| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 2 |
| Forrest at al. (procyclic) | no | yes: 2 |
| Silverman et al. | no | yes: 0 |
| Pissara et al. | no | yes: 12 |
| 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: 27 |
| NetGPI | no | yes: 0, no: 27 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 28 |
| GO:0110165 | cellular anatomical entity | 1 | 28 |
| GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A0A3S7X7B0
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000041 | transition metal ion transport | 7 | 1 |
| GO:0006810 | transport | 3 | 1 |
| GO:0006811 | monoatomic ion transport | 4 | 1 |
| GO:0006812 | monoatomic cation transport | 5 | 1 |
| GO:0006829 | zinc ion transport | 8 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0030001 | metal ion transport | 6 | 1 |
| GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
| GO:0051179 | localization | 1 | 1 |
| GO:0051234 | establishment of localization | 2 | 1 |
| GO:0055085 | transmembrane transport | 2 | 1 |
| GO:0071577 | zinc ion transmembrane transport | 6 | 1 |
| GO:0098655 | monoatomic cation transmembrane transport | 4 | 1 |
| GO:0098660 | inorganic ion transmembrane transport | 4 | 1 |
| GO:0098662 | inorganic cation transmembrane transport | 5 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 28 |
| GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 28 |
| GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 28 |
| GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 28 |
| GO:0022857 | transmembrane transporter activity | 2 | 28 |
| GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 28 |
| GO:0046873 | metal ion transmembrane transporter activity | 5 | 28 |
| GO:0005385 | zinc ion transmembrane transporter activity | 7 | 1 |
| GO:0046915 | transition metal ion transmembrane transporter activity | 6 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_MEL_PAP_1 | 45 | 51 | PF00089 | 0.172 |
| CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.273 |
| CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.273 |
| CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.329 |
| CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.240 |
| DEG_APCC_DBOX_1 | 309 | 317 | PF00400 | 0.504 |
| DOC_PP1_RVXF_1 | 120 | 126 | PF00149 | 0.204 |
| DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.426 |
| DOC_PP4_FxxP_1 | 52 | 55 | PF00568 | 0.526 |
| DOC_PP4_FxxP_1 | 98 | 101 | PF00568 | 0.276 |
| DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.336 |
| DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.618 |
| DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.506 |
| DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.289 |
| DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.230 |
| DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.309 |
| DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.384 |
| DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.524 |
| LIG_14-3-3_CanoR_1 | 48 | 55 | PF00244 | 0.393 |
| LIG_Actin_WH2_2 | 66 | 82 | PF00022 | 0.449 |
| LIG_AP2alpha_1 | 124 | 128 | PF02296 | 0.366 |
| LIG_APCC_ABBA_1 | 121 | 126 | PF00400 | 0.385 |
| LIG_CSL_BTD_1 | 7 | 10 | PF09270 | 0.327 |
| LIG_eIF4E_1 | 285 | 291 | PF01652 | 0.270 |
| LIG_FHA_1 | 231 | 237 | PF00498 | 0.536 |
| LIG_FHA_1 | 269 | 275 | PF00498 | 0.310 |
| LIG_FHA_1 | 65 | 71 | PF00498 | 0.320 |
| LIG_FHA_2 | 13 | 19 | PF00498 | 0.434 |
| LIG_LIR_Apic_2 | 50 | 55 | PF02991 | 0.376 |
| LIG_LIR_Gen_1 | 201 | 211 | PF02991 | 0.353 |
| LIG_LIR_Gen_1 | 21 | 32 | PF02991 | 0.208 |
| LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.522 |
| LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.471 |
| LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.311 |
| LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.256 |
| LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.282 |
| LIG_PCNA_PIPBox_1 | 289 | 298 | PF02747 | 0.230 |
| LIG_Pex14_2 | 124 | 128 | PF04695 | 0.376 |
| LIG_Pex14_2 | 211 | 215 | PF04695 | 0.321 |
| LIG_PTAP_UEV_1 | 156 | 161 | PF05743 | 0.348 |
| LIG_SH2_SRC | 57 | 60 | PF00017 | 0.478 |
| LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.352 |
| LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.399 |
| LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.261 |
| LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.318 |
| LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.409 |
| LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.281 |
| LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.231 |
| LIG_SH3_3 | 154 | 160 | PF00018 | 0.533 |
| LIG_SH3_3 | 303 | 309 | PF00018 | 0.480 |
| LIG_SH3_3 | 4 | 10 | PF00018 | 0.511 |
| LIG_UBA3_1 | 75 | 80 | PF00899 | 0.439 |
| MOD_CDK_SPK_2 | 305 | 310 | PF00069 | 0.371 |
| MOD_CK1_1 | 138 | 144 | PF00069 | 0.402 |
| MOD_CK1_1 | 164 | 170 | PF00069 | 0.366 |
| MOD_CK1_1 | 184 | 190 | PF00069 | 0.339 |
| MOD_CK1_1 | 64 | 70 | PF00069 | 0.350 |
| MOD_CK1_1 | 85 | 91 | PF00069 | 0.253 |
| MOD_CK2_1 | 12 | 18 | PF00069 | 0.439 |
| MOD_Cter_Amidation | 45 | 48 | PF01082 | 0.334 |
| MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.403 |
| MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.263 |
| MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.250 |
| MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.209 |
| MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.234 |
| MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.458 |
| MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.319 |
| MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.346 |
| MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.528 |
| MOD_GSK3_1 | 161 | 168 | PF00069 | 0.390 |
| MOD_GSK3_1 | 33 | 40 | PF00069 | 0.258 |
| MOD_GSK3_1 | 8 | 15 | PF00069 | 0.364 |
| MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.436 |
| MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.527 |
| MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.449 |
| MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.428 |
| MOD_NEK2_1 | 145 | 150 | PF00069 | 0.410 |
| MOD_NEK2_1 | 181 | 186 | PF00069 | 0.286 |
| MOD_NEK2_1 | 241 | 246 | PF00069 | 0.289 |
| MOD_NEK2_1 | 299 | 304 | PF00069 | 0.524 |
| MOD_NEK2_1 | 33 | 38 | PF00069 | 0.259 |
| MOD_NEK2_2 | 207 | 212 | PF00069 | 0.445 |
| MOD_NEK2_2 | 227 | 232 | PF00069 | 0.395 |
| MOD_PIKK_1 | 138 | 144 | PF00454 | 0.504 |
| MOD_PIKK_1 | 145 | 151 | PF00454 | 0.467 |
| MOD_PIKK_1 | 268 | 274 | PF00454 | 0.255 |
| MOD_PKA_1 | 47 | 53 | PF00069 | 0.376 |
| MOD_PKA_2 | 47 | 53 | PF00069 | 0.376 |
| MOD_Plk_1 | 82 | 88 | PF00069 | 0.265 |
| MOD_Plk_4 | 184 | 190 | PF00069 | 0.285 |
| MOD_Plk_4 | 201 | 207 | PF00069 | 0.234 |
| MOD_Plk_4 | 263 | 269 | PF00069 | 0.267 |
| MOD_Plk_4 | 322 | 328 | PF00069 | 0.324 |
| MOD_Plk_4 | 33 | 39 | PF00069 | 0.286 |
| MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.378 |
| MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.524 |
| TRG_DiLeu_BaEn_1 | 140 | 145 | PF01217 | 0.399 |
| TRG_DiLeu_BaEn_1 | 201 | 206 | PF01217 | 0.213 |
| TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.312 |
| TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.251 |
| TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.423 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P2E9 | Leptomonas seymouri | 32% | 100% |
| A0A0N0P5K7 | Leptomonas seymouri | 63% | 100% |
| A0A1X0NR51 | Trypanosomatidae | 42% | 90% |
| A0A1X0NSB9 | Trypanosomatidae | 36% | 82% |
| A0A1X0NSI7 | Trypanosomatidae | 35% | 88% |
| A0A3R7LZX6 | Trypanosoma rangeli | 38% | 95% |
| A0A3S7X1N7 | Leishmania donovani | 35% | 100% |
| A0A422MUI2 | Trypanosoma rangeli | 33% | 90% |
| A4HGP7 | Leishmania braziliensis | 36% | 99% |
| A4HJU6 | Leishmania braziliensis | 44% | 100% |
| A4HJU9 | Leishmania braziliensis | 33% | 100% |
| A4HJV0 | Leishmania braziliensis | 33% | 100% |
| A4HM27 | Leishmania braziliensis | 76% | 100% |
| A4I3R9 | Leishmania infantum | 35% | 100% |
| A4I9G1 | Leishmania infantum | 100% | 100% |
| D0A885 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 85% |
| D0A886 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 85% |
| D0A887 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 85% |
| D0A888 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 85% |
| D0A889 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 87% |
| E9B012 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
| E9B4F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
| O23039 | Arabidopsis thaliana | 25% | 93% |
| O64738 | Arabidopsis thaliana | 25% | 98% |
| O81123 | Arabidopsis thaliana | 29% | 94% |
| O81850 | Arabidopsis thaliana | 27% | 95% |
| O82643 | Arabidopsis thaliana | 26% | 97% |
| O94639 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 82% |
| P32804 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 89% |
| Q38856 | Arabidopsis thaliana | 28% | 96% |
| Q4Q3L6 | Leishmania major | 90% | 100% |
| Q6L8G0 | Oryza sativa subsp. japonica | 31% | 95% |
| Q6L8G1 | Oryza sativa subsp. japonica | 28% | 90% |
| Q6ZJ91 | Oryza sativa subsp. japonica | 25% | 84% |
| Q75HB1 | Oryza sativa subsp. japonica | 28% | 89% |
| Q7XLD4 | Oryza sativa subsp. japonica | 27% | 92% |
| Q852F6 | Oryza sativa subsp. japonica | 24% | 93% |
| Q8S3W4 | Arabidopsis thaliana | 26% | 96% |
| Q8W245 | Arabidopsis thaliana | 29% | 92% |
| Q8W246 | Arabidopsis thaliana | 24% | 92% |
| Q9FIS2 | Arabidopsis thaliana | 27% | 94% |
| Q9SLG3 | Arabidopsis thaliana | 26% | 99% |
| V5AWN3 | Trypanosoma cruzi | 36% | 90% |
| V5BC34 | Trypanosoma cruzi | 34% | 90% |
| V5DCU2 | Trypanosoma cruzi | 42% | 90% |