Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| Q9NWB6 | ARGLU1 | Arginine and glutamate-rich protein 1 | Homo sapiens (Human) | 273 aa |
Protein Details: Q9NWB6 (ARGLU1)
Protein Information
| Accession | Q9NWB6 |
|---|---|
| Protein Names | Arginine and glutamate-rich protein 1 |
| Gene Symbol | ARGLU1 |
| Organism | Homo sapiens (Human) |
| Length | 273 aa |
| Isoforms | No isoforms |
| Related PMIDs | 31382980 |
| Database Sources | SwissPalm |
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
Experimental Database High Prediction Non-palmitylated Cys
1-501MGRSRSRSSS11RSKHTKSSKH21NKKRSRSRSR31SRDKERVRKR41SKSRESKRNR
51-10051RRESRSRSRS61TNTAVSRRER71DRERASSPPD81RIDIFGRTVS91KRSSLDEKQK
101-150101REEEEKKAEF111ERQRKIRQQE121IEEKLIEEET131ARRVEELVAK141RVEEELEKRK
151-200151DEIEREVLRR161VEEAKRIMEK171QLLEELERQR181QAELAAQKAR191EEEERAKREE
201-250201LERILEENNR211KIAEAQAKLA221EEQLRIVEEQ231RKIHEERMKL241EQERQRQQKE
251-273251EQKIILGKGK261SRPKLSFSLK271TQD
Palmitoylation Sites Details
No known palmitoylation sites
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
1
U937 cell
Specificity: 1.000
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.000Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID).
Blue bars: Literature data, Orange bars: Mass Spectrometry data.
The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples.
TCGA Cysteine Mutation Information
Note: Mutations indicate amino acid changes that may create potential palmitoylation sites.
| Position | Amino Acid Change | Frequency | Type | Function | Cancer Type |
|---|---|---|---|---|---|
| 166 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 195 | R → C | 0.001764 | SNP | Missense Mutation | LUAD |