Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| O00220 | TNFRSF10A; APO2; DR4; TRAILR1 | Tumor necrosis factor receptor superfamily … | Homo sapiens (Human) | 468 aa |
Protein Details: O00220 (TNFRSF10A)
Protein Information
| Accession | O00220 |
|---|---|
| Protein Names | Tumor necrosis factor receptor superfamily member 10A (Death receptor 4) (TNF-related apoptosis-inducing ligand receptor 1) (TRAIL receptor 1) (TRAIL-R1) (CD antigen CD261) |
| Gene Symbol | TNFRSF10A; APO2; DR4; TRAILR1 |
| Organism | Homo sapiens (Human) |
| Length | 468 aa |
| Isoforms | No isoforms |
| Related PMIDs | 19801377 29575903 31251020 |
| Database Sources | dbPTM SwissPalm |
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.897
Bubble Size: Positive Samples Count
Color Intensity: Positive Ratio
26
LNCaP cells
Specificity: 0.897
26/46 (56.5%)
2
DU145 cells
Specificity: 0.069
2/2 (100.0%)
1
HeLa cells
Specificity: 0.034
1/1 (100.0%)
0
Jurkat T cells
Specificity: 0.000
0/25 (0.0%)
0
U937 cells
Specificity: 0.000
0/1 (0.0%)
0
PC3 cells
Specificity: 0.000
0/4 (0.0%)
0
T cells
Specificity: 0.000
0/4 (0.0%)
0
HAP1 cells
Specificity: 0.000
0/10 (0.0%)
0
293T cells
Specificity: 0.000
0/10 (0.0%)
0
CEMx174 cells
Specificity: 0.000
0/3 (0.0%)
0
Endothelial cells
Specificity: 0.000
0/2 (0.0%)
0
Prefrontal cortex
Specificity: 0.000
0/1 (0.0%)
0
Cerebral cortex
Specificity: 0.000
0/4 (0.0%)
0
Liver membrane
Specificity: 0.000
0/1 (0.0%)
Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID).
The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples.
Bars are grouped by tissue/cell line for easy comparison.
Protein Sequence
Single Types:
Experimental Database High Prediction Medium Prediction Low Prediction
Experimental Database High Prediction Medium Prediction Low Prediction
Combined Types:
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
1-501MAPPPARVHL11GAFLAVTPNP21GSAASGTEAA31AATPSKVWGS41SAGRIEPRGG
51-10051GRGALPTSMG61QHGPSARARA71GRAPGPRPAR81EASPRLRVHK91TFKFVVVGVL
101-150101LQVVPSSAAT111IKLHDQSIGT121QQWEHSPLGE131LCPPGSHRSE141HPGACNRCTE
151-200151GVGYTNASNN161LFACLPCTAC171KSDEEERSPC181TTTRNTACQC191KPGTFRNDNS
201-250201AEMCRKCSRG211CPRGMVKVKD221CTPWSDIECV231HKESGNGHNI241WVILVVTLVV
251-300251PLLLVAVLIV261CCCIGSGCGG271DPKCMDRVCF281WRLGLLRGPG291AEDNAHNEIL
301-350301SNADSLSTFV311SEQQMESQEP321ADLTGVTVQS331PGEAQCLLGP341AEAEGSQRRR
351-400351LLVPANGADP361TETLMLFFDK371FANIVPFDSW381DQLMRQLDLT391KNEIDVVRAG
401-450401TAGPGDALYA411MLMKWVNKTG421RNASIHTLLD431ALERMEERHA441REKIQDLLVD
451-468451SGKFIYLEDG461TGSAVSLE
Palmitoylation Sites Details
| Position | Sources | Domains | Experimental PMIDs |
|---|---|---|---|
| 167 | Prediction (Low) | - | - |
| 188 | Prediction (Medium) | - | - |
| 190 | Prediction (Low) | - | - |
| 211 | Prediction (Medium) | - | - |
| 261 | DBPTM SWISSPALM Prediction (High) | - | - |
| 262 | DBPTM SWISSPALM Prediction (High) | - | - |
| 263 | DBPTM SWISSPALM Prediction (High) | - | - |
| 268 | Prediction (Medium) | - | - |
| 274 | Prediction (Low) | - | - |
| 279 | Prediction (Medium) | - | - |
Conservation Scores
PhyloP
PhastCons
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 |
|---|---|---|---|---|---|
| 132 | C → F | 0.002294 | SNP | Missense Mutation | OV |
| 136 | S → C | 0.002545 | SNP | Missense Mutation | GBM |
| 164 | C → Y | 0.001887 | SNP | Missense Mutation | UCEC |
| 180 | C → Afs*63 | 0.002545 | DEL | Frame Shift Del | GBM |
| 190 | C → W | 0.002294 | SNP | Missense Mutation | OV |
| 267 | G → C | 0.002506 | SNP | Missense Mutation | COAD |