Q9USN1
Gene name |
snx12 (SPCC16A11.04) |
Protein name |
Sorting nexin-12 |
Names |
|
Species |
Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) |
KEGG Pathway |
spo:SPCC16A11.04 |
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 Q9USN1
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q9USN1-F1 | Predicted | AlphaFoldDB |
No variants for Q9USN1
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for Q9USN1 | |||||
No associated diseases with Q9USN1
5 GO annotations of cellular component
| Name | Definition |
|---|---|
| endoplasmic reticulum-vacuole membrane contact site | A zone of apposition between endoplasmic-reticulum and lytic vacuole membranes, structured by bridging complexes. |
| 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. |
| intracellular membrane-bounded organelle | Organized structure of distinctive morphology and function, bounded by a single or double lipid bilayer membrane and occurring within the cell. Includes the nucleus, mitochondria, plastids, vacuoles, and vesicles. Excludes the plasma membrane. |
| nucleus-vacuole junction | An organelle membrane contact site formed between the vacuole membrane and the outer nuclear membrane. In S. cerevisiae these contacts are mediated through direct physical interaction between Vac8p and Nvj1p. |
| vacuole | A closed structure, found only in eukaryotic cells, that is completely surrounded by unit membrane and contains liquid material. Cells contain one or several vacuoles, that may have different functions from each other. Vacuoles have a diverse array of functions. They can act as a storage organelle for nutrients or waste products, as a degradative compartment, as a cost-effective way of increasing cell size, and as a homeostatic regulator controlling both turgor pressure and pH of the cytosol. |
1 GO annotations of molecular function
| Name | Definition |
|---|---|
| phosphatidylinositol binding | Binding to an inositol-containing glycerophospholipid, i.e. phosphatidylinositol (PtdIns) and its phosphorylated derivatives. |
2 GO annotations of biological process
| Name | Definition |
|---|---|
| protein transport | The directed movement of proteins into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. |
| vacuole-ER tethering | The attachment of a lytic vacuole to the endoplasmic reticulum, which may facilitate exchange of metabolites between the organelles. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MYQQHIFYFI | TGGIFILWIL | AHSFFVKIIY | LWASGCLLWY | CLETRTFENK | NNLGTSEPFL |
| 70 | 80 | 90 | 100 | 110 | 120 |
| VNPAIFQKRA | RQLALSKLLL | RQPLYPGIPE | ISEEIESIIS | HFMQKYIKVW | SYQIIPEPTI |
| 130 | 140 | 150 | 160 | 170 | 180 |
| SNSIESHLRK | CLMVLLSRVD | EIDLADVLVK | TVLPLITKHL | RLFVEAEQLV | VGNKAVSFTD |
| 190 | 200 | 210 | 220 | 230 | 240 |
| HSELSREVAA | KYDHGRLHEA | VLLSGNPMVA | QKRYLRNWTT | QVLSIILPNY | YETSPLVLSL |
| 250 | 260 | 270 | 280 | 290 | 300 |
| VTEVIINTTL | LPLVSYISDP | DFFNYLIIQA | SGSIIQRRRK | IRRLKRAIRK | QSNHFQVGAR |
| 310 | 320 | 330 | 340 | 350 | 360 |
| RLRLKDSQHS | FEQYIHEIKK | ISNISDARRL | RSELMVQRRQ | LEQTEAFDFE | FKQYRERLQI |
| 370 | 380 | 390 | 400 | 410 | 420 |
| AIITAEKRIS | LLSGTPFQHK | EAVLFEQVQS | LLQILSDSAA | VSCFLEFMER | KNRSRYLHFW |
| 430 | 440 | 450 | 460 | 470 | 480 |
| LVVEGLKESQ | DDPLNAHMIA | PFSDIVSDHT | DFTAIVKSYF | ESVDNPLDIP | KPLTNTINKF |
| 490 | 500 | 510 | 520 | 530 | 540 |
| VNQSKDNLNP | DLWVEARNAM | LMAQEHVFDI | MQNSDYSEFV | NSEIYYRFLA | QDVVSDHKST |
| 550 | 560 | 570 | 580 | 590 | 600 |
| NSSATFSRLE | ELGENIPAIS | KQPSYLSISS | SSKSINSSPS | PSIQLSVSSS | ISRDKNLSPL |
| 610 | 620 | 630 | 640 | 650 | 660 |
| DLELDDPTYS | DEEEVLFAPP | GDLQLSESID | ELNNNIEELK | AQLNAINTLI | KKAELVADQK |
| 670 | 680 | 690 | 700 | 710 | 720 |
| QLKSLTKNHQ | EIEKAIHRKE | RQRDQYMSQE | EDSKLFNRSR | VSIDSFKISK | EENTPDFAVY |
| 730 | 740 | 750 | 760 | 770 | 780 |
| TIRIERLENG | HVRSGWMVAR | RYREFAELHK | QLKQTYPGVR | SLKFPQKSII | TSLNKNVLEY |
| 790 | 800 | 810 | 820 | 830 | 840 |
| RRGALEEYLQ | SLFRMPEVCD | SKMLRMFLSQ | QNITAPQMFN | PKEVGKKWKQ | LLEVLGFEVN |
| 850 | 860 | 870 | 880 | 890 | 900 |
| NSFNASNVNT | NSSFSGPISE | FLVELFSPND | DAKQQWLPKK | TYISILEQLF | GGALEKRIRL |
| 910 | 920 | 930 | 940 | 950 | 960 |
| QLFQLFTPEK | IYRKLREFRR | GLEGKSNHDH | SKDRRHSRAR | KPAYADRNQL | KAEAGILLAS |
| 970 | 980 | 990 | 1000 | ||
| MFPGYTPDIA | VKRIFRILQN | QSLNAHVIYT | LLDEILLALK | KHARSTNKAT |