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: 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: 27 |
NetGPI | no | yes: 0, no: 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 4 |
GO:0016020 | membrane | 2 | 28 |
GO:0110165 | cellular anatomical entity | 1 | 28 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: Q4Q3L6
Term | Name | Level | Count |
---|---|---|---|
GO:0000041 | transition metal ion transport | 7 | 4 |
GO:0006810 | transport | 3 | 4 |
GO:0006811 | monoatomic ion transport | 4 | 4 |
GO:0006812 | monoatomic cation transport | 5 | 4 |
GO:0006829 | zinc ion transport | 8 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0030001 | metal ion transport | 6 | 4 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 4 |
GO:0051179 | localization | 1 | 4 |
GO:0051234 | establishment of localization | 2 | 4 |
GO:0055085 | transmembrane transport | 2 | 4 |
GO:0071577 | zinc ion transmembrane transport | 6 | 4 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 4 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 4 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 4 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 1 |
GO:0006882 | intracellular zinc ion homeostasis | 7 | 1 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0046916 | obsolete intracellular transition metal ion homeostasis | 7 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055069 | obsolete zinc ion homeostasis | 8 | 1 |
GO:0055076 | obsolete transition metal 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:0005215 | transporter activity | 1 | 28 |
GO:0005385 | zinc ion transmembrane transporter activity | 7 | 4 |
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:0046915 | transition metal ion transmembrane transporter activity | 6 | 4 |
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_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.251 |
DEG_APCC_DBOX_1 | 309 | 317 | PF00400 | 0.505 |
DOC_PP1_RVXF_1 | 120 | 126 | PF00149 | 0.190 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.439 |
DOC_PP4_FxxP_1 | 52 | 55 | PF00568 | 0.386 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.321 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.299 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.210 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.300 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.378 |
LIG_Actin_WH2_2 | 66 | 82 | PF00022 | 0.210 |
LIG_AP2alpha_1 | 124 | 128 | PF02296 | 0.360 |
LIG_APCC_ABBA_1 | 121 | 126 | PF00400 | 0.378 |
LIG_eIF4E_1 | 285 | 291 | PF01652 | 0.279 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.196 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.554 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.246 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.333 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.415 |
LIG_LIR_Gen_1 | 18 | 28 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 201 | 211 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 234 | 245 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.280 |
LIG_PCNA_PIPBox_1 | 289 | 298 | PF02747 | 0.210 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.367 |
LIG_Pex14_2 | 211 | 215 | PF04695 | 0.335 |
LIG_Pex14_2 | 237 | 241 | PF04695 | 0.232 |
LIG_SH2_SRC | 57 | 60 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.250 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.437 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.475 |
LIG_SUMO_SIM_anti_2 | 325 | 330 | PF11976 | 0.170 |
LIG_UBA3_1 | 75 | 80 | PF00899 | 0.422 |
MOD_CDK_SPK_2 | 305 | 310 | PF00069 | 0.364 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.563 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.303 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.370 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.431 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.260 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.454 |
MOD_Cter_Amidation | 45 | 48 | PF01082 | 0.286 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.281 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.214 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.259 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.309 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.664 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.542 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.447 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.472 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.526 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.264 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.432 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.445 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.422 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.356 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.534 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.288 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.291 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.249 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.522 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.301 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.255 |
MOD_NEK2_2 | 207 | 212 | PF00069 | 0.448 |
MOD_NEK2_2 | 227 | 232 | PF00069 | 0.397 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.528 |
MOD_PIKK_1 | 145 | 151 | PF00454 | 0.556 |
MOD_PIKK_1 | 168 | 174 | PF00454 | 0.342 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.240 |
MOD_PK_1 | 165 | 171 | PF00069 | 0.342 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.336 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.268 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.358 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.277 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.230 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.270 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.382 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.301 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.388 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.378 |
TRG_DiLeu_BaEn_1 | 140 | 145 | PF01217 | 0.386 |
TRG_DiLeu_BaEn_1 | 18 | 23 | PF01217 | 0.219 |
TRG_DiLeu_BaEn_1 | 201 | 206 | PF01217 | 0.200 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.195 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.259 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.430 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2E9 | Leptomonas seymouri | 34% | 100% |
A0A0N0P5K7 | Leptomonas seymouri | 60% | 100% |
A0A1X0NR51 | Trypanosomatidae | 41% | 90% |
A0A1X0NSB9 | Trypanosomatidae | 35% | 82% |
A0A1X0NSI7 | Trypanosomatidae | 35% | 88% |
A0A3R7LZX6 | Trypanosoma rangeli | 38% | 95% |
A0A3S7X1N7 | Leishmania donovani | 33% | 72% |
A0A3S7X7B0 | Leishmania donovani | 90% | 100% |
A0A422MUI2 | Trypanosoma rangeli | 33% | 90% |
A4HGP7 | Leishmania braziliensis | 35% | 95% |
A4HM27 | Leishmania braziliensis | 74% | 100% |
A4I3R9 | Leishmania infantum | 33% | 72% |
A4I9G1 | Leishmania infantum | 90% | 100% |
D0A885 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 85% |
D0A886 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 85% |
D0A887 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 85% |
D0A888 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 85% |
D0A889 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 87% |
E9B012 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 74% |
E9B2A5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B2A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 77% |
E9B4F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
O23039 | Arabidopsis thaliana | 25% | 93% |
O64738 | Arabidopsis thaliana | 26% | 98% |
O81123 | Arabidopsis thaliana | 28% | 94% |
O81850 | Arabidopsis thaliana | 25% | 95% |
O82643 | Arabidopsis thaliana | 26% | 97% |
O94639 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 82% |
P32804 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 89% |
Q38856 | Arabidopsis thaliana | 28% | 96% |
Q4Q5V1 | Leishmania major | 34% | 77% |
Q4Q873 | Leishmania major | 34% | 100% |
Q6L8G0 | Oryza sativa subsp. japonica | 32% | 95% |
Q6L8G1 | Oryza sativa subsp. japonica | 28% | 90% |
Q6ZJ91 | Oryza sativa subsp. japonica | 25% | 84% |
Q75HB1 | Oryza sativa subsp. japonica | 26% | 89% |
Q7XLD4 | Oryza sativa subsp. japonica | 27% | 92% |
Q852F6 | Oryza sativa subsp. japonica | 26% | 93% |
Q8S3W4 | Arabidopsis thaliana | 25% | 96% |
Q8W245 | Arabidopsis thaliana | 28% | 92% |
Q8W246 | Arabidopsis thaliana | 24% | 92% |
Q94EG9 | Arabidopsis thaliana | 23% | 100% |
Q9FIS2 | Arabidopsis thaliana | 25% | 94% |
Q9SLG3 | Arabidopsis thaliana | 25% | 99% |
V5AWN3 | Trypanosoma cruzi | 36% | 90% |
V5BC34 | Trypanosoma cruzi | 34% | 90% |
V5DCU2 | Trypanosoma cruzi | 41% | 90% |