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UniProt ID Gene Symbol Protein Name Organism Length Action
L0R6D2 ATP2B2 Alternative protein ATP2B2 Homo sapiens (Human) 66 aa

Protein Details: L0R6D2 (ATP2B2)

Protein Information
AccessionL0R6D2
Protein NamesAlternative protein ATP2B2
Gene SymbolATP2B2
OrganismHomo sapiens (Human)
Length66 aa
IsoformsNo isoforms
Related PMIDs 26876311
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MRATREKSHS11QLGGPTSGWR21WKNLRVWGSK31SAHPTWQNPP41GRRTFKSASP
51-6651ECREEVSLNV61SRRGTA
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
52 - - -
GPS-Palm: 0.68
Deep-Palm: 0.86
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
1
frontal cortex
Specificity: 1.000
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