovani | 70% | 100% | 
| A4HJR6 | Leishmania braziliensis | 32% | 100% | 
| A4I783 | Leishmania infantum | 70% | 100% | 
| Q4Q5Y2 | Leishmania major | 63% | 100% |