| 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: 10 |
| NetGPI | no | yes: 0, no: 10 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 3 |
| GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4HZD9
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 237 | 241 | PF00656 | 0.570 |
| CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.444 |
| CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.646 |
| CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.589 |
| CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.530 |
| CLV_PCSK_FUR_1 | 252 | 256 | PF00082 | 0.635 |
| CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.441 |
| CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.596 |
| CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.478 |
| CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.530 |
| CLV_PCSK_PC7_1 | 224 | 230 | PF00082 | 0.529 |
| CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.661 |
| CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.529 |
| CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.482 |
| CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.453 |
| CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.552 |
| DEG_SPOP_SBC_1 | 89 | 93 | PF00917 | 0.590 |
| DOC_AGCK_PIF_1 | 42 | 47 | PF00069 | 0.504 |
| DOC_CYCLIN_RxL_1 | 15 | 24 | PF00134 | 0.496 |
| DOC_PP1_RVXF_1 | 65 | 71 | PF00149 | 0.519 |
| DOC_PP1_RVXF_1 | 80 | 87 | PF00149 | 0.544 |
| DOC_PP2B_LxvP_1 | 108 | 111 | PF13499 | 0.600 |
| DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.663 |
| DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.649 |
| DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.653 |
| LIG_14-3-3_CanoR_1 | 155 | 164 | PF00244 | 0.565 |
| LIG_14-3-3_CanoR_1 | 172 | 181 | PF00244 | 0.603 |
| LIG_14-3-3_CanoR_1 | 259 | 266 | PF00244 | 0.667 |
| LIG_14-3-3_CanoR_1 | 40 | 45 | PF00244 | 0.464 |
| LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.620 |
| LIG_APCC_ABBA_1 | 193 | 198 | PF00400 | 0.529 |
| LIG_APCC_ABBAyCdc20_2 | 192 | 198 | PF00400 | 0.529 |
| LIG_CaM_IQ_9 | 27 | 42 | PF13499 | 0.454 |
| LIG_Clathr_ClatBox_1 | 116 | 120 | PF01394 | 0.479 |
| LIG_Clathr_ClatBox_1 | 20 | 24 | PF01394 | 0.396 |
| LIG_CtBP_PxDLS_1 | 111 | 115 | PF00389 | 0.529 |
| LIG_deltaCOP1_diTrp_1 | 253 | 258 | PF00928 | 0.622 |
| LIG_FHA_1 | 200 | 206 | PF00498 | 0.422 |
| LIG_FHA_2 | 142 | 148 | PF00498 | 0.560 |
| LIG_LIR_Gen_1 | 184 | 195 | PF02991 | 0.443 |
| LIG_LIR_Gen_1 | 39 | 50 | PF02991 | 0.466 |
| LIG_LIR_Gen_1 | 7 | 17 | PF02991 | 0.590 |
| LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.538 |
| LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.446 |
| LIG_LIR_Nem_3 | 46 | 50 | PF02991 | 0.495 |
| LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.553 |
| LIG_Pex14_1 | 221 | 225 | PF04695 | 0.563 |
| LIG_Pex14_2 | 44 | 48 | PF04695 | 0.534 |
| LIG_PTB_Apo_2 | 216 | 223 | PF02174 | 0.491 |
| LIG_REV1ctd_RIR_1 | 83 | 89 | PF16727 | 0.612 |
| LIG_SH2_CRK | 210 | 214 | PF00017 | 0.482 |
| LIG_SH2_CRK | 9 | 13 | PF00017 | 0.523 |
| LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.521 |
| LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.522 |
| LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.379 |
| LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.410 |
| LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.533 |
| LIG_SUMO_SIM_anti_2 | 112 | 120 | PF11976 | 0.515 |
| LIG_SUMO_SIM_par_1 | 112 | 120 | PF11976 | 0.489 |
| LIG_WRC_WIRS_1 | 44 | 49 | PF05994 | 0.511 |
| MOD_CK1_1 | 128 | 134 | PF00069 | 0.561 |
| MOD_CK1_1 | 160 | 166 | PF00069 | 0.622 |
| MOD_CK1_1 | 167 | 173 | PF00069 | 0.610 |
| MOD_CK1_1 | 262 | 268 | PF00069 | 0.595 |
| MOD_CK1_1 | 43 | 49 | PF00069 | 0.487 |
| MOD_CK1_1 | 72 | 78 | PF00069 | 0.465 |
| MOD_CK1_1 | 92 | 98 | PF00069 | 0.404 |
| MOD_CK2_1 | 141 | 147 | PF00069 | 0.664 |
| MOD_CK2_1 | 172 | 178 | PF00069 | 0.460 |
| MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.667 |
| MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.460 |
| MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.674 |
| MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.680 |
| MOD_GSK3_1 | 121 | 128 | PF00069 | 0.505 |
| MOD_GSK3_1 | 156 | 163 | PF00069 | 0.636 |
| MOD_GSK3_1 | 164 | 171 | PF00069 | 0.533 |
| MOD_GSK3_1 | 172 | 179 | PF00069 | 0.649 |
| MOD_GSK3_1 | 181 | 188 | PF00069 | 0.553 |
| MOD_GSK3_1 | 229 | 236 | PF00069 | 0.494 |
| MOD_GSK3_1 | 88 | 95 | PF00069 | 0.667 |
| MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.577 |
| MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.449 |
| MOD_NEK2_1 | 146 | 151 | PF00069 | 0.576 |
| MOD_NEK2_1 | 181 | 186 | PF00069 | 0.522 |
| MOD_NEK2_1 | 201 | 206 | PF00069 | 0.250 |
| MOD_NEK2_1 | 4 | 9 | PF00069 | 0.566 |
| MOD_PIKK_1 | 121 | 127 | PF00454 | 0.592 |
| MOD_PKA_1 | 229 | 235 | PF00069 | 0.482 |
| MOD_PKA_2 | 229 | 235 | PF00069 | 0.482 |
| MOD_PKA_2 | 4 | 10 | PF00069 | 0.580 |
| MOD_PKA_2 | 95 | 101 | PF00069 | 0.613 |
| MOD_Plk_1 | 141 | 147 | PF00069 | 0.606 |
| MOD_Plk_1 | 185 | 191 | PF00069 | 0.522 |
| MOD_Plk_1 | 40 | 46 | PF00069 | 0.452 |
| MOD_Plk_2-3 | 141 | 147 | PF00069 | 0.627 |
| MOD_Plk_4 | 125 | 131 | PF00069 | 0.499 |
| MOD_Plk_4 | 229 | 235 | PF00069 | 0.399 |
| TRG_DiLeu_BaEn_1 | 112 | 117 | PF01217 | 0.565 |
| TRG_DiLeu_BaEn_2 | 177 | 183 | PF01217 | 0.547 |
| TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.454 |
| TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.470 |
| TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.522 |
| TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.414 |
| TRG_ER_diArg_1 | 254 | 256 | PF00400 | 0.605 |
| TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.525 |
| TRG_ER_diArg_1 | 65 | 68 | PF00400 | 0.612 |
| TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.442 |
| TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.606 |
| TRG_Pf-PMV_PEXEL_1 | 82 | 87 | PF00026 | 0.584 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P3V9 | Leptomonas seymouri | 60% | 98% |
| A0A0S4IH77 | Bodo saltans | 30% | 100% |
| A0A1X0NHE8 | Trypanosomatidae | 42% | 100% |
| A0A3S7WWT7 | Leishmania donovani | 100% | 100% |
| A4HBY9 | Leishmania braziliensis | 80% | 100% |
| D0A146 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
| E9AVC6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
| Q4QC53 | Leishmania major | 93% | 100% |
| V5B1U8 | Trypanosoma cruzi | 39% | 100% |