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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
AccessionL8E7Z2
Protein NamesAlternative protein DLG1
Gene SymbolDLG1
OrganismHomo sapiens (Human)
Length65 aa
IsoformsNo isoforms
Related PMIDs 26876311
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MAQMQIMNMK11KSHLKGEIQG21LVSALQEVRT31THTLEMTQVF41SLPKLSQGEQ
51-6551PPKMEDCGSM61TVYYE
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
57 - - -
Deep-Palm: 0.02
Score Interpretation:
GPS-Palm: Thresholds - High (≥0.8920), Medium (≥0.7766), Low (≥0.6484), Very Low (<0.6484)
Deep-Palm: Higher score indicates higher probability of palmitoylation (High ≥0.9)
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
1
frontal cortex
Specificity: 1.000
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.000
Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID). Blue bars: Literature data, Orange bars: Mass Spectrometry data. The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples.
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