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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
H3BUU3 ATP2A1 ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting … Homo sapiens (Human) 26 aa

Protein Details: H3BUU3 (ATP2A1)

Protein Information
Accession H3BUU3
Protein Names ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 1
Gene Symbol ATP2A1
Organism Homo sapiens (Human)
Length 26 aa
Isoforms No isoforms
Related PMIDs 26876311
Database Sources No database sources
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
1
Prefrontal cortex
Specificity: 1.000
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
HeLa cells
Specificity: 0.000
0/1 (0.0%)
0
LNCaP cells
Specificity: 0.000
0/46 (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
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
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
1-261MGKVYRADRK11SVQRIKARDI21VPGDIV
Palmitoylation Sites Details

No known palmitoylation sites

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
265 S → C 0.007299 SNP Missense Mutation READ
268 C → C 0.001887 SNP Silent UCEC
346 S → C 0.001969 SNP Missense Mutation HNSC
420 C → C 0.001887 SNP Silent UCEC
516 G → C 0.002506 SNP Missense Mutation COAD
553 G → C 0.001887 SNP Missense Mutation UCEC
651 R → C 0.001887 SNP Missense Mutation UCEC
670 C → R 0.002506 SNP Missense Mutation COAD
836 R → C 0.005618 SNP Missense Mutation PAAD
471* C → ? 0.002506 SNP Nonsense Mutation COAD
498* C → ? 0.005587 SNP Nonsense Mutation PCPG