A bacterial-type Mg2+ transporter found in kinetoplastids.. Expanded extensively on multiple lineages, especially T cruzi
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. | yes | yes: 25 |
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:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9AXI8
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 6 |
GO:0006811 | monoatomic ion transport | 4 | 6 |
GO:0006812 | monoatomic cation transport | 5 | 6 |
GO:0051179 | localization | 1 | 6 |
GO:0051234 | establishment of localization | 2 | 6 |
GO:0015693 | magnesium ion transport | 7 | 5 |
GO:0030001 | metal ion transport | 6 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 15 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 15 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 15 |
GO:0015095 | magnesium ion transmembrane transporter activity | 6 | 10 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 15 |
GO:0022857 | transmembrane transporter activity | 2 | 15 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 15 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 15 |
GO:0015562 | efflux transmembrane transporter activity | 3 | 1 |
GO:0046583 | monoatomic cation efflux transmembrane transporter activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.343 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.326 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.276 |
CLV_Separin_Metazoa | 171 | 175 | PF03568 | 0.525 |
DEG_APCC_DBOX_1 | 2 | 10 | PF00400 | 0.651 |
DEG_APCC_DBOX_1 | 70 | 78 | PF00400 | 0.483 |
DOC_CKS1_1 | 192 | 197 | PF01111 | 0.484 |
DOC_CKS1_1 | 269 | 274 | PF01111 | 0.593 |
DOC_PP2B_LxvP_1 | 230 | 233 | PF13499 | 0.512 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.581 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.738 |
LIG_14-3-3_CanoR_1 | 249 | 259 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 27 | 32 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 325 | 335 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.546 |
LIG_Actin_WH2_2 | 34 | 50 | PF00022 | 0.463 |
LIG_APCC_ABBA_1 | 287 | 292 | PF00400 | 0.593 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.522 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.484 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.485 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.642 |
LIG_DLG_GKlike_1 | 251 | 258 | PF00625 | 0.593 |
LIG_eIF4E_1 | 260 | 266 | PF01652 | 0.512 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.575 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.516 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.602 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.494 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.587 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.775 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.593 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.563 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.547 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 56 | 67 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 253 | 258 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 368 | 373 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.504 |
LIG_LYPXL_yS_3 | 370 | 373 | PF13949 | 0.322 |
LIG_PTB_Apo_2 | 116 | 123 | PF02174 | 0.583 |
LIG_PTB_Phospho_1 | 116 | 122 | PF10480 | 0.583 |
LIG_SH2_SRC | 109 | 112 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.556 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.613 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.564 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.512 |
LIG_SUMO_SIM_anti_2 | 225 | 232 | PF11976 | 0.496 |
LIG_SUMO_SIM_anti_2 | 341 | 347 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 154 | 160 | PF11976 | 0.506 |
LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.558 |
LIG_UBA3_1 | 157 | 164 | PF00899 | 0.567 |
LIG_UBA3_1 | 258 | 264 | PF00899 | 0.516 |
LIG_WRC_WIRS_1 | 252 | 257 | PF05994 | 0.564 |
MOD_CDK_SPxxK_3 | 268 | 275 | PF00069 | 0.564 |
MOD_CDK_SPxxK_3 | 63 | 70 | PF00069 | 0.516 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.456 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.634 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.531 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.613 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.495 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.440 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.524 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.387 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.295 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.400 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.405 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.752 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.483 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.534 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.517 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.652 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.532 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.550 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.646 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.419 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.448 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.784 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.532 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.494 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.594 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.485 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.510 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.349 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.457 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.512 |
MOD_PIKK_1 | 324 | 330 | PF00454 | 0.512 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.564 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.669 |
MOD_PKA_1 | 250 | 256 | PF00069 | 0.508 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.489 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.483 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.512 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.553 |
MOD_PKB_1 | 249 | 257 | PF00069 | 0.543 |
MOD_PKB_1 | 25 | 33 | PF00069 | 0.653 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.595 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.571 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.489 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.569 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.491 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.436 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.480 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.634 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.362 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.504 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.731 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.575 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.564 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.607 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.739 |
MOD_SUMO_rev_2 | 329 | 337 | PF00179 | 0.514 |
TRG_DiLeu_BaEn_1 | 226 | 231 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_3 | 68 | 74 | PF01217 | 0.595 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.284 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.692 |
TRG_Pf-PMV_PEXEL_1 | 165 | 170 | PF00026 | 0.316 |
TRG_Pf-PMV_PEXEL_1 | 264 | 268 | PF00026 | 0.319 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3I5 | Leptomonas seymouri | 73% | 100% |
A0A1X0NLW5 | Trypanosomatidae | 43% | 95% |
A0A1X0NUD3 | Trypanosomatidae | 30% | 100% |
A0A3Q8IND2 | Leishmania donovani | 94% | 100% |
A0A3R7KXL6 | Trypanosoma rangeli | 37% | 100% |
A0A3R7R8A9 | Trypanosoma rangeli | 44% | 97% |
A4HE45 | Leishmania braziliensis | 84% | 100% |
A4I1F1 | Leishmania infantum | 94% | 100% |
C9ZK17 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZK26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 96% |
C9ZXP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
Q4Q9Y4 | Leishmania major | 93% | 100% |
V5B7S4 | Trypanosoma cruzi | 42% | 100% |
V5D3L0 | Trypanosoma cruzi | 43% | 94% |