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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005743 | mitochondrial inner membrane | 5 | 9 |
GO:0016020 | membrane | 2 | 9 |
GO:0019866 | organelle inner membrane | 4 | 9 |
GO:0031090 | organelle membrane | 3 | 9 |
GO:0031966 | mitochondrial membrane | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4HBN3
Term | Name | Level | Count |
---|---|---|---|
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 9 |
GO:0006874 | intracellular calcium ion homeostasis | 7 | 9 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0019725 | cellular homeostasis | 2 | 9 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 9 |
GO:0042592 | homeostatic process | 3 | 9 |
GO:0048878 | chemical homeostasis | 4 | 9 |
GO:0050801 | monoatomic ion homeostasis | 5 | 9 |
GO:0051560 | mitochondrial calcium ion homeostasis | 8 | 9 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 9 |
GO:0055074 | calcium ion homeostasis | 8 | 9 |
GO:0055080 | monoatomic cation homeostasis | 6 | 9 |
GO:0055082 | intracellular chemical homeostasis | 3 | 9 |
GO:0065007 | biological regulation | 1 | 9 |
GO:0065008 | regulation of biological quality | 2 | 9 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 9 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 9 |
GO:0098771 | inorganic ion homeostasis | 6 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 9 |
GO:0005216 | monoatomic ion channel activity | 4 | 9 |
GO:0005261 | monoatomic cation channel activity | 5 | 9 |
GO:0005262 | calcium channel activity | 6 | 9 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 9 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 9 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 9 |
GO:0015267 | channel activity | 4 | 9 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 9 |
GO:0015292 | uniporter activity | 5 | 9 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 9 |
GO:0022803 | passive transmembrane transporter activity | 3 | 9 |
GO:0022804 | active transmembrane transporter activity | 3 | 9 |
GO:0022857 | transmembrane transporter activity | 2 | 9 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 9 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.415 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.183 |
CLV_PCSK_PC1ET2_1 | 95 | 97 | PF00082 | 0.192 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.185 |
CLV_Separin_Metazoa | 5 | 9 | PF03568 | 0.508 |
DEG_APCC_DBOX_1 | 95 | 103 | PF00400 | 0.408 |
DOC_MAPK_gen_1 | 8 | 15 | PF00069 | 0.623 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.179 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.652 |
DOC_USP7_UBL2_3 | 210 | 214 | PF12436 | 0.526 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.557 |
LIG_Actin_WH2_2 | 74 | 91 | PF00022 | 0.479 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.538 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.526 |
LIG_deltaCOP1_diTrp_1 | 137 | 145 | PF00928 | 0.340 |
LIG_eIF4E_1 | 9 | 15 | PF01652 | 0.511 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.281 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.588 |
LIG_LIR_Gen_1 | 137 | 148 | PF02991 | 0.208 |
LIG_LIR_Gen_1 | 158 | 169 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 173 | 183 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 185 | 194 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.204 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.358 |
LIG_LYPXL_yS_3 | 116 | 119 | PF13949 | 0.379 |
LIG_PCNA_PIPBox_1 | 121 | 130 | PF02747 | 0.379 |
LIG_PDZ_Class_3 | 217 | 222 | PF00595 | 0.496 |
LIG_Pex14_2 | 143 | 147 | PF04695 | 0.205 |
LIG_SH2_STAP1 | 157 | 161 | PF00017 | 0.223 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.157 |
LIG_TRAF2_1 | 218 | 221 | PF00917 | 0.457 |
MOD_CDK_SPK_2 | 67 | 72 | PF00069 | 0.560 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.668 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.557 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.328 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.335 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.503 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.505 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.701 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.675 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.617 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.482 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.646 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.458 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.329 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.581 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.380 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.263 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.568 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.557 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.516 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.487 |
MOD_PK_1 | 72 | 78 | PF00069 | 0.524 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.531 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.616 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.340 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.609 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.323 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.637 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.558 |
MOD_SUMO_for_1 | 105 | 108 | PF00179 | 0.379 |
MOD_SUMO_rev_2 | 203 | 212 | PF00179 | 0.553 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.219 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.464 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 181 | 185 | PF00026 | 0.247 |
TRG_Pf-PMV_PEXEL_1 | 217 | 221 | PF00026 | 0.405 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEX8 | Leptomonas seymouri | 42% | 100% |
A0A0S4JH33 | Bodo saltans | 29% | 100% |
A0A1X0NNH4 | Trypanosomatidae | 27% | 91% |
A0A1X0NXF2 | Trypanosomatidae | 36% | 93% |
A0A422MZA0 | Trypanosoma rangeli | 38% | 97% |
A0A422NQP4 | Trypanosoma rangeli | 27% | 94% |
D0A1N3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |