| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 4 |
| Forrest at al. (procyclic) | no | yes: 4 |
| Silverman et al. | no | yes: 0 |
| Pissara et al. | yes | yes: 15 |
| 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: 31 |
| NetGPI | no | yes: 0, no: 31 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 2 |
| GO:0005886 | plasma membrane | 3 | 5 |
| GO:0016020 | membrane | 2 | 32 |
| GO:0110165 | cellular anatomical entity | 1 | 32 |
Related structures:
AlphaFold database: Q4Q873
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000041 | transition metal ion transport | 7 | 5 |
| GO:0006810 | transport | 3 | 5 |
| GO:0006811 | monoatomic ion transport | 4 | 5 |
| GO:0006812 | monoatomic cation transport | 5 | 5 |
| GO:0006829 | zinc ion transport | 8 | 5 |
| GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 2 |
| GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 2 |
| GO:0006882 | intracellular zinc ion homeostasis | 7 | 2 |
| GO:0009987 | cellular process | 1 | 5 |
| GO:0019725 | cellular homeostasis | 2 | 2 |
| GO:0030001 | metal ion transport | 6 | 5 |
| GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 2 |
| GO:0034220 | monoatomic ion transmembrane transport | 3 | 5 |
| GO:0042592 | homeostatic process | 3 | 2 |
| GO:0046916 | obsolete intracellular transition metal ion homeostasis | 7 | 2 |
| GO:0048878 | chemical homeostasis | 4 | 2 |
| GO:0050801 | monoatomic ion homeostasis | 5 | 2 |
| GO:0051179 | localization | 1 | 5 |
| GO:0051234 | establishment of localization | 2 | 5 |
| GO:0055065 | obsolete metal ion homeostasis | 7 | 2 |
| GO:0055069 | obsolete zinc ion homeostasis | 8 | 2 |
| GO:0055076 | obsolete transition metal ion homeostasis | 8 | 2 |
| GO:0055080 | monoatomic cation homeostasis | 6 | 2 |
| GO:0055082 | intracellular chemical homeostasis | 3 | 2 |
| GO:0055085 | transmembrane transport | 2 | 5 |
| GO:0065007 | biological regulation | 1 | 2 |
| GO:0065008 | regulation of biological quality | 2 | 2 |
| GO:0071577 | zinc ion transmembrane transport | 6 | 5 |
| GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 2 |
| GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 2 |
| GO:0098655 | monoatomic cation transmembrane transport | 4 | 5 |
| GO:0098660 | inorganic ion transmembrane transport | 4 | 5 |
| GO:0098662 | inorganic cation transmembrane transport | 5 | 5 |
| GO:0098771 | inorganic ion homeostasis | 6 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 32 |
| GO:0005385 | zinc ion transmembrane transporter activity | 7 | 5 |
| GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 32 |
| GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 32 |
| GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 32 |
| GO:0022857 | transmembrane transporter activity | 2 | 32 |
| GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 32 |
| GO:0046873 | metal ion transmembrane transporter activity | 5 | 32 |
| GO:0046915 | transition metal ion transmembrane transporter activity | 6 | 5 |
| GO:0005381 | iron ion transmembrane transporter activity | 7 | 1 |
| GO:0015093 | ferrous iron transmembrane transporter activity | 8 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.504 |
| CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.560 |
| CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.552 |
| CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.603 |
| CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.287 |
| CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.604 |
| CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.222 |
| CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.287 |
| CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.254 |
| CLV_PCSK_PC7_1 | 394 | 400 | PF00082 | 0.187 |
| CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.553 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.355 |
| DOC_MAPK_gen_1 | 101 | 108 | PF00069 | 0.574 |
| DOC_MAPK_MEF2A_6 | 101 | 108 | PF00069 | 0.422 |
| DOC_MAPK_MEF2A_6 | 294 | 302 | PF00069 | 0.265 |
| DOC_MAPK_MEF2A_6 | 321 | 330 | PF00069 | 0.546 |
| DOC_MAPK_NFAT4_5 | 321 | 329 | PF00069 | 0.483 |
| DOC_PP4_FxxP_1 | 334 | 337 | PF00568 | 0.305 |
| DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.373 |
| DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.401 |
| DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.499 |
| DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.269 |
| DOC_USP7_MATH_2 | 4 | 10 | PF00917 | 0.387 |
| LIG_14-3-3_CanoR_1 | 107 | 112 | PF00244 | 0.418 |
| LIG_14-3-3_CanoR_1 | 37 | 43 | PF00244 | 0.437 |
| LIG_APCC_ABBA_1 | 25 | 30 | PF00400 | 0.385 |
| LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.206 |
| LIG_Clathr_ClatBox_1 | 381 | 385 | PF01394 | 0.432 |
| LIG_deltaCOP1_diTrp_1 | 154 | 160 | PF00928 | 0.216 |
| LIG_DLG_GKlike_1 | 107 | 115 | PF00625 | 0.382 |
| LIG_eIF4E_1 | 376 | 382 | PF01652 | 0.321 |
| LIG_FHA_1 | 119 | 125 | PF00498 | 0.368 |
| LIG_FHA_1 | 13 | 19 | PF00498 | 0.351 |
| LIG_FHA_1 | 342 | 348 | PF00498 | 0.267 |
| LIG_FHA_1 | 356 | 362 | PF00498 | 0.245 |
| LIG_FHA_2 | 225 | 231 | PF00498 | 0.512 |
| LIG_FHA_2 | 29 | 35 | PF00498 | 0.414 |
| LIG_LIR_Apic_2 | 333 | 337 | PF02991 | 0.305 |
| LIG_LIR_Gen_1 | 154 | 164 | PF02991 | 0.211 |
| LIG_LIR_Gen_1 | 357 | 366 | PF02991 | 0.322 |
| LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.265 |
| LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.360 |
| LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.349 |
| LIG_PDZ_Wminus1_1 | 418 | 420 | PF00595 | 0.354 |
| LIG_Pex14_1 | 156 | 160 | PF04695 | 0.463 |
| LIG_Pex14_2 | 302 | 306 | PF04695 | 0.381 |
| LIG_Pex14_2 | 379 | 383 | PF04695 | 0.371 |
| LIG_SH2_CRK | 359 | 363 | PF00017 | 0.216 |
| LIG_SH2_NCK_1 | 359 | 363 | PF00017 | 0.216 |
| LIG_SH2_SRC | 111 | 114 | PF00017 | 0.514 |
| LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.499 |
| LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.300 |
| LIG_SH3_1 | 189 | 195 | PF00018 | 0.413 |
| LIG_SH3_3 | 189 | 195 | PF00018 | 0.516 |
| LIG_SH3_3 | 249 | 255 | PF00018 | 0.573 |
| LIG_SUMO_SIM_anti_2 | 233 | 239 | PF11976 | 0.382 |
| LIG_SUMO_SIM_anti_2 | 325 | 330 | PF11976 | 0.447 |
| LIG_SxIP_EBH_1 | 89 | 102 | PF03271 | 0.340 |
| LIG_TYR_ITSM | 355 | 362 | PF00017 | 0.216 |
| LIG_UBA3_1 | 95 | 101 | PF00899 | 0.248 |
| LIG_WRC_WIRS_1 | 331 | 336 | PF05994 | 0.278 |
| MOD_CK1_1 | 355 | 361 | PF00069 | 0.311 |
| MOD_CK1_1 | 52 | 58 | PF00069 | 0.530 |
| MOD_CK2_1 | 145 | 151 | PF00069 | 0.233 |
| MOD_Cter_Amidation | 99 | 102 | PF01082 | 0.321 |
| MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.604 |
| MOD_GlcNHglycan | 30 | 34 | PF01048 | 0.775 |
| MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.361 |
| MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.366 |
| MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.316 |
| MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.804 |
| MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.784 |
| MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.729 |
| MOD_GSK3_1 | 14 | 21 | PF00069 | 0.558 |
| MOD_GSK3_1 | 29 | 36 | PF00069 | 0.591 |
| MOD_GSK3_1 | 316 | 323 | PF00069 | 0.502 |
| MOD_GSK3_1 | 38 | 45 | PF00069 | 0.437 |
| MOD_GSK3_1 | 6 | 13 | PF00069 | 0.425 |
| MOD_GSK3_1 | 87 | 94 | PF00069 | 0.296 |
| MOD_N-GLC_2 | 202 | 204 | PF02516 | 0.213 |
| MOD_NEK2_1 | 272 | 277 | PF00069 | 0.370 |
| MOD_NEK2_1 | 285 | 290 | PF00069 | 0.276 |
| MOD_NEK2_1 | 330 | 335 | PF00069 | 0.334 |
| MOD_NEK2_1 | 354 | 359 | PF00069 | 0.290 |
| MOD_NEK2_1 | 87 | 92 | PF00069 | 0.322 |
| MOD_NEK2_2 | 316 | 321 | PF00069 | 0.446 |
| MOD_PIKK_1 | 18 | 24 | PF00454 | 0.513 |
| MOD_PKA_1 | 38 | 44 | PF00069 | 0.403 |
| MOD_PKA_2 | 180 | 186 | PF00069 | 0.523 |
| MOD_PKA_2 | 38 | 44 | PF00069 | 0.458 |
| MOD_Plk_1 | 202 | 208 | PF00069 | 0.600 |
| MOD_Plk_1 | 316 | 322 | PF00069 | 0.430 |
| MOD_Plk_4 | 107 | 113 | PF00069 | 0.438 |
| MOD_Plk_4 | 202 | 208 | PF00069 | 0.382 |
| MOD_Plk_4 | 233 | 239 | PF00069 | 0.389 |
| MOD_Plk_4 | 275 | 281 | PF00069 | 0.326 |
| MOD_Plk_4 | 87 | 93 | PF00069 | 0.323 |
| MOD_SUMO_for_1 | 208 | 211 | PF00179 | 0.382 |
| TRG_DiLeu_BaEn_2 | 153 | 159 | PF01217 | 0.256 |
| TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.311 |
| TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.305 |
| TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.373 |
| TRG_ER_diArg_1 | 37 | 39 | PF00400 | 0.440 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PCU5 | Leptomonas seymouri | 41% | 98% |
| A0A1X0NR51 | Trypanosomatidae | 46% | 100% |
| A0A1X0NSB9 | Trypanosomatidae | 37% | 100% |
| A0A1X0NSI7 | Trypanosomatidae | 37% | 100% |
| A0A3R7LZX6 | Trypanosoma rangeli | 40% | 100% |
| A0A3S7X1N7 | Leishmania donovani | 84% | 91% |
| A0A3S7X501 | Leishmania donovani | 41% | 97% |
| A0A422MUI2 | Trypanosoma rangeli | 36% | 100% |
| A4HGP7 | Leishmania braziliensis | 78% | 100% |
| A4HJU9 | Leishmania braziliensis | 42% | 99% |
| A4HJV0 | Leishmania braziliensis | 42% | 99% |
| A4HJV1 | Leishmania braziliensis | 36% | 100% |
| A4HM27 | Leishmania braziliensis | 32% | 100% |
| A4I3R9 | Leishmania infantum | 86% | 91% |
| A4I7B1 | Leishmania infantum | 41% | 97% |
| D0A885 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
| D0A886 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
| D0A887 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
| D0A888 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
| D0A889 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
| E9B012 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 93% |
| E9B2A5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 97% |
| E9B2A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 97% |
| E9B4F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
| O04089 | Arabidopsis thaliana | 28% | 100% |
| O23039 | Arabidopsis thaliana | 30% | 100% |
| O64738 | Arabidopsis thaliana | 24% | 100% |
| O81123 | Arabidopsis thaliana | 24% | 100% |
| O81850 | Arabidopsis thaliana | 25% | 100% |
| O82643 | Arabidopsis thaliana | 30% | 100% |
| O94639 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
| P32804 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
| Q38856 | Arabidopsis thaliana | 24% | 100% |
| Q4Q3L6 | Leishmania major | 34% | 100% |
| Q4Q5V0 | Leishmania major | 40% | 97% |
| Q4Q5V1 | Leishmania major | 40% | 97% |
| Q6L8F7 | Oryza sativa subsp. japonica | 28% | 100% |
| Q6L8G0 | Oryza sativa subsp. japonica | 29% | 100% |
| Q6L8G1 | Oryza sativa subsp. japonica | 29% | 100% |
| Q75HB1 | Oryza sativa subsp. japonica | 28% | 100% |
| Q7XLD4 | Oryza sativa subsp. japonica | 28% | 100% |
| Q8S3W4 | Arabidopsis thaliana | 22% | 100% |
| Q8W245 | Arabidopsis thaliana | 22% | 100% |
| Q8W246 | Arabidopsis thaliana | 26% | 100% |
| Q9FIS2 | Arabidopsis thaliana | 26% | 100% |
| Q9SLG3 | Arabidopsis thaliana | 29% | 100% |
| V5AWN3 | Trypanosoma cruzi | 38% | 100% |
| V5BC34 | Trypanosoma cruzi | 36% | 100% |
| V5DCU2 | Trypanosoma cruzi | 46% | 100% |