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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
E5RIU8 ANXA6 Annexin A6 Homo sapiens (Human) 95 aa

Protein Details: E5RIU8 (ANXA6)

Protein Information
AccessionE5RIU8
Protein NamesAnnexin A6
Gene SymbolANXA6
OrganismHomo sapiens (Human)
Length95 aa
IsoformsNo isoforms
Related PMIDs 21076176 31251020 32944167 36430497
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MAKPAQGAKY11RGSIHDFPGF21DPNQDAEALY31TAMKGFGSDK41EAILDIITSR
51-9551SNRQRQEVCQ61SYKSLYGKDL71IADLKYELTG81KFERLIVGGL91SDVGT
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
59 - - -
Deep-Palm: 0.97
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): 0.444
4
PC3
Specificity: 0.444
4/4 (100.0%)
3
cerebral cortex
Specificity: 0.333
3/3 (100.0%)
1
LNCaP
Specificity: 0.111
1/1 (100.0%)
1
Jurkat T cell
Specificity: 0.111
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.
Conservation score for cysteine
PhyloP for Cysteine
PhastCons Conservation Scores for Cysteine
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
59 C → C 0.001887 SNP Silent UCEC
206 R → C 0.002506 SNP Missense Mutation COAD
206 R → C 0.001887 SNP Missense Mutation UCEC
248 C → Y 0.002294 SNP Missense Mutation OV
302 Y → C 0.001014 SNP Missense Mutation BRCA
393 R → C 0.001887 SNP Missense Mutation UCEC
669 C → R 0.001887 SNP Missense Mutation UCEC