Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
L8E9B9 YES1 Alternative protein YES1 Homo sapiens (Human) 43 aa

Protein Details: L8E9B9 (YES1)

Protein Information
Accession L8E9B9
Protein Names Alternative protein YES1
Gene Symbol YES1
Organism Homo sapiens (Human)
Length 43 aa
Isoforms No isoforms
Related PMIDs 19801377 22496122 32944167
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.571
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
4
PC3 cells
Specificity: 0.571
4/4 (100.0%)
2
DU145 cells
Specificity: 0.286
2/2 (100.0%)
1
Endothelial cells
Specificity: 0.143
1/2 (50.0%)
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
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
1-431MFRRSVDGNM11EWNHESSNQN21TKTRYNDARS31FPSRSSDNEK41IKT
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
75 S → C 0.002427 SNP Missense Mutation BLCA
199 R → C 0.002545 SNP Missense Mutation GBM
223 Y → _I224insYCSWRLQHLSL 0.002545 INS In Frame Ins GBM
489 Y → C 0.002427 SNP Missense Mutation BLCA
? ? → ? 0.001887 SNP Missense Mutation UCEC