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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
F8VXK3 CHST11 Carbohydrate sulfotransferase (EC 2.8.2.-) Homo sapiens (Human) 158 aa

Protein Details: F8VXK3 (CHST11)

Protein Information
AccessionF8VXK3
Protein NamesCarbohydrate sulfotransferase (EC 2.8.2.-)
Gene SymbolCHST11
OrganismHomo sapiens (Human)
Length158 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
1-501MRRNPFGVDI11CCRKGSRSPL21QELYNPIQLE31LSNTAVLHQM41RRDQVTDTCR
51-10051ANSATSRKRR61VLTPNDLKHL71VVDEDHELIY81CYVPKVACTN91WKRLMMVLTG
101-150101RGKYSDPMEI111PANEAHVSAN121LKTLNQYSIP131EINHRLKSYM141KFLFVREPFE
151-158151RLVSAYRN
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
11 - - -
GPS-Palm: 0.93
Deep-Palm: 0.02
12 - - -
GPS-Palm: 0.91
Deep-Palm: 0.03
49 - - -
GPS-Palm: 0.81
Deep-Palm: 0.88
81 - - -
Deep-Palm: 0.26
88 - - -
GPS-Palm: 0.70
Deep-Palm: 0.29
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