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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0AAG2TDY5 CANX Calnexin Homo sapiens (Human) 168 aa

Protein Details: A0AAG2TDY5 (CANX)

Protein Information
AccessionA0AAG2TDY5
Protein NamesCalnexin
Gene SymbolCANX
OrganismHomo sapiens (Human)
Length168 aa
IsoformsNo isoforms
Related PMIDs 19801377 21076176 22496122 32944167
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MEGKWLLCML11LVLGTAIVEA21HDGHDDDVID31IEDDLDDVIE41EVEDSKPDTT
51-10051APPSSPKVTY61KAPVPTGEVY71FADSFDRGTL81SGWILSKAKK91DDTDDEIAKY
101-150101DGKWEVEEMK111ESKLPGDKGL121VLMSRAKHHA131ISAKLNKPFL141FDTKPLIVQY
151-168151EVNFQNGIEC161GGAYVKLL
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
8 - - -
Deep-Palm: 0.05
160 - - -
Deep-Palm: 0.03
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): 0.571
4
PC3
Specificity: 0.571
4/4 (100.0%)
1
Jurkat T cell
Specificity: 0.143
1/1 (100.0%)
1
EC cell
Specificity: 0.143
1/1 (100.0%)
1
DU145 cell
Specificity: 0.143
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
438 F → C 0.001887 SNP Missense Mutation UCEC
456 G → C 0.001764 SNP Missense Mutation LUAD
480 R → C 0.001887 SNP Missense Mutation UCEC