| 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: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005739 | mitochondrion | 5 | 1 |
| GO:0032991 | protein-containing complex | 1 | 1 |
| GO:0034702 | monoatomic ion channel complex | 4 | 1 |
| GO:0034703 | cation channel complex | 5 | 1 |
| GO:0034704 | calcium channel complex | 6 | 1 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
| GO:0098796 | membrane protein complex | 2 | 1 |
| GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
| GO:0098800 | inner mitochondrial membrane protein complex | 3 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 4 |
| GO:1902495 | transmembrane transporter complex | 3 | 1 |
| GO:1990246 | uniplex complex | 4 | 1 |
| GO:1990351 | transporter complex | 2 | 1 |
| GO:0016020 | membrane | 2 | 3 |
Related structures:
AlphaFold database: A4H4V4
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 12 |
| GO:0006811 | monoatomic ion transport | 4 | 12 |
| GO:0006812 | monoatomic cation transport | 5 | 12 |
| GO:0006816 | calcium ion transport | 7 | 12 |
| GO:0006851 | mitochondrial calcium ion transmembrane transport | 4 | 12 |
| GO:0009987 | cellular process | 1 | 12 |
| GO:0030001 | metal ion transport | 6 | 12 |
| GO:0034220 | monoatomic ion transmembrane transport | 3 | 12 |
| GO:0051179 | localization | 1 | 12 |
| GO:0051234 | establishment of localization | 2 | 12 |
| GO:0055085 | transmembrane transport | 2 | 12 |
| GO:0070588 | calcium ion transmembrane transport | 6 | 12 |
| GO:0098655 | monoatomic cation transmembrane transport | 4 | 12 |
| GO:0098660 | inorganic ion transmembrane transport | 4 | 12 |
| GO:0098662 | inorganic cation transmembrane transport | 5 | 12 |
| GO:1990542 | mitochondrial transmembrane transport | 3 | 12 |
| GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
| GO:0006874 | intracellular calcium ion homeostasis | 7 | 1 |
| GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 1 |
| GO:0019725 | cellular homeostasis | 2 | 1 |
| GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
| GO:0036444 | calcium import into the mitochondrion | 5 | 1 |
| GO:0042592 | homeostatic process | 3 | 1 |
| GO:0048878 | chemical homeostasis | 4 | 1 |
| GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
| GO:0051560 | mitochondrial calcium ion homeostasis | 8 | 1 |
| GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
| GO:0055074 | calcium ion homeostasis | 8 | 1 |
| GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
| GO:0055082 | intracellular chemical homeostasis | 3 | 1 |
| GO:0065007 | biological regulation | 1 | 1 |
| GO:0065008 | regulation of biological quality | 2 | 1 |
| GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 1 |
| GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 1 |
| GO:0098771 | inorganic ion homeostasis | 6 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005488 | binding | 1 | 12 |
| GO:0005509 | calcium ion binding | 5 | 12 |
| GO:0043167 | ion binding | 2 | 12 |
| GO:0043169 | cation binding | 3 | 12 |
| GO:0046872 | metal ion binding | 4 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.305 |
| CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.429 |
| CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.320 |
| CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.595 |
| CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.567 |
| CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.359 |
| CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.413 |
| CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.285 |
| CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.567 |
| CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.435 |
| CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.339 |
| CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.420 |
| CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.486 |
| CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.431 |
| CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.291 |
| CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.465 |
| CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.579 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.401 |
| DOC_CKS1_1 | 25 | 30 | PF01111 | 0.387 |
| DOC_CYCLIN_RxL_1 | 148 | 161 | PF00134 | 0.455 |
| DOC_CYCLIN_RxL_1 | 162 | 174 | PF00134 | 0.302 |
| DOC_CYCLIN_yCln2_LP_2 | 76 | 82 | PF00134 | 0.255 |
| DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.409 |
| DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.458 |
| LIG_14-3-3_CanoR_1 | 106 | 112 | PF00244 | 0.391 |
| LIG_14-3-3_CanoR_1 | 178 | 183 | PF00244 | 0.329 |
| LIG_14-3-3_CanoR_1 | 287 | 292 | PF00244 | 0.389 |
| LIG_14-3-3_CanoR_1 | 331 | 337 | PF00244 | 0.473 |
| LIG_14-3-3_CanoR_1 | 339 | 345 | PF00244 | 0.574 |
| LIG_BIR_III_4 | 93 | 97 | PF00653 | 0.261 |
| LIG_deltaCOP1_diTrp_1 | 195 | 201 | PF00928 | 0.293 |
| LIG_DLG_GKlike_1 | 178 | 185 | PF00625 | 0.469 |
| LIG_FHA_1 | 131 | 137 | PF00498 | 0.404 |
| LIG_FHA_1 | 15 | 21 | PF00498 | 0.560 |
| LIG_FHA_1 | 299 | 305 | PF00498 | 0.391 |
| LIG_FHA_2 | 145 | 151 | PF00498 | 0.472 |
| LIG_FHA_2 | 211 | 217 | PF00498 | 0.456 |
| LIG_FHA_2 | 279 | 285 | PF00498 | 0.423 |
| LIG_FHA_2 | 298 | 304 | PF00498 | 0.133 |
| LIG_FHA_2 | 58 | 64 | PF00498 | 0.289 |
| LIG_LIR_Apic_2 | 24 | 28 | PF02991 | 0.423 |
| LIG_LIR_Gen_1 | 137 | 146 | PF02991 | 0.361 |
| LIG_LIR_Gen_1 | 215 | 225 | PF02991 | 0.420 |
| LIG_LIR_Gen_1 | 284 | 291 | PF02991 | 0.279 |
| LIG_LIR_Gen_1 | 303 | 310 | PF02991 | 0.351 |
| LIG_LIR_Gen_1 | 320 | 330 | PF02991 | 0.275 |
| LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.259 |
| LIG_LIR_Nem_3 | 104 | 108 | PF02991 | 0.230 |
| LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.353 |
| LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.154 |
| LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.286 |
| LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.312 |
| LIG_LIR_Nem_3 | 284 | 288 | PF02991 | 0.339 |
| LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.328 |
| LIG_LIR_Nem_3 | 320 | 325 | PF02991 | 0.257 |
| LIG_LIR_Nem_3 | 41 | 46 | PF02991 | 0.300 |
| LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.259 |
| LIG_MYND_1 | 29 | 33 | PF01753 | 0.258 |
| LIG_MYND_2 | 28 | 32 | PF01753 | 0.259 |
| LIG_NRBOX | 107 | 113 | PF00104 | 0.245 |
| LIG_PCNA_yPIPBox_3 | 158 | 171 | PF02747 | 0.421 |
| LIG_Pex14_1 | 197 | 201 | PF04695 | 0.291 |
| LIG_Rb_pABgroove_1 | 303 | 311 | PF01858 | 0.170 |
| LIG_SH2_CRK | 25 | 29 | PF00017 | 0.322 |
| LIG_SH2_CRK | 334 | 338 | PF00017 | 0.600 |
| LIG_SH2_CRK | 46 | 50 | PF00017 | 0.364 |
| LIG_SH2_NCK_1 | 25 | 29 | PF00017 | 0.464 |
| LIG_SH2_NCK_1 | 334 | 338 | PF00017 | 0.600 |
| LIG_SH2_SRC | 30 | 33 | PF00017 | 0.354 |
| LIG_SH2_STAP1 | 262 | 266 | PF00017 | 0.452 |
| LIG_SH2_STAT3 | 262 | 265 | PF00017 | 0.364 |
| LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.377 |
| LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.307 |
| LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.319 |
| LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.320 |
| LIG_SUMO_SIM_anti_2 | 300 | 306 | PF11976 | 0.236 |
| LIG_SUMO_SIM_par_1 | 131 | 138 | PF11976 | 0.391 |
| LIG_TRAF2_1 | 135 | 138 | PF00917 | 0.310 |
| LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.462 |
| LIG_TYR_ITIM | 230 | 235 | PF00017 | 0.472 |
| LIG_TYR_ITIM | 44 | 49 | PF00017 | 0.371 |
| LIG_UBA3_1 | 122 | 130 | PF00899 | 0.277 |
| LIG_UBA3_1 | 304 | 311 | PF00899 | 0.168 |
| LIG_UBA3_1 | 323 | 329 | PF00899 | 0.329 |
| LIG_WW_3 | 336 | 340 | PF00397 | 0.550 |
| MOD_CDC14_SPxK_1 | 71 | 74 | PF00782 | 0.492 |
| MOD_CDK_SPxK_1 | 68 | 74 | PF00069 | 0.464 |
| MOD_CK1_1 | 110 | 116 | PF00069 | 0.474 |
| MOD_CK1_1 | 191 | 197 | PF00069 | 0.489 |
| MOD_CK1_1 | 24 | 30 | PF00069 | 0.579 |
| MOD_CK1_1 | 276 | 282 | PF00069 | 0.341 |
| MOD_CK2_1 | 132 | 138 | PF00069 | 0.334 |
| MOD_CK2_1 | 144 | 150 | PF00069 | 0.388 |
| MOD_CK2_1 | 178 | 184 | PF00069 | 0.374 |
| MOD_CK2_1 | 210 | 216 | PF00069 | 0.467 |
| MOD_CK2_1 | 287 | 293 | PF00069 | 0.319 |
| MOD_CK2_1 | 98 | 104 | PF00069 | 0.261 |
| MOD_GlcNHglycan | 129 | 133 | PF01048 | 0.402 |
| MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.399 |
| MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.377 |
| MOD_GlcNHglycan | 293 | 297 | PF01048 | 0.361 |
| MOD_GSK3_1 | 107 | 114 | PF00069 | 0.378 |
| MOD_GSK3_1 | 128 | 135 | PF00069 | 0.356 |
| MOD_GSK3_1 | 272 | 279 | PF00069 | 0.501 |
| MOD_N-GLC_1 | 298 | 303 | PF02516 | 0.168 |
| MOD_NEK2_1 | 107 | 112 | PF00069 | 0.327 |
| MOD_NEK2_1 | 272 | 277 | PF00069 | 0.410 |
| MOD_NEK2_1 | 278 | 283 | PF00069 | 0.261 |
| MOD_NEK2_1 | 340 | 345 | PF00069 | 0.488 |
| MOD_PKA_1 | 178 | 184 | PF00069 | 0.422 |
| MOD_PKA_2 | 340 | 346 | PF00069 | 0.586 |
| MOD_Plk_1 | 292 | 298 | PF00069 | 0.319 |
| MOD_Plk_4 | 107 | 113 | PF00069 | 0.332 |
| MOD_Plk_4 | 118 | 124 | PF00069 | 0.459 |
| MOD_Plk_4 | 15 | 21 | PF00069 | 0.503 |
| MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.396 |
| MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.464 |
| TRG_DiLeu_BaEn_1 | 104 | 109 | PF01217 | 0.245 |
| TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.388 |
| TRG_DiLeu_BaEn_2 | 317 | 323 | PF01217 | 0.250 |
| TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.496 |
| TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.326 |
| TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.245 |
| TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.275 |
| TRG_ER_diArg_1 | 338 | 341 | PF00400 | 0.571 |
| TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.560 |
| TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.430 |
| TRG_ER_diArg_1 | 49 | 52 | PF00400 | 0.380 |
| TRG_NLS_MonoCore_2 | 49 | 54 | PF00514 | 0.494 |
| TRG_NLS_MonoExtN_4 | 50 | 55 | PF00514 | 0.492 |
| TRG_Pf-PMV_PEXEL_1 | 168 | 173 | PF00026 | 0.362 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P773 | Leptomonas seymouri | 73% | 83% |
| A0A0S4IPF8 | Bodo saltans | 44% | 91% |
| A0A1X0NK53 | Trypanosomatidae | 50% | 90% |
| A0A3S5H5W0 | Leishmania donovani | 87% | 100% |
| A0A422NT64 | Trypanosoma rangeli | 47% | 90% |
| A2VEI2 | Drosophila melanogaster | 22% | 69% |
| A4HT58 | Leishmania infantum | 87% | 100% |
| A4IG32 | Danio rerio | 22% | 74% |
| B1H2N3 | Xenopus tropicalis | 21% | 76% |
| C9ZUW0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 76% |
| D2HZB0 | Ailuropoda melanoleuca | 21% | 75% |
| E9AL21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 81% |
| Q0IIL1 | Bos taurus | 21% | 76% |
| Q4QIT3 | Leishmania major | 86% | 100% |
| Q4R518 | Macaca fascicularis | 22% | 76% |
| Q8CD10 | Mus musculus | 21% | 84% |
| Q8IYU8 | Homo sapiens | 21% | 83% |
| Q99P63 | Rattus norvegicus | 21% | 84% |
| Q9BPX6 | Homo sapiens | 22% | 76% |
| Q9SZ45 | Arabidopsis thaliana | 26% | 72% |
| V5B8U7 | Trypanosoma cruzi | 48% | 78% |
| V5BRA1 | Trypanosoma cruzi | 20% | 78% |