Q9R155
Gene name |
Slc26a4 (Pds) |
Protein name |
Pendrin |
Names |
Sodium-independent chloride/iodide transporter, Solute carrier family 26 member 4 |
Species |
Mus musculus (Mouse) |
KEGG Pathway |
mmu:23985 |
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
11 structures for Q9R155
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| 7WK1 | EM | 325 A | A/B | 1-780 | PDB |
| 7WK7 | EM | 349 A | A/B | 1-780 | PDB |
| 7WL2 | EM | 325 A | A/B | 1-780 | PDB |
| 7WL7 | EM | 351 A | A/B | 1-780 | PDB |
| 7WL8 | EM | 340 A | A/B | 1-780 | PDB |
| 7WL9 | EM | 378 A | A/B | 1-780 | PDB |
| 7WLA | EM | 376 A | A/B | 1-780 | PDB |
| 7WLB | EM | 410 A | A/B | 1-780 | PDB |
| 7WLE | EM | 362 A | A/B | 1-780 | PDB |
| 8HZN | EM | 325 A | A/B | 1-780 | PDB |
| AF-Q9R155-F1 | Predicted | AlphaFoldDB |
27 variants for Q9R155
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| rs264545196 | 65 | V>I | No | EVA | |
| rs3389243177 | 123 | P>L | No | EVA | |
| rs251373153 | 168 | G>R | No | EVA | |
| rs3389204166 | 226 | A>V | No | EVA | |
| rs107752849 | 264 | I>V | No | EVA | |
| rs3389235228 | 273 | I>V | No | EVA | |
| rs3389237822 | 292 | F>I | No | EVA | |
| rs3403238383 | 326 | G>S | No | EVA | |
| rs3389222232 | 334 | G>E | No | EVA | |
| rs3389210682 | 347 | S>T | No | EVA | |
| rs3389250127 | 350 | L>* | No | EVA | |
| rs3389250132 | 370 | V>L | No | EVA | |
| rs37181502 | 422 | V>M | No | EVA | |
| rs3389245941 | 488 | M>V | No | EVA | |
| rs3389229027 | 578 | Y>* | No | EVA | |
| rs226477703 | 608 | I>V | No | EVA | |
| rs3389228974 | 615 | F>I | No | EVA | |
| rs3389231108 | 615 | F>L | No | EVA | |
| rs3389210648 | 634 | I>N | No | EVA | |
| rs3389167551 | 669 | D>Y | No | EVA | |
| rs3389222245 | 736 | R>I | No | EVA | |
| rs217848809 | 738 | G>S | No | EVA | |
| rs3389233867 | 749 | I>E | No | EVA | |
| rs3389235196 | 750 | R>W | No | EVA | |
| rs36982362 | 766 | E>G | No | EVA | |
| rs3389210658 | 767 | E>* | No | EVA | |
| rs3389210658 | 767 | E>K | No | EVA |
No associated diseases with Q9R155
1 regional properties for Q9R155
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | Alpha crystallin/Hsp20 domain | 67 - 180 | IPR002068 |
Functions
5 GO annotations of cellular component
| Name | Definition |
|---|---|
| apical plasma membrane | The region of the plasma membrane located at the apical end of the cell. |
| brush border membrane | The portion of the plasma membrane surrounding the brush border. |
| extracellular exosome | A vesicle that is released into the extracellular region by fusion of the limiting endosomal membrane of a multivesicular body with the plasma membrane. Extracellular exosomes, also simply called exosomes, have a diameter of about 40-100 nm. |
| integral component of plasma membrane | The component of the plasma 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. |
| membrane | A lipid bilayer along with all the proteins and protein complexes embedded in it an attached to it. |
7 GO annotations of molecular function
| Name | Definition |
|---|---|
| anion transmembrane transporter activity | Enables the transfer of a negatively charged ion from one side of a membrane to the other. |
| bicarbonate transmembrane transporter activity | Enables the transfer of bicarbonate from one side of a membrane to the other. Bicarbonate is the hydrogencarbonate ion, HCO3-. |
| chloride transmembrane transporter activity | Enables the transfer of chloride ions from one side of a membrane to the other. |
| iodide transmembrane transporter activity | Enables the transfer of iodide ions from one side of a membrane to the other. |
| oxalate transmembrane transporter activity | Enables the transfer of oxalate from one side of a membrane to the other. Oxalate, or ethanedioic acid, occurs in many plants and is highly toxic to animals. |
| secondary active sulfate transmembrane transporter activity | Enables the secondary active transfer of sulfate from one side of a membrane to the other. Secondary active transport is the transfer of a solute across a membrane, up its concentration gradient. The transporter binds the solute and undergoes a series of conformational changes. Transport works equally well in either direction and is driven by a chemiosmotic source of energy. Secondary active transporters include symporters and antiporters. |
| sulfate transmembrane transporter activity | Enables the transfer of sulfate ions, SO4(2-), from one side of a membrane to the other. |
4 GO annotations of biological process
| Name | Definition |
|---|---|
| animal organ morphogenesis | Morphogenesis of an animal organ. An organ is defined as a tissue or set of tissues that work together to perform a specific function or functions. Morphogenesis is the process in which anatomical structures are generated and organized. Organs are commonly observed as visibly distinct structures, but may also exist as loosely associated clusters of cells that work together to perform a specific function or functions. |
| inorganic anion transport | The directed movement of inorganic anions into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Inorganic anions are atoms or small molecules with a negative charge which do not contain carbon in covalent linkage. |
| regulation of pH | Any process involved in the maintenance of an internal equilibrium of hydrogen ions, thereby modulating the internal pH, within an organism or cell. |
| regulation of protein localization | Any process that modulates the frequency, rate or extent of any process in which a protein is transported to, or maintained in, a specific location. |
15 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| A6QNW6 | SLC26A8 | Testis anion transporter 1 | Bos taurus (Bovine) | PR |
| P50443 | SLC26A2 | Sulfate transporter | Homo sapiens (Human) | PR |
| P58743 | SLC26A5 | Prestin | Homo sapiens (Human) | PR |
| Q8TE54 | SLC26A7 | Anion exchange transporter | Homo sapiens (Human) | PR |
| Q86WA9 | SLC26A11 | Sodium-independent sulfate anion transporter | Homo sapiens (Human) | PR |
| Q96RN1 | SLC26A8 | Testis anion transporter 1 | Homo sapiens (Human) | PR |
| Q99NH7 | Slc26a5 | Prestin | Mus musculus (Mouse) | PR |
| Q9WVC8 | Slc26a3 | Chloride anion exchanger | Mus musculus (Mouse) | PR |
| Q8R0C3 | Slc26a8 | Testis anion transporter 1 | Mus musculus (Mouse) | PR |
| Q924C9 | Slc26a3 | Chloride anion exchanger | Rattus norvegicus (Rat) | PR |
| Q9EPH0 | Slc26a5 | Prestin | Rattus norvegicus (Rat) | PR |
| Q02920 | Early nodulin-70 | Glycine max (Soybean) (Glycine hispida) | PR | |
| Q9FY46 | SULTR4;1 | Sulfate transporter 4.1, chloroplastic | Arabidopsis thaliana (Mouse-ear cress) | PR |
| Q9SV13 | SULTR3;1 | Sulfate transporter 3.1 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| Q8GYH8 | SULTR4;2 | Probable sulfate transporter 4.2 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MAARGGRSEP | PQLAEYSCSY | TVSRPVYSEL | AFQQQRERRL | PERRTLRDSL | ARSCSCSRKR |
| 70 | 80 | 90 | 100 | 110 | 120 |
| AFGVVKTLLP | ILDWLPKYRV | KEWLLSDIIS | GVSTGLVGTL | QGMAYALLAA | VPVQFGLYSA |
| 130 | 140 | 150 | 160 | 170 | 180 |
| FFPILTYFVF | GTSRHISVGP | FPVVSLMVGS | VVLSMAPDDH | FLVPSGNGSA | LNSTTLDTGT |
| 190 | 200 | 210 | 220 | 230 | 240 |
| RDAARVLLAS | TLTLLVGIIQ | LVFGGLQIGF | IVRYLADPLV | GGFTTAAAFQ | VLVSQLKIVL |
| 250 | 260 | 270 | 280 | 290 | 300 |
| NVSTKNYNGI | LSIIYTLIEI | FQNIGDTNIA | DFIAGLLTII | VCMAVKELND | RFKHRIPVPI |
| 310 | 320 | 330 | 340 | 350 | 360 |
| PIEVIVTIIA | TAISYGANLE | KNYNAGIVKS | IPSGFLPPVL | PSVGLFSDML | AASFSIAVVA |
| 370 | 380 | 390 | 400 | 410 | 420 |
| YAIAVSVGKV | YATKHDYVID | GNQEFIAFGI | SNVFSGFFSC | FVATTALSRT | AVQESTGGKT |
| 430 | 440 | 450 | 460 | 470 | 480 |
| QVAGLISAVI | VMVAIVALGR | LLEPLQKSVL | AAVVIANLKG | MFMQVCDVPR | LWKQNKTDAV |
| 490 | 500 | 510 | 520 | 530 | 540 |
| IWVFTCIMSI | ILGLDLGLLA | GLLFALLTVV | LRVQFPSWNG | LGSVPSTDIY | KSITHYKNLE |
| 550 | 560 | 570 | 580 | 590 | 600 |
| EPEGVKILRF | SSPIFYGNVD | GFKKCINSTV | GFDAIRVYNK | RLKALRRIQK | LIKKGQLRAT |
| 610 | 620 | 630 | 640 | 650 | 660 |
| KNGIISDIGS | SNNAFEPDED | VEEPEELNIP | TKEIEIQVDW | NSELPVKVNV | PKVPIHSLVL |
| 670 | 680 | 690 | 700 | 710 | 720 |
| DCGAVSFLDV | VGVRSLRMIV | KEFQRIDVNV | YFALLQDDVL | EKMEQCGFFD | DNIRKDRFFL |
| 730 | 740 | 750 | 760 | 770 | |
| TVHDAILHLQ | NQVKSREGQD | SLLETVARIR | DCKDPLDLME | AEMNAEELDV | QDEAMRRLAS |