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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A2VBC8 ATP2B2 ATPase, Ca++ transporting, plasma membrane … Homo sapiens (Human) 117 aa

Protein Details: A2VBC8 (ATP2B2)

Protein Information
AccessionA2VBC8
Protein NamesATPase, Ca++ transporting, plasma membrane 2
Gene SymbolATP2B2
OrganismHomo sapiens (Human)
Length117 aa
IsoformsNo isoforms
Related PMIDs 26876311 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
1-501TIPTSRLKFL11KEAGRLTQKE21EIPEEELNED31VEEIDHAERE41LRRGQILWFR
51-10051GLNRIQTQIE61VVNTFKSGAS71FQGALRRQSS81VTSQSQDVAS91LSSPSRVSLS
101-117101NALSSPTSLP111PAAAGQG
Palmitoylation Sites Details

No known palmitoylation sites

Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.800
4
cerebral cortex
Specificity: 0.800
4/4 (100.0%)
1
frontal cortex
Specificity: 0.200
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
32 R → C 0.002141 SNP Missense Mutation SKCM
32 R → C 0.001887 SNP Missense Mutation UCEC
59 R → C 0.002294 SNP Missense Mutation OV
86 F → C 0.007299 SNP Missense Mutation READ
151 W → C 0.001887 SNP Missense Mutation UCEC
185 R → C 0.001764 SNP Missense Mutation LUAD
249 R → C 0.002288 SNP Missense Mutation STAD
249 R → C 0.002506 SNP Missense Mutation COAD
432 C → S 0.006944 SNP Missense Mutation TGCT
491 G → C 0.002033 SNP Missense Mutation LUSC
497 C → S 0.001764 SNP Missense Mutation LUAD
559 G → C 0.002288 SNP Missense Mutation STAD
588 R → C 0.001887 SNP Missense Mutation UCEC
597 Y → C 0.001887 SNP Missense Mutation UCEC
606 R → C 0.001969 SNP Missense Mutation HNSC
606 R → C 0.002020 SNP Missense Mutation PRAD
606 R → C 0.001887 SNP Missense Mutation UCEC
621 R → C 0.001764 SNP Missense Mutation LUAD
621 R → C 0.002141 SNP Missense Mutation SKCM
651 R → C 0.001887 SNP Missense Mutation UCEC
666 C → C 0.001887 SNP Silent UCEC
673 C → C 0.001887 SNP Silent UCEC
677 R → C 0.005435 SNP Missense Mutation ESCA
699 C → C 0.001887 SNP Silent UCEC
869 R → C 0.001887 SNP Missense Mutation UCEC
1014 R → C 0.001887 SNP Missense Mutation UCEC
1020 R → C 0.001887 SNP Missense Mutation UCEC
1055 S → C 0.002747 SNP Missense Mutation LIHC
1067 C → C 0.003460 SNP Silent CESC
1142 R → C 0.002141 SNP Missense Mutation SKCM
1178 S → C 0.002294 SNP Missense Mutation OV
1211 S → C 0.001764 SNP Missense Mutation LUAD