Q9FWY7
SS
Gene name |
IMPA6 (At1g02690, T14P4.3) |
Protein name |
Importin subunit alpha-6 |
Names |
IMPa-6 |
Species |
Arabidopsis thaliana (Mouse-ear cress) |
KEGG Pathway |
ath:AT1G02690 |
EC number |
|
Protein Class |
|
Descriptions
Importin-α is a nuclear import receptor that facilitates the transport of proteins with nuclear localization sequences (NLSs) into the nucleus. It is autoinhibited by its N-terminal region, which occupies the NLS-binding site, preventing unnecessary binding and import activity. Importin-α is autoinhibited in the absence of importin-β and the binding of importin-β alleviates this autoinhibition, which displaces the autoinhibitory sequence.
Autoinhibitory domains (AIDs)
Target domain |
142-234 (Major NLS-binding site);310-399 (Minor NLS-binding site) |
Relief mechanism |
Partner binding |
Assay |
|
Accessory elements
No accessory elements
References
- Fontes MR et al. (2000) "Structural basis of recognition of monopartite and bipartite nuclear localization sequences by mammalian importin-alpha", Journal of molecular biology, 297, 1183-94
- Fontes MR et al. (2003) "Structural basis for the specificity of bipartite nuclear localization sequence binding by importin-alpha", The Journal of biological chemistry, 278, 27981-7
- Catimel B et al. (2001) "Biophysical characterization of interactions involving importin-alpha during nuclear import", The Journal of biological chemistry, 276, 34189-98
- Pumroy RA et al. (2015) "Molecular determinants for nuclear import of influenza A PB2 by importin α isoforms 3 and 7", Structure (London, England : 1993), 23, 374-84
Autoinhibited structure
Activated structure
1 structures for Q9FWY7
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q9FWY7-F1 | Predicted | AlphaFoldDB |
27 variants for Q9FWY7
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| ENSVATH04509509 | 20 | V>L | No | 1000Genomes | |
| ENSVATH04509510 | 53 | F>V | No | 1000Genomes | |
| ENSVATH04509511 | 71 | T>M | No | 1000Genomes | |
| tmp_1_584924_C_G | 96 | A>G | No | 1000Genomes | |
| ENSVATH00003074 | 123 | H>R | No | 1000Genomes | |
| ENSVATH01006574 | 130 | R>K | No | 1000Genomes | |
| tmp_1_585247_C_T | 141 | A>V | No | 1000Genomes | |
| tmp_1_585255_C_G | 144 | L>V | No | 1000Genomes | |
| tmp_1_585330_A_G | 169 | K>E | No | 1000Genomes | |
| ENSVATH13849959 | 172 | S>T | No | 1000Genomes | |
| ENSVATH04509543 | 206 | M>V | No | 1000Genomes | |
| tmp_1_585912_G_A | 288 | G>D | No | 1000Genomes | |
| ENSVATH10495193 | 318 | G>R | No | 1000Genomes | |
| ENSVATH00003081 | 329 | S>N | No | 1000Genomes | |
| tmp_1_586463_C_T | 376 | R>W | No | 1000Genomes | |
| tmp_1_586544_G_T | 403 | G>C | No | 1000Genomes | |
| tmp_1_586742_A_C | 441 | E>D | No | 1000Genomes | |
| ENSVATH13849964 | 461 | L>M | No | 1000Genomes | |
| tmp_1_586838_C_G | 473 | D>E | No | 1000Genomes | |
| ENSVATH00003083 | 507 | I>V | No | 1000Genomes | |
| ENSVATH00003084 | 508 | G>S | Plants were checked bi-weekly for presence of first buds and the average flowering time of 4 plants of the same accession were collected [10c and 16 hrs daylight] [EnsemblGenome] | No | 1000Genomes |
| ENSVATH04509553 | 518 | S>A | No | 1000Genomes | |
| ENSVATH10495270 | 518 | S>F | No | 1000Genomes | |
| tmp_1_586978_G_T | 520 | G>V | No | 1000Genomes | |
| ENSVATH00003085 | 528 | G>V | No | 1000Genomes | |
| tmp_1_587010_C_G | 531 | P>A | No | 1000Genomes | |
| ENSVATH04509555 | 535 | F>L | No | 1000Genomes |
No associated diseases with Q9FWY7
7 regional properties for Q9FWY7
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| repeat | Armadillo | 108 - 191 | IPR000225-1 |
| repeat | Armadillo | 193 - 234 | IPR000225-2 |
| repeat | Armadillo | 236 - 320 | IPR000225-3 |
| repeat | Armadillo | 319 - 402 | IPR000225-4 |
| repeat | Armadillo | 405 - 445 | IPR000225-5 |
| domain | Importin-alpha, importin-beta-binding domain | 1 - 97 | IPR002652 |
| repeat | Atypical Arm repeat | 460 - 506 | IPR032413 |
3 GO annotations of cellular component
| Name | Definition |
|---|---|
| cytoplasm | The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures. |
| nuclear envelope | The double lipid bilayer enclosing the nucleus and separating its contents from the rest of the cytoplasm; includes the intermembrane space, a gap of width 20-40 nm (also called the perinuclear space). |
| nucleus | A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent. |
2 GO annotations of molecular function
| Name | Definition |
|---|---|
| nuclear import signal receptor activity | Combining with a nuclear import signal (NIS) on a cargo to be transported, to mediate transport of the cargo through the nuclear pore, from the cytoplasm to the nuclear lumen. The cargo can be either a RNA or a protein. |
| nuclear localization sequence binding | Binding to a nuclear localization sequence, a specific peptide sequence that acts as a signal to localize the protein within the nucleus. |
1 GO annotations of biological process
| Name | Definition |
|---|---|
| NLS-bearing protein import into nucleus | The directed movement of a protein bearing a nuclear localization signal (NLS) from the cytoplasm into the nucleus, across the nuclear envelope. |
30 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| Q02821 | SRP1 | Importin subunit alpha | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) | SS |
| A2VE08 | KPNA1 | Importin subunit alpha-5 | Bos taurus (Bovine) | SS |
| C1JZ66 | KPNA7 | Importin subunit alpha-8 | Bos taurus (Bovine) | PR |
| Q0V7M0 | KPNA6 | Importin subunit alpha-7 | Bos taurus (Bovine) | SS |
| Q5ZML1 | KPNA1 | Importin subunit alpha-5 | Gallus gallus (Chicken) | SS |
| P52295 | Pen | Importin subunit alpha | Drosophila melanogaster (Fruit fly) | SS |
| A9QM74 | KPNA7 | Importin subunit alpha-8 | Homo sapiens (Human) | EV |
| O00505 | KPNA3 | Importin subunit alpha-4 | Homo sapiens (Human) | SS |
| O00629 | KPNA4 | Importin subunit alpha-3 | Homo sapiens (Human) | SS |
| O15131 | KPNA5 | Importin subunit alpha-6 | Homo sapiens (Human) | SS |
| O60684 | KPNA6 | Importin subunit alpha-7 | Homo sapiens (Human) | SS |
| P52292 | KPNA2 | Importin subunit alpha-1 | Homo sapiens (Human) | EV |
| P52294 | KPNA1 | Importin subunit alpha-5 | Homo sapiens (Human) | SS |
| P52293 | Kpna2 | Importin subunit alpha-1 | Mus musculus (Mouse) | EV |
| C0LLJ0 | Kpna7 | Importin subunit alpha-8 | Mus musculus (Mouse) | SS |
| O35343 | Kpna4 | Importin subunit alpha-3 | Mus musculus (Mouse) | SS |
| O35344 | Kpna3 | Importin subunit alpha-4 | Mus musculus (Mouse) | SS |
| O35345 | Kpna6 | Importin subunit alpha-7 | Mus musculus (Mouse) | PR |
| Q60960 | Kpna1 | Importin subunit alpha-5 | Mus musculus (Mouse) | SS |
| C6K7I2 | KPNA7 | Importin subunit alpha-8 | Sus scrofa (Pig) | SS |
| P83953 | Kpna1 | Importin subunit alpha-5 | Rattus norvegicus (Rat) | SS |
| Q56R16 | Kpna5 | Importin subunit alpha-6 | Rattus norvegicus (Rat) | SS |
| Q71VM4 | Os01g0253300 | Importin subunit alpha-1a | Oryza sativa subsp. japonica (Rice) | SS |
| P91276 | ima-2 | Importin subunit alpha-2 | Caenorhabditis elegans | SS |
| Q19969 | ima-3 | Importin subunit alpha-3 | Caenorhabditis elegans | SS |
| O04294 | IMPA3 | Importin subunit alpha-3 | Arabidopsis thaliana (Mouse-ear cress) | SS |
| Q9FJ09 | IMPA5 | Importin subunit alpha-5 | Arabidopsis thaliana (Mouse-ear cress) | SS |
| Q9M9X7 | IMPA7 | Importin subunit alpha-7 | Arabidopsis thaliana (Mouse-ear cress) | SS |
| O22478 | Importin subunit alpha | Solanum lycopersicum (Tomato) (Lycopersicon esculentum) | SS | |
| Q503E9 | kpna5 | Importin subunit alpha-6 | Danio rerio (Zebrafish) (Brachydanio rerio) | SS |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MSYKPSAKTE | VRRNRYKVSV | DADEGRRRRE | DNMVEIRKNK | REENLQKKRR | EGFNPSMASQ |
| 70 | 80 | 90 | 100 | 110 | 120 |
| PGQDFSSSLP | TETRLENIQQ | MIAGVMSEDR | DLQLEATASF | RRLLSIERNP | PINEVVQSGV |
| 130 | 140 | 150 | 160 | 170 | 180 |
| VPHIVQFLSR | DDFTQLQFEA | AWALTNIASG | TSENTRVIID | SGAVPLFVKL | LSSASEEVRE |
| 190 | 200 | 210 | 220 | 230 | 240 |
| QAVWALGNVA | GDSPKCRDHV | LSCEAMMSLL | AQFHEHSKLS | MLRNATWTLS | NFCRGKPQPA |
| 250 | 260 | 270 | 280 | 290 | 300 |
| FEQTKAALPA | LERLLHSTDE | EVLTDASWAL | SYLSDGTNEK | IQTVIDAGVI | PRLVQLLAHP |
| 310 | 320 | 330 | 340 | 350 | 360 |
| SPSVLIPALR | TIGNIVTGDD | IQTQAVISSQ | ALPGLLNLLK | NTYKKSIKKE | ACWTISNITA |
| 370 | 380 | 390 | 400 | 410 | 420 |
| GNTSQIQEVF | QAGIIRPLIN | LLEIGEFEIK | KEAVWAISNA | TSGGNHDQIK | FLVSQGCIRP |
| 430 | 440 | 450 | 460 | 470 | 480 |
| LCDLLPCPDP | RVVTVTLEGL | ENILKVGEAE | KNLGNTGNDN | LYAQMIEDAD | GLDKIENLQS |
| 490 | 500 | 510 | 520 | 530 | |
| HDNNEIYEKA | VKILESYWAA | DDEEEDIGGV | DAPENVQSSG | FQFGNQSGNA | PTGGFNFG |