Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
H0YK32 ADAM10 ADAM metallopeptidase domain 10 Homo sapiens (Human) 38 aa

Protein Details: H0YK32 (ADAM10)

Protein Information
Accession H0YK32
Protein Names ADAM metallopeptidase domain 10
Gene Symbol ADAM10
Organism Homo sapiens (Human)
Length 38 aa
Isoforms No isoforms
Related PMIDs 19801377 32944167
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.667
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
4
PC3 cells
Specificity: 0.667
4/4 (100.0%)
2
DU145 cells
Specificity: 0.333
2/2 (100.0%)
0
Jurkat T cells
Specificity: 0.000
0/25 (0.0%)
0
U937 cells
Specificity: 0.000
0/1 (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
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
1-381MVLLRVLILL11LSWAAGMGVP21TMGKLHSKEK31PIKSSSPN
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
108 Y → C 0.002427 SNP Missense Mutation BLCA
389 F → C 0.002506 SNP Missense Mutation COAD
536 C → G 0.002545 SNP Missense Mutation GBM
594 C → W 0.001887 SNP Missense Mutation UCEC
607 C → F 0.002747 SNP Missense Mutation LIHC
639 C → Y 0.001764 SNP Missense Mutation LUAD
734 R → C 0.001887 SNP Missense Mutation UCEC
344* C → ? 0.002294 DEL Frame Shift Del OV