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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q9UMN3 ACTB ACTB protein Homo sapiens (Human) 17 aa

Protein Details: Q9UMN3 (ACTB)

Protein Information
Accession Q9UMN3
Protein Names ACTB protein
Gene Symbol ACTB
Organism Homo sapiens (Human)
Length 17 aa
Isoforms No isoforms
Related PMIDs 21076176
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
6
Jurkat T cells
Specificity: 1.000
6/25 (24.0%)
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
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
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
1-171MDDDIAALVV11DNGSGMC
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
17 Prediction (High) - -
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
69 Y → C 0.001764 SNP Missense Mutation LUAD
86 W → C 0.027027 SNP Missense Mutation DLBC
91 Y → C 0.001764 SNP Missense Mutation LUAD
156 G → C 0.002545 SNP Missense Mutation GBM
177 R → C 0.002020 SNP Missense Mutation PRAD
177 R → C 0.001887 SNP Missense Mutation UCEC
196 R → C 0.002288 SNP Missense Mutation STAD
196 R → C 0.002427 SNP Missense Mutation BLCA
210 R → C 0.001887 SNP Missense Mutation UCEC
217 C → Y 0.027027 SNP Missense Mutation DLBC
217 C → C 0.001969 SNP Silent LGG
240 Y → C 0.001764 SNP Missense Mutation LUAD
265 S → C 0.002141 SNP Missense Mutation SKCM
279 F → C 0.002545 SNP Missense Mutation GBM
281 S → C 0.002427 SNP Missense Mutation BLCA
294 Y → C 0.002288 SNP Missense Mutation STAD
335 R → C 0.003774 SNP Missense Mutation UCEC
372 R → C 0.002506 SNP Missense Mutation COAD