| 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: 14 | 
| NetGPI | no | yes: 0, no: 14 | 
Related structures:
AlphaFold database: E9B243
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 227 | 231 | PF00656 | 0.480 | 
| CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.591 | 
| CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.406 | 
| CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.518 | 
| CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.779 | 
| CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.532 | 
| CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.779 | 
| CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.637 | 
| CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.506 | 
| CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.569 | 
| CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.430 | 
| CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.451 | 
| DEG_APCC_DBOX_1 | 140 | 148 | PF00400 | 0.514 | 
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.546 | 
| DOC_CYCLIN_RxL_1 | 137 | 146 | PF00134 | 0.462 | 
| DOC_MAPK_gen_1 | 90 | 97 | PF00069 | 0.488 | 
| DOC_MAPK_MEF2A_6 | 90 | 97 | PF00069 | 0.509 | 
| DOC_MAPK_NFAT4_5 | 90 | 98 | PF00069 | 0.511 | 
| DOC_PP1_RVXF_1 | 198 | 205 | PF00149 | 0.299 | 
| DOC_PP2B_PxIxI_1 | 20 | 26 | PF00149 | 0.406 | 
| DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.654 | 
| DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.436 | 
| DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.550 | 
| DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.369 | 
| DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.378 | 
| LIG_14-3-3_CanoR_1 | 33 | 43 | PF00244 | 0.390 | 
| LIG_deltaCOP1_diTrp_1 | 216 | 225 | PF00928 | 0.350 | 
| LIG_FHA_1 | 169 | 175 | PF00498 | 0.465 | 
| LIG_FHA_1 | 36 | 42 | PF00498 | 0.415 | 
| LIG_FHA_1 | 47 | 53 | PF00498 | 0.428 | 
| LIG_FHA_2 | 175 | 181 | PF00498 | 0.432 | 
| LIG_FHA_2 | 225 | 231 | PF00498 | 0.505 | 
| LIG_FHA_2 | 96 | 102 | PF00498 | 0.427 | 
| LIG_LIR_Gen_1 | 83 | 94 | PF02991 | 0.504 | 
| LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.433 | 
| LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.510 | 
| LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.507 | 
| LIG_MYND_1 | 153 | 157 | PF01753 | 0.560 | 
| LIG_PDZ_Class_3 | 229 | 234 | PF00595 | 0.721 | 
| LIG_Pex14_1 | 172 | 176 | PF04695 | 0.373 | 
| LIG_SH2_CRK | 63 | 67 | PF00017 | 0.480 | 
| LIG_SH2_CRK | 86 | 90 | PF00017 | 0.355 | 
| LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.442 | 
| LIG_SUMO_SIM_anti_2 | 183 | 188 | PF11976 | 0.478 | 
| LIG_SUMO_SIM_par_1 | 37 | 44 | PF11976 | 0.436 | 
| LIG_SUMO_SIM_par_1 | 48 | 53 | PF11976 | 0.452 | 
| LIG_TYR_ITIM | 61 | 66 | PF00017 | 0.564 | 
| LIG_UBA3_1 | 187 | 193 | PF00899 | 0.503 | 
| LIG_WRC_WIRS_1 | 111 | 116 | PF05994 | 0.402 | 
| MOD_CK1_1 | 121 | 127 | PF00069 | 0.565 | 
| MOD_CK1_1 | 178 | 184 | PF00069 | 0.459 | 
| MOD_CK2_1 | 174 | 180 | PF00069 | 0.438 | 
| MOD_CK2_1 | 226 | 232 | PF00069 | 0.693 | 
| MOD_CK2_1 | 95 | 101 | PF00069 | 0.552 | 
| MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.611 | 
| MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.706 | 
| MOD_GSK3_1 | 102 | 109 | PF00069 | 0.542 | 
| MOD_GSK3_1 | 110 | 117 | PF00069 | 0.465 | 
| MOD_GSK3_1 | 121 | 128 | PF00069 | 0.510 | 
| MOD_GSK3_1 | 132 | 139 | PF00069 | 0.643 | 
| MOD_GSK3_1 | 153 | 160 | PF00069 | 0.589 | 
| MOD_GSK3_1 | 162 | 169 | PF00069 | 0.578 | 
| MOD_GSK3_1 | 174 | 181 | PF00069 | 0.431 | 
| MOD_GSK3_1 | 226 | 233 | PF00069 | 0.559 | 
| MOD_GSK3_1 | 35 | 42 | PF00069 | 0.415 | 
| MOD_GSK3_1 | 46 | 53 | PF00069 | 0.468 | 
| MOD_LATS_1 | 224 | 230 | PF00433 | 0.374 | 
| MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.450 | 
| MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.755 | 
| MOD_NEK2_1 | 114 | 119 | PF00069 | 0.348 | 
| MOD_NEK2_1 | 15 | 20 | PF00069 | 0.441 | 
| MOD_NEK2_1 | 62 | 67 | PF00069 | 0.451 | 
| MOD_NEK2_1 | 95 | 100 | PF00069 | 0.507 | 
| MOD_PKA_2 | 34 | 40 | PF00069 | 0.518 | 
| MOD_PKB_1 | 33 | 41 | PF00069 | 0.417 | 
| MOD_Plk_1 | 100 | 106 | PF00069 | 0.445 | 
| MOD_Plk_1 | 129 | 135 | PF00069 | 0.637 | 
| MOD_Plk_4 | 110 | 116 | PF00069 | 0.610 | 
| MOD_Plk_4 | 118 | 124 | PF00069 | 0.554 | 
| MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.429 | 
| MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.552 | 
| MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.352 | 
| MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.376 | 
| MOD_SUMO_for_1 | 192 | 195 | PF00179 | 0.399 | 
| TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.460 | 
| TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.432 | 
| TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.552 | 
| TRG_NLS_MonoExtC_3 | 53 | 58 | PF00514 | 0.440 | 
| TRG_Pf-PMV_PEXEL_1 | 39 | 44 | PF00026 | 0.466 | 
| TRG_Pf-PMV_PEXEL_1 | 64 | 69 | PF00026 | 0.582 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1I730 | Leptomonas seymouri | 23% | 100% | 
| A0A0N1I8Q6 | Leptomonas seymouri | 41% | 100% | 
| A0A0N1ILD5 | Leptomonas seymouri | 28% | 83% | 
| A0A0N1PCW5 | Leptomonas seymouri | 33% | 100% | 
| A0A3Q8IF19 | Leishmania donovani | 40% | 100% | 
| A0A3S5H7Q5 | Leishmania donovani | 81% | 99% | 
| A4HJM7 | Leishmania braziliensis | 50% | 100% | 
| A4HJM8 | Leishmania braziliensis | 38% | 100% | 
| A4I749 | Leishmania infantum | 82% | 100% | 
| A4I750 | Leishmania infantum | 40% | 100% | 
| E9B244 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% | 
| Q4Q617 | Leishmania major | 39% | 100% | 
| Q4Q618 | Leishmania major | 76% | 100% |