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. | 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: 34 |
NetGPI | no | yes: 0, no: 34 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 35 |
GO:0110165 | cellular anatomical entity | 1 | 35 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005886 | plasma membrane | 3 | 4 |
Related structures:
AlphaFold database: E9B4F9
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: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:0009987 | cellular process | 1 | 4 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030001 | metal ion transport | 6 | 4 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 4 |
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:0051179 | localization | 1 | 4 |
GO:0051234 | establishment of localization | 2 | 4 |
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:0055085 | transmembrane transport | 2 | 4 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071577 | zinc ion transmembrane transport | 6 | 4 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 1 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 1 |
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:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 35 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 35 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 35 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 35 |
GO:0022857 | transmembrane transporter activity | 2 | 35 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 35 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 35 |
GO:0005385 | zinc ion transmembrane transporter activity | 7 | 4 |
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_MEL_PAP_1 | 45 | 51 | PF00089 | 0.168 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.275 |
DEG_APCC_DBOX_1 | 309 | 317 | PF00400 | 0.511 |
DEG_APCC_KENBOX_2 | 16 | 20 | PF00400 | 0.250 |
DOC_CYCLIN_yCln2_LP_2 | 243 | 249 | PF00134 | 0.279 |
DOC_CYCLIN_yCln2_LP_2 | 98 | 104 | PF00134 | 0.151 |
DOC_PP1_RVXF_1 | 120 | 126 | PF00149 | 0.191 |
DOC_PP2B_LxvP_1 | 132 | 135 | PF13499 | 0.483 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.447 |
DOC_PP4_FxxP_1 | 52 | 55 | PF00568 | 0.524 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.317 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.210 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.302 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.352 |
LIG_14-3-3_CanoR_1 | 300 | 304 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 48 | 55 | PF00244 | 0.413 |
LIG_Actin_WH2_2 | 66 | 82 | PF00022 | 0.452 |
LIG_APCC_ABBA_1 | 121 | 126 | PF00400 | 0.373 |
LIG_BRCT_BRCA1_1 | 243 | 247 | PF00533 | 0.313 |
LIG_BRCT_BRCA1_1 | 308 | 312 | PF00533 | 0.395 |
LIG_Clathr_ClatBox_1 | 290 | 294 | PF01394 | 0.351 |
LIG_CSL_BTD_1 | 7 | 10 | PF09270 | 0.316 |
LIG_eIF4E_1 | 285 | 291 | PF01652 | 0.295 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.182 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.559 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.266 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.346 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.416 |
LIG_LIR_Apic_2 | 50 | 55 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 21 | 32 | PF02991 | 0.185 |
LIG_LIR_Gen_1 | 210 | 219 | PF02991 | 0.243 |
LIG_LIR_Gen_1 | 234 | 245 | PF02991 | 0.224 |
LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.247 |
LIG_PCNA_PIPBox_1 | 289 | 298 | PF02747 | 0.210 |
LIG_PCNA_yPIPBox_3 | 289 | 300 | PF02747 | 0.159 |
LIG_PDZ_Class_2 | 329 | 334 | PF00595 | 0.141 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.371 |
LIG_Pex14_2 | 211 | 215 | PF04695 | 0.345 |
LIG_Pex14_2 | 237 | 241 | PF04695 | 0.237 |
LIG_SH2_SRC | 57 | 60 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.271 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.530 |
LIG_SUMO_SIM_par_1 | 289 | 294 | PF11976 | 0.169 |
LIG_TRAF2_1 | 137 | 140 | PF00917 | 0.526 |
LIG_UBA3_1 | 75 | 80 | PF00899 | 0.440 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.409 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.308 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.380 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.375 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.249 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.257 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.433 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.206 |
MOD_Cter_Amidation | 45 | 48 | PF01082 | 0.293 |
MOD_GlcNHglycan | 166 | 170 | PF01048 | 0.238 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.311 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.327 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.653 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.171 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.222 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.422 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.269 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.382 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.431 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.146 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.567 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.350 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.391 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.306 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.306 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.237 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.535 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.285 |
MOD_NEK2_2 | 207 | 212 | PF00069 | 0.454 |
MOD_NEK2_2 | 227 | 232 | PF00069 | 0.396 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.506 |
MOD_PIKK_1 | 145 | 151 | PF00454 | 0.374 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.246 |
MOD_PKA_1 | 47 | 53 | PF00069 | 0.371 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.533 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.525 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.371 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.347 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.274 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.216 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.296 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.290 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.268 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.297 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.345 |
TRG_DiLeu_BaEn_1 | 140 | 145 | PF01217 | 0.387 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2E9 | Leptomonas seymouri | 34% | 100% |
A0A0N0P5K7 | Leptomonas seymouri | 59% | 100% |
A0A1X0NR51 | Trypanosomatidae | 41% | 90% |
A0A1X0NSB9 | Trypanosomatidae | 36% | 82% |
A0A1X0NSI7 | Trypanosomatidae | 36% | 88% |
A0A3R7LZX6 | Trypanosoma rangeli | 38% | 95% |
A0A3S7X1N7 | Leishmania donovani | 34% | 72% |
A0A3S7X501 | Leishmania donovani | 35% | 77% |
A0A3S7X7B0 | Leishmania donovani | 86% | 100% |
A0A422MUI2 | Trypanosoma rangeli | 34% | 90% |
A4HGP7 | Leishmania braziliensis | 36% | 100% |
A4HJU6 | Leishmania braziliensis | 41% | 100% |
A4HJU9 | Leishmania braziliensis | 33% | 100% |
A4HJV0 | Leishmania braziliensis | 33% | 100% |
A4HM27 | Leishmania braziliensis | 73% | 100% |
A4I3R9 | Leishmania infantum | 34% | 72% |
A4I7B1 | Leishmania infantum | 35% | 77% |
A4I9G1 | Leishmania infantum | 86% | 100% |
D0A885 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 85% |
D0A886 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 85% |
D0A887 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 85% |
D0A888 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 85% |
D0A889 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 87% |
E9B012 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B2A5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B2A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
O23039 | Arabidopsis thaliana | 25% | 93% |
O64738 | Arabidopsis thaliana | 26% | 98% |
O81123 | Arabidopsis thaliana | 27% | 94% |
O81850 | Arabidopsis thaliana | 26% | 95% |
O82643 | Arabidopsis thaliana | 26% | 97% |
O94639 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 82% |
P32804 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 89% |
Q38856 | Arabidopsis thaliana | 26% | 96% |
Q4Q3L6 | Leishmania major | 85% | 100% |
Q4Q5V0 | Leishmania major | 35% | 100% |
Q4Q5V1 | Leishmania major | 35% | 100% |
Q4Q873 | Leishmania major | 35% | 100% |
Q6L8G0 | Oryza sativa subsp. japonica | 32% | 95% |
Q6L8G1 | Oryza sativa subsp. japonica | 28% | 90% |
Q75HB1 | Oryza sativa subsp. japonica | 27% | 89% |
Q7XLD4 | Oryza sativa subsp. japonica | 27% | 92% |
Q852F6 | Oryza sativa subsp. japonica | 25% | 93% |
Q8S3W4 | Arabidopsis thaliana | 26% | 96% |
Q8W245 | Arabidopsis thaliana | 28% | 92% |
Q8W246 | Arabidopsis thaliana | 25% | 92% |
Q94DG6 | Oryza sativa subsp. japonica | 24% | 95% |
Q9FIS2 | Arabidopsis thaliana | 25% | 94% |
Q9SLG3 | Arabidopsis thaliana | 24% | 99% |
V5AWN3 | Trypanosoma cruzi | 36% | 90% |
V5BC34 | Trypanosoma cruzi | 33% | 90% |
V5DCU2 | Trypanosoma cruzi | 40% | 90% |