Q9FMF7
Gene name |
DIT2-1 (DIT2, At5g64290, MSJ1.13) |
Protein name |
Dicarboxylate transporter 2.1, chloroplastic |
Names |
AtpDCT1, Glutamate/malate translocator |
Species |
Arabidopsis thaliana (Mouse-ear cress) |
KEGG Pathway |
ath:AT5G64290 |
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 Q9FMF7
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q9FMF7-F1 | Predicted | AlphaFoldDB |
21 variants for Q9FMF7
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| tmp_5_25716539_G_T | 35 | T>N | No | 1000Genomes | |
| ENSVATH12925755 | 35 | T>P | No | 1000Genomes | |
| ENSVATH00750827 | 62 | I>T | No | 1000Genomes | |
| tmp_5_25716415_G_T | 76 | N>K | No | 1000Genomes | |
| ENSVATH07477120 | 84 | S>F | No | 1000Genomes | |
| tmp_5_25716375_A_C | 90 | S>A | No | 1000Genomes | |
| tmp_5_25716372_G_A | 91 | P>S | No | 1000Genomes | |
| tmp_5_25716174_C_T | 157 | V>I | No | 1000Genomes | |
| ENSVATH14647706 | 162 | S>P | No | 1000Genomes | |
| ENSVATH03473172 | 256 | S>F | No | 1000Genomes | |
| tmp_5_25715877_A_G | 256 | S>P | No | 1000Genomes | |
| tmp_5_25715413_T_A | 317 | I>F | No | 1000Genomes | |
| tmp_5_25715146_C_G | 377 | E>D | No | 1000Genomes | |
| tmp_5_25715148_C_G | 377 | E>Q | No | 1000Genomes | |
| tmp_5_25715087_A_T | 397 | L>Q | No | 1000Genomes | |
| tmp_5_25714992_T_C | 429 | T>A | No | 1000Genomes | |
| ENSVATH00750806 | 437 | M>I | No | 1000Genomes | |
| tmp_5_25714910_A_C | 456 | F>C | No | 1000Genomes | |
| tmp_5_25714763_T_C | 505 | N>S | No | 1000Genomes | |
| ENSVATH07477110 | 555 | F>Y | No | 1000Genomes | |
| ENSVATH12925690 | 559 | F>C | No | 1000Genomes |
No associated diseases with Q9FMF7
No regional properties for Q9FMF7
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| No domain, repeats, and functional sites for Q9FMF7 | |||
6 GO annotations of cellular component
| Name | Definition |
|---|---|
| chloroplast | A chlorophyll-containing plastid with thylakoids organized into grana and frets, or stroma thylakoids, and embedded in a stroma. |
| chloroplast envelope | The double lipid bilayer enclosing the chloroplast and separating its contents from the rest of the cytoplasm; includes the intermembrane space. |
| chloroplast inner membrane | The inner, i.e. lumen-facing, lipid bilayer of the chloroplast envelope; also faces the chloroplast stroma. |
| chloroplast thylakoid | Sac-like membranous structures (cisternae) in a chloroplast combined into stacks (grana) and present singly in the stroma (stroma thylakoids or frets) as interconnections between grana. An example of this component is found in Arabidopsis thaliana. |
| 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. |
| plastid | Any member of a family of organelles found in the cytoplasm of plants and some protists, which are membrane-bounded and contain DNA. Plant plastids develop from a common type, the proplastid. |
3 GO annotations of molecular function
| Name | Definition |
|---|---|
| L-glutamate transmembrane transporter activity | Enables the transfer of L-glutamate from one side of a membrane to the other. L-glutamate is the anion of 2-aminopentanedioic acid. |
| malate transmembrane transporter activity | Enables the transfer of malate from one side of a membrane to the other. Malate is a chiral hydroxydicarboxylic acid, hydroxybutanedioic acid. The (+) enantiomer is an important intermediate in metabolism as a component of both the TCA cycle and the glyoxylate cycle. |
| oxaloacetate transmembrane transporter activity | Enables the transfer of oxaloacetate, the anion of oxobutanedioic acid, from one side of a membrane to the other. |
5 GO annotations of biological process
| Name | Definition |
|---|---|
| ammonia assimilation cycle | The pathway by which ammonia is processed and incorporated into a cell. In an energy-rich (glucose-containing), nitrogen-poor environment, glutamine synthetase and glutamate synthase form an ammonia assimilatory cycle, in which ammonia is incorporated into L-glutamate to form L-glutamine, which then combines with alpha-ketoglutarate to regenerate L-glutamate. This ATP-dependent cycle is essential for nitrogen-limited growth and for steady-state growth with some sources of nitrogen. |
| L-glutamate transmembrane transport | The directed movement of L-glutamate across a membrane. |
| malate transmembrane transport | A process in which a malate ion is transported across a membrane. |
| oxaloacetate transport | The directed movement of oxaloacetate, the anion of oxobutanedioic acid, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. |
| response to nematode | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus from a nematode. |
1 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| Q9FMF8 | DIT2-2 | Dicarboxylate transporter 2.2, chloroplastic | Arabidopsis thaliana (Mouse-ear cress) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MESFALHSLS | TTATSTLLSH | HHHHHPSRLS | LLRRTSSRSP | PSTISLRSLS | VQPLSFPLLK |
| 70 | 80 | 90 | 100 | 110 | 120 |
| PIPRFSTRIA | AAPQDNAPPP | PPPSPSPSPS | PQGAKLIPLI | LSISVGLILR | FAVPVPEGVT |
| 130 | 140 | 150 | 160 | 170 | 180 |
| PQGWQLLSIF | LSTIAGLVLS | PLPVGAWAFI | GLTASIVTKT | LSFSAAFSAF | TSEVIWLIVI |
| 190 | 200 | 210 | 220 | 230 | 240 |
| SFFFARGFVK | TGLGDRIATY | FVKWLGKSTL | GLSYGLTLSE | ALIAPAMPST | TARAGGIFLP |
| 250 | 260 | 270 | 280 | 290 | 300 |
| IIKSLSLSAG | SKPNDSSSRK | LGSYLIQSQF | QCAGNSSALF | LTAAAQNLLC | LKLAEELGVV |
| 310 | 320 | 330 | 340 | 350 | 360 |
| ISNPWVSWFK | AASLPAIISL | LCTPLILYKL | YPPETKDTPE | APGIAATKLK | QMGPVTKNEW |
| 370 | 380 | 390 | 400 | 410 | 420 |
| IMVGTMLLAV | TLWICGETLG | IPSVVAAMIG | LSILLVLGVL | NWDDCLSEKS | AWDTLAWFAV |
| 430 | 440 | 450 | 460 | 470 | 480 |
| LVGMAGQLTN | LGVVTWMSDC | VAKVLQSLSL | SWPAAFGLLQ | AAYFFIHYLF | ASQTGHVGAL |
| 490 | 500 | 510 | 520 | 530 | 540 |
| FSAFLAMHIA | AGVPGILAAL | ALAYNTNLFG | ALTHYSSGQA | AVYYGAGYVD | LPDVFKIGFV |
| 550 | 560 | ||||
| MATINAIIWG | VVGTFWWKFL | GLY |