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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
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: A4HE45
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 7 |
GO:0006811 | monoatomic ion transport | 4 | 7 |
GO:0006812 | monoatomic cation transport | 5 | 7 |
GO:0015693 | magnesium ion transport | 7 | 6 |
GO:0030001 | metal ion transport | 6 | 6 |
GO:0051179 | localization | 1 | 7 |
GO:0051234 | establishment of localization | 2 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 17 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 17 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 17 |
GO:0015095 | magnesium ion transmembrane transporter activity | 6 | 11 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 17 |
GO:0022857 | transmembrane transporter activity | 2 | 17 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 17 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 17 |
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_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.409 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.334 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 165 | 167 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.280 |
CLV_Separin_Metazoa | 172 | 176 | PF03568 | 0.536 |
DEG_APCC_DBOX_1 | 70 | 78 | PF00400 | 0.480 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.596 |
DOC_CYCLIN_RxL_1 | 24 | 35 | PF00134 | 0.638 |
DOC_MAPK_MEF2A_6 | 175 | 183 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 297 | 305 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 25 | 32 | PF00149 | 0.626 |
DOC_PP2B_LxvP_1 | 231 | 234 | PF13499 | 0.511 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.580 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.726 |
LIG_14-3-3_CanoR_1 | 250 | 260 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 326 | 336 | PF00244 | 0.536 |
LIG_APCC_ABBA_1 | 288 | 293 | PF00400 | 0.596 |
LIG_BRCT_BRCA1_1 | 137 | 141 | PF00533 | 0.552 |
LIG_DLG_GKlike_1 | 252 | 259 | PF00625 | 0.596 |
LIG_eIF4E_1 | 261 | 267 | PF01652 | 0.511 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.583 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.571 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.565 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.482 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.592 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.756 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.603 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.596 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.563 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.542 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.549 |
LIG_LIR_Gen_1 | 57 | 67 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 254 | 259 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 57 | 62 | PF02991 | 0.521 |
LIG_SH2_SRC | 109 | 112 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.670 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.707 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.571 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.522 |
LIG_SUMO_SIM_anti_2 | 226 | 233 | PF11976 | 0.498 |
LIG_SUMO_SIM_anti_2 | 342 | 348 | PF11976 | 0.363 |
LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.566 |
LIG_UBA3_1 | 158 | 165 | PF00899 | 0.573 |
LIG_UBA3_1 | 259 | 265 | PF00899 | 0.510 |
LIG_UBA3_1 | 284 | 292 | PF00899 | 0.409 |
LIG_WRC_WIRS_1 | 253 | 258 | PF05994 | 0.571 |
MOD_CDK_SPxxK_3 | 269 | 276 | PF00069 | 0.571 |
MOD_CDK_SPxxK_3 | 63 | 70 | PF00069 | 0.510 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.529 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.527 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.639 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.498 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.494 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.603 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.519 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.297 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.426 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.486 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.711 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.466 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.505 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.524 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.677 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.553 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.545 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.422 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.493 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.783 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.504 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.556 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.556 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.690 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.489 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.544 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.506 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.369 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.273 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.451 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.472 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.522 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.420 |
MOD_PKA_1 | 251 | 257 | PF00069 | 0.512 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.486 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.481 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.531 |
MOD_PKB_1 | 250 | 258 | PF00069 | 0.552 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.553 |
MOD_Plk_2-3 | 127 | 133 | PF00069 | 0.543 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.497 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.771 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.482 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.481 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.651 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.370 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.521 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.580 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.571 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.597 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.730 |
MOD_SUMO_rev_2 | 330 | 338 | PF00179 | 0.525 |
TRG_DiLeu_BaEn_1 | 227 | 232 | PF01217 | 0.481 |
TRG_DiLeu_BaEn_3 | 68 | 74 | PF01217 | 0.597 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.671 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.780 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.712 |
TRG_Pf-PMV_PEXEL_1 | 166 | 171 | PF00026 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 265 | 269 | PF00026 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 56 | 61 | PF00026 | 0.335 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3I5 | Leptomonas seymouri | 73% | 100% |
A0A1X0NLW5 | Trypanosomatidae | 43% | 96% |
A0A1X0NLX5 | Trypanosomatidae | 37% | 100% |
A0A1X0NUD3 | Trypanosomatidae | 30% | 100% |
A0A3Q8IND2 | Leishmania donovani | 84% | 100% |
A0A3R7KXL6 | Trypanosoma rangeli | 37% | 100% |
A0A3R7R8A9 | Trypanosoma rangeli | 45% | 97% |
A0A3S5IQJ8 | Trypanosoma rangeli | 26% | 100% |
A4I1F1 | Leishmania infantum | 84% | 100% |
C9ZK17 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
C9ZK26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 97% |
C9ZWQ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 73% |
C9ZXP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AXI8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q9Y4 | Leishmania major | 84% | 100% |
V5B7S4 | Trypanosoma cruzi | 43% | 100% |
V5D3L0 | Trypanosoma cruzi | 45% | 95% |