Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| K7EQQ5 | ATP9B | ATPase phospholipid transporting 9B (putative) | Homo sapiens (Human) | 200 aa |
Protein Details: K7EQQ5 (ATP9B)
Protein Information
| Accession | K7EQQ5 |
|---|---|
| Protein Names | ATPase phospholipid transporting 9B (putative) |
| Gene Symbol | ATP9B |
| Organism | Homo sapiens (Human) |
| Length | 200 aa |
| Isoforms | No isoforms |
| Related PMIDs | 29575903 31251020 |
| Database Sources | No database sources |
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.973
Bubble Size: Positive Samples Count
Color Intensity: Positive Ratio
36
LNCaP cells
Specificity: 0.973
36/46 (78.3%)
1
HeLa cells
Specificity: 0.027
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
DU145 cells
Specificity: 0.000
0/2 (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
1-501LVISGDSLEV11CLKYYEHEFV21ELACQCPAVV31CCRCSPTQKA41RIVTLLQQHT
51-10051GRRTCAIGDG61GNDVSMIQAA71DCGIGIEGKE81GKQASLAADF91SITQFRHIGR
101-150101LLMVHGRNSY111KRSAALGQFV121MHRGLIISTM131QVCHHIHHVP141SVLLSAGPGR
151-200151EARDGDALPG161AVQGPHQGKI171LVLQNLPHLG181FNKYLPRRHP191HVWGPGALRV
Palmitoylation Sites Details
| Position | Sources | Domains | Experimental PMIDs |
|---|---|---|---|
| 31 | Prediction (High) | - | - |
| 32 | Prediction (High) | - | - |
| 34 | Prediction (Low) | - | - |
| 55 | Prediction (Low) | - | - |
| 72 | Prediction (Low) | - | - |
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 |
|---|---|---|---|---|---|
| 180 | Y → C | 0.001969 | SNP | Missense Mutation | HNSC |
| 216 | Y → C | 0.005435 | SNP | Missense Mutation | ESCA |
| 229 | S → C | 0.019608 | SNP | Missense Mutation | CHOL |
| 252 | F → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 321 | S → C | 0.002747 | SNP | Missense Mutation | LIHC |
| 401 | F → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 425 | R → C | 0.003774 | SNP | Missense Mutation | UCEC |
| 435 | Y → C | 0.002288 | SNP | Missense Mutation | STAD |
| 461 | R → C | 0.002545 | SNP | Missense Mutation | GBM |
| 557 | V → Cfs*59 | 0.001887 | DEL | Frame Shift Del | UCEC |
| 756 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 814 | C → Y | 0.003460 | SNP | Missense Mutation | CESC |
| 856 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 868 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 870 | C → C | 0.001887 | SNP | Silent | UCEC |
| 949 | F → Cfs*34 | 0.002747 | INS | Frame Shift Ins | LIHC |
| 1022 | Y → C | 0.002545 | SNP | Missense Mutation | GBM |
| 1135 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 1135 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1135 | R → C | 0.003460 | SNP | Missense Mutation | CESC |