Q9UT18
Gene name |
thi9 (SPAC9.10) |
Protein name |
Thiamine transporter thi9 |
Names |
|
Species |
Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) |
KEGG Pathway |
spo:SPAC9.10 |
EC number |
|
Protein Class |
|
Descriptions
The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.
Autoinhibitory domains (AIDs)
Target domain |
|
Relief mechanism |
|
Assay |
cis-regPred |
Accessory elements
No accessory elements
Autoinhibited structure
Activated structure
1 structures for Q9UT18
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q9UT18-F1 | Predicted | AlphaFoldDB |
8 variants for Q9UT18
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| I_1482918_C_T | 29 | P>S | No | Jeffares_SNPs | |
| I_1482924_C_T | 31 | L>F | No | Jeffares_SNPs | |
| I_1482942_G_A | 37 | D>N | No | Jeffares_SNPs | |
| I_1483008_A_C | 59 | N>H | No | Jeffares_SNPs | |
| I_1483366_T_C | 178 | I>T | No | Jeffares_SNPs | |
| I_1483489_T_C | 219 | V>A | No | Jeffares_SNPs | |
| I_1483491_T_C | 220 | F>L | No | Jeffares_SNPs | |
| I_1484037_G_A | 402 | V>I | No | Jeffares_SNPs |
No associated diseases with Q9UT18
No regional properties for Q9UT18
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| No domain, repeats, and functional sites for Q9UT18 | |||
6 GO annotations of cellular component
| Name | Definition |
|---|---|
| endoplasmic reticulum | The irregular network of unit membranes, visible only by electron microscopy, that occurs in the cytoplasm of many eukaryotic cells. The membranes form a complex meshwork of tubular channels, which are often expanded into slitlike cavities called cisternae. The ER takes two forms, rough (or granular), with ribosomes adhering to the outer surface, and smooth (with no ribosomes attached). |
| endoplasmic reticulum membrane | The lipid bilayer surrounding the endoplasmic reticulum. |
| integral component of membrane | The component of a membrane consisting of the gene products and protein complexes having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane. |
| medial membrane band | A sterol-rich region of the plasma membrane which forms at the cell surface overlying the contractile ring and spreads into the invaginating plasma membrane surrounding the septum. |
| plasma membrane | The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins. |
| plasma membrane of cell tip | The portion of the plasma membrane surrounding the cell tip. |
1 GO annotations of molecular function
| Name | Definition |
|---|---|
| high-affinity thiamine:proton symporter activity | Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: thiamine(out) + H+(out) = thiamine(in) + H+(in). In high-affinity transport the transporter is able to bind the solute even if it is only present at very low concentrations. |
2 GO annotations of biological process
| Name | Definition |
|---|---|
| amino acid transport | The directed movement of amino acids, organic acids containing one or more amino substituents, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. |
| thiamine import across plasma membrane | The directed movement of thiamine from outside of a cell, across the plasma membrane and into the cytosol. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MPSSQISHQD | PELGQTSSGS | SSIKEKAEPQ | LYAGPIDPAR | RPDVFQEGFE | DVSVTDDDND |
| 70 | 80 | 90 | 100 | 110 | 120 |
| NELLRKMGYQ | PVLHRSFEFF | ESFAASFASL | DVVSGVRLTF | SWGISFGGPA | AYWSAMLVTG |
| 130 | 140 | 150 | 160 | 170 | 180 |
| FCSIVTAACL | AEICSALPAA | GSIYLWAAES | AGPRFGRFVS | FLVAWWSTTA | WTTFVASITQ |
| 190 | 200 | 210 | 220 | 230 | 240 |
| STANFIFAEV | STFNNPWPTN | DSDVKFRAVQ | WIVAEVLLVF | TILLNQVPPR | YYKWIFKASM |
| 250 | 260 | 270 | 280 | 290 | 300 |
| LLMFIDYVMN | IIWVPVATSK | KPDGFRSAKW | VFTETIYDQA | GYIKEVDDAN | GNPIASLSKI |
| 310 | 320 | 330 | 340 | 350 | 360 |
| VPKGWQWCLS | YFATAGVIVG | YDASGHIAEE | TKDASIKAAR | GIFYSTVTSF | IVAFSLAILY |
| 370 | 380 | 390 | 400 | 410 | 420 |
| LFCCPDLDTF | TAILYNDNSP | QPFVNFYSYL | LGRGGHVVMN | VVIILEIFLN | GVVSVLACSR |
| 430 | 440 | 450 | 460 | 470 | 480 |
| LVFAVSRDGV | LPFSNWISQV | SKTGQPKNAI | TVIYIVSALL | LCTILPSAVA | FTSLVSAAGA |
| 490 | 500 | 510 | 520 | 530 | 540 |
| PSFAAYAVLA | FCRLFITRDK | FPKGRWSLGW | LSKPCLVITL | VYNLFALVVN | VSPYTYPVTG |
| 550 | 560 | 570 | 580 | 590 | |
| PSFNYAVVIM | GGVSIFAIIC | TIVIPKSRWV | ANRYRYESDS | EHSASVKELK | V |