Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| M0R2D3 | TUBB4A | Tubulin beta 4A class IVa | Homo sapiens (Human) | 340 aa |
Protein Details: M0R2D3 (TUBB4A)
Protein Information
| Accession | M0R2D3 |
|---|---|
| Protein Names | Tubulin beta 4A class IVa |
| Gene Symbol | TUBB4A |
| Organism | Homo sapiens (Human) |
| Length | 340 aa |
| Isoforms | No isoforms |
| Related PMIDs | 31251020 |
| Database Sources | CysModDB dbPTM SwissPalm |
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
Bubble Size: Positive Samples Count
Color Intensity: Positive Ratio
35
LNCaP cells
Specificity: 1.000
35/46 (76.1%)
0
Jurkat T cells
Specificity: 0.000
0/25 (0.0%)
0
U937 cells
Specificity: 0.000
0/1 (0.0%)
0
DU145 cells
Specificity: 0.000
0/2 (0.0%)
0
HeLa 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
1-501MREIVHLQAG11QCGNQIGAKF21WEVISDEHGI31DPTGTYHGDS41DLQLERINVY
51-10051YNEEFPDRIM61NTFSVVPSPK71VSDTVVEPYN81ATLSVHQLVE91NTDETYCIDN
101-150101EALYDICFRT111LKLTTPTYGD121LNHLVSATMS131GVTTCLRFPG141QLNADLRKLA
151-200151VNMVPFPRLH161FFMPGFAPLT171SRGSQQYRAL181TVPELTQQMF191DAKNMMAACD
201-250201PRHGRYLTVA211AVFRGRMSMK221EVDEQMLSVQ231SKNSSYFVEW241IPNNVKTAVC
251-300251DIPPRGLKMA261ATFIGNSTAI271QELFKRISEQ281FTAMFRRKAF291LHWYTGEGMD
301-340301EMEFTEAESN311MNDLVSEYQQ321YQDATAEEGE331FEEEAEEEVA
Palmitoylation Sites Details
| Position | Sources | Domains | Experimental PMIDs |
|---|---|---|---|
| 12 | Prediction (Low) | - | - |
| 107 | Prediction (Medium) | - | - |
| 135 | CYSMODDB SWISSPALM DBPTM Prediction (High) | - | - |
| 199 | Prediction (High) | - | - |
| 250 | Prediction (High) | - | - |
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 |
|---|---|---|---|---|---|
| 77 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 127 | C → C | 0.001887 | SNP | Silent | UCEC |
| 156 | R → C | 0.002020 | SNP | Missense Mutation | PRAD |
| 162 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 183 | Y → C | 0.002033 | SNP | Missense Mutation | LUSC |
| 213 | R → C | 0.001969 | SNP | Missense Mutation | HNSC |
| 251 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 251 | R → C | 0.001969 | SNP | Missense Mutation | LGG |
| 262 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 303 | C → C | 0.002545 | SNP | Silent | GBM |
| 309 | R → C | 0.002545 | SNP | Missense Mutation | GBM |
| 309 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 354 | C → C | 0.002506 | SNP | Silent | COAD |
| 354 | C → C | 0.003774 | SNP | Silent | UCEC |
| 380 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 391 | R → C | 0.002020 | SNP | Missense Mutation | PRAD |
| 391 | R → C | 0.002294 | SNP | Missense Mutation | OV |