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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
F8VXK7 CHST11 Carbohydrate sulfotransferase 11 Homo sapiens (Human) 77 aa

Protein Details: F8VXK7 (CHST11)

Protein Information
AccessionF8VXK7
Protein NamesCarbohydrate sulfotransferase 11
Gene SymbolCHST11
OrganismHomo sapiens (Human)
Length77 aa
IsoformsNo isoforms
Related PMIDs 19137006
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MKPALLEVMR11MNRICRMVLA21TCLGSFILVI31FYFQSMLHPV41MRRNPFGVDI
51-7751CCRKGSRSPL61QELYNPIQVS71FKHSVSM
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
15 - - -
GPS-Palm: 0.90
Deep-Palm: 0.83
22 - - -
GPS-Palm: 0.86
Deep-Palm: 0.29
51 - - -
GPS-Palm: 0.93
Deep-Palm: 0.62
52 - - -
GPS-Palm: 0.91
Deep-Palm: 0.68
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
2
Jurkat T cell
Specificity: 1.000
2/2 (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
35 S → Cfs*50 0.001969 DEL Frame Shift Del LGG
64 Y → C 0.001887 SNP Missense Mutation UCEC
121 C → Y 0.010870 SNP Missense Mutation ACC
230 R → C 0.001887 SNP Missense Mutation UCEC
331 Y → C 0.002033 SNP Missense Mutation LUSC
343 Y → C 0.002506 SNP Missense Mutation COAD