Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| M0QXF2 | ATP1A3 | ATPase Na+/K+ transporting subunit alpha … | Homo sapiens (Human) | 251 aa |
Protein Details: M0QXF2 (ATP1A3)
Protein Information
| Accession | M0QXF2 |
|---|---|
| Protein Names | ATPase Na+/K+ transporting subunit alpha 3 |
| Gene Symbol | ATP1A3 |
| Organism | Homo sapiens (Human) |
| Length | 251 aa |
| Isoforms | No isoforms |
| Related PMIDs | 19137006 29575903 36430497 |
| Database Sources | No database sources |
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
1-501MTEHKMSVEE11VCRKYNTDCV21QGLTHSKAQE31ILARDGPNAL41TPPPTTPEWV
51-10051KFCRQLFGGF61SILLWIGAIL71CFLAYGIQAG81TEDDPSGDNL91YLGIVLAAVV
101-150101IITGCFSYYQ111EAKSSKIMES121FKNMVPQQAL131VIREGEKMQV141NAEEVVVGDL
151-200151VEIKGGDRVP161ADLRIISAHG171CKVDNSSLTG181ESEPQTRSPD191CTHDNPLETR
201-250201NITFFSTNCV211EGTARGVVVA221TGDRTVMGRI231ATLASGLEVG241KTPIAIEIEH
251-251251F
Palmitoylation Sites Details
| Position | Database | Domains | Literature (PMID/Cell-Tissue) | Mass(PMID/Cell-Tissue) | Prediction Scores |
|---|---|---|---|---|---|
| 12 | Cation-transporting P-type ATPase, N-terminal P-type ATPase, transmembrane domain superfamily | - |
cerebral cortex
(36430497)
|
Deep-Palm: 0.03
|
|
| 19 | Cation transport ATPase (P-type) P-type ATPase, transmembrane domain superfamily Cation-transporting P-type ATPase, N-terminal | - |
cerebral cortex
(36430497)
|
Deep-Palm: 0.77
|
|
| 53 | - | - | - |
GPS-Palm: 0.77
Deep-Palm: 0.88
|
|
| 71 | - | - | - |
Deep-Palm: 0.80
|
|
| 105 | - | - | - |
GPS-Palm: 0.81
Deep-Palm: 0.91
|
|
| 171 | - | - | - |
GPS-Palm: 0.73
Deep-Palm: 0.96
|
|
| 191 | - | - |
cerebral cortex
(36430497)
|
Deep-Palm: 0.40
|
|
| 209 | - | - |
cerebral cortex
(36430497)
|
Deep-Palm: 0.95
|
Score Interpretation:
• GPS-Palm: Thresholds - High (≥0.8920), Medium (≥0.7766), Low (≥0.6484), Very Low (<0.6484)
• Deep-Palm: Higher score indicates higher probability of palmitoylation (High ≥0.9)
• GPS-Palm: Thresholds - High (≥0.8920), Medium (≥0.7766), Low (≥0.6484), Very Low (<0.6484)
• Deep-Palm: Higher score indicates higher probability of palmitoylation (High ≥0.9)
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.667
4
cerebral cortex
Specificity: 0.667
4/4 (100.0%)
1
HeLa cell
Specificity: 0.167
1/1 (100.0%)
1
Jurkat T cell
Specificity: 0.167
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.
Conservation score for cysteine
PhyloP for Cysteine
PhastCons Conservation Scores for Cysteine
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 |
|---|---|---|---|---|---|
| 19 | R → C | 0.007299 | SNP | Missense Mutation | READ |
| 19 | R → C | 0.003460 | SNP | Missense Mutation | CESC |
| 185 | G → C | 0.004219 | SNP | Missense Mutation | SARC |
| 217 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 259 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 340 | R → C | 0.002545 | SNP | Missense Mutation | GBM |
| 346 | C → C | 0.001887 | SNP | Silent | UCEC |
| 346 | C → S | 0.006993 | SNP | Missense Mutation | LAML |
| 375 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 420 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 420 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 461 | R → C | 0.002427 | SNP | Missense Mutation | BLCA |
| 463 | R → C | 0.027027 | SNP | Missense Mutation | DLBC |
| 478 | Y → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 541 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 546 | C → S | 0.002545 | SNP | Missense Mutation | GBM |
| 682 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 756 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 793 | G → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 803 | G → C | 0.005435 | SNP | Missense Mutation | ESCA |
| 980 | C → Vfs*136 | 0.002294 | DEL | Frame Shift Del | OV |
| 995 | R → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 995 | R → C | 0.001969 | SNP | Missense Mutation | HNSC |
| 1000 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |