Forms a well-defined channel with 6 helices. Some paralogs tend to have an additional hydrophobic segment that might be a transit or signal peptide. It is unclear if the N-peptide is a signal or transit peptide. Localization: Mitochondrial (by homology)
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: 3 |
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: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 14 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005743 | mitochondrial inner membrane | 5 | 14 |
GO:0016020 | membrane | 2 | 14 |
GO:0019866 | organelle inner membrane | 4 | 14 |
GO:0031090 | organelle membrane | 3 | 14 |
GO:0031966 | mitochondrial membrane | 4 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0020023 | kinetoplast | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: A4HNB1
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 16 |
GO:0006811 | monoatomic ion transport | 4 | 16 |
GO:0006817 | phosphate ion transport | 7 | 16 |
GO:0006820 | monoatomic anion transport | 5 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0015698 | inorganic anion transport | 6 | 16 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 16 |
GO:0035435 | phosphate ion transmembrane transport | 6 | 16 |
GO:0051179 | localization | 1 | 16 |
GO:0051234 | establishment of localization | 2 | 16 |
GO:0055085 | transmembrane transport | 2 | 16 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 16 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 16 |
GO:0098661 | inorganic anion transmembrane transport | 5 | 16 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 16 |
GO:1990547 | mitochondrial phosphate ion transmembrane transport | 4 | 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 16 |
GO:0005315 | inorganic phosphate transmembrane transporter activity | 4 | 16 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 16 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 16 |
GO:0022804 | active transmembrane transporter activity | 3 | 16 |
GO:0022857 | transmembrane transporter activity | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.392 |
CLV_PCSK_PC1ET2_1 | 295 | 297 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.622 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.291 |
DOC_AGCK_PIF_2 | 75 | 80 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 295 | 303 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 95 | 103 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 198 | 206 | PF00069 | 0.386 |
DOC_PP4_FxxP_1 | 189 | 192 | PF00568 | 0.430 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.168 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.578 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.308 |
LIG_14-3-3_CanoR_1 | 34 | 39 | PF00244 | 0.460 |
LIG_APCC_ABBA_1 | 181 | 186 | PF00400 | 0.204 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.334 |
LIG_BRCT_BRCA1_1 | 150 | 154 | PF00533 | 0.410 |
LIG_BRCT_BRCA1_1 | 202 | 206 | PF00533 | 0.389 |
LIG_DLG_GKlike_1 | 34 | 42 | PF00625 | 0.460 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.437 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.394 |
LIG_GBD_Chelix_1 | 38 | 46 | PF00786 | 0.204 |
LIG_LIR_Apic_2 | 186 | 192 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 246 | 257 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 83 | 89 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 239 | 243 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.332 |
LIG_PCNA_yPIPBox_3 | 47 | 61 | PF02747 | 0.392 |
LIG_REV1ctd_RIR_1 | 173 | 183 | PF16727 | 0.321 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.448 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.419 |
LIG_SH2_CRK | 249 | 253 | PF00017 | 0.414 |
LIG_SH2_GRB2like | 249 | 252 | PF00017 | 0.456 |
LIG_SH2_GRB2like | 85 | 88 | PF00017 | 0.334 |
LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.465 |
LIG_SH2_SRC | 185 | 188 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.296 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.334 |
LIG_SH2_STAT3 | 67 | 70 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.450 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.368 |
LIG_SH3_4 | 191 | 198 | PF00018 | 0.543 |
LIG_SUMO_SIM_par_1 | 259 | 266 | PF11976 | 0.387 |
MOD_CDK_SPK_2 | 127 | 132 | PF00069 | 0.401 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.399 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.494 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.311 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.357 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.454 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.343 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.446 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.416 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.468 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.330 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.282 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.344 |
MOD_N-GLC_2 | 251 | 253 | PF02516 | 0.437 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.306 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.458 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.384 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.436 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.405 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.427 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.308 |
MOD_SUMO_for_1 | 46 | 49 | PF00179 | 0.419 |
MOD_SUMO_rev_2 | 287 | 297 | PF00179 | 0.355 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.330 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I993 | Leptomonas seymouri | 85% | 97% |
A0A0S4JBC4 | Bodo saltans | 40% | 79% |
A0A0S4JNX4 | Bodo saltans | 72% | 91% |
A0A0S4KJX8 | Bodo saltans | 27% | 88% |
A0A1D6N272 | Zea mays | 23% | 91% |
A0A1X0P0K9 | Trypanosomatidae | 39% | 100% |
A0A1X0P561 | Trypanosomatidae | 74% | 96% |
A0A3R7KY11 | Trypanosoma rangeli | 38% | 100% |
A0A3S5IRV4 | Trypanosoma rangeli | 77% | 97% |
A0A3S7X9V4 | Leishmania donovani | 94% | 97% |
A0A3S7X9Y0 | Leishmania donovani | 94% | 97% |
A4HNB2 | Leishmania braziliensis | 100% | 97% |
A4IBY2 | Leishmania infantum | 89% | 97% |
A4IBY3 | Leishmania infantum | 94% | 97% |
B0G143 | Dictyostelium discoideum | 24% | 100% |
B4FIJ0 | Zea mays | 23% | 91% |
C9ZYM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 76% | 97% |
D0A4I3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 81% |
E9AFR9 | Leishmania major | 94% | 100% |
E9AFS0 | Leishmania major | 94% | 100% |
E9B6X2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 97% |
O61703 | Choristoneura fumiferana | 52% | 88% |
P12234 | Bos taurus | 53% | 85% |
P16036 | Rattus norvegicus | 51% | 86% |
P23641 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 40% | 99% |
P40035 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 44% | 100% |
P40614 | Caenorhabditis elegans | 55% | 90% |
Q00325 | Homo sapiens | 52% | 85% |
Q54BF6 | Dictyostelium discoideum | 41% | 100% |
Q5R7W2 | Pongo abelii | 52% | 85% |
Q7DNC3 | Arabidopsis thaliana | 41% | 99% |
Q8VEM8 | Mus musculus | 51% | 86% |
Q9FMU6 | Arabidopsis thaliana | 52% | 82% |
Q9LJX5 | Arabidopsis thaliana | 23% | 88% |
Q9M2Z8 | Arabidopsis thaliana | 50% | 85% |
Q9P7V8 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 48% | 99% |
V5BT68 | Trypanosoma cruzi | 76% | 97% |