Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
L8E7Z2 DLG1 Alternative protein DLG1 Homo sapiens (Human) 65 aa

Protein Details: L8E7Z2 (DLG1)

Protein Information
Accession L8E7Z2
Protein Names Alternative protein DLG1
Gene Symbol DLG1
Organism Homo sapiens (Human)
Length 65 aa
Isoforms No isoforms
Related PMIDs 26876311 32944167
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.500
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
1
PC3 cells
Specificity: 0.500
1/4 (25.0%)
1
Prefrontal cortex
Specificity: 0.500
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
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
1-501MAQMQIMNMK11KSHLKGEIQG21LVSALQEVRT31THTLEMTQVF41SLPKLSQGEQ
51-6551PPKMEDCGSM61TVYYE
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
69 R → C 0.002141 SNP Missense Mutation SKCM
100 S → C 0.001764 SNP Missense Mutation LUAD
574 G → C 0.002288 SNP Missense Mutation STAD
645 R → C 0.002427 SNP Missense Mutation BLCA
645 R → C 0.001887 SNP Missense Mutation UCEC
693 Y → C 0.001887 SNP Missense Mutation UCEC
789 Y → C 0.001014 SNP Missense Mutation BRCA
844 R → C 0.002506 SNP Missense Mutation COAD